methionine (SAM)

This page contains educational material about S-adenosylmethionine (SAM or also called SAMe). This information is for educational purposes only. Nothing in this text is intended to serve as medical advice. All medical decisions should be made only with the guidance of your own personal medical authority. I am doing my best to get this data up quickly and correctly. If you find errors in this data, please let me know.


S-Adenosylmethionine (SAM, was listed as SAMe in the past) acts a methyl donor for over 200 (Some research data claims 300) methylation reactions. SAM also serves as a precursor for biosynthesis of polyamines and is the substrate used for numerous reactions, including vitamin biosyntheses and nucleotide modifications. Therefore SAM is believed to be the second most often used biological compound in use d by the body in normal biochemical reactions. The first is of course ATP. SAM is very important in cellular homeostasis.

The reason SAM is used so much as a methyl donor rather than 5-methyltetrahydrofolate (5MTHF/active folate) is that the transfer potential for 5MTHF is not verty high. The activated methyl carriar of choice is SAM. SAM is produced by the transfer of an adenosyl group from ATP to methionine. The methyl group of the methionine group is activated by the positive charge on the adjacent sulfur atom. This positive charge make the methyl transfer more energetic than from 5-MTHF.

So to reiterate SAM is a molecule composed of adenosine (derived from ATP) and methionine. Methionine is an amino acid that comes from your diet and can be recycled in the body.

When SAM is used to donate a methyl group, SAM is converted to S-adenosylhomocysteine (SAH), an inhibitor of methylation reactions. Hence, the ratio SAM/SAH is termed as the methylation capacity of the cell.

The methylation pathway not only has to produce SAM, it also has to recycle it. Once SAM has given up its methyl groups to help create neurotransmitters, it is then “recycled” or in scientific terms, re-methylated. After SAM has received its new methyl groups, it can perform its job all over again. Due to methylation pathway weaknesses, some people can neither produce nor recycle SAM very well. Fortunately, we can supplement SAM or better yet support the folate or methionine pathway to bypass mutations and attain its many benefits.

The methionine/methylation cycle is shown below. This gives you an idea of how SAM is made and recycled. It is explained in greater detail on the methylation page.

methionine comprehensive cycle



Once SAM provides a methyl group, it becomes S-adenosylhomocysteine and then homocysteine. Homocysteine is now ready to be changed back into methionine which will once again be used to synthesize SAM.

As a Queen of the methylators, SAM does all the things a methylator does. Without enough of it you see all the diseases associated with poor methylation. So for a good understanding of how important SAM is, just read about methylation here.

Here are a few of the things SAM does.

Needed for glutathione synthesis.

Needed for stabalization of many proteins, including myelin, the nerve sheaths that are so important to proper nerve firing.

Converts acetylserotonin to melatonin, which is necessary for a good nights sleep.

Converts the neurotransmitter norepinephrine into epinephrine ( adrenaline)

Converts guanidinoacetate into creatine

Converts creatine into creatinine.

Converts phophatidylethanolamine into phosphatidylcholine

Converts nucleotides to methylated nucleotides.

Needed in the creation of CoQ10 and carnitine. These are all compounds essential to the work of the mitochondria, which is the energy power house in our cells.

Involved in synthesis of methylcobalamin. Needed to also convert between various forms of B12.

Some varoius factoids about SAM

Because of its essential role in reactions involving neurotransmitters, it’s not surprising that a lack of SAM plays a role in neurodegenerative conditions.

If you are hypothyroid, you may not be making enough SAM. T4 is needed to convert riboflavin to FAD (flavin adenine dinucleotide) the active form of B
(FAD) controls MTHFR which is needed to make methylfolate which produces SAMe

Although SAM is the principle methyl donor in all cells of the body, SAM is mainly synthesized, utilized, and degraded in the liver. Up to 80% of liver methionine is converted to SAM, which is the source of glutathione, a principle antioxidant required for liver detoxificiation reactions (Bottiglieri,2002). Low SAM levels in the liver associated with the removal of liver tissue is a stimulus for liver tissue regeneration ( Lu,SC,2008).

SAM has proven to be effective in the treatment of depression, with fewer side effects than is seen with conventional antidepressants (Chiaie,RD, 2002) and (Papakostas,2010). Nearly a third of severely depressed patients have folic acid deficiency accompanied by high plasma homocysteine (Bottiglieri, 2000).

SAM is able to inactivate hormones such as estrogens (through methylation), supporting the use of methionine in conditions of estrogen excess. Its effects in preventing estrogen-induced cholestasis (stagnation of bile in the gall bladder) have been demonstrated in pregnant women and those on oral contraceptives. In addition to its role in promoting estrogen excretion, methionine has been shown to increase the membrane fluidity that is typically decreased by estrogens, thereby restoring several factors that promote bile flow.

Methionine also promotes the flow of lipids to and from the liver in humans. Methionine is a major source of numerous sulfur-containing compounds, including the amino acids cysteine and taurine.

SAM is necessary to make adequate levels of CoQ10. Clinically, CoQ10 has been used in the treatment of angina, heart failure, and after coronary artery bypass and cardiomyopathy, as well as inflammation and weakening of the heart muscle. The synthesis of CoQ10 requires components of the methylation pathway, in particular, adequate levels of SAM.

SAM effects geme tramscription. SAM methylates specific cytosines in DNA, and this regulates gene transcription. If cellular SAM is depleted, it leads to DNA hypomethylation

Low SAM is Risk Factor for:
Alzheimer's Disease,

Supplementing SAM & Instability of Supplements

SAM can cause insomnia if not taken in the morning, and is best taken on an empty stomach.

S-adenosyl-l-methionine is chemically unstable, both in solution and in dry state, and forms different degradation products. The chemical instability represents al problem during the preparation of therapeutic formulations. One research study showed the disaccharide trehalose exercises a protective effect towards the lyophilized SAM, decreasing its degradation (65% of SAM was detected after 50 days at 37 °C). A parallel study, performed to stabilize the SAM into lyophilized yeast cells enriched in the sulfonium compound, assessed the positive effect of trehalose also in whole cells, but in lesser measure. It is possible hat using trehalose with SAMe in the future will protect it and make it more shelf stable.What is currently done is to put it in an acid resistant capsule and the product is kept cool. It can’t be heat treated. SAme needs to be kept refrigerated. Best if it is in blister pack.

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