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酒精代谢的生化与病理生理方面(作者译)

[Biochemical and pathophysiological aspects of alcohol metabolism (author's transl)].

作者信息

Teschke R, Lieber C S

出版信息

Leber Magen Darm. 1978 Oct;8(5):237-45.

PMID:30009
Abstract

The metabolism of ethanol to acetaldehyde proceeds in the liver via alcohol dehydrogenase (ADH) and the microsomal ethanol oxidizing system (MEOS), whereas catalase plays no significant role. ADH is localized in the cytosol, required required NAD+ as cofactor and exhibits a pH optimum in the alkaline range and a Km of less than 2 mM for ethanol. Conversely, the MEOS resides in the endoplasmic reticulum, requires NADPH and O2, is inhibited by CO, and exhibits a Km of about 10 mM for ethanol. The microsomal system also metabolizes higher aliphatic alcohols such as butanol which is not a substrate for catalase. Moreover, it could be separated from ADH and catalase by column chromatography. The MEOS exhibits a variety of properties similar to those of other microsomal drug metabolizing enzymes and is characterized by inducibility of its activity following chronic alcohol consumption, which suggests the involvement of the microsomal system in the adaptive enhancement of ethanol clearance commonly observed in alcoholics.

摘要

乙醇代谢为乙醛在肝脏中通过乙醇脱氢酶(ADH)和微粒体乙醇氧化系统(MEOS)进行,而过氧化氢酶不起重要作用。ADH定位于胞质溶胶中,需要NAD⁺作为辅因子,在碱性范围内表现出最适pH值,对乙醇的Km值小于2 mM。相反,MEOS存在于内质网中,需要NADPH和O₂,受CO抑制,对乙醇的Km值约为10 mM。微粒体系统还代谢高级脂肪醇,如丁醇,丁醇不是过氧化氢酶的底物。此外,它可以通过柱色谱与ADH和过氧化氢酶分离。MEOS表现出与其他微粒体药物代谢酶相似的多种特性,其特征是长期饮酒后其活性可诱导,这表明微粒体系统参与了在酗酒者中常见的乙醇清除适应性增强过程。

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