HealthBeat News

Are Your Supplements Safe? What You Should Know

So, why all the fuss? Why are our Senators getting involved? Are supplements really safe after all? How can you be sure that the supplements you are taking are safe and of good quality? “The dietary supplement market is the wild west” says California Democratic Congressman Henry Waxman. He’s right – Dr. Myatt has known this for a decade, and she has worked tirelessly to bring you the very best products through The Wellness Club.

Dietary and herbal supplements have been used safely for thousands of years. But make no mistake, they are as potent as any drug, and must be used with care. Some can have adverse interactions with medications or other herbs, some can cause adverse effects in the presence of certain medical conditions. Some concoctions can be downright dangerous.

Many supplements may not be all that they claim to be. The popular supplement Glucosamine Sulfate, used to stimulate joint repair and to relieve pain is a perfect example. It is a combination of Glucosamine which stimulates the production of glycosaminoglycans (GAG’s) which are the main structural material of our joints, and elemental Sulfate which is a carrier molecule for Glucosamine and which stimulates the production of joint substances (GAG’s) in it’s own right. When it is bound to Glucosamine, Sulfate acts to carry the Glucosamine molecule into the joint and it helps to activate joint substance production. But here is the rub. There is only one manufacturer that produces Glucosamine Sulfate that is molecularly bound together. This is so important that they have a patent on it. Other manufacturers throw glucosamine and sulfate together in the same capsule and tout it’s benefits based on the research done on molecularly bound Glucosamine Sulfate but it just isn’t the same. Dr. Myatt’s Wellness Club is one of the very few places where you can get the “good stuff” – the molecularly bound product. There are lots of other scams like this out there – poor quality or ineffective supplements, often sold at big prices. Other supplement concoctions claim to have amazing effects (like growing certain body parts “larger” or ending menopause symptoms) but contain only trace amounts of effective active ingredients – “fairy dust” we call them.

How do you protect yourself?

First, Be sure they are safe for you. Don’t take supplements based solely on advertising claims you see in magazines, tabloids, the internet, TV, or elsewhere. Don’t believe that what is good for your friend must be good for you too. A few minutes spent talking with a naturopathic doctor (not the clerk or salesperson in the health food store!) could save you a lot of grief. Secondly, be sure you are buying quality supplements. Don’t take the word of the clerk or salesperson – do the research, or let your holistic medical practitioner do it for you. If it looks like too good a deal, it probably is. When was quality ever cheap? Those supplements on sale for such a low price at your local superstore may have been sloppily manufactured, improperly shipped or stored (most supplements must be kept in carefully temperature controlled conditions), may contain impurities, or may just be old stock. There is usually a good reason for a really low price. Why risk it? Finally, if you have a medical condition or are taking any medications, you really must be in a good cooperative relationship with both your regular doctor and with your holistic health provider and / or Naturopathic Doctor. Only that way can you protect yourself from shoddy or unneeded products and potentially harmful side effects or interactions.


Hot Flashes:

Miracle beverage lowers cholesterol, blocks cancer, fights heart disease, and more!

A nice cup of Oriental Green Tea can be a delicious, relaxing, soothing break in your day. But more than that, recent research is pointing out other benefits as well. A recent article in the Archives of Internal Medicine found that enriched green tea extract may be effective in reducing low-density lipoprotein cholesterol (LDL-C). Subjects in a treatment study group showed decreases of 6.7% in total cholesterol and 9.6% in LDL-C after only 4 weeks of supplementation, and reductions of 11.3% and 16.4% after 12 weeks! Another study, done at the Linus Pauling Institute at Oregon State University and reported in the journal Carcinogenesis showed that green tea may be useful in the prevention of intestinal (colon) cancer in humans. Yet other studies show it useful in the prevention of heart disease, and there are studies suggesting it may be a potent antiviral, effective in combating HIV. It is further thought to have antimicrobial powers. What is so special about green tea? It is a rich source of catechins – flavinoid phytochemical compounds and polyphenols. Both are potent antioxidants, helping to prevent the damaging effects of free radicals.

Nurse Mark’s comment: Both Dr. Dana and I make green tea a part of our day. Traditional flavors are fine, and newer flavors such as fruit or spice offer a nice change. It is a great pick-me-up, and green tea is thought to have thermogenic properties, helping us to burn fat. There really is no down side, unless you just don’t like the taste of it, in which case you can obtain the benefits of green tea in capsule form as green tea extract capsules from the Wellness Club. Either way, you really owe it to yourself to make this simple, relaxing, and delicious addition to your daily wellness protocol.

N-Acetyl Cysteine (NAC) 60 caps

N-Acetyl Cysteine (NAC)Potent Antioxidant, Glutathione Precursor and Mucolytic

NAC (N-acetyl cysteine) is a form of the amino acid cysteine which is found in food and is also made by the body. NAC is a:

  • precursor to glutathione, a powerful antioxidant (1-8)
  • potent free-radical scavenger (9-15)
  • “mucolytic” (mucous-dissolving) agent (16-18)

NAC is used in conventional medicine to treat acetaminophen overdose, chronic bronchitis and COPD.

Uses of NAC include:

  • Chronic bronchitis – NAC is a safe and effective treatment to reduce the thickness of mucous.(16-18) A review of 39 clinical trials found the number of aggravations of chronic bronchitis was reduced in 50% of people who took NAC at a dose of 400-600mg per day. (19)
  • COPD – NAC supplies antioxidant protection to the lung and helps break down thick mucous, making it useful in Chronic Obstructive Pulmonary Disease (COPD). NAC was ineffective for COPD in patients taking steroids. (9,14-16)
  • Parkinson’s disease – NAC decreases the negative side effects of Levodopa and also decreases free radical production. (7, 20)
  • Infertility – as an adjuvant to clomiphene citrate in infertile patients with PCOS, NAC treatment results in higher ovulation and pregnancy rates, lower miscarriage rates and higher live birth rates. (21-24)
  • Kidney failure / hemodialysis. NAC improved residual renal function in patients on dialysis in a pilot study. (25)
  • IBS (Irritable Bowel Syndrome) – one study showed that NAC reduced inflammation and inflammatory cytokines in the small intestine. (26)
  • Liver Protection. Studies have found that NAC prevents liver damage due to environmental toxins, anaesthesia and elevated cholesterol levels.(12, 27)
  • Lupus – a pilot study shows that NAC may be helpful in lupus by blocking mTOR in T lymphocytes.(28)
  • Melanoma prevention. NAC reduces oxidative stress caused by UV-radiation.(29)
  • Schizophrenia and Bipolar Disorder. Both diseases are associated with glutathione depletion. Adding NAC to drug treatment improved depression in bipolar patients and overall symptoms in schizophrenic patients. (1-3,6)
  • Sickle Cell Anemia – NAC may decrease sickle cell crises. (10)
  • Cancer Prevention. (30)

Typical doses used for COPD, bronchitis and respiratory mucous are 600mg per day. Other studies have used 600-4,800 mg per day in divided doses. Most studies use 600-1,200mg per day. Rare side effects include nausea, usually only seen at the highest doses.

Suggested dose:
1 cap, 1-2 times per day or as directed by a physician.

Each (one) capsule contains:
NAC (N-Acetyl L-Cysteine) …………………. 600 mg

Other ingredients:
gelatin capsule (gelatin and water) and rice flour.

References

1.) Berk M, Copolov DL, Dean O, Lu K, Jeavons S, Schapkaitz I, Anderson-Hunt M, Bush AI.
N-acetyl cysteine for depressive symptoms in bipolar disorder–a double-blind randomized  placebo-controlled trial. Biol Psychiatry. 2008 Sep 15;64(6):468-75. Epub 2008 Jun 5.

2.) Berk M, Copolov D, Dean O, Lu K, Jeavons S, Schapkaitz I, et al. N-acetyl cysteine as a glutathione  precursor for schizophrenia–a double-blind, randomized, placebo-controlled trial. Biol Psychiatry.  2008 Sep 1;64(5):361-8. Epub 2008 Apr 23.

3.) Carmeli C, Knyazeva MG, Cuénod M, Do KQ. Glutathione precursor N-acetyl-cysteine modulates  EEG synchronization in schizophrenia patients: a double-blind, randomized, placebo-controlled trial. PLoS One. 2012;7(2):e29341. Epub 2012 Feb 22.

4.) Crinnion WJ. Do environmental toxicants contribute to allergy and asthma? Altern Med Rev. 2012 Mar;17(1):6-18.

5.) Krifka S, Hiller KA, Spagnuolo G, Jewett A, Schmalz G, Schweikl H. The influence of glutathione on  redox regulation by antioxidant proteins and apoptosis in macrophages exposed to 2-hydroxyethyl  methacrylate (HEMA). Biomaterials. 2012 Jul;33(21):5177-86. Epub 2012 Apr 24.

6.) Lavoie S, Murray MM, Deppen P, Knyazeva MG, et al. Glutathione precursor, N-acetyl-cysteine,  improves mismatch negativity in schizophrenia patients. Neuropsychopharmacology. 2008  Aug;33(9):2187-99. Epub 2007 Nov 14.

7.) Sun L, Gu L, Wang S, Yuan J, Yang H, Zhu J, Zhang H. N-acetylcysteine protects against apoptosis  through modulation of group I metabotropic glutamate receptor activity. PLoS One.  2012;7(3):e32503. Epub 2012 Mar 19.

8.) Fishman AI, Alexander B, Eshghi M, Choudhury M, Konno S. Nephrotoxin-induced renal cell injury  involving biochemical alterations and its prevention with antioxidant. J Clin Med Res. 2012  Apr;4(2):95-101. Epub 2012 Mar 23.

9.) Kao SJ, Wang D, Lin HI, Chen HI. N-acetylcysteine abrogates acute lung injury induced by endotoxin. Clin Exp Pharmacol Physiol. 2006 Jan-Feb;33(1-2):33-40.

10.) Nur E, Brandjes DP, Teerlink T, Otten HM, Oude Elferink RP, Muskiet F, Evers LM, Ten Cate H,  Biemond BJ, Duits AJ, Schnog JJ. N-acetylcysteine reduces oxidative stress in sickle cell patients. Ann Hematol. 2012 Feb 10. [Epub ahead of print]

11.) Faruqi RM, Poptic EJ, Faruqi TR, De La Motte C, DiCorleto PE. Distinct mechanisms for  N-acetylcysteine inhibition of cytokine-induced E-selectin and VCAM-1 expression.  Am J Physiol.1997 Aug;273 (2 Pt ):H817-26.

12.) Galicia-Moreno M, Favari L, Muriel P. Antifibrotic and antioxidant effects of N-acetylcysteine in an  experimental cholestatic model. Eur J Gastroenterol Hepatol. 2012 Feb;24(2):179-85.

13.) Koksel O, Ozdulger A, Ercil M, Tamer L, Ercan B, Atik U, Cinel L, Cinel I, Kanik A.
Effects of N-acetylcysteine on oxidant-antioxidant balance in oleic acid-induced lung injury.
Exp Lung Res. 2004 Sep;30(6):431-46.

14.) Akca T, Canbaz H, Tataroglu C, Caglikulekci M, Tamer L, Colak T, Kanik A, Bilgin O, Aydin S.
The effect of N-acetylcysteine on pulmonary lipid peroxidation and tissue damage. J Surg Res. 2005  Nov;129(1):38-45.

15.) Foschino Barbaro MP, Serviddio G, Resta O, Rollo T, Tamborra R, Elisiana Carpagnano G,  Vendemiale G, Altomare E. Oxygen therapy at low flow causes oxidative stress in chronic  obstructive pulmonary disease: Prevention by N-acetyl cysteine. Free Radic Res. 2005  Oct;39(10):1111-8.

16.) Sadowska AM. N-Acetylcysteine mucolysis in the management of chronic obstructive pulmonary disease. Ther Adv Respir Dis. 2012 Jun;6(3):127-35. Epub 2012 Feb 23.

17.) Jackson IM, Barnes J, Cooksey P. Efficacy and tolerability of oral acetylcysteine (Fabrol) in chronic bronchitis: a double-blind placebo controlled study. J Int Med Res 1984;12:198–206.

18.) Tattersall AB, Bridgman KM, Huitson A. Acetylcysteine (Fabrol) in chronic bronchitis—a study in general practice. J Int Med Res 1983;11:279–84.

19.) Stey C, Steurer J, Bachmann S, et al. The effect of oral N-acetylcysteine in chronic bronchitis: a quantitative systematic review. Eur Respir J 2000;16:253–62 [review].

20.) Martínez-Banaclocha MA. N-acetyl-cysteine in the treatment of Parkinson’s disease. What are we  waiting for? Med Hypotheses. 2012 Apr 28. [Epub ahead of print]

21.) Badawy A, State O, Abdelgawad S.N-Acetyl cysteine and clomiphene citrate for induction of  ovulation in polycystic ovary syndrome: a cross-over trial. Acta Obstet Gynecol Scand.  2007;86(2):218-22.

22.) Nasr A. Effect of N-acetyl-cysteine after ovarian drilling in clomiphene citrate-resistant PCOS  women: a pilot study. Reprod Biomed Online. 2010 Mar;20(3):403-9. Epub 2009 Dec 14.

23.) Rizk AY, Bedaiwy MA, Al-Inany HG. N-acetyl-cysteine is a novel adjuvant to clomiphene citrate in  clomiphene citrate-resistant patients with polycystic ovary syndrome. Fertil Steril. 2005  Feb;83(2):367-70.

24.) Salehpour S, Akbari Sene A, Saharkhiz N, Sohrabi MR, Moghimian F. N-acetylcysteine as an  adjuvant to clomiphene citrate for successful induction of ovulation in infertile patients with polycystic  ovary syndrome. J Obstet Gynaecol Res. 2012 Apr 30. doi: 10.1111/j.1447-0756.2012.01844.x.  [Epub ahead of print]

25.) Feldman L, Shani M, Sinuani I, Beberashvili I, Weissgarten J. N-acetylcysteine may improve residual  renal function in hemodialysis patients: A pilot study. Hemodial Int. 2012 Apr 30. doi:  10.1111/j.1542-4758.2012.00702.x. [Epub ahead of print]

26.) Hou Y, Wang L, Yi D, Ding B, Yang Z, Li J, Chen X, Qiu Y, Wu G. N-acetylcysteine reduces  inflammation in the small intestine by regulating redox, EGF and TLR4 signaling. Amino Acids. 2012 Apr 25. [Epub ahead of print]

27.) Beyaz SG, Yelken B, Kanbak G. The effects of N-acetylcysteine on hepatic function during  isoflurane anaesthesia for laparoscopic surgery patients. Indian J Anaesth. 2011 Nov;55(6):567-72.

28.) Lai ZW, Hanczko R, Bonilla E, Caza TN, Clair B, Bartos A, et al. N-acetylcysteine reduces disease  activity by blocking mTOR in T cells of lupus patients. Arthritis Rheum. 2012 May 1. doi:  10.1002/art.34502. [Epub ahead of print]

29.) Goodson AG, Cotter MA, Cassidy P, Wade M, Florell SR, Liu T, Boucher KM, Grossman D.
Use of oral N-acetylcysteine for protection of melanocytic nevi against UV-induced oxidative stress:  towards a novel paradigm for melanoma chemoprevention. Clin Cancer Res. 2009 Dec  1;15(23):7434-40. Epub 2009 Nov 17.

30.) Mates JM, Segura JA, Alonso FJ, Marquez J. Sulphur-containing non enzymatic antioxidants:  therapeutic tools against cancer. Front Biosci (Schol Ed). 2012 Jan 1;4:722-48.

Fertility Restore Acetyl L-Carnitine 500mg (30 Caps)

N-Acetyl Cysteine (NAC)

Potent Antioxidant, Glutathione Precursor and Mucolytic

NAC (N-acetyl cysteine) is a form of the amino acid cysteine which is found in food and is also made by the body. NAC is a:

  • precursor to glutathione, a powerful antioxidant (1-8)
  • potent free-radical scavenger (9-15)
  • “mucolytic” (mucous-dissolving) agent (16-18)

NAC is used in conventional medicine to treat acetaminophen overdose, chronic bronchitis and COPD.

Uses of NAC include:

  • Chronic bronchitis – NAC is a safe and effective treatment to reduce the thickness of mucous.(16-18) A review of 39 clinical trials found the number of aggravations of chronic bronchitis was reduced in 50% of people who took NAC at a dose of 400-600mg per day.(19)
  • COPD – NAC supplies antioxidant protection to the lung and helps break down thick mucous, making it useful in Chronic Obstructive Pulmonary Disease (COPD). NAC was ineffective for COPD in patients taking steroids. (9,14-16)
  • Parkinson’s disease – NAC decreases the negative side effects of Levodopa and also decreases free radical production. (7, 20)
  • Infertility – as an adjuvant to clomiphene citrate in infertile patients with PCOS, NAC treatment results in higher ovulation and pregnancy rates, lower miscarriage rates and higher live birth rates. (21-24)
  • Kidney failure / hemodialysis. NAC improved residual renal function in patients on dialysis in a pilot study. (25)
  • IBS (Irritable Bowel Syndrome) – one study showed that NAC reduced inflammation and inflammatory cytokines in the small intestine. (26)
  • Liver Protection. Studies have found that NAC prevents liver damage due to environmental toxins, anaesthesia and elevated cholesterol levels.(12, 27)
  • Lupus – a pilot study shows that NAC may be helpful in lupus by blocking mTOR in T lymphocytes.(28)
  • Melanoma prevention. NAC reduces oxidative stress caused by UV-radiation.(29)
  • Schizophrenia and Bipolar Disorder. Both diseases are associated with glutathione depletion. Adding NAC to drug treatment improved depression in bipolar patients and overall symptoms in schizophrenic patients. (1-3,6)
  • Sickle Cell Anemia – NAC may decrease sickle cell crisies. (10)
  • Cancer Prevention. (30)

Typical doses used for COPD, bronchitis and respiratory mucous are 600mg per day. Other studies have used 600-4,800 mg per day in divided doses. Most studies use 600-1,200mg per day. Rare side effects include nausea, usually only seen at the highest doses.

Suggested dose:
1 cap, 1-2 times per day or as directed by a physician.

Each (one) capsule contains:
NAC (N-Acetyl L-Cysteine) …………………. 600 mg

Other ingredients:
gelatin capsule (gelatin and water) and rice flour.

Product #N359 (60 Capsules) $16.97

Enter Quantity Desired and Click “Add To Cart” Button

 

 

References

1.) Berk M, Copolov DL, Dean O, Lu K, Jeavons S, Schapkaitz I, Anderson-Hunt M, Bush AI.
N-acetyl cysteine for depressive symptoms in bipolar disorder–a double-blind randomized  placebo-controlled trial. Biol Psychiatry. 2008 Sep 15;64(6):468-75. Epub 2008 Jun 5.

2.) Berk M, Copolov D, Dean O, Lu K, Jeavons S, Schapkaitz I, et al. N-acetyl cysteine as a glutathione  precursor for schizophrenia–a double-blind, randomized, placebo-controlled trial. Biol Psychiatry.  2008 Sep 1;64(5):361-8. Epub 2008 Apr 23.

3.) Carmeli C, Knyazeva MG, Cuénod M, Do KQ. Glutathione precursor N-acetyl-cysteine modulates  EEG synchronization in schizophrenia patients: a double-blind, randomized, placebo-controlled trial. PLoS One. 2012;7(2):e29341. Epub 2012 Feb 22.

4.) Crinnion WJ. Do environmental toxicants contribute to allergy and asthma? Altern Med Rev. 2012 Mar;17(1):6-18.

5.) Krifka S, Hiller KA, Spagnuolo G, Jewett A, Schmalz G, Schweikl H. The influence of glutathione on  redox regulation by antioxidant proteins and apoptosis in macrophages exposed to 2-hydroxyethyl  methacrylate (HEMA). Biomaterials. 2012 Jul;33(21):5177-86. Epub 2012 Apr 24.

6.) Lavoie S, Murray MM, Deppen P, Knyazeva MG, et al. Glutathione precursor, N-acetyl-cysteine,  improves mismatch negativity in schizophrenia patients. Neuropsychopharmacology. 2008  Aug;33(9):2187-99. Epub 2007 Nov 14.

7.) Sun L, Gu L, Wang S, Yuan J, Yang H, Zhu J, Zhang H. N-acetylcysteine protects against apoptosis  through modulation of group I metabotropic glutamate receptor activity. PLoS One.  2012;7(3):e32503. Epub 2012 Mar 19.

8.) Fishman AI, Alexander B, Eshghi M, Choudhury M, Konno S. Nephrotoxin-induced renal cell injury  involving biochemical alterations and its prevention with antioxidant. J Clin Med Res. 2012  Apr;4(2):95-101. Epub 2012 Mar 23.

9.) Kao SJ, Wang D, Lin HI, Chen HI. N-acetylcysteine abrogates acute lung injury induced by endotoxin. Clin Exp Pharmacol Physiol. 2006 Jan-Feb;33(1-2):33-40.

10.) Nur E, Brandjes DP, Teerlink T, Otten HM, Oude Elferink RP, Muskiet F, Evers LM, Ten Cate H,  Biemond BJ, Duits AJ, Schnog JJ. N-acetylcysteine reduces oxidative stress in sickle cell patients. Ann Hematol. 2012 Feb 10. [Epub ahead of print]

11.) Faruqi RM, Poptic EJ, Faruqi TR, De La Motte C, DiCorleto PE. Distinct mechanisms for  N-acetylcysteine inhibition of cytokine-induced E-selectin and VCAM-1 expression.  Am J Physiol.1997 Aug;273 (2 Pt ):H817-26.

12.) Galicia-Moreno M, Favari L, Muriel P. Antifibrotic and antioxidant effects of N-acetylcysteine in an  experimental cholestatic model. Eur J Gastroenterol Hepatol. 2012 Feb;24(2):179-85.

13.) Koksel O, Ozdulger A, Ercil M, Tamer L, Ercan B, Atik U, Cinel L, Cinel I, Kanik A.
Effects of N-acetylcysteine on oxidant-antioxidant balance in oleic acid-induced lung injury.
Exp Lung Res. 2004 Sep;30(6):431-46.

14.) Akca T, Canbaz H, Tataroglu C, Caglikulekci M, Tamer L, Colak T, Kanik A, Bilgin O, Aydin S.
The effect of N-acetylcysteine on pulmonary lipid peroxidation and tissue damage. J Surg Res. 2005  Nov;129(1):38-45.

15.) Foschino Barbaro MP, Serviddio G, Resta O, Rollo T, Tamborra R, Elisiana Carpagnano G,  Vendemiale G, Altomare E. Oxygen therapy at low flow causes oxidative stress in chronic  obstructive pulmonary disease: Prevention by N-acetyl cysteine. Free Radic Res. 2005  Oct;39(10):1111-8.

16.) Sadowska AM. N-Acetylcysteine mucolysis in the management of chronic obstructive pulmonary disease. Ther Adv Respir Dis. 2012 Jun;6(3):127-35. Epub 2012 Feb 23.

17.) Jackson IM, Barnes J, Cooksey P. Efficacy and tolerability of oral acetylcysteine (Fabrol) in chronic bronchitis: a double-blind placebo controlled study. J Int Med Res 1984;12:198–206.

18.) Tattersall AB, Bridgman KM, Huitson A. Acetylcysteine (Fabrol) in chronic bronchitis—a study in general practice. J Int Med Res 1983;11:279–84.

19.) Stey C, Steurer J, Bachmann S, et al. The effect of oral N-acetylcysteine in chronic bronchitis: a quantitative systematic review. Eur Respir J 2000;16:253–62 [review].

20.) Martínez-Banaclocha MA. N-acetyl-cysteine in the treatment of Parkinson’s disease. What are we  waiting for? Med Hypotheses. 2012 Apr 28. [Epub ahead of print]

21.) Badawy A, State O, Abdelgawad S.N-Acetyl cysteine and clomiphene citrate for induction of  ovulation in polycystic ovary syndrome: a cross-over trial. Acta Obstet Gynecol Scand.  2007;86(2):218-22.

22.) Nasr A. Effect of N-acetyl-cysteine after ovarian drilling in clomiphene citrate-resistant PCOS  women: a pilot study. Reprod Biomed Online. 2010 Mar;20(3):403-9. Epub 2009 Dec 14.

23.) Rizk AY, Bedaiwy MA, Al-Inany HG. N-acetyl-cysteine is a novel adjuvant to clomiphene citrate in  clomiphene citrate-resistant patients with polycystic ovary syndrome. Fertil Steril. 2005  Feb;83(2):367-70.

24.) Salehpour S, Akbari Sene A, Saharkhiz N, Sohrabi MR, Moghimian F. N-acetylcysteine as an  adjuvant to clomiphene citrate for successful induction of ovulation in infertile patients with polycystic  ovary syndrome. J Obstet Gynaecol Res. 2012 Apr 30. doi: 10.1111/j.1447-0756.2012.01844.x.  [Epub ahead of print]

25.) Feldman L, Shani M, Sinuani I, Beberashvili I, Weissgarten J. N-acetylcysteine may improve residual  renal function in hemodialysis patients: A pilot study. Hemodial Int. 2012 Apr 30. doi:  10.1111/j.1542-4758.2012.00702.x. [Epub ahead of print]

26.) Hou Y, Wang L, Yi D, Ding B, Yang Z, Li J, Chen X, Qiu Y, Wu G. N-acetylcysteine reduces  inflammation in the small intestine by regulating redox, EGF and TLR4 signaling. Amino Acids. 2012 Apr 25. [Epub ahead of print]

27.) Beyaz SG, Yelken B, Kanbak G. The effects of N-acetylcysteine on hepatic function during  isoflurane anaesthesia for laparoscopic surgery patients. Indian J Anaesth. 2011 Nov;55(6):567-72.

28.) Lai ZW, Hanczko R, Bonilla E, Caza TN, Clair B, Bartos A, et al. N-acetylcysteine reduces disease  activity by blocking mTOR in T cells of lupus patients. Arthritis Rheum. 2012 May 1. doi:  10.1002/art.34502. [Epub ahead of print]

29.) Goodson AG, Cotter MA, Cassidy P, Wade M, Florell SR, Liu T, Boucher KM, Grossman D.
Use of oral N-acetylcysteine for protection of melanocytic nevi against UV-induced oxidative stress:  towards a novel paradigm for melanoma chemoprevention. Clin Cancer Res. 2009 Dec  1;15(23):7434-40. Epub 2009 Nov 17.

30.) Mates JM, Segura JA, Alonso FJ, Marquez J. Sulphur-containing non enzymatic antioxidants:  therapeutic tools against cancer. Front Biosci (Schol Ed). 2012 Jan 1;4:722-48

Vitamin C

Master Immune Stimulant and Antioxidant

Vitamin C is a water-soluble vitamin that plays a major role in numerous biological functions including:

  • collagen synthesis (production of tendon, ligament, cartilage and skin)
  • immune function – increases white blood cell activity, interferon production and thymic hormone secretion.
  • cardiovascular health
  • cancer prevention

Levels of vitamin C are quickly depleted during infection. Our vitamin C is specially buffered to reduce acidity.

Vitamin C CapsulesVitamin C Buffered Capsules

One full gram of buffered vitamin C in every capsule.

An excellent source of antioxidant support, Buffered Vitamin C uses pure crystalline ascorbic acid to supply 1 gram of vitamin C in each capsule. This well-tolerated vitamin C formula supports a healthy immune system response and helps maintain healthy skin, collagen, and connective tissues.

Each (one) Capsule contains:
Vitamin C (ascorbic acid) – 1000 mg
Calcium (as calcium carbonate) – 20 mg
Magnesium (as magnesium carbonate) – 12 mg

Suggested dose: 1 capsule, 1-3 times per day, OR 1 capsule every 1-2 hours during acute illness, OR 1 capsule 3-4 times a day for accelerated vitamin C therapy.

Vitamin C Buffered Capsules – Product # 266 (60 Capsules) $15.95

Buffered Vitamin C Does Not Contain

  • artificial coloring
  • artificial flavoring
  • corn
  • dairy products
  • gluten
  • ingredients of animal origin
  • preservatives
  • salt
  • soy
  • sugar
  • wheat
  • yeast

Other Ingredients: vegetable capsule (modified cellulose), and ascorbyl palmitate.


Vitamin C Buffered Crystals

Description – High potency buffered vitamin Cpreparation in an effervescent, mineral-rich blend. Mixes easily in water or other beverages.

Each 1/4 teaspoon contains:
Vitamin C – 1066 mg
Calcium (calcium ascorbate) – 117 mg

Suggested dose: 1/4 teaspoon, 1-3 times per day, OR 1/4 teaspoon every 1-2 hours during acute illness, OR 1/4 teaspoon 3-4 times a day for accelerated vitamin C therapy.

Vitamin C Buffered Crystals – Product # 146 (8.8 ounces) $18.95

Buffered Vitamin C Crystals

Master Immune Stimulant and Antioxidant

Vitamin C is a water-soluble vitamin that plays a major role in numerous biological functions including:

  • collagen synthesis (production of tendon, ligament, cartilage and skin)
  • immune function – increases white blood cell activity, interferon production and thymic hormone secretion.
  • cardiovascular health
  • cancer prevention

Levels of vitamin C are quickly depleted during infection. Our vitamin C is specially buffered to reduce acidity.

Vitamin C Buffered Capsules

One full gram of buffered vitamin C in every capsule.

An excellent source of antioxidant support, Buffered Vitamin C uses pure crystalline ascorbic acid to supply 1 gram of vitamin C in each capsule. This well-tolerated vitamin C formula supports a healthy immune system response and helps maintain healthy skin, collagen, and connective tissues.

Each (one) Capsule contains:
Vitamin C (ascorbic acid) – 1000 mg
Calcium (as calcium carbonate) – 20 mg
Magnesium (as magnesium carbonate) – 12 mg

Suggested dose: 1 capsule, 1-3 times per day, OR 1 capsule every 1-2 hours during acute illness, OR 1 capsule 3-4 times a day for accelerated vitamin C therapy.

Vitamin C Buffered Capsules – Product # 266 (60 Capsules) $15.95
Buffered Vitamin C Does Not Contain

  • artificial coloring
  • artificial flavoring
  • corn
  • dairy products
  • gluten
  • ingredients of animal origin
  • preservatives
  • salt
  • soy
  • sugar
  • wheat
  • yeast

Other Ingredients: vegetable capsule (modified cellulose), and ascorbyl palmitate.


Vitamin C Buffered Crystals

Description – High potency buffered vitamin Cpreparation in an effervescent, mineral-rich blend. Mixes easily in water or other beverages.

Each 1/4 teaspoon contains:
Vitamin C – 1066 mg
Calcium (calcium ascorbate) – 117 mg

Suggested dose: 1/4 teaspoon, 1-3 times per day, OR 1/4 teaspoon every 1-2 hours during acute illness, OR 1/4 teaspoon 3-4 times a day for accelerated vitamin C therapy.

Vitamin C Buffered Crystals – Product # 146 (8.8 ounces) $18.95

Bone Health Marker Test

BONE HEALTH MARKERS TEST

Urine and saliva specimens measures rate of bone mineral loss and associated hormones by looking at a breakdown product of bone (DpD). This test also includes hormones DHEA and DHEA-S, estradiol, progesterone, testosterone, cortisol (x 2) and FSH (follicular stimulating hormones).

This is an excellent test for monitoring osteoporosis treatment and prevention in both men and women. It gives faster “feedback” about the efficacy of treatment than waiting a year to verify treatment by using a bone density scan. Collect samples in the privacy of home and mail in with a pre-paid mailer.

BONE MARKER TEST #994 $197.00

(Sorry – not available in New York state)

 

Buffered Vitamin C Capsules

Vitamin C

Master Immune Stimulant and Antioxidant

Vitamin C is a water-soluble vitamin that plays a major role in numerous biological functions including:

  • collagen synthesis (production of tendon, ligament, cartilage and skin)
  • immune function – increases white blood cell activity, interferon production and thymic hormone secretion.
  • cardiovascular health
  • cancer prevention

Levels of vitamin C are quickly depleted during infection. Our vitamin C is specially buffered to reduce acidity.

Vitamin C Buffered Capsules

One full gram of buffered vitamin C in every capsule.

An excellent source of antioxidant support, Buffered Vitamin C uses pure crystalline ascorbic acid to supply 1 gram of vitamin C in each capsule. This well-tolerated vitamin C formula supports a healthy immune system response and helps maintain healthy skin, collagen, and connective tissues.

Each (one) Capsule contains:
Vitamin C (ascorbic acid) – 1000 mg
Calcium (as calcium carbonate) – 20 mg
Magnesium (as magnesium carbonate) – 12 mg

Suggested dose: 1 capsule, 1-3 times per day, OR 1 capsule every 1-2 hours during acute illness, OR 1 capsule 3-4 times a day for accelerated vitamin C therapy.

Vitamin C Buffered Capsules – Product # 266 (60 Capsules) $15.95

Buffered Vitamin C Does Not Contain

  • artificial coloring
  • artificial flavoring
  • corn
  • dairy products
  • gluten
  • ingredients of animal origin
  • preservatives
  • salt
  • soy
  • sugar
  • wheat
  • yeast

Other Ingredients: vegetable capsule (modified cellulose), and ascorbyl palmitate.


Vitamin C Buffered Crystals

Description – High potency buffered vitamin Cpreparation in an effervescent, mineral-rich blend. Mixes easily in water or other beverages.

Each 1/4 teaspoon contains:
Vitamin C – 1066 mg
Calcium (calcium ascorbate) – 117 mg

Suggested dose: 1/4 teaspoon, 1-3 times per day, OR 1/4 teaspoon every 1-2 hours during acute illness, OR 1/4 teaspoon 3-4 times a day for accelerated vitamin C therapy.

Vitamin C Buffered Crystals – Product # 146 (8.8 ounces) $18.95

Fertility Restore Bromelain 120 caps

Bromelain

Nature’s Premier Anti-Inflammatory Herb

>Bromelain is a mixture of sulfur-containingprotein-digesting enzymes from the stem of Anansus cosmosis (pineapple). Since it was introduced as a medicinal agent in 1957, more than 200 scientific papers on bromelain’s medicinal uses have appeared in the medical literature.

Bromelain is one of the most well-studied anti-inflammatory herbs known. Unless an individual is allergic to pineapple (in which case, don’t use bromelain!) the safety profile of this herb is excellent.(2) Of all the anti-inflammatory substances available (including drugs), bromelain is the one I turn to first.

Bromelain has no direct immune or antimicrobial effects. Instead, it acts to increase the effect of other immune cells by dissolving the mucous coat that bacteria use to “shield” themselves from the immune system. Some studies have shown it to be as effective as antibiotics for treatment of pneumonia, bronchitis, sinusitis and dental, skin and kidney infection.

Bromelain’s actions include:

  • Antiinflammatory (1,2,7,8,10,11)
  • Antiedematous (reduces swelling) (1,2,11)
  • Antitumoral (13,20)
  • Antimetastatic (1,2,7,13)
  • Antithrombotic (1,2,4,5,11)
  • Fibrinolytic (1,2,3,4,7,11)
  • Immunomodulator (2)
  • Enhanced drug absorption (especially antibiotics) (2)
  • Decreased platelet aggregation (2,5,6,7)
  • Increase activity of the body’s defense system (2)

Based on it’s actions, bromelain may be useful in:

  • Thrombosis (1,2,4,5)
  • Cardiovascular disease (1-7,11)
  • Cancer (1,2,7,11,13,17,18,19,20)
  • All types of infection (sinusitis, pneumonia, bronchitis, sepsis) (2,8,23)
  • Osteo Arthritis (8,15,16)
  • Rheumatoid Arthritis (19,21,22)
  • Inflammatory bowel disease (8,10,12,15)

Suggested Dose: Begin with 2 capsules, 3 to 4 times per day between meals for acute infection or severe inflammation. Decrease dose  to 1 capsule, 3 to 4 times daily as symptoms improve.

Each (1) capsule contains: 400 mg of 2,400 mcu-strength bromelain.

This is one of the highest potencies of bromelain available. Don’t be fooled! It’s not just the “milligrams per capsule,” but the POTENCY of the enzyme (the “mcu”or GDU) that determines OVERALL potency. Our  Wellness Club brand of bromelain offers the highest potency and purityavailable!

Bromelain – Product # 183 (120 Caps) $32.00


References

 1.) Tysnes BB, Maurer HR, Porwol T, Probst B, Bjerkvig R, Hoover F. Bromelain reversibly inhibits invasive properties of glioma cells. Neoplasia. 2001 Nov-Dec;3(6):469-79.
2.) Maurer HR. Bromelain: biochemistry, pharmacology and medical use. Cell Mol Life Sci. 2001 Aug;58(9):1234-45.
3.) Ako H, Cheung AH, Matsuura PK. Isolation of a fibrinolysis enzyme activator from commercial bromelain. Arch Int Pharmacodyn Ther. 1981 Nov;254(1):157-67.
4.) Felton GE. Fibrinolytic and antithrombotic action of bromelain may eliminate thrombosis in heart patients. Med Hypotheses. 1980 Nov;6(11):1123-33.
5.) Metzig C, Grabowska E, Eckert K, Rehse K, Maurer HR. Bromelain proteases reduce human platelet aggregation in vitro, adhesion to bovine endothelial cells and thrombus formation in rat vessels in vivo. In Vivo. 1999 Jan-Feb;13(1):7-12.
6.) Gläser D, Hilberg T. The influence of bromelain on platelet count and platelet activity in vitro. Platelets. 2006 Feb;17(1):37-41.
7.) Taussig SJ, Batkin S.Bromelain, the enzyme complex of pineapple (Ananas comosus) and its clinical application. An update. J Ethnopharmacol. 1988 Feb-Mar;22(2):191-203.
8.) Hale LP, Greer PK, Trinh CT, James CL. Proteinase activity and stability of natural bromelain preparations. Int Immunopharmacol. 2005 Apr;5(4):783-93.
9.) Braun JM, Schneider B, Beuth HJ.Therapeutic use, efficiency and safety of the proteolytic pineapple enzyme Bromelain-POS in children with acute sinusitis in Germany.In Vivo. 2005 Mar-Apr;19(2):417-21.
10.) Hale LP.Proteolytic activity and immunogenicity of oral bromelain within the gastrointestinal tract of mice. Int Immunopharmacol. 2004 Feb;4(2):255-64.
11.) Lotz-Winter H. On the pharmacology of bromelain: an update with special regard to animal studies on dose-dependent effects. Planta Med. 1990 Jun;56(3):249-53.
12.) Hale LP, Greer PK, Trinh CT, Gottfried MR. Treatment with oral bromelain decreases colonic inflammation in the IL-10-deficient murine model of inflammatory bowel disease. Clin Immunol. 2005 Aug;116(2):135-42.
13.) Báez R, Lopes MT, Salas CE, Hernández M. In vivo antitumoral activity of stem pineapple (Ananas comosus) bromelain.Planta Med. 2007 Oct;73(13):1377-83. Epub 2007 Sep 24.
14.) Onken JE, Greer PK, Calingaert B, Hale LP.Bromelain treatment decreases secretion of pro-inflammatory cytokines and chemokines by colon biopsies in vitro. Clin Immunol. 2008 Mar;126(3):345-52. Epub 2007 Dec 21.
15.) Akhtar NM, Naseer R, Farooqi AZ, Aziz W, Nazir M. Oral enzyme combination versus diclofenac in the treatment of osteoarthritis of the knee–a double-blind prospective randomized study. Clin Rheumatol. 2004 Oct;23(5):410-5. Epub 2004 Jul 24.
16.)  Walker AF, Bundy R, Hicks SM, Middleton RW.Phytomedicine. 2002 Dec;9(8):681-6.Bromelain reduces mild acute knee pain and improves well-being in a dose-dependent fashion in an open study of otherwise healthy adults.
17.) Beuth J. Proteolytic enzyme therapy in evidence-based complementary oncology: fact or fiction? Integr Cancer Ther. 2008 Dec;7(4):311-6.
18.) Stopper H, Schinzel R, Sebekova K, Heidland A. Genotoxicity of advanced glycation end products in mammalian cells. Cancer Lett. 2003 Feb 20;190(2):151-6.
19.) Desser L, Holomanova D, Zavadova E, Pavelka K, Mohr T, Herbacek I. Oral therapy with proteolytic enzymes decreases excessive TGF-beta levels in human blood. Cancer Chemother Pharmacol. 2001 Jul;47 Suppl:S10-5.
20.) Eckert K, Grabowska E, Stange R, Schneider U, Eschmann K, Maurer HR. Effects of oral bromelain administration on the impaired immunocytotoxicity of mononuclear cells from mammary tumor patients. Oncol Rep. 1999 Nov-Dec;6(6):1191-9.
21.) Rovenská E, Svík K, Stancíková M, Rovenský J. Inhibitory effect of enzyme therapy and combination therapy with cyclosporin A on collagen-induced arthritis. Clin Exp Rheumatol. 2001 May-Jun;19(3):303-9.
22.) Leipner J, Iten F, Saller R. Therapy with proteolytic enzymes in rheumatic disorders. BioDrugs. 2001;15(12):779-89.
23.) Shahid SK, Turakhia NH, Kundra M, Shanbag P, Daftary GV, Schiess W. Efficacy and safety of phlogenzym–a protease formulation, in sepsis in children. J Assoc Physicians India. 2002 Apr;50:527-31.

 

Bromelain 120 caps New – Larger Size

Bromelain

Nature’s Premier Anti-Inflammatory Herb

Bromelain is a mixture of sulfur-containingprotein-digesting enzymes from the stem of Anansus cosmosis (pineapple). Since it was introduced as a medicinal agent in 1957, more than 200 scientific papers on bromelain’s medicinal uses have appeared in the medical literature.

Bromelain is one of the most well-studied anti-inflammatory herbs known. Unless an individual is allergic to pineapple (in which case, don’t use bromelain!) the safety profile of this herb is excellent.(2) Of all the anti-inflammatory substances available (including drugs), bromelain is the one I turn to first.

Bromelain has no direct immune or antimicrobial effects. Instead, it acts to increase the effect of other immune cells by dissolving the mucous coat that bacteria use to “shield” themselves from the immune system. Some studies have shown it to be as effective as antibiotics for treatment of pneumonia, bronchitis, sinusitis and dental, skin and kidney infection.

Bromelain’s actions include:

  • Antiinflammatory (1,2,7,8,10,11)
  • Antiedematous (reduces swelling) (1,2,11)
  • Antitumoral (13,20)
  • Antimetastatic (1,2,7,13)
  • Antithrombotic (1,2,4,5,11)
  • Fibrinolytic (1,2,3,4,7,11)
  • Immunomodulator (2)
  • Enhanced drug absorption (especially antibiotics) (2)
  • Decreased platelet aggregation (2,5,6,7)
  • Increase activity of the body’s defense system (2)

Based on it’s actions, bromelain may be useful in:

  • Thrombosis (1,2,4,5)
  • Cardiovascular disease (1-7,11)
  • Cancer (1,2,7,11,13,17,18,19,20)
  • All types of infection (sinusitis, pneumonia, bronchitis, sepsis) (2,8,23)
  • Osteo Arthritis (8,15,16)
  • Rheumatoid Arthritis (19,21,22)
  • Inflammatory bowel disease (8,10,12,15)

Suggested Dose: Begin with 2 capsules, 3 to 4 times per day between meals for acute infection or severe inflammation. Decrease dose  to 1 capsule, 3 to 4 times daily as symptoms improve.

Each (1) capsule contains: 400 mg of 2,400 mcu-strength bromelain.

This is one of the highest potencies of bromelain available. Don’t be fooled! It’s not just the “milligrams per capsule,” but the POTENCY of the enzyme (the “mcu”or GDU) that determines OVERALL potency. Our  Wellness Club brand of bromelain offers the highest potency and purity available!

References

 1.) Tysnes BB, Maurer HR, Porwol T, Probst B, Bjerkvig R, Hoover F. Bromelain reversibly inhibits invasive properties of glioma cells. Neoplasia. 2001 Nov-Dec;3(6):469-79.
2.) Maurer HR. Bromelain: biochemistry, pharmacology and medical use. Cell Mol Life Sci. 2001 Aug;58(9):1234-45.
3.) Ako H, Cheung AH, Matsuura PK. Isolation of a fibrinolysis enzyme activator from commercial bromelain. Arch Int Pharmacodyn Ther. 1981 Nov;254(1):157-67.
4.) Felton GE. Fibrinolytic and antithrombotic action of bromelain may eliminate thrombosis in heart patients. Med Hypotheses. 1980 Nov;6(11):1123-33.
5.) Metzig C, Grabowska E, Eckert K, Rehse K, Maurer HR. Bromelain proteases reduce human platelet aggregation in vitro, adhesion to bovine endothelial cells and thrombus formation in rat vessels in vivo. In Vivo. 1999 Jan-Feb;13(1):7-12.
6.) Gläser D, Hilberg T. The influence of bromelain on platelet count and platelet activity in vitro. Platelets. 2006 Feb;17(1):37-41.
7.) Taussig SJ, Batkin S.Bromelain, the enzyme complex of pineapple (Ananas comosus) and its clinical application. An update. J Ethnopharmacol. 1988 Feb-Mar;22(2):191-203.
8.) Hale LP, Greer PK, Trinh CT, James CL. Proteinase activity and stability of natural bromelain preparations. Int Immunopharmacol. 2005 Apr;5(4):783-93.
9.) Braun JM, Schneider B, Beuth HJ.Therapeutic use, efficiency and safety of the proteolytic pineapple enzyme Bromelain-POS in children with acute sinusitis in Germany.In Vivo. 2005 Mar-Apr;19(2):417-21.
10.) Hale LP.Proteolytic activity and immunogenicity of oral bromelain within the gastrointestinal tract of mice. Int Immunopharmacol. 2004 Feb;4(2):255-64.
11.) Lotz-Winter H. On the pharmacology of bromelain: an update with special regard to animal studies on dose-dependent effects. Planta Med. 1990 Jun;56(3):249-53.
12.) Hale LP, Greer PK, Trinh CT, Gottfried MR. Treatment with oral bromelain decreases colonic inflammation in the IL-10-deficient murine model of inflammatory bowel disease. Clin Immunol. 2005 Aug;116(2):135-42.
13.) Báez R, Lopes MT, Salas CE, Hernández M. In vivo antitumoral activity of stem pineapple (Ananas comosus) bromelain.Planta Med. 2007 Oct;73(13):1377-83. Epub 2007 Sep 24.
14.) Onken JE, Greer PK, Calingaert B, Hale LP.Bromelain treatment decreases secretion of pro-inflammatory cytokines and chemokines by colon biopsies in vitro. Clin Immunol. 2008 Mar;126(3):345-52. Epub 2007 Dec 21.
15.) Akhtar NM, Naseer R, Farooqi AZ, Aziz W, Nazir M. Oral enzyme combination versus diclofenac in the treatment of osteoarthritis of the knee–a double-blind prospective randomized study. Clin Rheumatol. 2004 Oct;23(5):410-5. Epub 2004 Jul 24.
16.)  Walker AF, Bundy R, Hicks SM, Middleton RW.Phytomedicine. 2002 Dec;9(8):681-6.Bromelain reduces mild acute knee pain and improves well-being in a dose-dependent fashion in an open study of otherwise healthy adults.
17.) Beuth J. Proteolytic enzyme therapy in evidence-based complementary oncology: fact or fiction? Integr Cancer Ther. 2008 Dec;7(4):311-6.
18.) Stopper H, Schinzel R, Sebekova K, Heidland A. Genotoxicity of advanced glycation end products in mammalian cells. Cancer Lett. 2003 Feb 20;190(2):151-6.
19.) Desser L, Holomanova D, Zavadova E, Pavelka K, Mohr T, Herbacek I. Oral therapy with proteolytic enzymes decreases excessive TGF-beta levels in human blood. Cancer Chemother Pharmacol. 2001 Jul;47 Suppl:S10-5.
20.) Eckert K, Grabowska E, Stange R, Schneider U, Eschmann K, Maurer HR. Effects of oral bromelain administration on the impaired immunocytotoxicity of mononuclear cells from mammary tumor patients. Oncol Rep. 1999 Nov-Dec;6(6):1191-9.
21.) Rovenská E, Svík K, Stancíková M, Rovenský J. Inhibitory effect of enzyme therapy and combination therapy with cyclosporin A on collagen-induced arthritis. Clin Exp Rheumatol. 2001 May-Jun;19(3):303-9.
22.) Leipner J, Iten F, Saller R. Therapy with proteolytic enzymes in rheumatic disorders. BioDrugs. 2001;15(12):779-89.
23.) Shahid SK, Turakhia NH, Kundra M, Shanbag P, Daftary GV, Schiess W. Efficacy and safety of phlogenzym–a protease formulation, in sepsis in children. J Assoc Physicians India. 2002 Apr;50:527-31.

Find Information on Potassium Iodide For Radiation Protection Here -> IODINE


The “Missing Mineral” for Thyroid, Heart, Healthy Immunity and Cancer Protection

Iodine is a non-metallic essential trace element in human nutrition. Currently considered in conventional medicine to be primarily a thyroid nutrient (thyroid hormones T4 and T3 are composed largely of iodine), Iodine is actually found in many organs and tissue in the body including salivary, parotid, submandibular and pituitary glands, pancreas, testis, breasts, prostate, ovary, adrenal gland, stomach, heart, thymus, and lung. (1,2,3).

Iodine is required for normal thyroid hormone production, it’s best-known role. But iodine also plays an important role in immune function, cancer prevention (especially of breast, thyroid and prostate cancer), diabetes prevention and reversal, atrial fibrillation correction, overweight and obesity, “brain fog” (low energy), breast and ovarian cysts, liver detoxification and menopausal symptoms.

Iodine is also an important anti-microbial and can often relieve skin, lung, GI tract and other infections when antibiotics fail. In fact, from 1900 to the 1960’s, virtually US physicians commonly used iodine (as Lugol’s solution) to treat low and high thyroid conditions, infections and many other conditions with excellent results.

Here’s the “short course” on iodine.

  • Studies show that we may need a LOT more iodine than the current RDI of 150 micrograms, and that many if not most Americans are iodine deficient.
     
  • Conventional doctors are “iodine-o-phobic” (afraid to recommend higher-than-RDA doses of iodine) because they are not familiar with the vast body of research showing that higher iodine levels are beneficial.
     
  • Low iodine levels are associated with higher rates of low and high thyroid function; breast and thyroid cancer (and possibly many other types of cancer); ovarian cysts (including polycystic ovaries); fibrocystic breast disease; heart arrhythmias; lung and other infections; fibromyalgia and chronic fatigue to name only a few.
     
  • Because very high doses of iodine can cause heart palpitations and excess thyroid function (both which resolve upon stopping supplementation), initial testing of iodine levels and monitoring by an holistic physician may be the safest way to take iodine.

More Iodine information:

Iodine Test (spot and 24-hour excretion test for total body iodine sufficiency)

Iodine Supplements (concentrated source of high-potency iodine)

Modfilan (Seaweed Source of Natural Iodine) (low dose, all-natural source of iodine)

References

1.) C. Spitzweg, W. Joba, W. Eisenmenger and A. E. Heufelder. “Analysis of Human Sodium Iodide Symporter Gene Expression in Extrathyroidal Tissues and Cloning of Its Complementary Deoxyribonucleic Acids from Salivary Gland, Mammary Gland, and Gastric Mucosa.” The Journal of Clinical Endocrinology & Metabolism Vol. 83, No. 5 1746-1751. (1)”Iodine in medicine and pharmacy since its discovery-1811-1961,” Proc R Soc Med, 1961:54:831-836.
2.) Dai G, Levy O, Carrasco N. 1996 “Cloning and characterization of the thyroid iodide transporter.” Nature. 379:458–460.
3.) Smanik PA, Ryu K-Y, Theil KS, Mazzaferri EL, Jhiang SM. 1997 “Expression, exon-intron organization, and chromosome mapping of the human sodium iodide symporter. Endocrinology.” 138:3555–3558.