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乙醚及其他麻醉剂对微粒体N-亚硝基二甲胺脱甲基酶的抑制作用。

Inhibition of microsomal N-nitrosodimethylamine demethylase by diethyl ether and other anesthetics.

作者信息

Tan Y Z, Keefer L K, Yang C S

出版信息

Biochem Pharmacol. 1987 Jun 15;36(12):1973-8. doi: 10.1016/0006-2952(87)90496-5.

Abstract

The inhibitory actions of diethyl ether and several other anesthetics on the metabolism of N-nitrosodimethylamine (NDMA) and other substrates were studied with rat liver microsomes. Diethyl ether was an effective inhibitor of the low Km NDMA demethylase, showing characteristics of a competitive inhibition. Inhibition of NDMA metabolism was also observed in the liver post-mitochondrial supernatant fraction prepared from ether-anesthetized rats. Selectivity in the inhibitory action of diethyl ether was demonstrated; the ether was most effective against NDMA demethylase, less potent against p-nitroanisole demethylase and N-nitrosomethylbenzylamine demethylase, and not effective against the metabolism of aminopyrine or benzphetamine. Other anesthetics such as chloroform, isoflurane, enflurane, and halothane also effectively inhibited NDMA demethylase. The work demonstrates that diethyl ether is an efficient inhibitor of NDMA metabolism by the microsomal monooxygenase systems.

摘要

用大鼠肝微粒体研究了乙醚和其他几种麻醉剂对N-亚硝基二甲胺(NDMA)及其他底物代谢的抑制作用。乙醚是低Km NDMA脱甲基酶的有效抑制剂,表现出竞争性抑制的特征。在由乙醚麻醉大鼠制备的肝线粒体后上清液部分中也观察到了对NDMA代谢的抑制作用。证明了乙醚抑制作用的选择性;乙醚对NDMA脱甲基酶最有效,对p-硝基苯甲醚脱甲基酶和N-亚硝基甲基苄胺脱甲基酶的效力较小,对氨基比林或苄非他明的代谢无效。其他麻醉剂如氯仿、异氟烷、恩氟烷和氟烷也有效抑制NDMA脱甲基酶。这项研究表明,乙醚是微粒体单加氧酶系统对NDMA代谢的有效抑制剂。

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