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长期摄入乙醇后二甲基亚硝胺代谢增强并激活为诱变剂。

Enhancement of dimethylnitrosamine metabolism and activation to a mutagen following chronic ethanol consumption.

作者信息

Garro A J, Seitz H K, Lieber C S

出版信息

Cancer Res. 1981 Jan;41(1):120-4.

PMID:7192597
Abstract

Chronic ethanol ingestion in rats results in an increase in hepatic microsomal dimethylnitrosamine (DMN) demethylase activity and in an increase in hepatic microsomal activation of DMN to a mutagen. These effects of ethanol on DMN metabolism were detectable in vitro at DMN concentrations as low as 0.3 to 1 mM and as high as 100 mM. This ability of ethanol to increase the rate of DMN metabolism over such a broad range of DMN concentrations is in marked contrast to the effects of other microsomal enzyme inducers, such as phenobarbital and 3-methylcholanthrene, which increase the rate of DMN metabolism only at relatively high DMN concentrations and repress its metabolism at low DMN concentrations.

摘要

大鼠长期摄入乙醇会导致肝脏微粒体二甲基亚硝胺(DMN)脱甲基酶活性增加,以及肝脏微粒体将DMN活化为诱变剂的能力增强。在体外,当DMN浓度低至0.3至1 mM以及高达100 mM时,均可检测到乙醇对DMN代谢的这些影响。乙醇在如此广泛的DMN浓度范围内增加DMN代谢速率的能力,与其他微粒体酶诱导剂(如苯巴比妥和3-甲基胆蒽)的作用形成显著对比,后者仅在相对较高的DMN浓度下增加DMN代谢速率,而在低DMN浓度下则抑制其代谢。

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