|Summary sheet: SAM-e|
|Common names||S-Adenosyl methionine, SAM-e, Methylguanidoacetic acid|
|Chemical class||Nitrogenous organic acid|
|Routes of Administration|
S-Adenosyl-L-methionine (also called S-Adenosyl methionine, Ademethionine and commonly as SAMe and SAM-e) is a common cosubstrate involved in methyl group transfers, transsulfuration, and aminopropylation in biological organisms. SAMe is an amino acid methionine bound to an ATP molecule that circulates in the blood naturally and acts as a 'methyl donor'. A methyl group in chemistry is simply a carbon molecule (bound to some hydrogens), and donating a methyl group to other molecules can accelerate or preserve reactions in the body as a form of metabolic 'maintenance'.
SAM-e is available over the counter and by prescription in the treatment of depression and osteoarthritis. It is generally distributed in enteric-coated tablets, which allows the supplement to pass through the low pH environment of the stomach to the gastrointestinal tract, raising the bioavaliability by 600%.
A review of trials assessing oral doses of SAM-e between 200mg and 1600mg notes that they appear to have similar efficacy to tricyclic antidepressants as well as being more effective than placebo.
S-adenosyl methionine is an endogenous molecule, found as a substrate synthesized by the sub-groups adenosine and methionine through an the enzyme methionine adenosyltransferase. The adenosine subcomponent is comprised of an adedine nucleobase bonded to a ribose chain. This ribose chain is attached to the terminal carbon of the methionine group. Methionine is a butyl carboxylic acid substituted at R2 with an amino group and at R4 with a methylthio (carbon-sulphur) group. It is an essential methyl donator in metabolic reactions.
SAM-e is an endogenous molecule that has numerous roles including methyl donation in neurotransmitter synthesis, antioxidative effects (radical scavenging, glutathione precursor), anti-inflammatory effects, and neuroprotective effects.
SAME-e, in addition to providing ATP to the cell, also can convert nicotinamine into N-methyl-nicotinamide (NMNA) via nicotinamide N-methyltransferase, NMNA which can prevent choline efflux from the brain and neuron, a process which may account for some of SAM-e's nootropic effects.
Disclaimer: The effects listed below cite the Subjective Effect Index (SEI), a research literature based on anecdotal reports and the personal experiences of PsychonautWiki contributors. As a result, they should be regarded with a healthy degree of skepticism. It is worth noting that these effects will not necessarily occur in a predictable or reliable manner, although higher doses are more liable to induce the full spectrum of effects. Likewise, adverse effects become much more likely with higher doses and may include addiction, serious injury, or death.
In comparison to the effects of other nootropics such as noopept, this compound is reported to produce by physical and cognitive stimulation.
- Stimulation - The stimulation which SAM-e presents can be considered as subtle, yet persistent and energetic comparable to that of caffeine, although less forced.
- Appetite suppression
- Bodily control enhancement - In addition to raising energy levels, SAM-e shows efficacy in improving joint mobility in those with osteoarthritis.
- Muscle spasms
- Pain relief - This appears to be about as effective as NSAIDS such as ibuprofen for joint inflammation and pain.
- Stamina enhancement
- Stomach cramps
- Tactile enhancement
There are currently no anecdotal reports which describe the effects of this compound within our experience index. Additional experience reports can be found here:
Toxicity and harm potential
This toxicity and harm potential section is a stub.
As a result, it may contain incomplete or even dangerously wrong information. You can help by expanding upon or correcting it.
There are no clinically significant side-effects of acute SAM-e supplementation. Although side-effects are not commonly reported with SAMe, numerous studies note a small set of participants who experience mania after supplementing SAM-e. While not common, it appears to be related to SAMe supplementation for unknown reasons; it has been reported in some persons without history of mania as well and does not appear to be related to any pathological condition per se.
SAM-e is also hypothesized to raise homocystine to harmful levels, but this has yet to be proven in a laboratory environment.  Still, it is advised to take Sam-e along with folate and B12.
Regardless, it is strongly recommended that one be familiar with harm reduction practices when using this substance.
Tolerance and addiction potential
SAM-e is not habit-forming with a low potential for abuse. It does not seem to be capable of causing psychological or physiological dependence among users.
Tolerance to many of the effects of S-adenosyl methionine develops over several weeks of prolonged and repeated use. This results in users having to administer increasingly larger doses to achieve the same effects. After that, it takes about 3 - 7 days for the tolerance to be reduced to half and 1 - 2 weeks to be back at baseline (in the absence of further consumption).
- United States - SAM-e is approved and legal over the counter for purchase.
- Germany - SAM-e is sold as a dietary supplement.
- Russia - SAM-e is available by prescription.
- United Kingdom - It is illegal to produce, supply, or import this drug under the Psychoactive Substance Act, which came into effect on May 26th, 2016.
- Homocysteine. | https://www.ncbi.nlm.nih.gov/pubmed/10762063
- Bioavailability of S-adenosyl methionine and impact on response in a randomized, double-blind, placebo-controlled trial in major depressive disorder. | http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4156851/
- A vitamin/nutriceutical formulation improves memory and cognitive performance in community-dwelling adults without dementia. | http://www.ncbi.nlm.nih.gov/pubmed/20191258
- Role of S-adenosyl-L-methionine in the treatment of depression: a review of the evidence. | http://www.ncbi.nlm.nih.gov/pubmed/12420702/
- Nicotinamide homeostasis: a xenobiotic pathway that is key to development and degenerative diseases. | http://www.ncbi.nlm.nih.gov/pubmed/15922112
- [Meta-analysis of the efficacy of adenosylmethionine and oxaceprol in the treatment of osteoarthritis]. | http://www.ncbi.nlm.nih.gov/pubmed/12436324
- Italian double-blind multicenter study comparing S-adenosylmethionine, naproxen, and placebo in the treatment of degenerative joint disease. | http://www.ncbi.nlm.nih.gov/pubmed/3318442
- A Case Report of a Manic Episode Triggered by S-Adenosylmethionine (SAMe) | http://www.ncbi.nlm.nih.gov/pmc/articles/PMC315487/
- S-adenosylmethionine (SAM-e) for the treatment of depression in people living with HIV/AIDS | http://www.ncbi.nlm.nih.gov/pmc/articles/PMC535560/
- Role of S-adenosyl-L-methionine in the treatment of depression: a review of the evidence. | http://www.ncbi.nlm.nih.gov/pubmed/12420702
- Influence of oral S-adenosylmethionine on plasma 5-methyltetrahydrofolate, S-adenosylhomocysteine, homocysteine and methionine in healthy humans. | http://www.ncbi.nlm.nih.gov/pubmed/9262350
- Psychoactive Substances Act 2016 (Legislation.gov.uk) | http://www.legislation.gov.uk/ukpga/2016/2/contents/enacted