Glutathione is the most powerful intracellular antioxidant, offering superior antioxidant support in a form that is easily absorbed.*
Setria® Glutathione helps prevent free radical damage by supporting glutathione-dependent enzymes that aid in the elimination of toxins and prevention of free radicals.* It is recognized as the great protector.
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This reduced form of glutathione is required for many stages of immune response, and when taking more than 1000 mg daily, has been shown to enhance the body’s normal immune cell function.* Setria® Glutathione supports the detoxification of drugs, pesticides, or carcinogens and alcohol in the liver.*
Our bodies obtain glutathione in two ways: from the foods we eat and from our own internal production. Under some conditions, however, the body’s need for glutathione is outpaced by its ability to produce it. Glutathione levels can be depleted by poor diet, pollution, toxins, stress, aging, and infections.
Setria® Glutathione is a unique tripeptide form of glutathione that has been clinically shown to raise blood glutathione levels.* It consists of three amino acids: glutamate, cysteine, and glycine. It is found to varying degrees in all cells, tissues, body fluids, and organ systems. It aids in detoxification by supporting liver, kidney, and digestive function to eliminate ingested toxins and intercept toxins in the GI tract before they get absorbed.* It maintains normal immune function by supporting white blood cells including T cell lymphocytes, the body’s frontline of defense.*
Setria Glutathione’s pure, allergen-free form is manufactured through a proprietary fermentation process. Its three primary benefits are:
Published studies show:
Setria glutathione supplementation effectively increases the body’s stores of glutathione and supports the immune system.*
Learn more from Setria’s website »
Suggested intake of glutathione for a healthy person is 100-150 mg daily. During times of need, however, daily requirements can be significantly higher. Larger amounts of glutathione may be required for adequate supplementation.
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2. Pastore, A., et al., Analysis of glutathione: implication in redox and detoxification. Clin Chim Acta, 2004. 333(1): p. 19-39.
3. Balendiran, G.K., R. Dabur, and D. Fraser, The role of glutathione in cancer. Cell Biochem Funct, 2004. 22(6): p. 343-52.
4. Richie JP Jr, Nichenametla S, Neidig W, Calcagnotto A, Haley JS, Schell TD, Muscat JE. Randomized controlled trial of oral glutathione supplementation on body stores of glutathione. European Journal of Nutrition. May 2014:1436-6207. doi: 10.1007/s00394-014-0706-z.
5. Ballatori, N., et al., Glutathione dysregulation and the etiology and progression of human diseases. Biol Chem, 2009. 390(3): p. 191-214.
6. Hunjan, M.K. and D.F. Evered, Absorption of glutathione from the gastro-intestinal tract. Biochim Biophys Acta, 1985. 815(2): p. 184-8.
7. Iantomasi, T., et al., Glutathione transport system in human small intestine epithelial cells. Biochim Biophys Acta, 1997. 1330(2): p. 274-82.
8. van Haaften, R.I., et al., Effect of Vitamin E on glutathione-dependent enzymes. Drug Metab Rev, 2003. 35(2-3): p. 215-53.
9. Schafer, M. and S. Werner, Oxidative Stress in normal and impaired wound repair. Pharmacol Res, 2008. 58(2): p. 165-71.
10. Hunjan MK, Evered DF, Absorption of glutathione from the gastro-intestinal tract, Biochim Biophys Acta. 1985 May 14;815(2):184-8.
11. Hagen TM1, Bai C, Jones DP, Stimulation of glutathione absorption in rat small intestine by alpha-adrenergic agonists, FASEB J. 1991 Sep;5(12):2721-7.
12. Richie JP Jr1, Nichenametla S, Neidig W, Calcagnotto A, Haley JS, Schell TD, Muscat JE, Randomized controlled trial of oral glutathione supplementation on body stores of glutathione, Eur J Nutr. March 2015, Volume 54, Issue 2, pp 251-263
13. McKinley-Barnard S, Andre T, Morita M2, Willoughby DS, Combined L-citrulline and glutathione supplementation increases the concentration of markers indicative of nitric oxide synthesis, J Int Soc Sports Nutr.2015 Jun 10;12:27.
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