Saturated Fats and The Big Fat Lie 


“For every complicated problem there is a solution that is simple, direct, understandable, and wrong.” — H.L. Mencken

 Everybody knows that saturated fats are unhealthy, just like everybody knew once upon a time that the earth was flat. The saturated fat myth has seriously compromised the heart-health of Americans, and it’s all based on a Big Fat Lie. Here’s how this fairy tale came to be….

How Bad Science (And Urban Health Legends) Get Started

Once upon a time, not so very long ago in a place called Nebraska (where the corn grows as high as an elephant’s eye) there lived a handsome young man who was very wealthy and powerful and kept himself very fit. This young man worked hard making millions of dollars in the construction industry and he loved to eat hamburgers. Though he was a very happy young man with a fine family and a successful business, all was not well. One day the young man became very sick. He suffered a heart attack, and almost died.

The young man’s doctors were very skilled and they saved the his life, but this turn of events frightened the young man very much and he set out to discover why such a dreadful thing happened to him. He found out that his blood cholesterol was high and his doctors told him that this was the cause of his heart attack. Without questioning whether this was true or not, the young man made up his mind to ensure that this would never happen again. He set out to learn as much as he could about heart disease and cholesterol, and quickly decided that the foods he was eating were to blame for his troubles. You see, the experts at that time believed that certain kinds of fats called saturated fats would cause high blood cholesterol and dangerous buildups of a substance called plaque in peoples blood vessels. The young man listened carefully to these “experts,” and being a fine young man who wished to help others avoid the troubles that he had experienced, he decided that he would do everything in his power to make sure that saturated fats never ever harmed anyone again.

The young man wrote many letters and spent much of his own money to take out big newspaper ads telling people how they were being poisoned by saturated fats. He made a lot of people believe in the same things that he believed – that is, that saturated fats were bad and would make them sick and had no place in a healthy diet. The young man’s efforts were quite successful and many big companies were forced to change the way they cooked their foods. They stopped using the saturated fats, and began to use fats that were created especially for them by big industries in big factories. They said that these fats were healthier, and the young man was pleased.

The young man became very popular, and dedicated the rest of his life to his mission of spreading the word about “bad saturated fats” and cholesterol to all who would listen. He didn’t live happily ever after, but he did live a long life, and became known as “America’s Number One Cholesterol Fighter” before he became sick with heart failure and passed away just a few years ago.

While this sounds like a fairy tale, it really isn’t. Philip Sokolof was a handsome and wealthy young man who suffered a heart attack that was blamed on high cholesterol and who dedicated himself and his millions to becoming a self-described “amateur cardiologist” and championing the cause of removing the saturated fats that he believed caused elevated blood cholesterol levels from the American diet. While his intentions were good, his science was shaky (he was a high school graduate, not a biochemist or a doctor – much less a cardiologist) and his misguided campaign resulted in the replacement of stable, healthy saturated fats with artificially created trans fatty acids that we now know as extremely dangerous “trans fats.”

Big Business (Can You Say “Proctor and Gamble”?) Helps Promote the Sat Fat Myth

While Sokolof was largely responsible for the vilification of saturated fats in America, he was not alone. The campaign against saturated fats actually began many years earlier, and Sokolof’s efforts were going on at the same time as the efforts from other political organizations were gathering momentum. A few years prior to Sokolof’s efforts, in 1986, the American Soybean Association began a campaign protesting the importation of competing palm and coconut oils. Two years later the “watchdog” organization, the Center for Science in the Public Interest, took up the cry against saturated fats with the publication of a booklet that was later found to contain mistakes, errors of biochemistry, and erroneous statements about the fat composition of foods. This concerted campaign against saturated tropical oils paid off, and ” fats” have been considered poison ever since by mainstream medicine and nutrition “experts.”

To discover why saturated fats have been given such a bad rap we need to go a little further back into history – perhaps as far back as the riverboat days of Mark Twain, but at least to the Second World War, when Japanese forces occupied much of the south Pacific and supplies of most of the tropical oils in the US were cut off for a number of years. Americans turned to home-grown substitutes: polyunsaturated oils such as corn, peanut, cottonseed, and a product of the aforementioned American Soybean Association, soy oil. As the use of these oils grew the growers and industries involved in their production became more powerful and eager to protect their market at any cost.

At this same time, in the early 1950′s, America began to notice a sharp increase in rates of cardiovascular disease and researchers were looking for answers. A study conducted by a Russian researcher found that rabbits, fed with animal fats (cholesterol) added to their feed developed fatty deposits in their skin and other tissues, including their blood vessels. (I’ll bet those normally vegetarian bunnies wondered what they were being fed!) Another sensational study relied on autopsies of American soldiers that had died in the Korean conflict and found that many of those examined had buildups of arterial plaque – atherosclerosis. (Which surely couldn’t have had anything to do with the military diet of the day, right? Or with the popularity of cigarette smoking?) This study, which made major news at the time, overshadowed other studies of the period which showed similar degrees of atherosclerosis in populations which had less mortality from heart disease despite high fat and high meat diets, or that ate far more vegetarian diets and suffered similar degrees of atherosclerosis, and generally indicated that the thickening of the arterial walls is a natural and unavoidable process. The press took the headline-grabbing autopsy results and ran with them using their usual logic of “the rooster crows every morning, and then the sun rises: therefore, the crowing of the rooster is what makes sunrise happen!”

During the 1960′s the attack on saturated fats continued with unabated vigor: despite scientific studies showing a decided lack of benefits companies such as Mazola and Proctor and Gamble promoted their vegetable oil creations as being especially healthy, and medical journals of the day promoted Fleischman’s unsalted margarine as being especially good for patients with high blood pressure. The American Medical Association was initially skeptical of all this hype but after the American Heart Association published its dietary guidelines damning animal fats and praising vegetable oils the AMA quickly fell into line. In 1966 a little self-help book called “Your Heart Has Nine Lives” advocated the substitution of vegetable oils for butter and other so-called “artery clogging” saturated fats. This book was sponsored by makers of Mazola Corn Oil and Mazola Margarine – no surprise – and was widely and freely circulated.

And that brings us to the handsome young man with his clogged arteries. Despite volumes of evidence to the contrary, saturated fats have been the “fall guy” for coronary artery disease since the 1950′s when in fact, as early as 1956 one researcher had suggested that the increasing use of hydrogenated vegetable oils might be the underlying cause of the CAD epidemic. Unwilling to stand idly by and let profits be imperiled by such things as health or humanitarian concerns, the massive and powerful edible oil industry in the United States has obfuscated, bullied, manipulated, and outright lied to protect it’s burgeoning market share. Supporting the flawed science of Philip Sokolof and pressuring legislators to adopt the anti-saturated fat / tropical oils legislation that he promoted was just good business.

Setting the Record Straight about Sat Fats

So, just what are these so-called saturated fats, where do they come from, and what are they used for? Well, the answers to these questions might be a surprise – sat fats are not what we have been led to believe. The most exact answers to the question “what is a saturated fat?” require some tedious and complicated science, and there are varying degrees of saturation. It is easier to simply think of the properties of “hardness” of fats.

A fat that is fully “saturated” would be as hard as wax, and quite indigestible. Fats that are almost totally “unsaturated” are very liquid, easily absorbed, and not at all common in the natural food supply. This “hardness” of fats is also dependant upon temperature. Many fats are liquid when warm, and solid when cold. Butter, for example, is quite hard when refrigerated, but soft at room temperature. Animal fats such as beef fat, lard, or chicken fat, while usually called “saturated fats” are actually not so: they are mixtures of naturally occurring fats and are actually less than half “saturated.” So-called “saturated fats” include things such as cocoa butter, dairy fats (milk fats and butter for example), palm oil, and tallow. Even breast milk is high in saturated fats! Monounsaturated fats include most animal fats, olive oil, canola oil, and peanut oil. Polyunsaturated fats include corn, cotton, and soybean oils, borage and primrose oil, flax seed oil, and fish oil.

Then there are the “modified” oils: oils that have been altered through a process called “hydrogenation” to make them more useful for certain applications. Margarine is a perfect example of hydrogenation: liquid oil such as cottonseed oil or corn oil, something that humans would never eat in nature, is altered to make it more solid and hard at room temperature. Crisco is another example – the name stands for CRyStalized Cottonseed Oil. The degree of hydrogenation is varied according to the desired use of the oil. Heavily hydrogenated oils might become stick margarine, while less hydrogenated or “partially hydrogenated” oils would become “spreads” or other “food products.”

Then there are the “trans fats” that have been in the news lately. These are fats that have had their molecular geometry altered, either on purpose or accidentally, and they are with very few and minor exceptions, not found in nature. Trans fats, when eaten by humans, tend to have some very bad effects on our bodies as they enter our cells and change how the cell walls function. Effects of trans fats in humans (and animals too) range from unfavorable changes in cholesterol levels to causing blood to become more “sticky”, to reduced ability to utilize insulin and increased blood sugar levels and increased weight, to alterations in hormone balances, and more. Trans fats are really only a very small step away from polyunsaturated fats – many polyunsaturated fats can be turned “trans” simply by heating them too much in cooking!

So, what does all this mean in more practical terms? It means that we must choose our fats carefully, and use them wisely. It means that we must cautiously weigh the claimed benefits of the vegetable-based hydrogenated “designer fats” that are so very commonplace in our modern “fast foods / prepared foods” diet against the known benefits of those traditional and natural fats that have been a part of mankind’s diet for millions of years.

We humans have evolved over the millennia as creatures that are well-adapted to, and in fact require, animal fats and proteins in our diets for optimal health – the claims of the vegetarian and vegan folks notwithstanding. Indeed, our very first meal, at our mother’s breast, supplied us with a high energy drink that gave our tiny bodies the cholesterol needed for development, and a special fat called Lauric Acid. This Lauric Acid, which is also found in the now-vilified tropical oils coconut oil and palm kernel oil has very strong antifungal and antibacterial properties and helps our tiny infant bodies develop strong immune systems. We are very well equipped to utilize fatty acids in the form of saturated fats such as dairy fats, and monounsaturated fats such as animal fats and olive oil. It is only with the advent of modern industrial processes that polyunsaturated fats such as corn and soybean oils have been available for our consumption – though fish oils (a form of polyunsaturated animal fat) have historically been considered to be healthy.

Why You Should Eat Butter and Lard

Butter, as another example, has a far healthier composition as a saturated fat than the synthesized creations that are the various margarines. Being a combination of saturated, monounsaturated, and polyunsaturated fats it is not as “stable” as margarine – that is, it will turn rancid (a form of turning “trans”) if not refrigerated. But then, who would eat rancid butter? It also contains a variety of health-giving vitamins, minerals, and other nutrients.

Does anyone remember the jar of bacon grease that was a fixture in every kitchen before the days of “spray-on” cooking oils, non-stick fry pans and fat-phobia? My mother carefully saved the grease from the morning bacon, and it was used to cook all sorts of wonderful things, from our morning eggs to delectable entrees and even desserts. We keep a jar of bacon grease in our own kitchen – it is far healthier than the canola oil and soy lecithin and “propellants” (your guess?) that are in our can of “no stick cooking spray.”

Then there is our obsession with “vegetable oils” as found in the aforementioned Crisco shortening. It is interesting to note that Proctor and Gamble, perhaps seeing the writing on the wall, or perhaps in a belated fit of conscience, has sold off the Crisco name and product. This “all vegetable oil” creation, once made from cottonseed oil, is now made from canola oil which must be hydrogenated (as was the cottonseed oil) to make it semi-solid. Smuckers, the new owners of Crisco, claims “Our entire line of Crisco Shortening products have been reformulated to contain zero grams trans fat per serving”. Can anyone reading this remember the days when lard was used? All-natural, no-trans-fat lard that made such wonderfully fluffy pastries and flaky pie crusts? Do we really think that humans are well-equipped to consume the kinds of oils that require bushels of rape seed or corn or soybeans per gallon to produce? Any more than we might be equipped to consume petroleum oils – no matter how they are “modified”?

Just like our handsome young man who made it his life’s mission to vilify healthful fats, we live in a fairy-tale world where we are led to believe that with a little help from chemistry and science we can fool mother nature into allowing us to consume “food products” that our bodies were never intended to have to deal with. Unfortunately, life in that fairy tale world is having very real and very serious consequences for Americans and people around the world who are buying into the anti-sat-fat fantasy being promoted by the vegetable oils industry. We are gambling our health and our lives and our future on a grand industrial experiment, and it is paying off with increasing rates of heart disease, cancer, diabetes, obesity, and more.

At the beginning of the last century, most of the fats in our forefathers diet were either saturated or monounsaturated, mostly from butter, lard, tallow, coconut oil and small amounts of olive oil. Today most of the fats in our diet are polyunsaturated from vegetable oils mostly from soy, as well as from corn, safflower and canola. Before 1920 coronary heart disease was a rarity in America, causing no more than 10% of all deaths. Today heart disease accounts for at least 40% of all deaths. Is there a connection? We believe there is, and a growing body of scientists, researchers, and health care professionals is beginning to stand up to the politically correct diet dogma that is dictating low fat diets and vegetable fats instead of animal or tropical fats. For a historically interesting end to this article we go back to 1956 when Dr. Dudley White, in a television interview, noted that heart disease in the form of myocardial infarction (heart attack) was almost nonexistent in 1900 when egg consumption was three times what it was in 1956 and when corn oil was unavailable. When pressed to support the low-fat, vegetable oil based “Prudent Diet”, Dr. White replied: “See here, I began my practice as a cardiologist in 1921 and I never saw an MI patent until 1928. Back in the MI free days before 1920, the fats were butter and lard and I think that we would all benefit from the kind of diet that we had at a time when no one had ever heard the word corn oil.”

Former surgeon general Dr. C. Everett Koop even said, during congressional hearings in 1988: “the coconut scare is foolishness. . . To get the word to commercial interests terrorizing the public about nothing is another matter.” Could it be that it is time to turn away from the dangerous designer oils and fats of Big Industry and return to the animal and tropical fats that served our ancestors so well? We think it is!

Finally, let’s look briefly at this current medical fad that demands that we reduce cholesterol levels in our bloodstream to the lowest possible levels. Remember, cholesterol is essential to life; so essential that your liver will make it “de novo” – from new – if your body senses that it doesn’t have enough of this precious material. Even conventional medicine, in the form of The Framingham Report – the oldest, longest, and biggest study into heart disease in history – determined that when total serum cholesterol is reduced below 160 the risk of heart disease actually increases. Even more interestingly, the Director of The Framingham Study, Dr. William Castelli said in the July 1992 issue of the Archives of Internal Medicine “At Framingham, we found that the people who ate the most saturated fat, the most cholesterol and the most calories weighed the least, were more physically active and had the lowest serum cholesterol levels.” We can only imagine the dismay that this information must have cause for Philip Sokolof; he must have been aware of it as it was published over a decade before his death. Nevertheless, Sokolof persisted in his efforts to vilify saturated fats and remove cholesterol from the American diet and we can only guess as to why he would continue these efforts in the face of research showing them to be wrong, even harmful. Was he simply too stubborn to accept the facts that proved him wrong, or was he too fully caught up in the whirlwind of Big Politics, Big Industry, Big Agriculture, and Big Pharmacy to be able to change? We’ll never know…

References
1.) Sokolof article http://www.cbsnews.com/stories/2003/11/26/health/main585849.shtml
2.) Sokolof death http://www.blogofdeath.com/archives/000902.html
3.) D Groom, “Population Studies of Atherosclerosis,” Annals of Int Med , July 1961, 55:1:51-62; W F Enos, et al, “Pathogenesis of Coronary Disease in American Soldiers Killed in Korea,” JAMA , 1955, 158:912
4.) “Hydrogenated vegetable oils might be the underlying cause of the CAD epidemic”
A Keys, “Diet and Development of Coronary Heart Disease,” J Chron Dis, Oct 1956, 4(4):364-380
5.) Excerpt from “The Coconut Diet: The Secret Ingredient That Helps You Lose Weight While You Eat Your Favorite Foods” by Cherie Calbom http://www.enotalone.com/article/3242.html
6.) http://easydiagnosis.com/articles/oiling.html “The Oiling of America” by Enig and Fallon – many rerferences following this 4 part series.
7.) http://www.westonaprice.org/knowyourfats/skinny.html#lipid
The Weston A Price Society Enig & Fallon article “The Skinny on Fats”
8.) Framingham Study reports re: total cholesterol <160:
“There is a direct association between falling cholesterol levels over the first 14 years and mortality over the following 18 years” (11% overall and 14% CVD death rate increase per 1 mg/dL per year drop in cholesterol levels). Anderson KM JAMA 1987
9.) The Honolulu Heart Study:
“Our data accord with previous findings of increased mortality in elderly people with low serum cholesterol, and show that long-term persistence of low cholesterol concentration actually increases the risk of death. Thus, the earlier that patients start to have lower cholesterol concentrations, the greater the risk of death.” Lancet Aug 2001.

 

Fertility Supplements Questions and Answers

There is a lot of misinformation out there and it can cause a lot of distress and worry to women trying to conceive.

On this page Dr. Myatt will address some of these concerns regarding natural supplementation, vitamins, herbs, and more.

Using Flavones to Lower IL-6: Which is better – Luteolin / Diosmin or Maxi Flavone?

Milk Thistle – is it safe?

Green Tea – Causes Inflammation?

Myo-inositol in the Treatment of PCOS and Non-PCOS Infertility

What’s So Special About Maxi Greens?


Using Flavones to Lower IL-6: Which is better – Luteolin / Diosmin or Maxi Flavone?

Interleukin 6 (IL-6) is both a pro-inflammatory and anti-inflammatory cytokine. (1-3)

As a class, flavones lower inflammation and inflammatory cytokines including IL-1, IL-6,
IL-18 and TNF-a. (4) Flavone-containing herbs have a synergistic effect when used in combination.(5-6)

The flavones contained in Maxi Flavone all have IL-6 lowering properties.

These IL-6 lowering herbs include Pycnogenol (pine bark) (7-8), red grape seed extract (resveretrol) (9-17), bilberry (Vaccinum myrtillus) (18-19), green tea (Camellia sinensis) polyphenols (20-23), ginkgo (24-26), milk thistle (27) and citrus bioflavonoids (4,28)

Further, the IL-6 lowering properties of the herbs in Maxi Flavone have been studied in humans. (8,12-14,16-19,25,27)

Luteolin and its semi-synthetic structural analog diosmin have been studied only in rodents for their IL-6-lowering properties. (29)

Maxi Flavone Or Luteolin/Diosmin for IL-6?

Maxi Flavone contains a combination of flavonoid herbs. Benefits of Maxi Flavone include:

  • Each herb in this formula has demonstrated IL-6 lowering properties (4,7-28)
  • The IL-6 lowering properties of these flavones have been studied in humans (8,12-14,16-19, 25, 27)
  • Safety of these flavones has been documented in humans (8,12-14,16-19, 25, 27)
  • Flavones work synergistically so that a combination of flavones may be more effective than an isolated flavone. (5,6)

Luteolin / Diosmin:

  • Has been studied only in rodents for IL-6 lowering properties and in only one study (29)
  • Has strong estrogenic properties that may not be desirable for many infertile women (30)
  • Isolated flavones may not be as effective as an array of flavones for lowering inflammatory cytokines.(5,6)

Until more research is available on luteolin/diosmin, Maxi Flavone multi-flavone formula would appear a superior choice for addressing elevated IL-6 than any single flavonoid including luteolin or its semi-synthetic analogue diosmin.

References

1.) Scheller J, Chalaris A, Schmidt-Arras D, Rose-John S.
The pro- and anti-inflammatory properties of the cytokine interleukin-6.
Biochim Biophys Acta. 2011 May;1813(5):878-88.
2.) Z Xing, J Gauldie, G Cox, H Baumann, M Jordana, X F Lei, and M K Achong
IL-6 is an antiinflammatory cytokine required for controlling local or systemic acute
inflammatory responses. J Clin Invest. 1998 January 15; 101(2): 311320.
3.) Rose-John S, Scheller J, Elson G, Jones SA. Interleukin-6 biology is coordinated by membrane-bound
and soluble receptors: role in inflammation and cancer. J Leukoc Biol. 2006 Aug;80(2):227-36. Epub 2006 May 17.
4.) Landberg R, Sun Q, Rimm EB, Cassidy A, Scalbert A, Mantzoros CS, Hu FB, van Dam RM. Selected dietary
flavonoids are associated with markers of inflammation and endothelial dysfunction in U.S. women. J Nutr. 2011 Apr 1;141(4):618-25.
5.) Rahman MM, Ichiyanagi T, Komiyama T, Hatano Y, Konishi T. Superoxide radical- and peroxynitrite-scavenging activity of anthocyanins; structure-activity relationship and their synergism. Free Radic Res. 2006 Sep;40(9):993-1002.
6.) Sagar SM, Yance D, Wong RK. Natural health products that inhibit angiogenesis: a potential source for investigational new agents to treat cancer-Part 1. Curr Oncol. 2006 Feb;13(1):14-26.
7.) Ozer Sehirli A, Sener G, Ercan F. Protective effects of pycnogenol against ischemia reperfusion-induced oxidative renal injury in rats.Ren Fail. 2009;31(8):690-7.
8.) Scheff SW, Ansari MA, Roberts KN.Neuroprotective effect of Pycnogenol® following traumatic brain injury. Exp Neurol. 2013 Jan;239:183-91.
9.) Cullberg KB, Olholm J, Paulsen SK, Foldager CB, Lind M, Richelsen B, Pedersen SB. Resveratrol has inhibitory effects on the hypoxia-induced inflammation and angiogenesis in human adipose tissue in vitro.
Eur J Pharm Sci. 2013 May 13;49(2):251-7.
10.) Gatson JW, Liu MM, Abdelfattah K, Wigginton JG, Smith S, Wolf S, Minei JP. Resveratrol decreases inflammation in the brain of mice with mild traumatic brain injury. J Trauma Acute Care Surg. 2013 Feb;74(2):470-4; discussion 474-5.
11.) Marier JF, Chen K, Prince P, Scott G, del Castillo JR, Vachon P.
Production of ex vivo lipopolysaccharide-induced tumor necrosis factor-alpha, interleukin-1beta, and interleukin-6 is suppressed by trans-resveratrol in a concentration-dependent manner. Can J Vet Res. 2005 Apr;69(2):151-4.
12.) Rizzo A, Bevilacqua N, Guida L, Annunziata M, Romano Carratelli C, Paolillo R. Effect of resveratrol and modulation of cytokine production on human periodontal ligament cells. Cytokine. 2012 Oct;60(1):197-204.
13.) Su YC, Li SC, Wu YC, Wang LM, Chao KS, Liao HF.
Resveratrol downregulates interleukin-6-stimulated sonic hedgehog signaling in human acute myeloid leukemia. Evid Based Complement Alternat Med. 2013;2013:547430.
14.) Tomé-Carneiro J, Gonzálvez M, Larrosa M, Yáñez-Gascón MJ, García-Almagro FJ, Ruiz-Ros JA, García-Conesa MT, Tomás-Barberán FA, Espín JC. One-year consumption of a grape nutraceutical containing resveratrol improves the inflammatory and fibrinolytic status of patients in primary prevention of cardiovascular disease. Am J Cardiol. 2012 Aug 1;110(3):356-63.
15.) Wight RD, Tull CA, Deel MW, Stroope BL, Eubanks AG, Chavis JA, Drew PD, Hensley LL.Resveratrol effects on astrocyte function: relevance to neurodegenerative diseases. Biochem Biophys Res Commun. 2012 Sep 14;426(1):112-5.
16.) Wuertz K, Quero L, Sekiguchi M, Klawitter M, Nerlich A, Konno S, Kikuchi S, Boos N. The red wine polyphenol resveratrol shows promising potential for the treatment of nucleus pulposus-mediated pain in vitro and in vivo.
Spine (Phila Pa 1976). 2011 Oct 1;36(21):E1373-84.
17.) Xie XH, Zang N, Li SM, Wang LJ, Deng Y, He Y, Yang XQ, Liu EM.
Resveratrol Inhibits respiratory syncytial virus-induced IL-6 production, decreases viral replication, and downregulates TRIF expression in airway epithelial cells. Inflammation. 2012 Aug;35(4):1392-401.
18.) Karlsen A, Paur I, Bøhn SK, Sakhi AK, Borge GI, Serafini M, Erlund I, Laake P, Tonstad S, Blomhoff R. Bilberry juice modulates plasma concentration of NF-kappaB related inflammatory markers in subjects at increased risk of CVD. Eur J Nutr. 2010 Sep;49(6):345-55.
19.) Kolehmainen M, Mykkänen O, Kirjavainen PV, Leppänen T, Moilanen E, Adriaens M, Laaksonen DE, Hallikainen M, Puupponen-Pimiä R, Pulkkinen L, Mykkänen H, Gylling H, Poutanen K, Törrönen R. Bilberries reduce low-grade inflammation in individuals with features of metabolic syndrome. Mol Nutr Food Res. 2012 Oct;56(10):1501-10.
20.) Ahmed S, Marotte H, Kwan K, Ruth JH, Campbell PL, Rabquer BJ, Pakozdi A, Koch AE. Epigallocatechin-3-gallate inhibits IL-6 synthesis and suppresses transsignaling by enhancing soluble gp130 production. Proc Natl Acad Sci U S A. 2008 Sep 23;105(38):14692-7.
21.) Cavet ME, Harrington KL, Vollmer TR, Ward KW, Zhang JZ. Anti-inflammatory and anti-oxidative effects of the green tea polyphenol epigallocatechin gallate in human corneal epithelial cells. Mol Vis. 2011 Feb 18;17:533-42.
22.) Hosokawa Y, Hosokawa I, Ozaki K, Nakanishi T, Nakae H, Matsuo T.
Tea polyphenols inhibit IL-6 production in tumor necrosis factor superfamily 14-stimulated human gingival fibroblasts. Mol Nutr Food Res. Mol Nutr Food Res. 2010 Jul;54 Suppl 2:S151-8.
23.) Katiyar SK, Raman C. Green tea: a new option for the prevention or control of osteoarthritis. Arthritis Res Ther. 2011 Aug 10;13(4):121.
24.) Chen JS, Chen YH, Huang PH, Tsai HY, Chen YL, Lin SJ, Chen JW.
Ginkgo biloba extract reduces high-glucose-induced endothelial adhesion by inhibiting the redox-dependent interleukin-6 pathways. Cardiovasc Diabetol. 2012 May 3;11:49.
25.) Ching-Hsiang L, Chiao-Wen H, Nan-Fu C, Wen-Sheng L, Ya-Fen H, Wen-Tung W. In vivo effects of Ginkgo biloba extract on interleukin-6 cytokine levels in patients with neurological disorders. Indian J Pharmacol. 2012 Jan;44(1):118-21.
26.) Zhou YH, Yu JP, Liu YF, Teng XJ, Ming M, Lv P, An P, Liu SQ, Yu HG.
Effects of Ginkgo biloba extract on inflammatory mediators (SOD, MDA, TNF-alpha, NF-kappaBp65, IL-6) in TNBS-induced colitis in rats. Mediators Inflamm. 2006;2006(5):92642.
27.) Täger M, Dietzmann J, Thiel U, Hinrich Neumann K, Ansorge S.
Restoration of the cellular thiol status of peritoneal macrophages from CAPD patients by the flavonoids silibinin and silymarin.
Free Radic Res. 2001 Feb;34(2):137-51.
28.) Kim JA, Park HS, Kang SR, Park KI, Lee DH, Nagappan A, Shin SC, Lee WS, Kim EH, Kim GS. Suppressive effect of flavonoids from Korean Citrus aurantium L. on the expression of inflammatory mediators in L6 skeletal muscle cells. Phytother Res. 2012 Dec;26(12):1904-12.
29.) Parker-Athill E, Luo D, Bailey A, Giunta B, Tian J, Shytle RD, Murphy T, Legradi G, Tan J. Flavonoids, a prenatal prophylaxis via targeting JAK2/STAT3 signaling to oppose IL-6/MIA associated autism. J Neuroimmunol. 2009 Dec 10;217(1-2):20-7.
30.) Zand RS, Jenkins DJ, Diamandis EP. Steroid hormone activity of flavonoids and related compounds.Breast Cancer Res Treat. 2000 Jul;62(1):35-49.


“An IVF Doctor Said Not to Take MilkThistle” and Other Uninformed Medical Advice

From an infertility forum website, where the patient quoted an IVF doc as saying not to take milk thistle because “It makes the liver work better / metabolize things faster so it can metabolize your drugs too and hence shouldn’t be taken during an IVF cycle.”  There are no studies cited.

Unsubstantiated comments like this occur when a doctor steps outside of his/her area of expertise. That’s unfortunate, because it can cause a lot of needless alarm AND potentially drive patients away from helpful treatments. So, let’s set the record straight about this unsupported statement and about the usefulness of milk thistle in infertility.

The dose of milk thistle required to upregulate liver enzymes and therefor increase drug metabolism is of a 10 to 30-fold magnitude higher than anything Dr. Braverman or I use for infertility. A woman would have to take 24 doses of Maxi Flavone daily to achieve this increased drug metabolism effect, if even that would do it.

In the one lab rat study cited, an equivalent human female dose would be 2400mg+ per day.(1) Maxi Flavone contains 100mg per dose, maximum 200mg per day at the highest recommended intake. At this dose, there is not one study which shows that liver enzymes are upregulated enough to alter blood levels of any drug.(2-5)

Dr. Braverman and I are going for antioxidant, anti-inflammatory, and TNFa inhibitory effect of milk thistle but we are well below any liver-enzyme upregulating (and therefor IVF drug-changing) effect. (16-20)

600mg of milk thistle per day in HUMANS (not just lab rats) did not show any significant effect on drug-metabolizing liver enzymes. (6) Other studies have shown a minimal effect on liver enzymes (P450, CYP’s, etc) even at concentrations much higher than doses found in Maxi Flavone.(7)

Only at very high concentrations has milk thistle been shown to affect liver enzymes. According the the FDA, “In view of the clinically relevant plasma concentration of approx. 0.2 microM measured as silibinin, it is evident that there is no drug-drug interaction problem with silymarin.” (8)

Any by the way, many foods and drugs affect this same liver enzyme system far more than milk thistle. Did you know that many “health foods” such as kale, cabbage, Brussels sprouts, broccoli, arugula, watercress, grapefruit, pomegranate, and others can all have a profound effect on this important enzyme system?

http://dmd.aspetjournals.org/content/early/2006/01/13/dmd.105.007930.full.pdf
http://en.wikipedia.org/wiki/Cruciferous_vegetables

HOLD THE MAYO

Milk Thistle according to Mayo Clinic’s website:

“Theoretically, because milk thistle plant extract might have estrogenic effects, women with hormone sensitive conditions should avoid milk thistle above ground parts. Some of these conditions include breast, uterine, and ovarian cancer, endometriosis, and uterine fibroids.” http://www.mayoclinic.com/health/silymarin/NS_patient-milkthistle/DSECTION=safety

Mayo clinic has some incredibly poorly referenced, contradictory articles on their site. I would not rely on them for authoritative herbal information. It is outside their area of expertise. (Don’t expect your brain surgeon to be an expert in acupuncture and don’t expect your acupuncturist to be an expert in brain surgery.)

For example, the cited Mayo clinic article on milk thistle actually contradicts itself. In one place it says “silymarin and silibinin in milk thistle reduce the growth of human breast, cervical and prostate cancer cells” and in another place it says “…should avoid milk thistle in… breast, uterine, and ovarian cancer…”  Which is it, Mayo?

Contrary to Mayo’s “theoretical” (read that: “unreferenced”) concerns, milk thistle has actually proven to be beneficial for the hormone-related conditions cited above in numerous studies. (9-15)

Next, someone thought they were revealing a smoking gun by quoting, “Silybin, an extract from seeds of milk thistle (Silybum marianum), is known to have hepato-protective, anticarcinogenic, and estrogenic effects.” http://www.ncbi.nlm.nih.gov/pubmed/20183284

Be sure to look at the doses when reading abstracts or medical journal articles. Dose makes a big difference. (I addressed this issue in a recent previous email)

This rat study used 18mg/kg given twice per day. That would equate to 2,454 mg per day for a 150-pound female. Maxi Flavone has 100mg total to be taken once per day. This is less than 1/24th the dose that has demonstrated estrogenic effects. (1)

Let’s Dump In Some Totally Unrelated Studies for Good Measure…

What was said: Reservatol increases Nk cell activity: http://www.ncbi.nlm.nih.gov/pubmed/20082299

Dr. Myatt’s Comment: Resveretrol has potent antioxidant and anti-inflammatory effects. Resveretrol also suppresses TNF-alpha. Please see the extensive reference list here: Grape Seed Extract. Repeat after me, “preponderance of evidence” and “dose” (see below).

What was said: Grape seed extract and pycnogenol are aromatase inhibitors. Aromatase is an enzyme present in fat tissue and in ovaries that converts testosterone to estrogen. When it is inhibited, there will be more testosterone. Sometimes in short doses this is ok, as femara is works by being an aromatase inhibitor. “But it is not good to take this for longer times as it can inhibit ovulation and lead to high testosterone levels which are toxic to our eggs.”

Dr. Myatt’s comment: Here we have a medical opinion from a layperson. Would this really be the best source of information about improving fertility? Again, dose. The amount of aromatase effect from the doses of grape seed and pycnogenol in Maxi Flavone are insufficient to cause a hormone shift. Besides, your infertility specialist can easily measure hormone levels and would know if such a shift were occurring.

Dr. Myatt’s Caution About “References” and “Experts”

For any question you type into Pub Med (the medical journal article abstract website), you will find references that support both sides of the question. There’s almost never “black and white.” Instead, there are “ten thousand shades of gray.” Here’s what you need to know:

One reference does not make “proof” and an isolated lab rat study does not “prove” anything. The “preponderance of evidence,” including number of studies, how well-conducted the studies were, whether the studies were test-tube or lab rat studies versus human studies, who funded the studies, all must be taken into account.

I see a lot of women quoting single lab-rat or test-tube studies without any knowledge or consideration of the above-mentioned factors. So, when you are reading such “proofs” posted by non-physicians, please keep these factors in mind and “consider the source.”

Also, I believe any statement that has absolutely NO references should be dismissed on its face. References might not constitute “proof,” but at least they need to be there. Otherwise, any one of us can sit in our easy chair and “theorize.”

Theorizing won’t get you pregnant; it will simply waste your time.

Fertility is not individual brush strokes; it is the whole picture taken together. Dr. Braverman takes the “whole picture” view.

He is an expert in IVF, one of the most renown in the world. But when he is out of his area of expertise, he turns to me or another expert for their evaluation. He doesn’t just “make stuff up” like some so-called “experts.” THAT is the mark of a true professional.

References

1.) El-Shitany NA, Hegazy S, El-Desoky K. Evidences for antiosteoporotic and selective estrogen receptor modulator activity of silymarin compared with ethinylestradiol in ovariectomized rats. Phytomedicine. 2010 Feb;17(2):116-25. Epub 2009 Jul 3.
2.) Breinholt V, Lauridsen ST, Dragsted LO. Differential effects of dietary flavonoids on drug metabolizing and antioxidant enzymes in female rat. Xenobiotica. 1999 Dec;29(12):1227-40.
3.) Doehmer J, Weiss G, McGregor GP, Appel K. Assessment of a dry extract from milk thistle (Silybum marianum) for interference with human liver cytochrome-P450 activities. Toxicol In Vitro. 2011 Feb;25(1):21-7. Epub 2010 Sep 7.
4.) Gurley B, Hubbard MA, Williams DK, Thaden J, Tong Y, Gentry WB, Breen P, Carrier DJ, Cheboyina S. Assessing the clinical significance of botanical supplementation on human cytochrome P450 3A activity: comparison of a milk thistle and black cohosh product to rifampin and clarithromycin. J Clin Pharmacol. 2006 Feb;46(2):201-13.
5.) Gurley BJ, Barone GW, Williams DK, Carrier J, Breen P, Yates CR, Song PF, Hubbard MA, Tong Y, Cheboyina S. Effect of milk thistle (Silybum marianum) and black cohosh (Cimicifuga racemosa) supplementation on digoxin pharmacokinetics in humans. Drug Metab Dispos. 2006 Jan;34(1):69-74. Epub 2005 Oct 12.
6.) van Erp NP, Baker SD, Zhao M, Rudek MA, Guchelaar HJ, Nortier JW, Sparreboom A, Gelderblom H. Effect of milk thistle (Silybum marianum) on the pharmacokinetics of irinotecan. Clin Cancer Res. 2005 Nov 1;11(21):7800-6.
7.) Gurley BJ, Gardner SF, Hubbard MA, Williams DK, Gentry WB, Carrier J, Khan IA, Edwards DJ, Shah A. In vivo assessment of botanical supplementation on human cytochrome P450 phenotypes: Citrus aurantium, Echinacea purpurea, milk thistle, and saw palmetto. Clin Pharmacol Ther. 2004 Nov;76(5):428-40.
8.) Doehmer J, Tewes B, Klein KU, Gritzko K, Muschick H, Mengs U.
Assessment of drug-drug interaction for silymarin. Toxicol In Vitro. 2008 Apr;22(3):610-7. Epub 2007 Dec 8.
9.) Agarwal R, Agarwal C, Ichikawa H, Singh RP, Aggarwal BB. Anticancer potential of silymarin: from bench to bed side. Anticancer Res. 2006 Nov-Dec;26(6B):4457-98.
10.) Kim S, Han J, Kim JS, Kim JH, Choe JH, Yang JH, Nam SJ, Lee JE.
Silibinin suppresses EGFR ligand-induced CD44 expression through inhibition of EGFR activity in breast cancer cells. Anticancer Res. 2011 Nov;31(11):3767-73.
11.) Lu W, Lin C, King TD, Chen H, Reynolds RC, Li Y.
Silibinin inhibits Wnt/ -catenin signaling by suppressing Wnt co-receptor LRP6 expression in human prostate and breast cancer cells. Cell Signal. 2012 Dec;24(12):2291-6. doi: 10.1016/j.cellsig.2012.07.009. Epub 2012 Jul 20.
12.) Nejati-Koshki K, Zarghami N, Pourhassan-Moghaddam M, Rahmati-Yamchi M, Mollazade M, Nasiri M, Esfahlan RJ, Barkhordari A, Tayefi-Nasrabadi H. Inhibition of leptin gene expression and secretion by silibinin: possible role of estrogen receptors. Cytotechnology. 2012 Apr 17. [Epub ahead of print]
13.) Noh EM, Yi MS, Youn HJ, Lee BK, Lee YR, Han JH, Yu HN, Kim JS, Jung SH.
Silibinin enhances ultraviolet B-induced apoptosis in mcf-7 human breast cancer cells. J Breast Cancer. 2011 Mar;14(1):8-13. Epub 2011 Mar 31.
14.) Scambia G, De Vincenzo R, Ranelletti FO, Panici PB, Ferrandina G, D’Agostino G, Fattorossi A, Bombardelli E, Mancuso S.Antiproliferative effect of silybin on gynaecological malignancies: synergism with cisplatin and doxorubicin. Eur J Cancer. 1996 May;32A(5):877-82.
15.) Yu HC, Chen LJ, Cheng KC, Li YX, Yeh CH, Cheng JT. Silymarin inhibits cervical cancer cell through an increase of phosphatase and tensin homolog. Phytother Res. 2012 May;26(5):709-15. doi: 10.1002/ptr.3618. Epub 2011 Oct 20.
16.) Manna SK, Mukhopadhyay A, Van NT, Aggarwal BB. Silymarin suppresses TNF-induced activation of NF-kappa B, c-Jun N-terminal kinase, and apoptosis.J Immunol. 1999 Dec 15;163(12):6800-9.
17.) Johnson VJ, He Q, Osuchowski MF, Sharma RP. Physiological responses of a natural antioxidant flavonoid mixture, silymarin, in BALB/c mice: III. Silymarin inhibits T-lymphocyte function at low doses but stimulates inflammatory processes at high doses. Planta Med. 2003 Jan;69(1):44-9.
18.) Polyak SJ, Morishima C, Shuhart MC, Wang CC, Liu Y, Lee DY. Inhibition of T-cell inflammatory cytokines, hepatocyte NF-kappaB signaling, and HCV infection by standardized Silymarin. Gastroenterology. 2007 May;132(5):1925-36. Epub 2007 Feb 21.
19.) Feher J, Lang I, Deak G, et al. Free radicals in tissue damage in liver diseases and therapeutic approach. Tokai J Exp Clin Med 1986;11:121–34.
20.) Toklu HZ, Tunali Akbay T, Velioglu-Ogunc A, Ercan F, Gedik N, Keyer-Uysal M, Sener G. Silymarin, the antioxidant component of Silybum marianum, prevents sepsis-induced acute lung and brain injury. J Surg Res. 2008 Apr;145(2):214-22. Epub 2007 Oct 22.


Green Tea – Causes Inflammation?

Green Tea (Camillia sinesis) is an antioxidant that suppresses TNF- .(44-48 )
Full references for this can be found on this page

There is one recent lab rat study which says HUGE DOSE of epigallocatechin-3-gallate, an isolate from green tea, promotes inflammation.  This dose was 1% of total food intake. A person would have to be eating GRAMS of pure epigallocatechin-3-gallate per day to achieve this dose. Maxi Flavone contains 180 milligrams of a 50% catechin mix. This is miniscule compared to doses used in this rodent study.

In the same study, as in numerous other studies, smaller doses were anti-inflammatory. (1)

Contrast this to NUMEROUS studies which show that green tea is anti-inflammatory. (2-14)

Bottom line: HUGE doses of isolated epigallocatechin-3-gallate from green tea may be inflammatory, at least in one lab-rat study.

Smaller doses are well-proven to be anti-inflammatory in numerous studies including human studies.

Dr. Myatt’s Additional Note: People have died from drinking too much water (electrolyte disturbance). Does this “prove” that water-drinking is dangerous? Hardly. All substances and their effects are dose-related.  “The dose makes the poison.” — Paracelsus

References
1.) Pae M, Ren Z, Meydani M, Shang F, Smith D, Meydani SN, Wu D. Dietary supplementation with high dose of epigallocatechin-3-gallate  promotes inflammatory response in mice. J Nutr Biochem. 2012 Jun;23(6):526-31. Epub 2011 Jun 17.
2.) Akhtar N, Haqqi TM. Epigallocatechin-3-gallate suppresses the global interleukin-1beta-induced inflammatory response in human chondrocytes.Arthritis Res Ther. 2011 Jun 17;13(3):R93.
3.) Babu PV, Si H, Liu D.Epigallocatechin gallate reduces vascular inflammation in db/db mice possibly through an NF-?B-mediated mechanism.Mol Nutr Food Res. 2012 Sep;56(9):1424-32. doi: 10.1002/mnfr.201200040. Epub 2012 Jul 2.
4.) Bogdanski P, Suliburska J, Szulinska M, Stepien M, Pupek-Musialik D, Jablecka A.Green tea extract reduces blood pressure, inflammatory biomarkers, and oxidative stress and improves parameters associated with insulin resistance in obese, hypertensive patients. Nutr Res. 2012 Jun;32(6):421-7. Epub 2012 Jun 20.
5.) Bornhoeft J, Castaneda D, Nemoseck T, Wang P, Henning SM, Hong MY.
The protective effects of green tea polyphenols: lipid profile, inflammation, and antioxidant capacity in rats fed an atherogenic diet and dextran sodium sulfate.J Med Food. 2012 Aug;15(8):726-32. Epub 2012 Jun 25.
6.) Cavet ME, Harrington KL, Vollmer TR, Ward KW, Zhang JZ. Anti-inflammatory and anti-oxidative effects of the green tea polyphenol epigallocatechin gallate in human corneal epithelial cells. Mol Vis. 2011 Feb 18;17:533-42.
7.) Chatterjee A, Saluja M, Agarwal G, Alam M. Green tea: A boon for periodontal and general health. J Indian Soc Periodontol. 2012 Apr;16(2):161-7. doi: 10.4103/0972-124X.99256.
8.) Chen J, Qin S, Xiao J, Tanigawa S, Uto T, Hashimoto F, Fujii M, Hou DX.
A genome-wide microarray highlights the antiinflammatory genes targeted by oolong tea theasinensin A in macrophages. Nutr Cancer. 2011;63(7):1064-73. Epub 2011 Aug 24.
9.) El-Mowafy AM, Al-Gayyar MM, Salem HA, El-Mesery ME, Darweish MM. Novel chemotherapeutic and renal protective effects for the green tea (EGCG): role of oxidative stress and inflammatory-cytokine signaling. Phytomedicine. 2010 Dec 1;17(14):1067-75. Epub 2010 Sep 18.
10.) Li J, Ye L, Wang X, Liu J, Wang Y, Zhou Y, Ho W. Epigallocatechin gallate inhibits endotoxin-induced expression of inflammatory cytokines in human cerebral microvascular endothelial cells. J Neuroinflammation. 2012 Jul 6;9:161.
11.) Lee YJ, Choi DY, Yun YP, Han SB, Oh KW, Hong JT. Epigallocatechin-3-gallate prevents systemic inflammation-induced memory deficiency and amyloidogenesis via its anti-neuroinflammatory properties. J Nutr Biochem. 2012 Sep 5. [Epub ahead of print]
12.) Park HJ, Lee JY, Chung MY, Park YK, Bower AM, Koo SI, Giardina C, Bruno RS. Green tea extract suppresses NF?B activation and inflammatory responses in diet-induced obese rats with nonalcoholic steatohepatitis. J Nutr. 2012 Jan;142(1):57-63. Epub 2011 Dec 7.
13.) Ramesh E, Geraldine P, Thomas PA.Regulatory effect of epigallocatechin gallate on the expression of C-reactive protein and other inflammatory markers in an experimental model of atherosclerosis. Chem Biol Interact. 2010 Jan 5;183(1):125-32.
14.) Syed DN, Afaq F, Kweon MH, Hadi N, Bhatia N, Spiegelman VS, Mukhtar H.
Green tea polyphenol EGCG suppresses cigarette smoke condensate-induced NF-kappaB activation in normal human bronchial epithelial cells. Oncogene. 2007 Feb 1;26(5):673-82. Epub 2006 Jul 24.


Myo-inositol in the Treatment of PCOS and Non-PCOS Infertility

Inositol is part of the vitamin B complex. It occurs as 9 different isomers, but only two of these are of interest in fertility: myo-inositol (MYO) and d-chiro-inositol (DCI)

Both MYO and DCI have been studied and found useful in the treatment of PCOS (PolyCystic Ovary Syndrome). (1-14)

However, only MI has been show to be present in follicular fluid and only MI was able to improve oocyte and embryo quality(1,2,9,12,15), ovulation induction (6-8,10-11) and hormone balance. (3-5,13)

DCI does not have even remotely as much research behind it as MYO. (16)

Therefor, for fertility issues with or without PCOS, I recommend the myo-inositol form.

Please note that some of these studies used melatonin in combination with myo-inositol (2,11-12). Melatonin alone has also been studied and found useful for improving egg quality. (17-18)

Myo-inositol may also improve other associated risks of PCOS (such as high triglycerides and blood sugars) with or without an effect on egg quality. (3,5,7)

Most forms of inositol available in health food stores are probably the myo-inositol form. However, many products do not specify this on the label. I would always want to verify the actual form with the manufacturer before using.

A product called “Pregnitude” is available, containing myo-inositol plus folic acid. Several studies used myo-inositol with folic acid and found improved egg quality in PCOS. (9,11)  All pre-pregnant women should already be getting folic acid from their multiple because of it’s importance in preventing spina bifida. This makes the “magic” in Pregnitude the myo-inositol. Pregnitude is individually packaged by 2 gram serving, which is convenient, but the price is double what what most myo-inositol powders are.

Daily dose of myo-inositol for improving egg quality is 2-4 grams per day. This can be taken as 2 grams, once or twice daily.

Myo-inositol product has a mild sweet taste and can be taken in water, smoothie, Super Shake — whatever makes it easiest.

Egg Quality Protocol, Especially for PCOS Patients (Dr. Myatt’s recommendation based on the studies)

  1. myo-inositol: 2-4 grams per day
  2. melatonin: 3mg per day (take this at bedtime)
  3. folic acid: 400mcg (this amount or more should already be in a good multi-vitamin)

[Nurse Mark comment: Any woman seeking to improve or enhance fertility should be using a good quality Optimal Dose multivitamin – we recommend Maxi Multi of course – but for those who want to shop around for something else, please use the ingredient list on the Maxi Multi page as a reference for what an Optimal Dose multivitamin should contain.]

References
1.) Ciotta L, Stracquadanio M, Pagano I, Carbonaro A, Palumbo M, Gulino F. Effects of myo-inositol supplementation on oocyte’s quality in PCOS patients: a double blind trial. Eur Rev Med Pharmacol Sci. 2011 May;15(5):509-14. [##myo for PCOS##]
2.) Carlomagno G, Nordio M, Chiu TT, Unfer V. Eur J Obstet Gynecol Reprod Biol. 2011 Dec;159(2):267-72. Epub 2011 Aug 10.
Contribution of myo-inositol and melatonin to human reproduction. http://www.ncbi.nlm.nih.gov/pubmed/21835536 [###myo and melatonin; egg quality##]
3.) Costantino D, Minozzi G, Minozzi E, Guaraldi C. Metabolic and hormonal effects of myo-inositol in women with polycystic ovary syndrome: a double-blind trial. Eur Rev Med Pharmacol Sci. 2009 Mar-Apr;13(2):105-10.  {## myo for PCOS; hormones and metabolic factors##]
4.) Donà G, Sabbadin C, Fiore C, Bragadin M, Giorgino FL, Ragazzi E, Clari G, Bordin L, Armanini D. Inositol administration reduces oxidative stress in erythrocytes of patients with polycystic ovary syndrome.Eur J Endocrinol. 2012 Apr;166(4):703-10. Epub 2012 Jan 5. [##MYO improves oxidative stress (decreases oxidative species), improves hormones in PCOS##]
5.) Genazzani AD, Lanzoni C, Ricchieri F, Jasonni VM. Myo-inositol administration positively affects hyperinsulinemia and hormonal parameters in overweight patients with polycystic ovary syndrome.Gynecol Endocrinol. 2008 Mar;24(3):139-44.[##MYO; menstrual cycle improvements; better non-fertility numbers; 2 grams per day##]
6.) Gerli S, Mignosa M, Di Renzo GC. Effects of inositol on ovarian function and metabolic factors in women with PCOS: a randomized double blind placebo-controlled trial. Eur Rev Med Pharmacol Sci. 2003 Nov-Dec;7(6):151-9. [##myo, PCOS, ovulation induction##]
7.) Gerli S, Papaleo E, Ferrari A, Di Renzo GC. Randomized, double blind placebo-controlled trial: effects of myo-inositol on ovarian function and metabolic factors in women with PCOS. Eur Rev Med Pharmacol Sci. 2007 Sep-Oct;11(5):347-54. [## MYO, PCOS, improved ovulation, improved non-fertility peramiters (including weight loss)}
8.) Morgante G, Orvieto R, Di Sabatino A, Musacchio MC, De Leo V. The role of inositol supplementation in patients with polycystic ovary syndrome, with insulin resistance, undergoing the low-dose gonadotropin ovulation induction regimen.Fertil Steril. 2011 Jun 30;95(8):2642-4. Epub 2011 Feb 5. [myo, PCOS, ovulation induction##]
9.) Papaleo E, Unfer V, Baillargeon JP, Fusi F, Occhi F, De Santis L. Fertil Steril. 2009 May;91(5):1750-4. Epub 2008 May 7. Myo-inositol may improve oocyte quality in intracytoplasmic sperm injection cycles. A prospective, controlled, randomized trial. [##myo+ folic acid for egg quality in PCOS##]
10.) Papaleo E, Unfer V, Baillargeon JP, De Santis L, Fusi F, Brigante C, Marelli G, Cino I, Redaelli A, Ferrari A. Myo-inositol in patients with polycystic ovary syndrome: a novel method for ovulation induction.Gynecol Endocrinol. 2007 Dec;23(12):700-3. Epub 2007 Oct 10. [##myo for ovulation in PCOS##]
11.) Rizzo P, Raffone E, Benedetto V. Effect of the treatment with myo-inositol plus folic acid plus melatonin in comparison with a treatment with myo-inositol plus folic acid on oocyte quality and pregnancy outcome in IVF cycles. A prospective, clinical trial. Eur Rev Med Pharmacol Sci. 2010 Jun;14(6):555-61. [##myo+folic acid+melatonin##]
12.) Unfer V, Raffone E, Rizzo P, Buffo S. Gynecol Endocrinol. 2011 Nov;27(11):857-61. Epub 2011 Apr 5. Effect of a supplementation with myo-inositol plus melatonin on oocyte quality in women who failed to conceive in previous in vitro fertilization cycles for poor oocyte quality: a prospective, longitudinal, cohort study. http://www.ncbi.nlm.nih.gov/pubmed/21463230  [##myo and melatonin##]
13.) Unfer V, Carlomagno G, Dante G, Facchinetti F. Effects of myo-inositol in women with PCOS: a systematic review of randomized controlled trials. Gynecol Endocrinol. 2012 Jul;28(7):509-15. doi: 10.3109/09513590.2011.650660. Epub 2012 Feb 1. {##myo and improved ovarian function##]
14.) Nestler JE, Jakubowicz DJ, Reamer P, Gunn RD, Allan G. Ovulatory and metabolic effects of D-chiro-inositol in the polycystic ovary syndrome. N Engl J Med. 1999 Apr 29;340(17):1314-20.[##DCI for PCO##]
15.) Galletta M, Grasso S, Vaiarelli A, Roseff SJ. Bye-bye chiro-inositol – myo-inositol: true progress in the treatment of polycystic ovary syndrome and ovulation induction. Eur Rev Med Pharmacol Sci. 2011 Oct;15(10):1212-4. {####myo for egg quality, not dci)
16.) Galazis N, Galazi M, Atiomo W. D-Chiro-inositol and its significance in polycystic ovary syndrome: a systematic review.Gynecol Endocrinol. 2011 Apr;27(4):256-62. Epub 2010 Dec 10.[##DCI not much research##]
17.) Batioglu AS, Sahin U, Gürlek B, Oztürk N, Unsal E. The efficacy of melatonin administration on oocyte quality. Gynecol Endocrinol. 2012 Feb;28(2):91-3. Epub 2011 Jul 20. [##melatonin##]
18.) Tamura H, Takasaki A, Miwa I, Taniguchi K, Maekawa R, Asada H, Taketani T, Matsuoka A, Yamagata Y, Shimamura K, Morioka H, Ishikawa H, Reiter RJ, Sugino N. Oxidative stress impairs oocyte quality and melatonin protects oocytes from free radical damage and improves fertilization rate. J Pineal Res. 2008 Apr;44(3):280-7.
[##melatonin##]


What’s So Special About Maxi Greens?

As with Maxi Flavone, Maxi Greens is designed to be a broad-spectrum anti-inflammatory and nutritional herbal formula. Maxi Greens contains:

1.) Anti-inflammatory herbs (the same ones as in Maxi Flavone): ginkgo biloba, bilberry,green tea, milk thistle, grape seed and pine bark (pycnogenols). See the full references for these herbs in the Maxi Flavone article.

2.) Nutrient-dense “super green foods.”

Maxi Greens includes wheat grass and several additional “green super foods” including: alfalfa, wheat grass, barley grass and wheat sprouts. Here is what the scientific literature says about these green food herbs.

I.) Alfalfa: a nutrient-rich herb high in chlorophyll, vitamins and micronutrients. Alfalfa is rich in vitamins A, B1, B6, C, E and K as well as calcium, potassium, iron and zinc.
Alfalfa has anti-inflammatory (1) and antioxidant properties.(2) Alfalfa reduced cytokine levels and ameliorated severity of auto-immune disease in animal models.(3,4)

II.) Wheat grass: contains vitamins A, B12, C and E, as well as amino acids lysine, tryptophan and phenylalanine. Wheat grass is 70% chlorophyll. Because of its high A,C, and E content, wheat grass is considered anti-inflammatory.(5)

III.) Barley grass: Has a high antioxidant activity. (6,7)

IV.) Wheat sprouts: contain meaningful amounts of A, B1, B2, B3, B5, B6, B12, B17, C, D, E, F, H, K, P, choline, folic acid, inositol, PABA, boron, calcium, chlorine, chromium, cobalt, copper, iodine, iron, magnesium, manganese, molybdenum, nickel, phosphorus, potassium, selenium, silicon, sodium, sulphur, zinc.(8) Wheat sprouts were shown to have antioxidant activity in bisphenol-induced ROS in young women.(9)

V.) Blue Green Algae contains dietary fiber, fatty acids, essential amino acids, and vitamins A, B, C, and E. (10) Blue green algae and other algal species exhibit immunomodulatory, antitumor, antithrombotic, anticoagulant, anti-mutagenic, anti-inflammatory, antimicrobial, and antiviral activities including anti-HIV infection, herpes, and hepatitis viruses. (11-13)
It is likely because of its immunomodulatory and antioxidant properties that algal species are anti-allergenic.(14)

VI.) Spirulina is high in proteins, acid, vitamins and minerals. It is anti-inflammatory.(15)

VII.) Chlorella contains 60 percent protein by weight. It is high in chlorophyll, vitamins, minerals and phytonutrients. It is rich in polysaccharides, nucleic acids, peptides, essential fatty acids and B vitamins. Chlorella is rich in vitamins A, C, E, niacin and folate. Chlorella has the complete vitamin B-complex with more B-12 than beef liver by weight. Chlorella contains more beta carotene than carrots and other green leafy green vegetables. Additional nutritional content of chlorella includes zinc, iron, calcium, magnesium, potassium, trace minerals and polysaccharides. (16)

Chlorella has anti-inflammatory properties. (17) It is also a biological response modifier. (18)

Because of its unique ability to bind with mercury, lead, and cadmium, chlorella can be used as a heavy metal chelator. Studies have shown that it has a superior ability to safely draw toxic metals that accumulate in the gut and intestinal tract. (19-22)

One study suggests that chlorella can stimulate cytokine production in human peripheral blood mononuclear cells. However, this study was performed ex vivo and at blood levels significantly higher (10 to 100mcg/ml) than would be expected from the dose contained in Maxi Greens. (23)

In addition to the “green” super-foods, we included flavonoid-rich super foods as well. Flavonoids, as a class of antioxidants, are anti-inflammatory.

Acerola Juice Powder
Acerola is high in vitaminc C, A, B1, B2 and B3, calcium, iron, carotenoids and bioflavonoids. (24)
Aceroal exerts potent antioxidant and anti-inflammatory properties. (24-27)

Beet Juice Powder:
Beet juice (also known as beetroot juice) is one of the richest sources of dietary antioxidants, with high total antioxidant capacity (TAC) and total polyphenol (TP) content. (28)

Beet root juice has been shown to protect against xenobiotic-induced oxidative stress in animal studies. (29,30)

Spinach Powder:
Spinach contains significant amounts if vitamin A, E, K, B2, B3, B6, folate and minerals calcium, magesiun, phosphorus, potassium, selenium, manganese and zinc. Spinach also has significant omega-3 fatty acids as linolenic acid. (24)

Because of its high polyphenol, flavonoid and carotene content, spinach has potent anti-inflammatory and antioxidant properties. (31-34)

Papaya (leaf) Papaya contains significant amounts of vitamins A, C, E, K and folate and minerals calcium, magnesium and potassium. (24) Papaya leaf suppresses inflammatory cytokines and exerts anti-inflammatory responses in both human and animal models. (35-37)

Dunaliella salina algae is a green algae that is a rich source of beta carotenoids including lycopene and zeaxanthin. (38-41) In studies, the synthetic beta carotene has had adverse effects in smokers while the natural form of beta carotene, as found in Dunaliella salina, has protective effects.(42,43)

Preliminary evidence suggests that natural beta-carotene supplementation results in better antioxidant activity and anticancer activity in humans than does supplementation with synthetic beta-carotene. (44,45)

Broccoli and Cauliflower are vegetables in the “Cruciferous” family. They are high in diindolylmethane (DIM), a metabolite of Indole-3-carbinol (I3C), a compound found in cruciferous vegetables including broccoli, cabbage, kale, bruseel sprouts and cauliflower. Diindolemethanes (DIM) is one of the major anticancer substances in the class of sulfur-containing chemicals called glucosinolates.(46)

DIMs help decrease estrogen metabolism by upregulating the P450 enzyme system. The net result of this effect is to decrease circulating estrogen levels and correct estrogen dominance. Because many causes of infertility including endometriosis, PCOS, ovarian cysts, and anovulation are all characterized by estrogen dominance, the addition of DIM by way of cruciferous vegetables can help balance hormones in favor of fertility.(47-49)

DIM inhibits the inflammatory response.(50-54) and possess antioxidant activity and decrease radical oxygen species (ROS) by acting as an ROS scavenger. (55-59)

Probiotic Cultures (dairy-free) Probiotics exert anti-inflammatory effects (60-61) and down-regulate inflammatory cytokines (62-63) including NF-êB, TNF-á, IL-6, and p-Akt (64-66)

References

1.) Hong YH, Chao WW, Chen ML, Lin BF. Ethyl acetate extracts of alfalfa (Medicago sativa L.) sprouts inhibit lipopolysaccharide-induced inflammation in vitro and in vivo. J Biomed Sci. 2009 Jul 14;16:64. doi: 10.1186/1423-0127-16-64.
2.) Yalinkilic O, Enginar H. Effect of X-radiation on lipid peroxidation and antioxidant systems in rats treated with saponin-containing compounds. Photochem Photobiol. 2008 Jan-Feb;84(1):236-42.
3.) Hong YH, Huang CJ, Wang SC, Lin BF. The ethyl acetate extract of alfalfa sprout ameliorates disease severity of autoimmune-prone MRL-lpr/lpr mice. Lupus. 2009 Mar;18(3):206-15.
4.) Apelgren LD, Bailey DL, Fouts RL, Short L, Bryan N, Evans GF, Sandusky GE, Zuckerman SH, Glasebrook A, Bumol TF. The effect of a selective estrogen receptor modulator on the progression of spontaneous autoimmune disease in MRL lpr/lpr mice. Cell Immunol. 1996 Oct 10;173(1):55-63.
5.) Seymour K. Wheat Grass. Illinois State University. http://horticulturecenter.illinoisstate.edu/gardens/documents/grain.pdf
6.) Kamiyama M, Shibamoto T. Flavonoids with potent antioxidant activity found in young green barley leaves. J Agric Food Chem. 2012 Jun 27;60(25):6260-7. doi: 10.1021/jf301700j. Epub 2012 Jun 18.
7.) Benedet JA, Umeda H, Shibamoto T. Antioxidant activity of flavonoids isolated from young green barley leaves toward biological lipid samples. J Agric Food Chem. 2007 Jul 11;55(14):5499-504. Epub 2007 Jun 1.
8.) USDA nutrition food table SR-21
9.) Yi B, Kasai H, Lee HS, Kang Y, Park JY, Yang M. Inhibition by wheat sprout (Triticum aestivum) juice of bisphenol A-induced oxidative stress in young women. Mutat Res. 2011 Sep 18;724(1-2):64-8. doi: 10.1016/j.mrgentox.2011.06.007. Epub 2011 Jun 28.
10.) Rajapakse N, Kim SK. Nutritional and digestive health benefits of seaweed.Adv Food Nutr Res. 2011;64:17-28.
11.) Mišurcová L, Škrovánková S, Samek D, Ambrožová J, Machù L. Health benefits of algal polysaccharides in human nutrition.Adv Food Nutr Res. 2012;66:75-145.
12.) Kim SK, Ta QV. Potential beneficial effects of marine algal sterols on human health.Adv Food Nutr Res. 2011;64:191-8.
13.) Jiao G, Yu G, Zhang J, Ewart HS. Chemical structures and bioactivities of sulfated polysaccharides from marine algae. Mar Drugs. 2011 Feb 8;9(2):196-223.
14.) Kim SK, Vo TS, Ngo DH. Antiallergic benefit of marine algae in medicinal foods. Adv Food Nutr Res. 2011;64:267-75.
15.) Joventino IP, Alves HG, Neves LC, Pinheiro-Joventino F, Leal LK, Neves SA, Ferreira FV, Brito GA, Viana GB. The microalga Spirulina platensis presents anti-inflammatory action as well as hypoglycemic and hypolipidemic properties in diabetic rats. J Complement Integr Med. 2012 Aug 10;9:Article 17.
16.) Nutritiondata.com
17.) Namsa ND, Tag H, Mandal M, Kalita P, Das AK. An ethnobotanical study of traditional anti-inflammatory plants used by the Lohit community of Arunachal Pradesh, India. J Ethnopharmacol. 2009 Sep 7;125(2):234-45. doi: 10.1016/j.jep.2009.07.004. Epub 2009 Jul 14.
18.) Miyazawa Y, Murayama T, Ooya N, Wang LF, Tung YC, Yamaguchi N. Immunomodulation by a unicellular green algae (Chlorella pyrenoidosa) in tumor-bearing mice. J Ethnopharmacol. 1988 Dec;24(2-3):135-46.
19.) Shim, Jae-Young; Shin, Hye-Seoung; Han, Jae-Gab; Park, Hyeung-Suk; Lim, Byung-Lak; Chung, Kyung-Won; Om, Ae-Son (2008). Protective Effects of Chlorella vulgaris on Liver Toxicity in Cadmium-Administered Rats. Journal of Medicinal Food 11 (3): 47985.
20.) Inthorn, Duangrat; Sidtitoon, Nalin; Silapanuntakul, Suthep; Incharoensakdi, Aran (2002). Sorption of mercury, cadmium and lead by microalgae. ScienceAsia 28 (3): 25361.
21.) Blas-Valdivia, Vanessa; Ortiz-Butrón, Rocio; Pineda-Reynoso, Marisol; Hernández-Garcia, Adelaida; Cano-Europa, Edgar (2010). Chlorella vulgaris administration prevents HgCl2-caused oxidative stress and cellular damage in the kidney. Journal of Applied Phycology 23: 538.
22.) Nakano, Shiro; Noguchi, Taketoshi; Takekoshi, Hideo; Suzuki, Go; Nakano, Masuo (2005). Maternal-fetal distribution and transfer of dioxins in pregnant women in Japan, and attempts to reduce maternal transfer with Chlorella (Chlorella pyrenoidosa) supplements. Chemosphere 61 (9): 124455. 23.) Ewart HS, Bloch O, Girouard GS, Kralovec J, Barrow CJ, Ben-Yehudah G, Suárez ER, Rapoport MJ. Stimulation of cytokine production in human peripheral blood mononuclear cells by an aqueous Chlorella extract. Planta Med. 2007 Jul;73(8):762-8. Epub 2007 Jul 5.
24.) Mezadri T, Villan˜o M, Fernandez-Pachon M, Garcia-Parrilla M, Troncoso A Antioxidant compounds and antioxidant activity in acerola(Malpighia emarginata DC.) fruits and derivatives. Journal of Food Composition and Analysis 21 (4): 282290.
25.) Guilhon-Simplicio F, Pinheiro CC, Conrado GG, Barbosa Gdos S, Santos PA, Pereira Mde M, Lima ES. Anti-inflammatory, anti-hyperalgesic, antiplatelet and antiulcer activities of Byrsonima japurensis A. Juss. (Malpighiaceae). J Ethnopharmacol. 2012 Mar 27;140(2):282-6. Epub 2012 Jan 21.
26.) Orlandi L, Vilela FC, Santa-Cecília FV, Dias DF, Alves-da-Silva G, Giusti-Paiva A.
27.) Anti-inflammatory and antinociceptive effects of the stem bark of Byrsonima intermedia A. Juss. J Ethnopharmacol. 2011 Oct 11;137(3):1469-76.
28.) Wootton-Beard P.C., Ryan L .A beetroot juice shot is a significant and convenient source of bioaccessible antioxidants.Journal of Functional Foods, Volume 3, Issue 4, October 2011, Pages 329334.
29.) Kujawska M, Ignatowicz E, Murias M, Ewertowska M, Miko³ajczyk K, Jodynis-Liebert J. Protective effect of red beetroot against carbon tetrachloride- and N-nitrosodiethylamine-induced oxidative stress in rats. J Agric Food Chem. 2009 Mar 25;57(6):2570-5.
30.) Krajka-KuŸniak V, Szaefer H, Ignatowicz E, Adamska T, Baer-Dubowska W. Beetroot juice protects against N-nitrosodiethylamine-induced liver injury in rats. Food Chem Toxicol. 2012 Jun;50(6):2027-33. doi: 10.1016/j.fct.2012.03.062. Epub 2012 Mar 24.
31.) Tiveron AP, Melo PS, Bergamaschi KB, Vieira TM, Regitano-d’Arce MA, Alencar SM. Antioxidant activity of brazilian vegetables and its relation with phenolic composition. Int J Mol Sci. 2012;13(7):8943-57.
32.) Otari KV, Gaikwad PS, Shete RV, Upasani CD.Protective effect of aqueous extract of Spinacia oleracea leaves in experimental paradigms of inflammatory bowel disease. Inflammopharmacology. 2012 Oct;20(5):277-87.
33.) [Proteggente AR, Pannala AS, Paganga G, Van Buren L, Wagner E, Wiseman S, Van De Put F, Dacombe C, Rice-Evans CA.The antioxidant activity of regularly consumed fruit and vegetables reflects their phenolic and vitamin C composition. Free Radic Res. 2002 Feb;36(2):217-33.
34.) Cao G, Russell RM, Lischner N, Prior RL.Serum antioxidant capacity is increased by consumption of strawberries, spinach, red wine or vitamin C in elderly women. J Nutr. 1998 Dec;128(12):2383-90.
35.) Abdullah M, Chai PS, Loh CY, Chong MY, Quay HW, Vidyadaran S, Seman Z, Kandiah M, Seow HF. Carica papaya increases regulatory T cells and reduces IFN-ã+ CD4+ T cells in healthy human subjects. Mol Nutr Food Res. 2011 May;55(5):803-6.
36.) Owoyele BV, Adebukola OM, Funmilayo AA, Soladoye AO. Anti-inflammatory activities of ethanolic extract of Carica papaya leaves.Inflammopharmacology. 2008 Aug;16(4):168-73.
37.) Juárez-Rojop IE, Díaz-Zagoya JC, Ble-Castillo JL, Miranda-Osorio PH, Castell-Rodríguez AE, Tovilla-Zárate CA, Rodríguez-Hernández A, Aguilar-Mariscal H, Ramón-Frías T, Bermúdez-Ocaña DY. Hypoglycemic effect of Carica papaya leaves in streptozotocin-induced diabetic rats. BMC Complement Altern Med. 2012 Nov 28;12:236.
38.)Ye ZW, Jiang JG. Analysis of an Essential Carotenogenic Enzyme: æ-Carotene Desaturase from Unicellular Alga Dunaliella salina. J Agric Food Chem. 2010 Oct 13.
39.) Zhu YH, Jiang JG, Chen Q. Characterization of cDNA of lycopene beta-cyclase responsible for a high level of beta-carotene accumulation in Dunaliella salina. Biochem Cell Biol. 2008 Jun;86(3):285-92.
40.) Thaipratum R, Melis A, Svasti J, Yokthongwattana K. Analysis of non-photochemical energy dissipating processes in wild type Dunaliella salina (green algae) and in zea1, a mutant constitutively accumulating zeaxanthin.J Plant Res. 2009 Jul;122(4):465-76. doi: 10.1007/s10265-009-0229-5. Epub 2009 Apr 1.
41.) Zhu YH, Jiang JG, Yan Y, Chen XW. Isolation and characterization of phytoene desaturase cDNA involved in the beta-carotene biosynthetic pathway in Dunaliella salina. J Agric Food Chem. 2005 Jul 13;53(14):5593-7.
42.) Omenn GS, Goodman GE, Thornquist MD, et al. Risk factors for lung cancer and for intervention effects in CARET, the Beta-Carotene and Retinol Efficacy Trial. J Natl Cancer Inst 1996;88:15509.
43.) The Alpha-Tocopherol, Beta Carotene Cancer Prevention Study Group. The effect of vitamin E and beta carotene on the incidence of lung cancer and other cancers in male smokers. N Engl J Med 1994;330:102935.
44.) Ben-Amotz A, Levy Y. Bioavailability of a natural isomer mixture compared with synthetic all-transß-carotene in human serum. Am J Clin Nutr 1996;63:72934.
45.) Yeum K-J, Zhu S, Xiao S, et al. ß-carotene intervention trial in premalignant gastric lesions. J Am Coll Nutr 1995;14:536.
46.) Stoewsand GS. Bioactive organosulfur phytochemicals in Brassica oleracea vegetablesa review. Food Chem Toxicol 1995;33:53743.
47.) Auborn KJ, Fan S, Rosen EM, Goodwin L, Chandraskaren A, Williams DE, Chen D, Carter TH. Indole-3-carbinol is a negative regulator of estrogen. J Nutr. 2003 Jul;133(7 Suppl):2470S-2475S.
48.) Rajoria S, Suriano R, Parmar PS, Wilson YL, Megwalu U, Moscatello A, Bradlow HL, Sepkovic DW, Geliebter J, Schantz SP, Tiwari RK. 3,3′-diindolylmethane modulates estrogen metabolism in patients with thyroid proliferative disease: a pilot study.Thyroid. 2011 Mar;21(3):299-304.
49.) Rogan EG. The natural chemopreventive compound indole-3-carbinol: state of the science. In Vivo. 2006 Mar-Apr;20(2):221-8.
50.) Cho HJ, Seon MR, Lee YM, Kim J, Kim JK, Kim SG, Park JH. 3,3′-Diindolylmethane suppresses the inflammatory response to lipopolysaccharide in murine macrophages. J Nutr. 2008 Jan;138(1):17-23.
51.) Kim EJ, Park H, Kim J, Park JH. 3,3′-diindolylmethane suppresses 12-O-tetradecanoylphorbol-13-acetate-induced inflammation and tumor promotion in mouse skin via the downregulation of inflammatory mediators. Mol Carcinog. 2010 Jul;49(7):672-83.
52.) De Miranda B, Miller J, Hansen R, Lunghofer P, Safe S, Gustafson D, Colagiovanni D, Tjalkens R.Neuroprotective efficacy and pharmacokinetic behavior of novel anti-inflammatory para-phenyl substituted diindolylmethanes in a mouse model of Parkinson’s disease. J Pharmacol Exp Ther. 2013 Jan 14. [Epub ahead of print]
53.) Dong L, Xia S, Gao F, Zhang D, Chen J, Zhang J.3,3′-Diindolylmethane attenuates experimental arthritis and osteoclastogenesis.Biochem Pharmacol. 2010 Mar 1;79(5):715-21.
54.) Kim YH, Kwon HS, Kim DH, Shin EK, Kang YH, Park JH, Shin HK, Kim JK. 3,3′-diindolylmethane attenuates colonic inflammation and tumorigenesis in mice. Inflamm Bowel Dis. 2009 Aug;15(8):1164-73.
55.) Yeh CT, Yen GC.Effect of vegetables on human phenolsulfotransferases in relation to their antioxidant activity and total phenolics.Free Radic Res. 2005 Aug;39(8):893-904.
56.) Huang Z, Zuo L, Zhang Z, Liu J, Chen J, Dong L, Zhang J. 3,3′-Diindolylmethane decreases VCAM-1 expression and alleviates experimental colitis via a BRCA1-dependent antioxidant pathway. Free Radic Biol Med. 2011 Jan 15;50(2):228-36.
57.) Arnao MB, Sanchez-Bravo J, Acosta M. Indole-3-carbinol as a scavenger of free radicals.Biochem Mol Biol Int. 1996 Aug;39(6):1125-34.
58.) Zhao F, Liu ZQ.Indole and its alkyl-substituted derivatives protect erythrocyte and DNA against radical-induced oxidation. J Biochem Mol Toxicol. 2009 Jul-Aug;23(4):273-9.
59.) Soung DY, Choi HR, Kim JY, No JK, Lee JH, Kim MS, Rhee SH, Park JS, Kim MJ, Yang R, Chung HY. Peroxynitrite scavenging activity of indole derivatives: interaction of indoles with peroxynitrite. J Med Food. 2004 Spring;7(1):84-9.
60.) Grompone G, Martorell P, Llopis S, González N, Genovés S, Mulet AP, Fernández-Calero T, Tiscornia I, Bollati-Fogolín M, Chambaud I, Foligné B, Montserrat A, Ramón D. Anti-Inflammatory Lactobacillus rhamnosus CNCM I-3690 Strain Protects against Oxidative Stress and Increases Lifespan in Caenorhabditis elegans. PLoS One. 2012;7(12):e52493.
61.) Jones SE, Versalovic J. Probiotic Lactobacillus reuteri biofilms produce antimicrobial and anti-inflammatory factors. BMC Microbiol. 2009 Feb 11;9:35.
62.) Chae CS, Kwon HK, Hwang JS, Kim JE, Im SH. Prophylactic effect of probiotics on the development of experimental autoimmune myasthenia gravis. PLoS One. 2012;7(12):e52119.
63.) Yoon HS, Ju JH, Lee JE, Park HJ, Lee JM, Shin HK, Holzapfel W, Park KY, Do MS. The probiotic Lactobacillus rhamnosus BFE5264 and Lactobacillus plantarum NR74 promote cholesterol efflux and suppress inflammation in THP-1 cells. J Sci Food Agric. 2012 Jul 17.
64.) Dai C, Zheng CQ, Meng FJ, Zhou Z, Sang LX, Jiang M. VSL#3 probiotics exerts the anti-inflammatory activity via PI3k/Akt and NF-êB pathway in rat model of DSS-induced colitis. Mol Cell Biochem. 2013 Feb;374(1-2):1-11.
65.) von Schillde MA, Hörmannsperger G, Weiher M, Alpert CA, Hahne H, Bäuerl C, van Huynegem K, Steidler L, Hrncir T, Pérez-Martínez G, Kuster B, Haller D. Lactocepin secreted by Lactobacillus exerts anti-inflammatory effects by selectively degrading proinflammatory chemokines. Cell Host Microbe. 2012 Apr 19;11(4):387-96.
66.) Thomas CM, Hong T, van Pijkeren JP, Hemarajata P, Trinh DV, Hu W, Britton RA, Kalkum M, Versalovic J. Histamine derived from probiotic Lactobacillus reuteri suppresses TNF via modulation of PKA and ERK signaling. PLoS One. 2012;7(2):e31951.

 

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Q – Is my order Secure? [Last updated 12/21/17]

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Maxi Marine O-3 (120 softgels) Temporary Product Substitute

High Potency Enteric Coated Ultra-Pure Essential Fatty Acids From Norwegian Arctic-Harvested Fish

July 2024: Many supplements have recently become extremely difficult to obtain. Dr. Myatt’s own special formulation of MaxiMarine O-3 is one of those supplements.

Fortunately, Dr. Myatt has been able to source a substitute product that meets her quality and purity standards.

Ultra Omega-3 provides 500mg EPA and 250mg DHA per softgel capsule and comes in a bottle of 180 softgel capsules.

Maxi Marine O-3 is an ultra-pure, ultra-high potency fish oil from anchovies and sardines harvested in pristine Norwegian Arctic waters. Purity is further assured by molecular distillation and every batch is verified by an independent third-party lab to be free of PCB’s, heavy metals and pesticides. Vitamin E (mixed tocopherols) is added to maintain maximum freshness and enteric coating ensures no “fishy” after-taste.

EPA and DHA, the “active ingredients” in fish oil, are long-chain Omega-3 Essential Fatty Acids that differ from short-chain Omega-3’s found in plant sources. EPA and DHA are beneficial for Cardiovascular (Heart) Health, Alzheimer’s Disease and other Dementias, Mental Health, Child Development, Attention-Deficit Disorders and Social/Cognitive Development, Diabetes, Inflammatory Diseases (rheumatoid arthritis, IBS/Crohn’s, asthma, infertility, etc.) and Cancer.

EPA/DHA (which occur together in fish oils) have numerous studies supporting their antiinflammatory properties and use in multiple hyper-inflammatory and autoimmune states. (14-24) EPA and DHA decrease NK cell activity (14,24-29), and this effect is synergistic when both EPA and DHA are used together.(18,28). EPA, but not ALA, also decreases TNF-alpha.(23-25).

While ALA (flax oil) has some similar benefits, it must be taken in significantly higher doses because ultimately the anti-inflammatory effect is seen when ALA is converted to EPA, as follows:

ALA (flax oil) >>> SDA (stearidonic acid) >>> EPA (fish oil) >>> Prostaglandin E3

An estimated 0.07% of ALA is converted to EPA in healthy people (30,31), but the conversion rate may be less when the delta-6-desaturase (d6d) enzyme is underfunctioning or when there is high competition from dietary Omega-6’s (both use the d6d enzyme). Assuming that converting enzymes are normal in a fertility clinic patient, a dose comparison would be 14 grams of flax oil vs. 1 grams of fish oil.

Studies have shown that ALA increases EPA but not DHA.(31) Some studies have shown that ALA does not reduce inflammatory markers (23,29). For these reasons, fish oil is preferrable to flax oil for raising EPA/DHA levels (33).

Several very informative pages about fish oil is found at the US Government website Medline. These pagse, from the NIH (National Institutes of Health) have an extensive list of uses and dosages with full references at these links:

Mayo Clinic also has a very informative webpage with dosing information: http://www.mayoclinic.org/drugs-supplements/omega-3-fatty-acids-fish-oil-alpha-linolenic-acid/dosing/hrb-20059372

Maxi Marine O3 (Fish Oil) and it’s use in CHF (Congestive Heart Failure):

http://www.ncbi.nlm.nih.gov/pubmed/8733172
“…Fish oil may decrease cardiac afterload by an antivasopressor action and by reducing blood viscosity, may reduce arrhythmic risk despite supporting the heart’s beta-adrenergic responsiveness, may decrease fibrotic cardiac remodeling by impeding the action of angiotensin II and, in patients with coronary disease, may reduce the risk of atherothrombotic ischemic complications. Since the measures recommended here are nutritional and carry little if any toxic risk, there is no reason why their joint application should not be studied as a comprehensive nutritional therapy for congestive heart failure. …”

Suggested Use: Adults take one or two capsules daily with meals or more if directed by your health care provider.

Please note that the EPA/DHA content of Maxi Marine O-3 (700mg total) is two and a half times more concentrated than most fish oils.

Dr. Myatt’s Comment:
Fish oil can be taken as an OTC supplement like Maxi Marine O3 or prescribed as an exorbitantly expensive “drug” Lovaza: http://www.lovaza.com/. The “drug” Lovaza costs about $200/month compared to around $20/month for Maxi Marine O3. The Rx. version is only slightly more potent than the OTC; there is no other “magic” about it.

Marine Lipid Concentrate: 1000mg – which provides:
EPA (eicosapentaenoic acid) 420mg
DHA (docosahexaenoic acid) 280mg

Because Maxi Marine is so concentrated it is a much more economical choice for those using higher doses of these important oils. Our regular brand of Ultra-Pure Fish Oil costs approximately 67 cents per gram while our higher-potency Maxi Marine O-3 is only 58 cents per gram. Higher potency means fewer capsules per day, representing significant cost savings.

STORAGE: Store in a cool place and keep out of reach of children.

Contains No wheat, gluten, corn protein, yeast, dairy, artificial colors, sweeteners or preservatives.

Product # N311 – Maxi Marine O3 – 120 softgels – $54.95

Enter Quantity Desired and Click “Add To Cart” Button

References:

14.) Mukaro VR, Costabile M, Murphy KJ, Hii CS, Howe PR, Ferrante A. Leukocyte numbers and function in subjects eating n-3 enriched foods: selective depression of natural killer cell levels. Arthritis Res Ther. 2008;10(3):R57. Epub 2008 May 14.
CONCLUSION: The data show that regular long-term consumption of n-3 enriched foods leads to lower numbers of NK cells and neutrophil iodination activity but higher lymphotoxin production by lymphocytes. These changes are consistent with decreased inflammatory reaction and tissue damage seen in patients with inflammatory disorders receiving n-3 LCPUFA supplementation.

15.) Calder PC. Dietary modification of inflammation with lipids. Proc Nutr Soc. 2002 Aug;61(3):345-58. CONCLUSION: EPA is anti-inflammatory

16.) Calder PC. N-3 polyunsaturated fatty acids and inflammation: from molecular biology to the clinic. Lipids. 2003 Apr;38(4):343-52. CONCLUSION: EPA is anti-inflammatory

17.) Simopoulos AP. Omega-3 fatty acids in inflammation and autoimmune diseases. J Am Coll Nutr. 2002 Dec;21(6):495-505.
CONCLUSION: Fish oil more biologically active than ALA; anti-inflammatory properties; useful in RA and MS among others

18.) Calder PC. Session 3: Joint Nutrition Society and Irish Nutrition and Dietetic Institute Symposium on ‘Nutrition and autoimmune disease’ PUFA, inflammatory processes and rheumatoid arthritis. Proc Nutr Soc. 2008 Nov;67(4):409-18.
CONCLUSION: fish oil (both EPA and DHA) are anti-inflammatory

19.) Rupp H, Wagner D, Rupp T, Schulte LM, Maisch B. Risk stratification by the “EPA+DHA level” and the “EPA/AA ratio” focus on anti-inflammatory and antiarrhythmogenic effects of long-chain omega-3 fatty acids. Herz. 2004 Nov;29(7):673-85.
CONCLUSION: DOSE:2-4 g/day of 84% EPA+DHA ethyl esters for anti-inflammatory effects

20.) Cleland LG, Caughey GE, James MJ, Proudman SM. Reduction of cardiovascular risk factors with longterm fish oil treatment in early rheumatoid arthritis.J Rheumatol. 2006 Oct;33(10):1973-9. Epub 2006 Aug 1.
CONCLUSION: anti-inflammatory effects of fish oil in RA patients; also reduced NSAID use with fish oil

21.) Cleland LG, James MJ, Proudman SM. The role of fish oils in the treatment of rheumatoid arthritis. Drugs. 2003;63(9):845-53. CONCLUSION: fish oil anti-inflammatory in RA

22.) Kremer JM, Lawrence DA, Petrillo GF, Litts LL, Mullaly PM, Rynes RI, Stocker RP, Parhami N, Greenstein NS, Fuchs BR, et al. Effects of high-dose fish oil on rheumatoid arthritis after stopping nonsteroidal antiinflammatory drugs. Clinical and immune correlates. Arthritis Rheum. 1995 Aug;38(8):1107-14. CONCLUSION: Fish oil anti-inflammatory in RA

23.) Pischon T, Hankinson SE, Hotamisligil GS, Rifai N, Willett WC, Rimm EB. Habitual dietary intake of n-3 and n-6 fatty acids in relation to inflammatory markers among US men and women. Circulation. 2003 Jul 15;108(2):155-60. Epub 2003 Jun 23. CONCLUSION: Fish oil but not ALA associated with decreased inflammatory markers; Fish oil decreased TNF

24.) Ferrucci L, Cherubini A, Bandinelli S, Bartali B, Corsi A, Lauretani F, Martin A, Andres-Lacueva C, Senin U, Guralnik JM. Relationship of plasma polyunsaturated fatty acids to circulating inflammatory markers. J Clin Endocrinol Metab. 2006 Feb;91(2):439-46. Epub 2005 Oct 18. CONCLUSION: Higher EFA’s accociated with lower inflammatory markers; n-3 lowers TNF-alpha and inflammation

25.) Sundrarjun T, Komindr S, Archararit N, Dahlan W, Puchaiwatananon O, Angthararak S, Udomsuppayakul U, Chuncharunee S. Effects of n-3 fatty acids on serum interleukin-6, tumour necrosis factor-alpha and soluble tumour necrosis factor receptor p55 in active rheumatoid arthritis. J Int Med Res. 2004 Sep-Oct;32(5):443-54. CONCLUSION: Fish oil decreaases TNF-alpha, soluble tumour necrosis factor receptor p55 (sTNF-R p55), CPR and I-6 in RA patients

26.) Yamashita N, Sugiyama E, Hamazaki T, Yano S.Inhibition of natural killer cell activity by eicosapentaenoic acid in vivo and in vitro.Biochem Biophys Res Commun. 1988 Jan 15;150(1):497-505. CONCLUSION: EPA decreases NK activity

27.) Yamashita N, Yokoyama A, Hamazaki T, Yano S. Inhibition of natural killer cell activity of human lymphocytes by eicosapentaenoic acid. Biochem Biophys Res Commun. 1986 Aug 14;138(3):1058-67. CONCLUSION: EPA decreases NK activity

28) Yamashita N, Maruyama M, Yamazaki K, Hamazaki T, Yano S. Effect of eicosapentaenoic and docosahexaenoic acid on natural killer cell activity in human peripheral blood lymphocytes. Clin Immunol Immunopathol. 1991 Jun;59(3):335-45.
CONCLUSION: EPA and DHA both inhibit NK cell activity; the effect is greater (synergistic) when both are used together

29.) Thies F, Nebe-von-Caron G, Powell JR, Yaqoob P, Newsholme EA, Calder PC. Dietary supplementation with eicosapentaenoic acid, but not with other long-chain n-3 or n-6 polyunsaturated fatty acids, decreases natural killer cell activity in healthy subjects aged >55 y. Am J Clin Nutr. 2001 Mar;73(3):539-48. CONCLUSION: NK cell activity was not significantly affected by the placebo, ALA, GLA, AA, or DHA treatment. Fish oil caused a significant reduction (mean decline: 48%) in NK cell activity that was fully reversed by 4 wk after supplementation had ceased. CONCLUSION: A moderate amount of EPA but not of other n-6 or n-3 polyunsaturated fatty acids can decrease NK cell activity in healthy subjects.” DOSE: 1 g EPA plus DHA (720 mg EPA + 280 mg DHA) daily

30.) James MJ, Ursin VM, Cleland LG. Metabolism of stearidonic acid in human subjects: comparison with the metabolism of other n-3 fatty acids. Am J Clin Nutr. 2003 May;77(5):1140-5. CONCLUSION: increases of EPA from various sources was 1:0.3:0.07 for EPA:SDA:ALA.

31.) Wallace FA, Miles EA, Calder PC. Comparison of the effects of linseed oil and different doses of fish oil on mononuclear cell function in healthy human subjects. Br J Nutr. 2003 May;89(5):679-89. CONCLUSION: ALA increases EPA but not DHA; higher dose needed

32.) Arterburn LM, Hall EB, Oken H. Distribution, interconversion, and dose response of n-3 fatty acids in humans. Am J Clin Nutr. 2006 Jun;83(6 Suppl):1467S-1476S. CONCLUSION: ALA not well-converted to EPA and DHA; DOSE: DHA 2 g/day for maximal tissue response

33.) Young GS, Conquer JA, Thomas R. Effect of randomized supplementation with high dose olive, flax or fish oil on serum phospholipid fatty acid levels in adults with attention deficit hyperactivity disorder. Reprod Nutr Dev. 2005 Sep-Oct;45(5):549-58. CONCLUSION: fish oil prefferable to flax oil for raising EPA/DHA levels and decreasing AA/EPA ratios

HealthBeat Newsletter Back Issues

HealthBeat Newsletter Back Issues

12/20/07 What’s Old Is New Again – Can You Say “Chia Pet?”

  • What’s Old Is New Again – Can You Say “Chia Pet?”
  • Fiber: Longevity Secret and More
  • More Questions About L-5-HTP and Paxil
  • Laughter is the best medicine: Age and Experience Beats Youth and Enthusiasm…

12/14/07 Where We Draw The Line On “Free Advice”

  • “Hot Flashes” from this Week’s Conventional Medical Journals
  • A Fitness Resource That We Use – And You Can Too!
  • Some Thoughts Regarding “Free Medical Advice” – A Nurse Mark Rant…
  • “But I really Miss Mashed Potatoes…” Our Secret Cauli-tato Recipe
  • Laughter is the best medicine: More Of The “Lowest Form Of Humor”…

12/07/07 Dr. Myatt’s Christmas Gift Ideas And Suggestions

  • Dr. Myatt’s Christmas Gift Ideas and suggestions
  • Laughter is the best medicine: Remembering Hollywood Squares

11/30/07 Mustard Plasters And A Grandmother’s Dilemma

  • Mustard Plasters And A Grandmother’s Dilemma
  • And Another Mustard Plaster Success Story
  • What About The “Good Sugars?”
  • What are “ketones” and “ketosis?” Isn’t Ketosis dangerous?
  • L5HTP vs Paxil vs St. Johns Wort: Which to use?
  • Laughter is the best medicine: 11 people on a rope…

11/19/07 Pneumonia – Deadly But Preventable – Here’s How:

  • Pneumonia – Deadly But Preventable – Here’s How:
  • Mom Wishmeyer’s Good Old-Fashioned Mustard Plaster For Chest Infections.
  • Common Sense For Colds And Flu…
  • We Get Letters: Peanut Oil And Label Claims – How To Know What’s What?
  • We get letters: When Will The Super Fast Diet Be Available In A “Paper Book?”
  • Laughter is Good Medicine: Test for Dementia

11/02/07 Special “Heart Health Report” Edition

  • Special “Heart Health Report” – Heart Attack and Stroke – what are your real risks?
  • Dave Checks in – What to do for shingles?
  • Laughter is the best medicine: From the kids…

10/26/07 Flu and Cold Season Is Coming – Get Natural Protection and Relief!

  • “Where Was My HealthBeat Last Week!?!” The Techno-Gremlins Ate It…
  • Flu and Cold Season Is Coming – But There Is Natural Relief!
  • Dr. Myatt’s Mighty Herbal First Aid Kit – For Colds and Flu Too!
  • Don’t Forget – Dr. Myatt Has A Crazy “No-Flu” money-back Guarantee!
  • Surprise And Disappointment – It Seems Everyone Figures Someone Else Will Do It…
  • Laughter is Good Medicine: A Skeletal Bit of Humor

10/12/07 HealthyTroops.com – What’s It All About?

  • HealthyTroops.com – What’s It All About?
  • We Get Letters – Complete With Lab Results…
  • We Get Letters – And Compliments!
  • Recent News From The FDA – “Power To The People!” NOT!
  • Laughter is Good Medicine: The Times, They Are A-Changin’

10/05/07 The Wellness Club Supports America’s Military Men and Women: HealthyTroops.com Goes Live!

  • Wellness Club Launches HealthyTroops.com
  • It’s Finally Here! The Wellness Club Website Has Had A Make-Over!
  • Seems The New Website Is A Hit! (With most folks, at least…)
  • Will the REAL Naturopathic Medical Doctor Please Stand Up?
  • Laughter is Good Medicine: Anger Management

09/27/07 It’s Finally Here! The Wellness Club Website Has Had A Make-Over!

  • It’s Finally Here! The Wellness Club Website Has Had A Make-Over!
  • Optimist or Pessimist — Does It Really Matter To Health?
  • What I Admire About My European Patients
  • A Lesson In How To Get Your Research Funded (And Your Salary Paid): A Look Behind The Scenes
  • Got Cancer? Two Reasons You Have My Deep Sympathy
  • We Get Questions: What Oil To Cook With?
  • Laughter is Good Medicine: Remembering Red Skelton

09/20/07 Rooster’s Crowing Is Determined Responsible For Sunrise – Learn More!

  • Something Wonderful Is Getting Ready To Happen At The Wellness Club!
  • The Problem With Research Article Abstracts – Or, How The Rooster Crows To Make The Sun Rise…
  • CT Scans And Radiation Risks In Children – Is It Really Worth It?
  • Phlebitis / Thrombophlebitis – A Dangerous Condition Much In The News Of Late
  • Some Fun With Politics
  • Laughter is Good Medicine: Some Truly Useful Information This Week – Conversion Units

09/13/07 Rheumatoid Arthritis – it’s a hopeless diagnosis, right? Not Here It Isn’t!

  • Extreme Sports, Nutrition, Vitamins, And Immunity – A conversation with my car mechanic got me to thinking and researching…
  • Lung Disease In A Bag: Why do insist on exposing ourselves to these toxic chemicals?
  • Patent Drugs: Prescription For Problems:
  • Ginkgo Biloba and Longevity
  • A New HealthBeat Feature: Readers Rants!
  • We Get Questions: A potpourri this week…
  • We Get Questions: Rheumatoid Arthritis – it’s a hopeless diagnosis, right?
  • Laughter is Good Medicine: Some Zen sarcasm…

09/06/07 The Flu Can Be a Brutal Enemy. Are You Relying on a Flu Shot Alone to Protect You? And How About A Money-Back Good Health Guarantee?

  • 3 Steps to A Natural Facelift – A More Youthful Appearance without Botox Or Surgery!
  • Cancer In a Can – Are You Really Still Drinking This Stuff?!?
  • More Great News For Grape Fans – Study Shows Prostate Cancer Benefit…
  • Green Tea Gets A Boost – Yet Another Study Shows It Stops Colon Cancer Tumors…
  • The Flu Can Be a Brutal Enemy. Are You Relying on a Flu Shot Alone to Protect You? And How About A Money-Back Good Health Guarantee?
  • We Get Questions: Seizures In Children…
  • We Get Questions: Hip Problems, Fosamax, Osteoporosis – And “Everything Hurts” For This One Senior – So, What To Do?
  • Laughter is Good Medicine: Simple Truths And Knowledge From Our Canine Friends

8/30/07 Surgical Dilemmas, Bad Knees, Infertility, And “Drug To Normalization”! A Potpourri Of Problems…

  • Damned If You Do, Damned If You Don’t! The dilemma of Big Surgery
  • Dave, With The “Bum Knees” Checks Back In… It still hurts – even after Big Surgery!
  • Fibroids, Fertility, and Working For Free… We get questions!
  • News Reports, Political Correctness, drugs, and Guns – One thing leads to another…
  • Kennedy, Roberts, and Burr – Meddling With Your Health Freedom Again…
  • Laughter is Good Medicine: The Latest In Diagnostic Technology, brought to you by Dr. Myatt!

08/23/07 Sugar More Addictive Than Cocaine According To New Research!

  • Yet More Good Reasons To Stop The Pop Habit – Metabolic Syndrome And Addiction
  • This week’s FDA “Warnings”…
  • The FDA Is “At It Again”… Keeping Us Safe From Mother Nature
  • We Get Letters I –  Comments and Questions…
  • We Get Letters II – Readers Ask Medical Questions…
  • Laughter is Good Medicine: Kids Say The Darndest Things – Part 2

08/16/07 Poisons Lurking In Common Plastic Items

  • Vitamins: What You Should be Taking, and Why
  • Readers Question Of The Week: What Dangers Lurk In Plastic?
  • US Ranks 42nd In World For Life Expectancy – What The Heck Is Wrong Here?
  • AstraZenca Profits Take Hit In Prilosec Heart Attack Scare
  • Problems with Diabetes Drugs continue
  • We Get Questions…
  • Laughter is Good Medicine: Kids Say The Darndest Things!

08/09/07 Got Mercury Amalgam Fillings? You Gotta See This Video!

  • Yet More Good News For Vitamin D!
  • Dr. Myatt’s Super Shake recipes
  • Alzheimer’s, Heartburn, Or Neither: What’s Your Pleasure?
  • Still have “Silver Fillings” in your teeth? You won’t want to after seeing this!
  • We Get Letters I – What Natural Treatments Are Available For MS?
  • We Get Letters II – Readers Ask Us Medical Questions…
  • Laughter is Good Medicine: “Pirates Of The West” stealing from Nature…

08/02/07 Detox Your Way To Better Health With Colon Cleansing

  • How To Have A Healthy Bowel – And A Healthy Body…
  • FDA Updates: “And The Beat Goes On…”
  • We Get Letters: Insurance Companies Out Of Control – And Something That You Can Do About It…
  • We Get Letters II – Readers Ask Us Medical Questions…
  • Laughter is Good Medicine: Wisdom From One Of Our Readers…

07/26/07 The Most Dangerous Food You Can Eat!

  • 10 Dangers of Carbohydrates – Carbs are NOT your friend!
  • Fungus, Yeasts and Molds: Hidden Cause of Many “Unexplained” Diseases
  • Those Not So Golden Years… and the story of a nice little truck.
  • Raw Almonds No More! Your Government, Hard At Work Protecting You…
  • Laughter is Good Medicine: Like it or not, a Compendium of Puntifications

07/18/07 Why Aerobic Exercise is a Waste of Time

  • Why Aerobic Exercise is a Waste of Time (Dr. Dana Myatt)
  • Strontium: The Missing Mineral for Osteoporosis Prevention and Reversal
  • FDA Tyranny Now Law: TWO Low Blows For Health Freedom and What It Will Mean to You
  • Ask Dr. Myatt:  Is Ostaderm Safe for Hot Flashes in a Woman on Breast Cancer Medication?
  • Laughter is Good Medicine: The Death of Common Sense

07/12/07

07/05/07

  • Neurological Disease: What You’re NOT Going To Hear From Your Conventional Doctor. You’ll NEVER hear any of this from your conventional medical doctor, for at least two reasons. First, there are no known cures for neurological diseases in conventional medicine. In fact, even our symptomatic treatments are fairly lame. Secondly, when a doctor does have information about a “non standard” (read that: “not conventional medicine”) approach, he or she could lose their medical license by telling you about it. So don’t be disappointed if your conventional medical doctor, no matter how good or well-respected, doesn’t have much hope to offer. That’s conventional medicine. If I found out tomorrow that I had a neurological disease, here are the steps I would take right away: Read the rest of Dr. Myatt’s article here…
  • Freedom – Ours to Keep or Lose. As the Founding Fathers knew, the way we remain free as individuals is because we each have a voice and a vote. If we fail to exercise our freedom to speak and to elect our officials, then we get the government we deserve. That is why I continually encourage you to be pro-active. It’s the only way we can continue to enjoy the freedoms that we do, health freedom included. Read the rest of Dr. Myatt’s article here:
  • The FDA’s Road Map to End Dietary Supplements. This document frightens me for the future of America’s access to nutritional supplements – In this document the FDA has laid out a very precise 3-year plan to decimate the nutritional supplement industry, reduce the availability of nutritional supplements to Americans, and to radically increase the price of those nutritional supplements that remain. Read the rest of Nurse Mark’s article here:
  • Mother Was Right: Drink Your Vegetables! “A French team now reports that diets rich in flavonoids – the antioxidant compounds in fruit, vegetables, coffee, tea, and chocolate – could reduce the decline in mental function associated with aging.” Following on Dr. Myatt’s article “Vitaminless Vegetables: the New Nutrient Deficiency” this article details important new proof of the value of veggies and fruits. Read this Craig Weatherby article here:
  • Letters: Mangosteen Juice – Hip or Hype? And “Dave” checks back in… Find out if this new MLM marvel is for real – Dr. Myatt shares her thoughts about Mangosteen. And, some updates on “Dave” as he works his way to better health – in his letters with Nurse Mark. Read it all here:
  • Laughter Really Is Good Medicine. Our readers like to share funnies with us – and this one makes you wonder: does all that healthy living really make you live longer, or does it just make it feel like longer? Read on…

06/26/07

06/21/07

06/14/07

  • Prescription Drugs In Your Drinking Water You are taking your neighbors drugs whether you like it or not! Read on to learn more, and find out how to protect yourself…
  • Vitamin D Cuts Cancer Risk By An Amazing 77%You won’t hear it from the American Cancer Society or the AMA or the FDA! Find out more about this latest research…
  • We Get Letters The American Cancer Society says the War On Cancer has been won! Do you believe it? We don’t, and neither does this savvy reader…
  • Upcoming Bill Strengthens FDA Power To Ban SupplementsThere are smokescreens being laid to keep us diverted from this threat to our health freedoms – read, learn, and act now!
  • The Decay Of Organic FoodsNo, the food isn’t rotting, but the standards are, under new USDA rules allowing non-organic ingredients in organic labeled foods…
  • Laughter – Not a funny this week, but a heartwarming story and a lesson for us of love and tolerance  from our furry friends…

06/09/07

06/02/07

05/25/07

05/15/07

05/10/07

  • What’s Burning You?Yes, you’ve got heartburn – but maybe not for the reasons that you think! Big Pharma and the Medical Mafia have hoodwinked you again – find out what you can do about it. Read about the simple test you can do at home…
  • Washington Updates: What matters more to your senator – money or your health and freedom? You’ve been sold out – read more…
  • Counterfeit Drugs: The FDA is warning us about them, but who is responsible? Nurse Mark shares his opinions…
  • Obscene Profits are what it’s all about – analysis and opinion by Nurse Mark…
  • Mother’s Day is coming: And just where do you think you would be without your mother…
  • Laughter:  Growing older ain’t for sissies – so you might as well laugh about it…

05/05/07 Political Activism Pays Off!

04/21/07 FDA To Regulate Healthy Foods as Drugs 04/30/07

04/06/07 Are GMO Foods Safe to Eat?

03/22/07

03/15/07

03/02/07 Killer Vitamins: Doctors of Spin Are At It Again

2/23/07 Sinister Things Afoot in US Medicine

02/15/07 LDL Cholesterol: Another Big Fat Lie

02/08/07 Valentine’s Day Special: Heart-Healthy Issue

02/02/2007 Senile Dementia Linked to Common Nutrient Deficiency

01/26/2007 FDA Outlaws Vitamins: Closer By The Minute

01/19/2007 Do We Really Need a “Trans Fat Ban”?

01/11/2007 Dying for Pain Relief

01/04/2007 Welcome to The New HealthBeat!

Sept 27, 2006 Three Hidden Causes of Disease Lurking in Your Mouth

April 14, 2006 Vitamin-less Vegetables

Sept 21, 2005 Antioxidants Explained

July 27, 2005 The End Of Free Access To Supplements?

June 9, 2005 A Special Look At Women’s Health

May 5, 2005 Lower Cholesterol Naturally

Jan. 5, 2005 New Years Resolutions: What value good  health?

Dec. 10, 2004 Vitamin Supplements Outlawed as of August, 2005 

Nov. 24, 2004 Healthy, Low Carb Thanksgiving Recipes

Oct. 19, 2004 Ingrown Toenails, and General Toenail Care.

Sept 16, 2004 The Truth About Cholesterol, Part II

Sept 3, 2004 The Truth About Cholesterol, Part I

Aug 11, 2004 Taking Good Health to Heart

July 13, 2004 Conjugated Linoleic Acid Reduces Body Fat Mass

June 17, 2004 Not Just Health News… Daily Health News!

June 7, 2004 Remembering Reagan, Avoiding Alzheimer’s

June 2, 2004 Your Health Freedom Under Siege!

May 12, 2004 Meet Your New HealthBeat Editor!

April 30, 2004 Heart Attack and Stroke: What are Your Real Risks?

April 5, 2004 The Ten Most Dangerous Foods: Part II

March 18, 2004 The Ten Most Dangerous Foods: Part I

March 2, 2004 When “Sorry” Doesn’t Help

Feb 12, 2004 5 Most Important Supplements For Health & Longevity

Feb 6, 2004 Dr. Myatt’s Super-Shake

Jan 22, 2004 Do You Really Take All That Stuff ???

Jan 12, 2004 Irritable Bowel Syndrome

Jan 1, 2004 “Liver Cleansing” – Worthwhile or Worthless?

Dec 20, 2003 Beat Flu & Colds The Natural Way

Dec 15, 2003 NurseBeat Update: Stress-Less Holidays

Dec 2, 2003 Memory-Boosting Supplements

Nov 12,  2003 NurseBeat Update: Green tea

November 2003 Life Extending Nutrients

September 2003 US Government Urges Higher Omega-3 Consumption

August 2003 Heart Health Breakthroughs

July 2003 Ten Proven Reasons to Take a Good Multiple Vitamin

June 2003 The Product Everyone Should Have on Hand

May 2003 7 Simple Ways to Decrease Your Cancer Risk

Health Resources

Recommended

Additional Health Products, Foods and Services

The Wellness Club doesn’t sell the following items, but the links will lead you to the websites where you will find foods and products that come highly recommended by Dr. Myatt.

Menu

 Healthy and Hard-to-Find Foods and Such    Shiritake (Konjac Noodles)    Wild Pacific Salmon and Other Organic Delicacies    Grass-fed Organic Beef, Chicken and Raw Milk Cheese    Water Filters

HEALTHY FOODS


Shiritake Noodles – Noodles and thickeners made from a tuber (Konjac root), not grain. Suitable for use in low carb, low calorie and anti-fungal diets.

Dr. Myatt’s Comment: These make a surprisingly good substitute for regular noodles. Rinse well in hot water or boil for 2 minutes to get rid of the “fishy” smell. (They come packed in sea water). You really need to try these, either in stir-fry or other oriental dishes or served with  pasta sauce.

Regardless of what the package says, here is the accurate “scoop” on nutrition composition: each one ounce of shiratake noodle contains 4 calories, 1 gram of carbohydrates and no fat or protein. (Compare this to regular pasta at approx. 38 calories and 7 grams of carbs per ounce!).


Wild Pacific Salmon Salmon is a “Super Food,” high in Omega-3 essential Fatty Acids. There’s one problem, though. Farm-raised fish don’t have a great Omega-3 content because of what they’re fed, and many ocean-caught salmon contain high levels of mercury.

The answer? Wild, sustainable Alaskan-caught salmon, tested for purity. This is the best, purest, highest Omega-3 salmon you can buy.

This company also features organic nuts and dried fruits, “salmon burgers” and other products made from salmon, scallops, halibut, shrimp, sablefish, organic cooking oils, teas and organic dark chocolate. Yum!


Grass-Fed Beef is a “Super Food,” especially when it is free of hormones, antibiotics and other synthetic additives. In fact, grass fed beef has an Omega content similar to fish, a very different food from “corn fed” or other types of beef. (Which not only contain hormones and antibiotics but are fed on fungus-containing grains).

This company offers all cuts of grass-fed, pure and wholesome beef plus free-range chicken and raw milk Amish cheese.


Quality Water Filters Eating right is important, but “drinking right” is even MORE important! Make sure your drinking water is clean and chemical-free. An at-the-sink water purifyer is a great health investment, better and less expensive than buying bottled water.

This highest-rate water filter company also offers whole-house purification units, shower filters, and an “auto-ship” filter service so you never have to worry about changing your filter


Paraliminal CD’s are here! Make positive changes without homework, exercises, memorizing or positive affirmations! Just put in a Paraliminal CD, kick back, listen, and enjoy the life-changing results.


* Luxury Cruises at guaranteed unbeatable prices. Relax! Luxury cruises are a relaxing, all-inclusive and stress-free way to travel. Many luxury cruises feature massage, spa treatments, gyms, full beauty services and world-class dining. Use our easy online cruise locator to find your ideal luxury cruise today.


* Inner Bonding – Grace Through Growth
We invite you to learn about the powerful emotional and spiritual healing process of Inner Bonding, created by Margaret Paul, Ph.D. and Erika Chopich, Ph.D. and recommended by Lindsay Wagner.


* Self Improvement, Inspiration, Happiness – Self Improvement Zone is a membership site dedicated to making self improvement your most gratifying, fascinating and liberating journey ever.


The Self-Help Advisor  Quality Books, Programs & Resources for Spiritual and Personal Growth. “Parables Series” Ebooks – on finding your Life Purpose. Free Monthly Ezine.


* Twenty years in medical offices watching the wrong treatments and information resulted in these books! http://www.antibiotic-alternatives.com


Subscribe to ‘The Glutathione Report’ for the latest news and updates on the
health benefits of Glutathione mailto:glutathione@pushbuttonresponder.com


Are you still smoking? Say it isn’t so! Here is a book that can help you kick the habit once and for ever! Check out quitsmoking4good.com and start your new smoke free life now!


O-zonelite Air Purifier Compact ozone light bulbs put out 6000 hours worth of environmentally friendly air filtration. Removes bad odors, eliminates many airborne irritants and microbes, and gives out the same light as a 100 watt incandescent.


HealthBeat News

In This Issue:

The Product EVERYONE should have on hand! This simple, inexpensive supplement can protect you from a serious consequence of radiation and nuclear fallout. Remember Chernobyl?

Skin Rejuvenation Protocol. Find out the best methods for renewing a youthful appearance to skin. Dr. Myatt summarizes the research, then puts it all together in a comprehensive “Skin Renewal” program. A MUST for Summer skin care!

Member News and Notes

*We heard your feedback and Thank You! By popular vote, HealthBeat will be delivered in “abstract”(summary) form to your mailbox. Simply click the underlined links to go to those articles you are interested in.

* Upcoming topics: by reader request, future topics will include natural hormone replacement therapy; Omega-3 Fatty Acids and how to obtain them; osteoporosis, prostate health, and more.

* Send a sample issue of HealthBeat to a Friend and let them share the medical updates. If they enjoy it, they can sign up at no charge.

The Product EVERYONE Should Have On Hand!

ARE YOU PREPARED FOR A RADIATION EMERGENCY?

Potassium Iodide (KI) Can Shield You From Thyroid Cancer

With 103 active commercial nuclear reactors in the United States, we live in constant threat of a nuclear emergency every day. A terrorist attack on any one of these facilities, or the release of a “dirty bomb” is also a possibility in today’s “highly charged” world. In fact, in an emergency, if you live within 200 miles of a nuclear reactor, you have a high risk of being exposed to significant doses of radioactive isotopes. In the event of a nuclear accident or attack radioactive materials can be released into the atmosphere, a high percentage of which is radioactive iodine. When a radioactive iodine cloud passes through a populated area, the radiation is concentrated into the thyroid gland of those exposed. The result is irreparable damage to the thyroid, which can lead to cancer. The 1986 Chernobyl accident in the Ukraine is a tragic example.

The best protection against thyroid damage and thyroid cancer induced by radioactive iodine exposure is Potassium Iodide. This simple compound protects the thyroid by saturating all of the iodine binding sites in the gland, leaving no room for the binding of radioactive iodine. Potassium Iodide is a low-cost way to protect yourself and your family against the long-term consequences of exposure to radiation. When used correctly, potassium iodide tablets can prevent or reduce the amount of radioactive iodine taken up by the thyroid gland. Even the government and the military stocks up on potassium iodide in case of nuclear disaster.

The body can’t distinguish between radioactive and the benign version of iodine, which is necessary for thyroid function. Taking 130 mg of potassium iodide, the dosage widely recommended for the blocking of radioactive iodine in the event of a nuclear disaster, can quickly and completely protect the thyroid gland, which is one of the organs most commonly damaged by radioactive fallout. Dr. Myatt’s Wellness Club offers a supplement that contains 14 x 130 mg tablets of potassium iodide. Tablets are scored for easy breakage in the case of any need for dosages smaller than 130 mg, as recommended for children and pets.

How many packages do you need?

The FDA recommends that you have one package per person available.* Remember that during an emergency, you may not be able to get to your home, thus it is recommended to have packages stored in several places as well. Since the shelf life of this product is virtually unlimited, you should have to purchase your supply only once. Have this on hand for your family, and remember the children, pets, grandchildren, too!

* To view home preparation procedures for emergency administration of potassium iodide, visit the FDA website at http://www.fda.gov/cder/drugprepare/kiprep.htm Only take potassium iodide tablets when guided by health officials in your area and follow guidelines included with each bottle.

Skin Rejuvenation Protocol

The skin (integument) is the body’s first line of defense in protection from the external environment. If it also one of the first things people notice about us. Healthy skin is both a cosmetic blessing and a sign of a healthy underlying system, yet few people know how best to take care of this important organ. Let’s focus on some of the most important things we can do to protect this amazing bit of our architecture!

A Basic Regimen for Skin Care

    1. Nutrition: Beauty from the Inside Out. Healthy skin requires water, essential fatty acids and nutrients to be truly healthy. No amount of topical cosmetics will make up the difference to skin that is under-nourished. The skin requires the following:

A.) Water ! The body is 60% or more water. Even a subtle dehydration makes lines and wrinkles appear deeper, whereas being well hydrated “plumps” skin and minimizes the appearance of lines. Drink 64 ounces of PURE water per day, especially in the Summer,

B.) UV Light: Small amounts of UV are beneficial to the skin, but excess amounts can cause premature aging and contribute to skin cancer. Ten minutes of early-morning sun several times per week is sufficient for skin health. Beyond that, always wear a UVA/UVB sunscreen with an SPF of 15, especially on the face.

C.) Smoking (and second-hand smoke): Causes a constriction of the small blood vessels that bring nutrients to the skin, depriving skin of both water, vitamins and minerals, and fatty acids. Smoking is one of the absolute WORST things you can do to skin. Don’t go there!

D.) Nutrients:

  1. Multiple Vitamin/Mineral Supplements: An optimal vitamin/mineral/trace mineral formula such as Maxi Multi supplies the important micronutrients required for healthy skin.
  2. Essential fatty Acids: The skin needs essential fats from the inside out to stay moisturized. EFA’s are supplied by flaxseed oil, flaxseed meal, or fish oil. Be sure to take 1-2 TBS of flax oil or 3 Caps of fish oil per day, and include fatty fish such as salmon in the diet twice per week. (You’ll learn more about Essential fats in upcoming installments of The New Keto Diet).
  3. Grape seed extract: 50-100 mg, 2-3 times per day is an optional “metanutrient” that aids the skin by improving collagen formation (the underlying structural material of skin) AND by acting as a potent antioxidant to protect skin from oxidation. (The human equivalent of “rust”!)
    1. A Basic Regimen for Skin Care

I.) Cleanse: The purpose is to gently remove surface debris without stripping natural oils. Most soaps are highly alkali and strip skin of natural oils. Wash skin twice per day in a mild soap like Dove or Ivory (both are highly recommended by many dermatologists).

II.) Skin Cream: Proven ingredients helpful for topical application include antioxidants (A,C,E, alpha lipoic acid) in a form that is easily absorbed by the skin (micronized). Glycolic acid helps break down old cells so they can be replaced more quickly with new cells from beneath. DMAE (dimethylaminoethanol) helps firm sagging skin, NaPCA aids moisture retention and Sunscreens that protect from UVA, UVB, and UVC are all useful in keeping skin radiant.

I have found it difficult if not impossible to find a good cream that contains all of these important ingredients until now. Rejuvenex is the first cosmetic preparation that I am aware of to combine the finest, proven ingredients into one easy formula. You can try to duplicate all of these skin essentials yourself, but you will be working hard and paying far more for the individual preparations. (Believe me, I know from experience. That’s how I’ve been making my own cream until now!).

In order to introduce you to the benefits of this formula, plus help you get started on a skin rejuvenation and protection program of your own (especially important as the Summer sun heats up), we have special-purchased Rejuvenex so we can offer it to you at a lower introductory price.

This cream is rich, wonderful, contains “all the right stuff” as listed above, and more, and a little goes a long way. You need only apply it morning and evening to get great results. Both men and women will benefit. As an alternative, you can do as I was doing and mix your own ingredients, just be sure to include the above-listed items for best results.

To order Rejuvenex, CLICK HEREor call 1-800-376-9288

Vitamin D A Special HealthBeat News Report



Vitamin D – You have been reading about it in the news, and you have wondered what is real and what is hype.

Dr. Myatt and Nurse Mark have researched and prepared this special report for HealthBeat News Readers.


Vitamin D — The Short Course

1.) Vit D is produced in our bodies in response to sun exposure. Vit D is also available from food and supplements.

2.) Vit D is FAR more important to health than was previously realized. I’m talking FAR more important.

3.) Vit D deficiency is widespread, including North America, even in sunny climates like Arizona. Many people who think they are getting enough Vitamin D from sunlight are mistaken.

4.) How to Optimize Vit D Levels for Good Health:

I.)  Vit D test, supplement accordingly, re-test

II.) Supplement at 5,000IU for 3 months, then test your levels.

III.) Don’t test, run the risk of being deficient, but take at least 2,000IU total per day. (This is still an extremely conservative dose, but much higher than the RDA of 400IU which hasn’t been changed yet to reflect the newer findings about Vit D). 

5.) Natural ways to obtain Vit D: Foods, supplements and sun exposure.


Vitamin D — Nutrient of the Decade: Are You Getting Enough?

The Consequences of Low Vitamin D

Vitamin D is called “the sunshine Vitamin” because our bodies make it in response to sun exposure.

Vit D is necessary for normal bone formation in both children and adults. In children, deficiencies of Vit D lead to rickets. In adults, deficiencies are associated with osteoporosis and osteomalacia (soft bones), decreased muscle strength and increased risk of fall. (1,12,14,22,43-48)Until recently, the bone-protecting effect was  about all that Vit D was known for, but the past decade of medical research has changed all that.

The newly appreciated Vitamin D deficiency risks include:

1.) heart disease: myocardial infarction, high blood pressure, heart failure, myopathy, sudden cardiac death, stroke (11,13-26, 30, 49-50)

2.) blood sugar problems: glucose intolerance, diabetes mellitus, metabolic syndrome (13-14,19,23-24,27-29)

3.) cancer prevention and improved cancer survival rates (7,8,11,14,15,24,31-37)

4.) upper respiratory tract infections, influenza and tuberculosis (24,30,38)

5.) cognitive impairment and low mood (38-40)

6.) autoimmune disease (multiple sclerosis, RA, systemic lupus erythromatosis (SLE) (15,24,26,29,30,32,41,42)

7.) misc. diseases: psoriasis, polycystic ovarian syndrome, inflammatory bowel disease

8.) urinary incontinence (54)

9.) and all-cause mortality! (5,6,7,24,30,51)

How “significant” are these associations? Here are some of the conclusions of various studies and meta-analyses (lots of studies looked at together) concerning Vit D. Italics are mine for emphasis.

“Research strongly supports the view … Vitamin D status would have significant protective effects against the development of cancer …. cancers of the breast, colon, prostate, ovary, lungs, and pancreas…” (8)

“High levels of Vitamin D among middle-age and elderly populations are associated with a substantial decrease in cardiovascular disease, type 2 diabetes and metabolic syndrome.” (9)

“Low levels of [Vitamin D] are independently predictive for fatal strokes” (10)

“It is estimated that there is a 30 to 50% reduction in risk for developing colorectal, breast, and prostate cancer by either increasing Vitamin D intake or increasing sun exposure…” (11)

“Oral Vitamin D supplementation between 700 to 800 IU/d appears to reduce the risk of hip and any nonvertebral fractures in ambulatory or institutionalized elderly persons” (12)

” 28 studies including 99,745 participants … highest levels of serum [Vit D] were associated with a 43% reduction in cardiometabolic disorders (cardiovascular disease, diabetes and metabolic syndrome) …” (9)

Are Your Vitamin D Levels Optimal? (Vitamin D Deficiency is Widespread)

One billion people worldwide are estimated to be Vit D deficient, and the problem affects us here in the United States as well. (2) One study found that more than half of North American women receiving drugs for prevention or treatment of osteoporosis were Vitamin D deficient. (1) Another study found 48% of pre-adolescent girls to be Vit D deficient (3). Other studies have found that 40% to 100% of older men and women in both the United States and Europe are Vitamin D deficient.[2] Because of the importance of Vit D and how widespread Vit D deficiency is, an estimated $100 to $200 billion is spent (wasted) each year on diseases which may really just be Vitamin D deficiencies. [4]

Age, overweight, dark skin color, use of sunscreen, and overprotection from the sun’s rays are causes of decreased production of Vit D in response to sunlight. (52,52)

How Much Vitamin D Should You Take?

Ideally, you should take whatever amount of Vitamin D puts you in the “optimal” range. Since the amount will be highly variable depending on age, sex, race, weight, daily sun exposure and diet, there is no “one size fits all” answer. Instead, blood testing of Vitamin D levels and increasing intake until optimal levels are reached is the surest way to obtain optimal concentrations of Vitamin D in the body.

Deficiency Insufficiency Sufficiency * Optimal Excess (Toxicity) <20ng/ml 20-32ng/ml 32-100ng/ml 40-80ng/ml > 150ng/ml

* – conventional medicine says that 30 ng/ml is “sufficient.” Chart references (59-62)

At the wellness Club we believe the most accurate and effective way to embark on a program of Vit D supplementation is to perform a Vit D test, supplement Vit D in accordance with the results, and then re-test in 3 months at which time your daily doses of Vit D can be fine-tuned for maintenance. March (right now!) is the best time to test initially because Vit. D stores tend to be lowest in this month.

The Vitamin D Council, a non-profit group dedicated to Vitamin D research and education recommends people take 5,000 IU per day for 2-3 months, then perform a Vitamin D test. They then suggest adjusting the dosage so that blood levels are between 50-80 ng/mL (or 125-200 nM/L) year-round. (55)

Alternately, some people opt to supplement without knowing their initial Vit D levels. A dose of 2000IU is quite conservative but certainly safe for almost anyone. In cases of significant Vit D deficiency conservative dosing such as this may take considerable time to rebuild healthy stores of this important Vitamin.

For those who wish to calculate their own Vit D requirements, 100 IU of Vitamin D could be expected to raise blood level of 25(OH)D by 1 ng/ml. (11)

Can too much Vitamin D can be toxic? Research shows that massive doses may eventually cause toxicity. One source found that in adults a sustained intake of 50,000 IU daily could produce toxicity within a few months (58) and 40,000 IU per day in infants has been shown to produce toxicity within 1 to 4 months. (56) That is ten times the recommended dose for each of those age groups! Vitamin D testing is good insurance that will allow you to safely fine-tune your dosage to your actual needs. Be careful though, since not all testing is the same and lab references and standards vary – be sure that you are comparing “apples to apples” and obtaining useable results when you are tested.

The 25-hydroxyVitamin D blood test (25(OH)D blood test) is a test that measures the amount of calcidiol circulating in the blood. This is the most accurate measure of the amount of Vitamin D in the body. The Wellness Club offers Vitamin D testing – performed by a lab that adheres to standardized references and values so that you know what you are getting when you receive your results. This can is performed at home with a “spot” (finger stick) blood test. Other tests that require a blood draw are also available.

How to Get to Your Optimal Vitamin D Levels

Start Vitamin D supplementation eight to twelve weeks before testing. Dr. John Cannell of the Vitamin D Council suggests a starting dose of 1,000 IU per 25 pounds of body weight. For example, a 150 pound person would take 6,000 IU Vitamin D per day. (150 divided by 25 = 6; 1,000IU x 6 = 6,000). Maintain this dose for 8-12 weeks, then test.

This dose may or may not put you in the optimal target range, but it certainly won’t put you in any “toxic” range. Remember, most adults can safely take up to 10,000IU per day and still be far away from Vitamin D toxicity which typically appears at 40,000-50,000IU taken for several months.

Although this dose should theoretically put you in an optimal range, numerous personal variations alter Vitamin D requirements. Some people will need a higher dose than this calculation affords. However, taking the calculated dose should at least put you “in the ballpark” for optimal dosing.

When you test results come back, you can use the number to help you know whether or not you need to increase your Vit D dose and by how much. It is estimated that each 1,000 IU increase in supplemental Vitamin D will generally produce a 10 ng/ml increase in the Vitamin D blood level (8). If your test result shows that you are 10ng/ml below your target, increase daily Vit D intake by 1,000IU per day for a total of 7,000IU per day from the above example. Continue this dose and re-test in another 3 months to verify that you are now in your optimal range.

Congratulations! You have found your optimal daily Vitamin D intake needed to maintain optimal Vitamin D blood levels.

How to Obtain Vitamin D Naturally

Exposure to sun is the most natural way to boost Vit D levels. Medical scientists have found that the skin produces approximately 10,000 IU of Vitamin D in response to as little as 30 minutes of unprotected summer sun exposure. (57)

Vitamin D can be obtained from food too. Since rickets in children is such a crippling but preventable condition, governments have long encouraged the “fortification” of dairy products and breads and cereals with token amounts of Vitamin D. In the United States and Canada, for example, fortified milk typically provides 100 IU per glass.

It is difficult to obtain optimal levels of Vitamin D from food alone.

Food IUs per serving* Percent DV** Cod liver oil, 1 tablespoon 1,360 340 Salmon (sockeye), cooked, 3 ounces 794 199 Mushrooms that have been exposed to ultraviolet light to increase vitamin D, 3 ounces (not yet commonly available) 400 100 Mackerel, cooked, 3 ounces 388 97 Tuna fish, canned in water, drained, 3 ounces 154 39 Milk, nonfat, reduced fat, and whole, vitamin D-fortified, 1 cup 115-124 29-31 Orange juice fortified with vitamin D, 1 cup (check product labels, as amount of added vitamin D varies) 100 25 Yogurt, fortified with 20% of the DV for vitamin D, 6 ounces (more heavily fortified yogurts provide more of the DV) 80 20 Margarine, fortified, 1 tablespoon 60 15 Sardines, canned in oil, drained, 2 sardines 46 12 Liver, beef, cooked, 3.5 ounces 46 12 Ready-to-eat cereal, fortified with 10% of the DV for vitamin D, 0.75-1 cup (more heavily fortified cereals might provide more of the DV) 40 10 Egg, 1 whole (vitamin D is found in yolk) 25 6 Cheese, Swiss, 1 ounce 6 2 *IUs = International Units.

**DV = Daily Value. DVs were developed by the U.S. Food and Drug Administration to help consumers compare the nutrient contents of products within the context of a total diet. The DV for vitamin D is 400 IU for adults and children age 4 and older. Food labels, however, are not required to list vitamin D content unless a food has been fortified with this nutrient.

Table courtesy of the U.S. Government National Institutes of Health Office of Dietary Supplements

Although cod liver oil is high in Vitamin D, it is also high in Vitamin A which interferes with Vit D uptake, so cod liver oil is not the best supplemental form of Vit D. Keep daily intake of pre-formed Vitamin A to a maximum of 5,000IU per day so as not to interfere with Vitamin D absorption. Beta carotene does not appear to interfere with Vit. D uptake.

Vegetarians need to be sure they are getting plenty of sunshine, because other than tiny amounts that may be found in UV-irradiated mushrooms, there are no vegetable sources of Vitamin D.

The Bottom Line on Vitamin D

Achieving Optimal Vitamin D  levels appears to be one of the most important things we can do for our overall health and life expectancy.

Please click on the image below enjoy an interesting and instructive video which discusses the relationship between Vitamin D and Cancer.

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References

1.) Holick MF, Siris ES, Binkley N, et al. Prevalence of Vitamin D inadequacy among postmenopausal North American women receiving osteoporosis therapy. J Clin Endocrinol Metab. 2005;90: 3215-3224.
2.) Holick MF. Vitamin D deficiency. N Engl J Med. 2007;357:266-281.
3.) Sullivan SS, Rosen CJ, Halteman WA, Chen TC, Holick MF. Adolescent girls in Maine at risk for Vitamin D insufficiency. J Am Diet Assoc. 2005;105:971-974.
4.) GrassrootsHealth. The Vitamin D deficiency epidemic. A call to D*action. http://www.grassrootshealth.org/daction/epidemic.php. Accessed May 8, 2009.
5.) GrassrootsHealth. Disease incidence prevention by serum 25(OH)D level. http://www.grassrootshealth.org/_download/disease_incidence_prev_chart_101608.pdf. Accessed May 8, 2009.
6.) Autier P, Gandini S. Vitamin D supplementation and total mortality. Arch Intern Med. 2007;167(16):1730-1737.
7.) Thomas L. Lenz. Vitamin D Supplementation and Cancer Prevention. Am J Lifestyle Med. 2009;3(5):365-368.
8.) Ingraham BA, Bragdon B, Nohe A. Molecular basis of the potential of Vitamin D to prevent cancer. Curr Med Res Opin. 2008 Jan;24(1):139-49.
9.) Parker J, Hashmi O, Dutton D, Mavrodaris A, Stranges S, Kandala NB, Clarke A, Franco OH. Levels of Vitamin D and cardiometabolic disorders: systematic review and meta-analysis. Maturitas. 2010 Mar;65(3):225-36. Epub 2009 Dec 23.
10.) Pilz S, Dobnig H, Fischer JE, Wellnitz B, Seelhorst U, Boehm BO, März W. Low Vitamin d levels predict stroke in patients referred to coronary angiography. Stroke. 2008 Sep;39(9):2611-3. Epub 2008 Jul 17.
11.) Holick MF. Vitamin D and sunlight: strategies for cancer prevention and other health benefits. Clin J Am Soc Nephrol. 2008 Sep;3(5):1548-54. Epub 2008 Jun 11.
12.) Bischoff-Ferrari HA, Willett WC, Wong JB, Giovannucci E, Dietrich T, Dawson-Hughes B. Fracture prevention with Vitamin D supplementation: a meta-analysis of randomized controlled trials. JAMA. 2005 May 11;293(18):2257-64.
13.) Anagnostis P, Athyros VG, Adamidou F, Florentin M, Karagiannis A. Vitamin D and Cardiovascular Disease: A Novel Agent for Reducing Cardiovascular Risk ? Curr Vasc Pharmacol. 2010 Feb 25. [Epub ahead of print]
14.) Holick MF. Vitamin D: importance in the prevention of cancers, type 1 diabetes, heart disease, and osteoporosis. Am J Clin Nutr. 2004 Mar;79(3):362-71.
15.) Holick MF. Vitamin D and sunlight: strategies for cancer prevention and other health benefits. Clin J Am Soc Nephrol. 2008 Sep;3(5):1548-54. Epub 2008 Jun 11.
16.) Judd SE, Tangpricha V. Vitamin D deficiency and risk for cardiovascular disease. Am J Med Sci. 2009 Jul;338(1):40-4.
17.) Kendrick J, Targher G, Smits G, Chonchol M.25-HydroxyVitamin D deficiency is independently associated with cardiovascular disease in the Third National Health and Nutrition Examination Survey. Atherosclerosis. 2009 Jul;205(1):255-60. Epub 2008 Nov 11.
18.) Lee W, Kang PM. Vitamin D deficiency and cardiovascular disease: Is there a role for Vitamin D therapy in heart failure? Curr Opin Investig Drugs. 2010 Mar;11(3):309-14.
19.) Martins D, Wolf M, Pan D, Zadshir A, Tareen N, Thadhani R, Felsenfeld A, Levine B, Mehrotra R, Norris K. Prevalence of cardiovascular risk factors and the serum levels of 25-hydroxyVitamin D in the United States: data from the Third National Health and Nutrition Examination Survey. Arch Intern Med. 2007 Jun 11;167(11):1159-65.
20.) McConnell JP, Foley KF, Vargas GM. HypoVitaminosis D: a new risk marker for cardiovascular disease. Clin Lab Sci. 2009 Fall;22(4):240-6.
21.) Mertens PR, Müller R. Vitamin D and cardiovascular risk. Int Urol Nephrol. 2009 Dec 29. [Epub ahead of print]
22.) Murlikiewicz K, Zawiasa A, Nowicki M. Vitamin D–a panacea in nephrology and beyond] Pol Merkur Lekarski. 2009 Nov;27(161):437-41.{article in Polish]
23.) Parker J, Hashmi O, Dutton D, Mavrodaris A, Stranges S, Kandala NB, Clarke A, Franco OH. Levels of Vitamin D and cardiometabolic disorders: systematic review and meta-analysis. Maturitas. 2010 Mar;65(3):225-36. Epub 2009 Dec 23.
24.) Pilz S, Dobnig H, Nijpels G, Heine RJ, Stehouwer CD, Snijder MB, van Dam RM, Dekker JM. Vitamin D and mortality in older men and women. Clin Endocrinol (Oxf). 2009 Nov;71(5):666-72. Epub 2009 Feb 18.
25.) Pilz S, März W, Wellnitz B, Seelhorst U, Fahrleitner-Pammer A, Dimai HP, Boehm BO, Dobnig H. Association of Vitamin D deficiency with heart failure and sudden cardiac death in a large cross-sectional study of patients referred for coronary angiography. J Clin Endocrinol Metab. 2008 Oct;93(10):3927-35. Epub 2008 Aug 5.
26.) Wu PW, Rhew EY, Dyer AR, Dunlop DD, Langman CB, Price H, Sutton-Tyrrell K, McPherson DD, Edmundowicz D, Kondos GT, Ramsey-Goldman R. 25-hydroxyVitamin D and cardiovascular risk factors in women with systemic lupus erythematosus. Arthritis Rheum. 2009 Oct 15;61(10):1387-95.
27.) Baz-Hecht M, Goldfine AB. The impact of Vitamin D deficiency on diabetes and cardiovascular risk. Curr Opin Endocrinol Diabetes Obes. 2010 Apr;17(2):113-9.
28.) Cheng S, Massaro JM, Fox CS, Larson MG, Keyes MJ, McCabe EL, Robins SJ, O’Donnell CJ, Hoffmann U, Jacques PF, Booth SL, Vasan RS, Wolf M, Wang TJ. Adiposity, cardiometabolic risk, and Vitamin D status: the Framingham Heart Study. Diabetes. 2010 Jan;59(1):242-8. Epub 2009 Oct 15.
29.) Holick MF. Sunlight and Vitamin D for bone health and prevention of autoimmune diseases, cancers, and cardiovascular disease. Am J Clin Nutr. 2004 Dec;80(6 Suppl):1678S-88S.
30.) Ginde AA, Scragg R, Schwartz RS, Camargo CA Jr. Prospective study of serum 25-hydroxyVitamin D level, cardiovascular disease mortality, and all-cause mortality in older U.S. adults. J Am Geriatr Soc. 2009 Sep;57(9):1595-603. Epub 2009 Jun 22.
31.) Grant WB. How strong is the evidence that solar ultraviolet B and Vitamin D reduce the risk of cancer?: An examination using Hill’s criteria for causality. Dermatoendocrinol. 2009 Jan;1(1):17-24.
32.) Holick MF, Chen TC. Vitamin D deficiency: a worldwide problem with health consequences. Am J Clin Nutr. 2008 Apr;87(4):1080S-6S.
33.) Holick MF. Vitamin D: its role in cancer prevention and treatment. Prog Biophys Mol Biol. 2006 Sep;92(1):49-59. Epub 2006 Mar 10.
34.) Ingraham BA, Bragdon B, Nohe A. Molecular basis of the potential of Vitamin D to prevent cancer. Curr Med Res Opin. 2008 Jan;24(1):139-49.
35.) Pilz S, Dobnig H, Winklhofer-Roob B, Riedmüller G, Fischer JE, Seelhorst U, Wellnitz B, Boehm BO, März W. Low serum levels of 25-hydroxyVitamin D predict fatal cancer in patients referred to coronary angiography. Cancer Epidemiol Biomarkers Prev. 2008 May;17(5):1228-33. Epub 2008 May 7.
36.) Pilz S, Tomaschitz A, Obermayer-Pietsch B, Dobnig H, Pieber TR. Epidemiology of Vitamin D insufficiency and cancer mortality. Anticancer Res. 2009 Sep;29(9):3699-704.
37.) Ginde AA, Mansbach JM, Camargo CA Jr. Association between serum 25-hydroxyVitamin D level and upper respiratory tract infection in the Third National Health and Nutrition Examination Survey. Arch Intern Med. 2009 Feb 23;169(4):384-90.
38.) Annweiler C, Schott AM, Allali G, Bridenbaugh SA, Kressig RW, Allain P, Herrmann FR, Beauchet O. Association of Vitamin D deficiency with cognitive impairment in older women: cross-sectional study. Neurology. 2010 Jan 5;74(1):27-32. Epub 2009 Sep 30.
39.) Cherniack EP, Troen BR, Florez HJ, Roos BA, Levis S. Some new food for thought: the role of Vitamin D in the mental health of older adults. Curr Psychiatry Rep. 2009 Feb;11(1):12-9.
40.) Wilkins CH, Sheline YI, Roe CM, Birge SJ, Morris JC. Vitamin D deficiency is associated with low mood and worse cognitive performance in older adults. Am J Geriatr Psychiatry. 2006 Dec;14(12):1032-40.
41.) Cutolo M, Otsa K. Review: Vitamin D, immunity and lupus. Lupus. 2008;17(1):6-10.
42.) Kamen DL, Cooper GS, Bouali H, Shaftman SR, Hollis BW, Gilkeson GS. Vitamin D deficiency in systemic lupus erythematosus. Autoimmun Rev. 2006 Feb;5(2):114-7. Epub 2005 Jun 21.
43.) Bischoff-Ferrari HA, Willett WC, Wong JB, Giovannucci E, Dietrich T, Dawson-Hughes B. Fracture prevention with Vitamin D supplementation: a meta-analysis of randomized controlled trials. JAMA. 2005 May 11;293(18):2257-64.
44.) Bischoff HA, Stähelin HB, Tyndall A, Theiler R. Relationship between muscle strength and Vitamin D metabolites: are there therapeutic possibilities in the elderly? Z Rheumatol. 2000;59 Suppl 1:39-41.
45.) DIPART (Vitamin D Individual Patient Analysis of Randomized Trials) Group. Patient level pooled analysis of 68 500 patients from seven major Vitamin D fracture trials in US and Europe. BMJ. 2010 Jan 12;340:b5463. doi: 10.1136/bmj.b5463.
46.) Houston DK, Cesari M, Ferrucci L, Cherubini A, Maggio D, Bartali B, Johnson MA, Schwartz GG, Kritchevsky SB. Association between Vitamin D status and physical performance: the InCHIANTI study. J Gerontol A Biol Sci Med Sci. 2007 Apr;62(4):440-6.
47.) Kwon J, Suzuki T, Yoshida H, Kim H, Yoshida Y, Iwasa H. Concomitant lower serum albumin and Vitamin D levels are associated with decreased objective physical performance among Japanese community-dwelling elderly. Gerontology. 2007;53(5):322-8. Epub 2007 May 29.
48.) Pfeifer M, Begerow B, Minne HW. Vitamin D and muscle function. Osteoporos Int. 2002 Mar;13(3):187-94.
49.) Judd SE, Nanes MS, Ziegler TR, Wilson PW, Tangpricha V. Optimal Vitamin D status attenuates the age-associated increase in systolic blood pressure in white Americans: results from the third National Health and Nutrition Examination Survey. Am J Clin Nutr. 2008 Jan;87(1):136-41.
50.) Pilz S, Dobnig H, Fischer JE, Wellnitz B, Seelhorst U, Boehm BO, März W. Low Vitamin d levels predict stroke in patients referred to coronary angiography. Stroke. 2008 Sep;39(9):2611-3. Epub 2008 Jul 17.
51.) Melamed ML, Michos ED, Post W, Astor B.25-hydroxyVitamin D levels and the risk of mortality in the general population. Arch Intern Med. 2008 Aug 11;168(15):1629-37.
52.) Jacobs ET, Alberts DS, Foote JA, Green SB, Hollis BW, Yu Z, Martínez ME. Vitamin D insufficiency in southern Arizona. Am J Clin Nutr. 2008 Mar;87(3):608-13.
53.) Park S, Johnson MA. Living in low-latitude regions in the United States does not prevent poor Vitamin D status. Nutr Rev. 2005 Jun;63(6 Pt 1):203-9.
54.) Low Vitamin D Levels Tied to Incontinence. WebMD March 22, 2010 http://www.webmd.com/urinary-incontinence-oab/news/20100322/low-Vitamin-d-linked-incontinence.
55.) The Vitamin D Council. Vitamin D Council
56.) Wikipedia: Vitamin D. Wikipedia Vitamine D
57.) Holick MF. Environmental factors thatinfluence the cutaneous production of Vitamin D. Am J Clin Nutr. 1995 Mar;61(3 Suppl):638S-645S.
58.) Vieth R. Vitamin D supplementation, 25-hydroxyVitamin D concentrations, and safety. Am J Clin Nutr. 1999 May;69(5):842-56.
59.) Holick MF. Vitamin D deficiency. N Engl J Med. 2007;357:266-281.
60.) GrassrootsHealth. Disease incidence prevention by serum 25(OH)D level.Grassroots Heaalth. Accessed May 8, 2009.
61.) Dall T, Anderson J. Vitamin D: merging research into clinical lipid practice. Lipid Spin. 2008;6(3):4-8.
62.) Heaney RP. What is a Vitamin D deficiency?Grassroots Health Vitamin D deficiency. Accessed May 8, 2009.

 

 

Potassium Iodide

Potassium Iodide (KI) Can Shield You From Thyroid Cancer

ARE YOU PREPARED FOR A RADIATION EMERGENCY?

With over 100 active commercial nuclear reactors in the United States, we live in constant threat of a nuclear emergency every day. A terrorist attack on any one of these facilities, or the release of a “dirty bomb” is also a possibility in today’s “highly charged” world. In fact, in an emergency, if you live within 200 miles of a nuclear reactor, you have a high risk of being exposed to significant doses of radioactive isotopes. In the event of a nuclear accident or attack radioactive materials can be released into the atmosphere, a high percentage of which is radioactive iodine. When a radioactive iodine cloud passes through a populated area, the radiation is concentrated into the thyroid gland of those exposed. The result is irreparable damage to the thyroid, which can lead to cancer. The 1986 Chernobyl accident in the Ukraine is a tragic example as is the Fukushima tragedy in Japan.

Even reactors in other countries can have adverse effects on people in the United States as prevailing winds can quickly spread the radioactive particulate matter from nuclear disasters.

The best protection against thyroid damage and thyroid cancer induced by radioactive iodine exposure is Potassium Iodide. This simple compound protects the thyroid by saturating all of the iodine binding sites in the gland, leaving no room for the binding of radioactive iodine. Potassium Iodide is a low-cost way to protect yourself and your family against the long-term consequences of exposure to radiation. When used correctly, potassium iodide tablets can prevent or reduce the amount of radioactive iodine taken up by the thyroid gland. Even the government and the military stocks up on potassium iodide in case of nuclear disaster.

The body can’t distinguish between radioactive and the benign version of iodine, which is necessary for thyroid function. Taking 130 mg of potassium iodide, the dosage widely recommended for the blocking of radioactive iodine in the event of a nuclear disaster, can quickly and completely protect the thyroid gland, which is one of the organs most commonly damaged by radioactive fallout.

It is important to remember that the precise dose of Potassium Iodide, whether it is 130mg or 125mg or 150mg (for a full-sized adult) is less critical than just simply offering the thyroid a good dose that will allow it to ignore the radioactive iodine that a person may have been exposed to.

Many Americans are cronically “undernourished” with iodine – iodine deficiency is common in North America. The FDA and CDC and other government agencies acknowledge this implicitly by recommending the use of Potassium Iodide in a radiation emergency since a thyroid gland that is not iodine deficient will not be prone to take up radioactive iodine.

Dr. Myatt’s Wellness Club offers a selection of supplements that contain potassium iodide.

Tablets are scored for easy breakage in the case of any need for exact or reduced dosages as recommended for children and pets.

How much do you need? The FDA recommends that you have one 130mg dose per person available for immediate use and up to 14 additional 130mg doses available for continuing use if needed.

Here is what the FDA recommends:

 What doses of potassium iodide (KI) should be taken for specific exposure levels?

Exposures greater than 5 cGy:
Birth through 1 mo.  – 16 mg.
1 mo. through 3 yrs.  – 32 mg.
3 yrs through 18 yrs.  – 65 mg. (Adolescents>150 pounds should take adult dose.)

Exposures greater than 10 cGy:
18 yrs through 40 yrs. – 130 mg

Exposures greater than 500 cGy:
Adults over 40 yrs – 130 mg.

7.  How long should potassium iodide (KI) be taken?

Since KI protects for approximately 24 hours, it should be dosed daily until the risk no longer exists.  Priority with regard to evacuation and sheltering should be given to pregnant females and neonates because of the potential for KI to suppress thyroid function in the fetus and neonate.  Unless other protective measures are not available, we do not recommend repeat dosing in pregnant females and neonates.

Remember that during an emergency, you may not be able to get to your home, thus it is recommended to have potassium iodide tablets stored in several places as well. Since the shelf life of this product is virtually unlimited, you should have to purchase your supply only once. Have this on hand for your family, and remember the children, pets, grandchildren, too!

Iodine for Radiation Protection

Iodoral – The Most Trusted Brand Of Natural Iodine

Iodoral (Iodine) For Healthy Thyroid FunctionIodoral® iodine tablets contain both iodine and iodide as the potassium salt. The preparation is absorbed into colloidal silica to prevent gastric irritation and specially coated with a thin film of pharmaceutical glaze to eliminate unpleasant taste.

Recommended Dose for daily use: 12.5 mg tablets – 1-2 tablets, 1-2 times per day as determined by iodine testing. A retest is suggested after 3 months. Best taken in the morning and afternoon to avoid nighttime stimulation.

Once whole body iodine sufficiency is achieved, Iodoral® maintenance dose is typically 1-4 tablets daily. People with thyroid disorders should work closely with their holistic physician or other health care professional.

NOTE: People with known iodine sensitivity should NOT use this product!

To make it easy to be prepared for a Radiation Emergency Dr. Myatt has Iodoral available:


Product # 309 Iodoral -90 tablets per bottle; 12.5mg iodine/iodide per tablet. $29.95


A More Convenient Product Is Also Available For Your Preparedness Kit:

Potassium Iodide Emergency Packs

Inexpensive protection – Click here to learn More.


Also Valuable for your Radiation Protection kit:

Modifilan (Laminaria japonica)

Thyroid and Immune Stimulant, Detoxification and Energizing Aid from the Sea

ModifilanThis “herb” (a variety of seaweed) might be the most important natural health discovery of the decade!

Modifilan was reportedly developed in Russia by scientists at the State Rehabilitation Institute, where victims of the Chernobyl nuclear catastrophe underwent treatment.

Hand-harvested from far Northern Pacific waters, Laminaria kelp has numerous health properties that set it apart from other species of seaweed.

Beneficial substances found in Modifilan include:

  • Organic iodine: Organic iodine feeds the thyroid gland, promoting normal metabolism and glandular function.
  • Fucoidan: a polysaccharide that promotes cancer cell death (apoptosis) and stimulates the immune system in animal studies. (1-4)
  • Laminarin: a polysaccharide that improves gut health in animal studies.(5)
  • Fucoxanthin: a natural pigment in the carotenoid family, is a potent antioxidant.(6-11)
  • Alginate: a natural polysaccharide that binds water and chelates radioactive toxins such as iodine-131 and strontium-90.(12-14)

Modifilan may be useful for:

  • Boosting the immune system with anti-viral and anti-cancer properties. (1-4, 15-21)
  • Helping lower blood sugar and cholesterol levels. (22-23)
  • Detoxifying the body from heavy metals, radioactive elements, free radicals and toxins.(12-14)
  • Aiding weight loss by improving thyroid, metabolism and GI-tract function.(24-25)
  • Helping smokers detoxify from heavy metals including strontium and cadmium.(12-14)

It takes 40 pounds or raw seaweed (conscientiously harvested to protect habitat) to make one pound of Modifilan.

Put some “pep in your step,” stimulate weight loss and energy while improving your immune system. This specially processed Laminaria is truly a unique gift from the sea.

Dr. Myatt’s Comment: Many of the “anti-cancer” and immune claims for Modifilan and other seaweed products have not yet been substantiated in humans. However, Modifilan is an excellent source of organic iodine and should be considered by anyone with low thyroid function.

Suggested dose:

For general health maintenance, 4-6 capsules per day.
For heavy metal chelation: 12 capsules per day.
For cancer: as directed by your physician (usually 6-12 capsules per day in divided doses).

#844 Modifilan (90 Caps) $29.97

Enter Quantity Desired and Click “Add To Cart” Button

References:

Potassium Iodide:

Food and Drug Administration (FDA) final Guidance on Potassium Iodide as a Thyroid Blocking Agent in Radiation Emergencies.

Food and Drug Administration (FDA) FAQ page on Potassium Iodide

Modifilan:

1.) Funahashi H, Imai T, Mase T, et al. Seaweed prevents breast cancer? Jpn J Cancer Res. 2001;92(5):483-487.
2.) Furusawa E, Furusawa S. Anticancer potential of Viva-Natural, a dietary seaweed extract, on Lewis lung carcinoma in comparison with chemical immunomodulators and on cyclosporine-accelerated AKR leukemia. Oncology. 1989;46(5):343-348.
3.) Itoh H, Noda H, Amano H, et al. Antitumor activity and immunological properties of marine algal polysaccharides, especially fucoidan, prepared from Sargassum thunbergii of Phaeophyceae. Anticancer Res. 1993;13(6A):2045-2052.
4.) Go H, Hwang HJ, Nam TJ. A glycoprotein from Laminaria japonica induces apoptosis in HT-29 colon cancer cells. Toxicol In Vitro. 2010 Sep;24(6):1546-53. Epub 2010 Jul 6.
5.) Lynch MB, Sweeney T, Callan JJ, O’Sullivan JT, O’Doherty JV. The effect of dietary Laminaria-derived laminarin and fucoidan on nutrient digestibility, nitrogen utilisation, intestinal microflora and volatile fatty acid concentration in pigs. J Sci Food Agric. 2010 Feb;90(3):430-7.
6.) Park PJ, Kim EK, Lee SJ, Park SY, Kang DS, Jung BM, Kim KS, Je JY, Ahn CB. Protective effects against H2O2-induced damage by enzymatic hydrolysates of an edible brown seaweed, sea tangle (Laminaria japonica). J Med Food. 2009 Feb;12(1):159-66.
7.) Wang J, Zhang Q, Zhang Z, Li Z. Antioxidant activity of sulfated polysaccharide fractions extracted from Laminaria japonica. Int J Biol Macromol. 2008 Mar 1;42(2):127-32. Epub 2007 Oct 9.
8.) Wang J, Wang F, Zhang Q, Zhang Z, Shi X, Li P. Synthesized different derivatives of low molecular fucoidan extracted from Laminaria japonica and their potential antioxidant activity in vitro. Int J Biol Macromol. 2009 Jun 1;44(5):379-84. Epub 2009 Feb 13.
9.) Wang J, Zhang Q, Zhang Z, Song H, Li P. Potential antioxidant and anticoagulant capacity of low molecular weight fucoidan fractions extracted from Laminaria japonica. Int J Biol Macromol. 2010 Jan 1;46(1):6-12. Epub 2009 Oct 31.
10.) Yan X, Chuda Y, Suzuki M, Nagata T. Fucoxanthin as the major antioxidant in Hijikia fusiformis, a common edible seaweed. Biosci Biotechnol Biochem 1999;63:605–7.
11.) Sachindra NM, Sato E, Maeda H, et al. Radical scavenging and singlet oxygen quenching activity of marine carotenoid fucoxanthin and its metabolites. J Agric Food Chem 2007;55:8516–22.
12.) Davis TA, Volesky B, Mucci A. A review of the biochemistry of heavy metal biosorption by brown algae. Water Res. 2003 Nov;37(18):4311-30.
13.) Sutton, A., Harrison, G. E., Carr, T. E., and Barltrop, D. Reduction in the absorption of dietary strontium in children by an alginate derivative. Br. J.Radiol. 44[523], 567. 1971.
14.) Sutton, A., Harrison, B. E., Carr, T. E., and Barltrop, D. Reduction in the absorption of dietary strontium in children by an alginate derivative. Int.J.Radiat.Biol.Relat Stud.Phys.Chem.Med. 19[1], 79-85. 1971
15.) [No authors listed][Production of cytokines by murine bone marrow dendritic cells in vitro mediated by sulfated polysaccharides obtained from sea brown algae].Zh Mikrobiol Epidemiol Immunobiol. 2010 Sep-Oct;(5):34-9. [Article in Russian]
16.) Damonte EB, Matulewicz MC, Cerezo AS. Sulfated seaweed polysaccharides as antiviral agents. Curr Med Chem. 2004 Sep;11(18):2399-419.
17.) Gerasimenko NI, Chaĭkina EL, Busarova NG, Anisimov MM. [Antimicrobic and hemolytic activity of low-molecular metabolits of brown seaweed Laminaria cichorioides Miyabe].Prikl Biokhim Mikrobiol. 2010 Jul-Aug;46(4):467-71. [Article in Russian]
18.) Ishikawa C, Tafuku S, Kadekaru T, Sawada S, Tomita M, Okudaira T, Nakazato T, Toda T, Uchihara JN, Taira N, Ohshiro K, Yasumoto T, Ohta T, Mori N. Anti-adult T-cell leukemia effects of brown algae fucoxanthin and its deacetylated product, fucoxanthinol. Int J Cancer. 2008 Dec 1;123(11):2702-12.
19.) Kim KN, Heo SJ, Kang SM, Ahn G, Jeon YJ. Fucoxanthin induces apoptosis in human leukemia HL-60 cells through a ROS-mediated Bcl-xL pathway. Toxicol In Vitro. 2010 Sep;24(6):1648-54. Epub 2010 Jun 8.
20.) Makarenkova ID, Deriabin PG, L’vov DK, Zviagintseva TN, Besednova NN. [Antiviral activity of sulfated polysaccharide from the brown algae Laminaria japonica against avian influenza A (H5N1) virus infection in the cultured cells]. Vopr Virusol. 2010 Jan-Feb;55(1):41-5. [Article in Russian].
21.) Yamamoto K, Ishikawa C, Katano H, Yasumoto T, Mori N. Fucoxanthin and its deacetylated product, fucoxanthinol, induce apoptosis of primary effusion lymphomas. Cancer Lett. 2010 Nov 13. [Epub ahead of print]
22.) Bu T, Liu M, Zheng L, Guo Y, Lin X. α-Glucosidase inhibition and the in vivo hypoglycemic effect of butyl-isobutyl-phthalate derived from the Laminaria japonica rhizoid. Phytother Res. 2010 Nov;24(11):1588-91. doi: 10.1002/ptr.3139.
23.) Woo MN, Jeon SM, Kim HJ, Lee MK, Shin SK, Shin YC, Park YB, Choi MS. Fucoxanthin supplementation improves plasma and hepatic lipid metabolism and blood glucose concentration in high-fat fed C57BL/6N mice. Chem Biol Interact. 2010 Aug 5;186(3):316-22. Epub 2010 May 16.
24.) Woo MN, Jeon SM, Shin YC, Lee MK, Kang MA, Choi MS. Anti-obese property of fucoxanthin is partly mediated by altering lipid-regulating enzymes and uncoupling proteins of visceral adipose tissue in mice. Mol Nutr Food Res. 2009 Dec;53(12):1603-11.
25.) You JS, Sung MJ, Chang KJ. Evaluation of 8-week body weight control program including sea tangle (Laminaria japonica) supplementation in Korean female college students. Nutr Res Pract. 2009 Winter;3(4):307-14. Epub 2009 Dec 31.

LugoTab / Iodoral 12.5mg – 90 tablets

 

Potassium Iodide (KI) Can Shield You From Thyroid Cancer

ARE YOU PREPARED FOR A RADIATION EMERGENCY?

With over 100 active commercial nuclear reactors in the United States, we live in constant threat of a nuclear emergency every day. A terrorist attack on any one of these facilities, or the release of a “dirty bomb” is also a possibility in today’s “highly charged” world. In fact, in an emergency, if you live within 200 miles of a nuclear reactor, you have a high risk of being exposed to significant doses of radioactive isotopes. In the event of a nuclear accident or attack radioactive materials can be released into the atmosphere, a high percentage of which is radioactive iodine. When a radioactive iodine cloud passes through a populated area, the radiation is concentrated into the thyroid gland of those exposed. The result is irreparable damage to the thyroid, which can lead to cancer. The 1986 Chernobyl accident in the Ukraine is a tragic example as is the Fukushima tragedy in Japan.

Even reactors in other countries can have adverse effects on people in the United States as prevailing winds can quickly spread the radioactive particulate matter from nuclear disasters.

The best protection against thyroid damage and thyroid cancer induced by radioactive iodine exposure is Potassium Iodide. This simple compound protects the thyroid by saturating all of the iodine binding sites in the gland, leaving no room for the binding of radioactive iodine. Potassium Iodide is a low-cost way to protect yourself and your family against the long-term consequences of exposure to radiation. When used correctly, potassium iodide tablets can prevent or reduce the amount of radioactive iodine taken up by the thyroid gland. Even the government and the military stocks up on potassium iodide in case of nuclear disaster.

The body can’t distinguish between radioactive and the benign version of iodine, which is necessary for thyroid function. Taking 130 mg of potassium iodide, the dosage widely recommended for the blocking of radioactive iodine in the event of a nuclear disaster, can quickly and completely protect the thyroid gland, which is one of the organs most commonly damaged by radioactive fallout.

It is important to remember that the precise dose of Potassium Iodide, whether it is 130mg or 125mg or 150mg (for a full-sized adult) is less critical than just simply offering the thyroid a good dose that will allow it to ignore the radioactive iodine that a person may have been exposed to.

Many Americans are cronically “undernourished” with iodine – iodine deficiency is common in North America. The FDA and CDC and other government agencies acknowledge this implicitly by recommending the use of Potassium Iodide in a radiation emergency since a thyroid gland that is not iodine deficient will not be prone to take up radioactive iodine.

Dr. Myatt’s Wellness Club offers a selection of supplements that contain potassium iodide.

Tablets are scored for easy breakage in the case of any need for exact or reduced dosages as recommended for children and pets.

How much do you need? The FDA recommends that you have one 130mg dose per person available for immediate use and up to 14 additional 130mg doses available for continuing use if needed.

Here is what the FDA recommends:

 What doses of potassium iodide (KI) should be taken for specific exposure levels?

Exposures greater than 5 cGy:
Birth through 1 mo.  – 16 mg.
1 mo. through 3 yrs.  – 32 mg.
3 yrs through 18 yrs.  – 65 mg. (Adolescents>150 pounds should take adult dose.)

Exposures greater than 10 cGy:
18 yrs through 40 yrs. – 130 mg

Exposures greater than 500 cGy:
Adults over 40 yrs – 130 mg.

7.  How long should potassium iodide (KI) be taken?

Since KI protects for approximately 24 hours, it should be dosed daily until the risk no longer exists.  Priority with regard to evacuation and sheltering should be given to pregnant females and neonates because of the potential for KI to suppress thyroid function in the fetus and neonate.  Unless other protective measures are not available, we do not recommend repeat dosing in pregnant females and neonates.

Remember that during an emergency, you may not be able to get to your home, thus it is recommended to have potassium iodide tablets stored in several places as well. Since the shelf life of this product is virtually unlimited, you should have to purchase your supply only once. Have this on hand for your family, and remember the children, pets, grandchildren, too!

Iodoral – The Most Trusted Brand Of Natural Iodine

Iodoral® iodine tablets contain both iodine and iodide as the potassium salt. The preparation is absorbed into colloidal silica to prevent gastric irritation and specially coated with a thin film of pharmaceutical glaze to eliminate unpleasant taste.

Recommended Dose for daily use: 12.5 mg tablets – 1-2 tablets, 1-2 times per day as determined by iodine testing. A retest is suggested after 3 months. Best taken in the morning and afternoon to avoid nighttime stimulation.

Once whole body iodine sufficiency is achieved, Iodoral® maintenance dose is typically 1-4 tablets daily. People with thyroid disorders should work closely with their holistic physician or other health care professional.

NOTE: People with known iodine sensitivity should NOT use this product!

To make it easy to be prepared for a Radiation Emergency Dr. Myatt has 2 sizes of Iodoral available:


Product # 309 Iodoral -90 tablets per bottle; 12.5mg iodine/iodide per tablet. $29.95

Enter Quantity Desired and Click “Add To Cart” Button


Product # N336 Iodoral -30 tablets per bottle; 50mg iodine/iodide per tablet. $36.95

Enter Quantity Desired and Click “Add To Cart” Button


A More Convenient Product Is Also Available For Your Preparedness Kit:

Inexpensive protection – Click here to learn More.


Also Valuable for your Radiation Protection kit:

Modifilan (Laminaria japonica)

Thyroid and Immune Stimulant, Detoxification and Energizing Aid from the Sea

This “herb” (a variety of seaweed) might be the most important natural health discovery of the decade!

Modifilan was reportedly developed in Russia by scientists at the State Rehabilitation Institute, where victims of the Chernobyl nuclear catastrophe underwent treatment.

Hand-harvested from far Northern Pacific waters, Laminaria kelp has numerous health properties that set it apart from other species of seaweed.

Beneficial substances found in Modifilan include:

  • Organic iodine: Organic iodine feeds the thyroid gland, promoting normal metabolism and glandular function.
  • Fucoidan: a polysaccharide that promotes cancer cell death (apoptosis) and stimulates the immune system in animal studies. (1-4)
  • Laminarin: a polysaccharide that improves gut health in animal studies.(5)
  • Fucoxanthin: a natural pigment in the carotenoid family, is a potent antioxidant.(6-11)
  • Alginate: a natural polysaccharide that binds water and chelates radioactive toxins such as iodine-131 and strontium-90.(12-14)

Modifilan may be useful for:

  • Boosting the immune system with anti-viral and anti-cancer properties. (1-4, 15-21)
  • Helping lower blood sugar and cholesterol levels. (22-23)
  • Detoxifying the body from heavy metals, radioactive elements, free radicals and toxins.(12-14)
  • Aiding weight loss by improving thyroid, metabolism and GI-tract function.(24-25)
  • Helping smokers detoxify from heavy metals including strontium and cadmium.(12-14)

It takes 40 pounds or raw seaweed (conscientiously harvested to protect habitat) to make one pound of Modifilan.

Put some “pep in your step,” stimulate weight loss and energy while improving your immune system. This specially processed Laminaria is truly a unique gift from the sea.

Dr. Myatt’s Comment: Many of the “anti-cancer” and immune claims for Modifilan and other seaweed products have not yet been substantiated in humans. However, Modifilan is an excellent source of organic iodine and should be considered by anyone with low thyroid function.

Suggested dose:

For general health maintenance, 4-6 capsules per day.
For heavy metal chelation: 12 capsules per day.
For cancer: as directed by your physician (usually 6-12 capsules per day in divided doses).

#844 Modifilan (90 Caps) $29.97

Enter Quantity Desired and Click “Add To Cart” Button

References:

Potassium Iodide:

Food and Drug Administration (FDA) final Guidance on Potassium Iodide as a Thyroid Blocking Agent in Radiation Emergencies.

Food and Drug Administration (FDA) FAQ page on Potassium Iodide

Modifilan:

1.) Funahashi H, Imai T, Mase T, et al. Seaweed prevents breast cancer? Jpn J Cancer Res. 2001;92(5):483-487.
2.) Furusawa E, Furusawa S. Anticancer potential of Viva-Natural, a dietary seaweed extract, on Lewis lung carcinoma in comparison with chemical immunomodulators and on cyclosporine-accelerated AKR leukemia. Oncology. 1989;46(5):343-348.
3.) Itoh H, Noda H, Amano H, et al. Antitumor activity and immunological properties of marine algal polysaccharides, especially fucoidan, prepared from Sargassum thunbergii of Phaeophyceae. Anticancer Res. 1993;13(6A):2045-2052.
4.) Go H, Hwang HJ, Nam TJ. A glycoprotein from Laminaria japonica induces apoptosis in HT-29 colon cancer cells. Toxicol In Vitro. 2010 Sep;24(6):1546-53. Epub 2010 Jul 6.
5.) Lynch MB, Sweeney T, Callan JJ, O’Sullivan JT, O’Doherty JV. The effect of dietary Laminaria-derived laminarin and fucoidan on nutrient digestibility, nitrogen utilisation, intestinal microflora and volatile fatty acid concentration in pigs. J Sci Food Agric. 2010 Feb;90(3):430-7.
6.) Park PJ, Kim EK, Lee SJ, Park SY, Kang DS, Jung BM, Kim KS, Je JY, Ahn CB. Protective effects against H2O2-induced damage by enzymatic hydrolysates of an edible brown seaweed, sea tangle (Laminaria japonica). J Med Food. 2009 Feb;12(1):159-66.
7.) Wang J, Zhang Q, Zhang Z, Li Z. Antioxidant activity of sulfated polysaccharide fractions extracted from Laminaria japonica. Int J Biol Macromol. 2008 Mar 1;42(2):127-32. Epub 2007 Oct 9.
8.) Wang J, Wang F, Zhang Q, Zhang Z, Shi X, Li P. Synthesized different derivatives of low molecular fucoidan extracted from Laminaria japonica and their potential antioxidant activity in vitro. Int J Biol Macromol. 2009 Jun 1;44(5):379-84. Epub 2009 Feb 13.
9.) Wang J, Zhang Q, Zhang Z, Song H, Li P. Potential antioxidant and anticoagulant capacity of low molecular weight fucoidan fractions extracted from Laminaria japonica. Int J Biol Macromol. 2010 Jan 1;46(1):6-12. Epub 2009 Oct 31.
10.) Yan X, Chuda Y, Suzuki M, Nagata T. Fucoxanthin as the major antioxidant in Hijikia fusiformis, a common edible seaweed. Biosci Biotechnol Biochem 1999;63:605–7.
11.) Sachindra NM, Sato E, Maeda H, et al. Radical scavenging and singlet oxygen quenching activity of marine carotenoid fucoxanthin and its metabolites. J Agric Food Chem 2007;55:8516–22.
12.) Davis TA, Volesky B, Mucci A. A review of the biochemistry of heavy metal biosorption by brown algae. Water Res. 2003 Nov;37(18):4311-30.
13.) Sutton, A., Harrison, G. E., Carr, T. E., and Barltrop, D. Reduction in the absorption of dietary strontium in children by an alginate derivative. Br. J.Radiol. 44[523], 567. 1971.
14.) Sutton, A., Harrison, B. E., Carr, T. E., and Barltrop, D. Reduction in the absorption of dietary strontium in children by an alginate derivative. Int.J.Radiat.Biol.Relat Stud.Phys.Chem.Med. 19[1], 79-85. 1971
15.) [No authors listed][Production of cytokines by murine bone marrow dendritic cells in vitro mediated by sulfated polysaccharides obtained from sea brown algae].Zh Mikrobiol Epidemiol Immunobiol. 2010 Sep-Oct;(5):34-9. [Article in Russian]
16.) Damonte EB, Matulewicz MC, Cerezo AS. Sulfated seaweed polysaccharides as antiviral agents. Curr Med Chem. 2004 Sep;11(18):2399-419.
17.) Gerasimenko NI, Chaĭkina EL, Busarova NG, Anisimov MM. [Antimicrobic and hemolytic activity of low-molecular metabolits of brown seaweed Laminaria cichorioides Miyabe].Prikl Biokhim Mikrobiol. 2010 Jul-Aug;46(4):467-71. [Article in Russian]
18.) Ishikawa C, Tafuku S, Kadekaru T, Sawada S, Tomita M, Okudaira T, Nakazato T, Toda T, Uchihara JN, Taira N, Ohshiro K, Yasumoto T, Ohta T, Mori N. Anti-adult T-cell leukemia effects of brown algae fucoxanthin and its deacetylated product, fucoxanthinol. Int J Cancer. 2008 Dec 1;123(11):2702-12.
19.) Kim KN, Heo SJ, Kang SM, Ahn G, Jeon YJ. Fucoxanthin induces apoptosis in human leukemia HL-60 cells through a ROS-mediated Bcl-xL pathway. Toxicol In Vitro. 2010 Sep;24(6):1648-54. Epub 2010 Jun 8.
20.) Makarenkova ID, Deriabin PG, L’vov DK, Zviagintseva TN, Besednova NN. [Antiviral activity of sulfated polysaccharide from the brown algae Laminaria japonica against avian influenza A (H5N1) virus infection in the cultured cells]. Vopr Virusol. 2010 Jan-Feb;55(1):41-5. [Article in Russian].
21.) Yamamoto K, Ishikawa C, Katano H, Yasumoto T, Mori N. Fucoxanthin and its deacetylated product, fucoxanthinol, induce apoptosis of primary effusion lymphomas. Cancer Lett. 2010 Nov 13. [Epub ahead of print]
22.) Bu T, Liu M, Zheng L, Guo Y, Lin X. α-Glucosidase inhibition and the in vivo hypoglycemic effect of butyl-isobutyl-phthalate derived from the Laminaria japonica rhizoid. Phytother Res. 2010 Nov;24(11):1588-91. doi: 10.1002/ptr.3139.
23.) Woo MN, Jeon SM, Kim HJ, Lee MK, Shin SK, Shin YC, Park YB, Choi MS. Fucoxanthin supplementation improves plasma and hepatic lipid metabolism and blood glucose concentration in high-fat fed C57BL/6N mice. Chem Biol Interact. 2010 Aug 5;186(3):316-22. Epub 2010 May 16.
24.) Woo MN, Jeon SM, Shin YC, Lee MK, Kang MA, Choi MS. Anti-obese property of fucoxanthin is partly mediated by altering lipid-regulating enzymes and uncoupling proteins of visceral adipose tissue in mice. Mol Nutr Food Res. 2009 Dec;53(12):1603-11.
25.) You JS, Sung MJ, Chang KJ. Evaluation of 8-week body weight control program including sea tangle (Laminaria japonica) supplementation in Korean female college students. Nutr Res Pract. 2009 Winter;3(4):307-14. Epub 2009 Dec 31.