SAMe 200mg Blister Pack

Life Extension

$25.00 

Add to Cart
✕

Save 15% forever Order Direct!

Sign up on next page to complete order

SAMe helps maintain stable mood and joint function without side effects. In addition, SAMe has multiple mechanisms of action that are used throughout the body, especially in the liver, which help maintain liver health. Largely known for its effects on optimal mood, SAMe has also shown benefits for the liver, brain, and joints.

Benefits at a glance:

  • Helps maintain stable mood
  • Helps maintain liver health
  • Helps maintain healthy jointfunction

Life Extension® first introduced SAMe (S-Adenosyl-Methionine) in 1997, and researchers continue to discover impressive benefits of this versatile nutrient.

SAMe is an amino acid derivative normally synthesized in the body that may become depleted with sickness or age. Supplementing with SAMe plus folate, trimethylglycine (TMG or betaine), vitamins B6 and B12 appears to be an effective way to overcome this deficiency.

SAMe is concentrated in the liver and brain and is a major methyl donor in the synthesis of hormones, nucleic acids, proteins, and phospholipids, and catecholamines and other neurotransmitters. SAMe is required for the synthesis of norepinephrine, dopamine, and serotonin.1-3 SAMe facilitates glutathione4, 5 usage, which improves the bodys antioxidant defense. It also helps maintain acetylcholine levels6, 7 which are necessary for cognitive function.

SAMe is used by the body in three important pathways:

  • Methylation (contributing methyl groups to activate certain molecules)8, 9
  • The synthesis of polyamines (for cell growth, gene expression, neuronal regeneration, etc.)10-14
  • Transsulfuration (synthesis of cysteine, glutathione, and other sulfate chemicals)15-17

In 2002, an agency of the U.S. Department of Health and Human Services conducted a meticulous evaluation of SAMe. Its findings show the efficacy of SAMe in helping to maintain stable mood and joint function without any side effects.18 Since aging people often suffer joint discomfort and immobilization, SAMe addresses multiple problems people face as they grow older.19-24

SAMe has multimodal mechanisms of action that are used throughout the body and especially in the liver.25-28 In order to perform its detoxification role, the liver continually performs large numbers of complex enzymatic reactions.29 SAMe facilitates healthy methylation enzymatic processes and boosts hepatic levels of glutathione, a critical antioxidant.28, 30, 31 When liver function is compromised, glutathione is depleted, which leads to free radical damage. In addition, SAMe acts as a methyl donor in the synthesis and formation of phosphatidylcholine and L-cysteine, both necessary for maintaining liver health.32, 33

A recent study conducted at Harvard Medical School and Massachusetts General Hospital cited the benefits of SAMe for mood elevation.34 In addition, a report published in Germany indicates that SAMe may help maintain healthy neurological function. The report revealed that:

SAMe increased glutathione levels by 50% and glutathione enzyme activity by 115%.35 SAMe decreased a measurement of free radical activity by 46%.35 SAMe inhibited lipid peroxidation by 55% in culture.35

SAMes ability to boost brain cell methylation facilitates youthful DNA enzymatic actions which may help account for SAMe’s mood-elevating properties. These enzymatic reactions are required for the healthy conversion of neurotransmitters such as serotonin and dopamine.

References

  1. Am J Clin Nutr. 2002 Nov;76(5):1151S-7S.
  2. Psychiatr Pol. 2011 Nov-Dec;45(6):923-31.
  3. Mol Cell Proteomics. 2012 Nov;11(11):1274-88.
  4. Clin Chem Lab Med. 2013 Mar 1;51(3):457-65.
  5. Toxicol Lett. 2012 Aug 3;212(3):320-8.
  6. Phys Biol. 2008 Dec 19;5(4):044002.
  7. J Nutr Health Aging. 2008 Apr;12(4):252-61.
  8. Science. 2011 Apr 29;332(6029):604-7.
  9. Pharmacol Biochem Behav. 2001 Sep;70(1):105-14.
  10. Neuroreport. 2001 Dec 21;12(18):3939-42.
  11. Drugs. 1994 Aug;48(2):137-52.
  12. J Clin Psychiatry. 2009;70 Suppl 5:18-22.
  13. J Cell Sci. 2014 Jan 1;127(Pt 1):50-9.
  14. Clin Rev Allergy Immunol. 2012 Feb;42(1):58-70.
  15. Toxicol Sci. 2010 May;115(1):131-9.
  16. World J Gastroenterol. 2010 Mar 21;16(11):1366-76.
  17. Am J Clin Nutr. 2002 Nov;76(5):1151S-7S.
  18. Evidence Report/Technology Assessment: Number 64 S-Adenosyl-L-Methionine for Treatment of Depression, Osteoarthritis, and Liver Disease http://archive.ahrq.gov/clinic/epcsums/samesum.htm
  19. Neuroreport. 2001 Dec 21;12(18):3939-42.
  20. J Nutr Health Aging. 2008 Apr;12(4):252-61.
  21. Proc Nutr Soc. 2011 Nov 4:1-9.
  22. J Nutr Health Aging. 2010 Mar;14(3):224-30.
  23. Vet Ther. 2008 Summer;9(2):69-82.
  24. Metabolism. 2011 May;60(5):673-80.25.
  25. Physiol Rev. 2012 Oct;92(4):1515-42.
  26. Am J Physiol Gastrointest Liver Physiol. 2007 Jul;293(1):G91-103.
  27. Rocz Akad Med Bialymst. 2005;50:7-20.
  28. World J Gastroenterol. 2006 Mar 28;12(12):1895-904.
  29. J Inherit Metab Dis. 1991;14(4):421-30.
  30. FASEB J. 1996 Mar;10(4):471-80.
  31. Alcohol. 2002 Jul;27(3):179-83.
  32. Minerva Gastroenterol Dietol. 1992 Jul-Sep;38(3):145-51.
  33. Pharmacol Biochem Behav. 2001 Sep;70(1):105-14.
  34. Am J Psychiatry. 2010 Aug;167(8):942-8.
  35. Naunyn Schmiedebergs Artch Pharmacol. 2000 Jan; 361 (1): 47-52.