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S-腺苷-L-甲硫氨酸的肠道吸收

Intestinal absorption of S-adenosyl-L-methionine.

作者信息

Stramentinoli G, Gualano M, Galli-Kienle M

出版信息

J Pharmacol Exp Ther. 1979 Jun;209(3):323-6.

PMID:439007
Abstract

The gastrointestinal absorption of S-adenosyl-L-methionine (SAMe) is demonstrated by evaluating plasma levels and gastrointestinal content of the unmodified molecule after oral administration. When [methyl-14C]SAMe is given orally, the radioactivity found in the liver is associated both with SAMe and phosphatidylcholine, a compound known to be derived from the methylation of phosphatidylethanolamine with SAMe as a methyl donor. These results and low plasma levels after the oral administration may be suggestive of a first-pass effect of SAMe characterized by an extensive uptake of the drug by the liver where it is rapidly metabolized.

摘要

通过评估口服给药后未修饰分子的血浆水平和胃肠道含量,证实了S-腺苷-L-蛋氨酸(SAMe)的胃肠道吸收情况。当口服[甲基-14C]SAMe时,在肝脏中发现的放射性与SAMe和磷脂酰胆碱都有关,磷脂酰胆碱是一种已知由磷脂酰乙醇胺以SAMe作为甲基供体进行甲基化而衍生的化合物。这些结果以及口服给药后的低血浆水平可能提示SAMe存在首过效应,其特征是肝脏对该药物有广泛摄取并迅速代谢。

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