
Conductor of whole body biochemistry
Few substances in the human body are involved in as many reactions as SAMe. This inconspicuous molecule, formed by the union of methionine and ATP energy, is at the heart of cellular biochemistry. Thanks to its ability to transfer methyl groups, it influences hundreds of processes ranging from gene regulation to the formation of cell building blocks. It is important in methylation, the formation of glutathione or the neurotransmitters dopamine and serotonin.


SAMe is closely linked to the production of neurotransmitters. Due to its role in methylation, it is involved in the synthesis of dopamine, serotonin and norepinephrine. Equally important is its action on cell membranes, where it helps the conversion of phospholipids and thus maintains the correct structure and flexibility of neuronal cells.

The majority of SAMe is formed in the liver, from where it is involved in many key metabolic pathways. It is a precursor of polyamines, such as spermidine, which are small molecules closely associated with regeneration. In addition, very important substances are formed from homocysteine, which is produced during the metabolism of SAMe:

| Nutritional component | Quantity in 1 dose |
|---|---|
| S-adenosyl-L-methionine | 400 mg |
1 capsule per day.
Package size:
60 vegetable capsules, 47.3 g.
Store at room temperature, in a dry and dark place. Do not remove the silica gel from the jar and make sure the cap is always securely closed.
Keep out of reach of children! The product is not intended for use by children, pregnant or nursing women unless recommended by a physician. Do not exceed the recommended daily dosage. The product is not intended as a substitute for a varied diet. Maintain a healthy lifestyle.
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Delle Chiaie, R., Pancheri, P., & Scapicchio, P. (2002). Efficacy and tolerability of oral and intramuscular S-adenosyl-L-methionine in the treatment of major depression: A meta-analysis of randomized controlled trials. The American Journal of Medicine, 113(6), 476-485.
Mischoulon, D., & Fava, M. (2014). Role of S-adenosyl-L-methionine in the treatment of depression: A review of the evidence. The American Journal of Clinical Nutrition, 100(suppl_1), 445S-449S.
Cuomo, A., Beccarini Crescenzi, B., Bolognesi, S., Goracci, Proietti, L., & Bolognesi, E. (2020). The efficacy and safety of S-adenosyl-L-methionine in major depressive disorder: A systematic review and meta-analysis of randomized clinical trials. Annals of General Psychiatry, 19, 8.
Anstee, Q. M., & Day, C. P. (2012). S-adenosylmethionine (SAMe) therapy in liver disease: A review of current evidence and clinical utility. Journal of Hepatology, 57(5), 1097-1109.
Hire, W. I., Reinsch, S., Hoehler, F., Tobis, J. S., & Harvey, P. W. (2004). S-adenosyl methionine (SAMe) versus celecoxib for the treatment of osteoarthritis symptoms: A double-blind cross-over trial. BMC Musculoskeletal Disorders, 5, 6.
BRAINMARKET s.r.o., Hladnovská. 83/93, Ostrava 702 00, Czech Republic, [email protected]
Specifications can be changed without notice. Images are for illustrative purposes only.