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[苯巴比妥对肝脏微粒体单加氧酶的底物型诱导作用]

[A substrate-type induction of liver microsomal monooxygenases by phenobarbital].

作者信息

Tsyrlov I B, Gromova O A, Rivkind N B, Vakulin G M, Liakhovich V V

出版信息

Biokhimiia. 1977 Jul;42(7):1184-94.

PMID:907792
Abstract

A possibility of step-wise induction of microsomal monooxygenases after injection of phenobarbital in the presence of 3-methylcholanthrene-caused induction was studied. It was found that the ratio of the high- and low-spin types of cytochrome, rather than the position of the CO-peak of its reduced form is a criterion for functional specificity of hemoprotein. Induction by phenobarbital appears possible under conditions when the inductor binding to microsomal hemoprotein is lacking, since cytochrome P-488 has no binding sites for phenobarbital. It is assumed that under microsomal monooxygenases induction by phenobarbital activation of genome and subsequent protein synthesis are operated by the substrate rather than by products of its primary metabolism in microsomes.

摘要

研究了在3-甲基胆蒽诱导存在的情况下注射苯巴比妥后微粒体单加氧酶逐步诱导的可能性。发现细胞色素高自旋和低自旋类型的比例,而非其还原形式的CO峰位置是血红素蛋白功能特异性的标准。由于细胞色素P-488没有苯巴比妥的结合位点,在缺乏诱导剂与微粒体血红素蛋白结合的条件下,苯巴比妥诱导似乎是可能的。据推测,在微粒体单加氧酶由苯巴比妥诱导的情况下,基因组的激活及随后的蛋白质合成是由底物而非其在微粒体中的初级代谢产物所操控。

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