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微粒体电子传递酶的诱导作用。

The induction of microsomal electron transport enzymes.

作者信息

Waterman M R, Estabrook R W

出版信息

Mol Cell Biochem. 1983;53-54(1-2):267-78. doi: 10.1007/BF00225259.

DOI:10.1007/BF00225259
PMID:6353196
Abstract

Liver endoplasmic reticulum contains as NADPH-dependent electron transport complex where the family of hemeproteins, termed cytochrome P-450, serve as catalysts for the oxidation of a variety of different organic chemicals. The content and inventory of the types of cytochrome P-450 is readily modified following in vivo treatment of animals with 'inducing agents' such as barbiturates, steroids and polycyclic hydrocarbons. Recent studies have applied the methods of molecular biology to evaluate changes in the transcription and translation of genomic information occurring concomitant with the initiation of synthesis of various types of cytochrome P-450. The ability to isolate unique cytochrome P-450 proteins and to prepare specific antibodies now permits the study of in vitro translation of mRNA and the preparation of specific cDNAs. The present review summarizes the historic background leading to current concepts of cytochrome P-450 induction and describes recent advances in our knowledge of the regulation of cytochrome P-450 synthesis in the liver.

摘要

肝脏内质网含有一种作为NADPH依赖电子传递复合物的物质,其中被称为细胞色素P - 450的血红素蛋白家族,作为多种不同有机化学物质氧化反应的催化剂。在用巴比妥酸盐、类固醇和多环烃等“诱导剂”对动物进行体内处理后,细胞色素P - 450类型的含量和存量很容易发生改变。最近的研究应用分子生物学方法来评估与各种类型细胞色素P - 450合成起始同时发生的基因组信息转录和翻译的变化。现在,分离独特细胞色素P - 450蛋白和制备特异性抗体的能力使得对mRNA的体外翻译研究以及特异性cDNA的制备成为可能。本综述总结了导致细胞色素P - 450诱导当前概念的历史背景,并描述了我们在肝脏中细胞色素P - 450合成调控知识方面的最新进展。

相似文献

1
The induction of microsomal electron transport enzymes.微粒体电子传递酶的诱导作用。
Mol Cell Biochem. 1983;53-54(1-2):267-78. doi: 10.1007/BF00225259.
2
Differential induction of peroxisomal and microsomal fatty-acid-oxidising enzymes by peroxisome proliferators in rat liver and kidney. Characterisation of a renal cytochrome P-450 and implications for peroxisome proliferation.过氧化物酶体增殖剂对大鼠肝脏和肾脏中过氧化物酶体及微粒体脂肪酸氧化酶的差异诱导作用。一种肾细胞色素P-450的特性及其对过氧化物酶体增殖的影响。
Eur J Biochem. 1989 Sep 1;184(1):69-78. doi: 10.1111/j.1432-1033.1989.tb14991.x.
3
Mechanism of induction of hepatic microsomal drug metabolizing enzymes by a series of barbiturates.一系列巴比妥类药物诱导肝微粒体药物代谢酶的机制。
J Pharm Pharmacol. 1975 Oct;27(10):739-46. doi: 10.1111/j.2042-7158.1975.tb09393.x.
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Diphasic action of the aliphatic amide, HOE 17879, on hepatic microsomal drug metabolizing enzymes in the mouse.脂肪族酰胺HOE 17879对小鼠肝脏微粒体药物代谢酶的双相作用。
Experientia. 1976 Mar 15;32(3):362-5. doi: 10.1007/BF01940840.
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引用本文的文献

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Pregnenolone 16 alpha-carbonitrile-inducible P-450 gene family: gene conversion and differential regulation.孕烯醇酮16α-腈诱导型P-450基因家族:基因转换与差异调控。
Mol Cell Biol. 1986 Aug;6(8):2969-76. doi: 10.1128/mcb.6.8.2969-2976.1986.
2
The 4S binding protein acts as a trans-regulator of the polycyclic hydrocarbon-inducible cytochrome P450.4S结合蛋白作为多环芳烃诱导型细胞色素P450的反式调节因子。
Cancer Metastasis Rev. 1988 Apr;7(1):51-65. doi: 10.1007/BF00048278.

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