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多种形式的诱导性药物代谢酶:一种任何生物体都能应对逆境的合理机制。

Multiple forms of inducible drug-metabolizing enzymes: a reasonable mechanism by which any organism can cope with adversity.

作者信息

Nebert D W

出版信息

Mol Cell Biochem. 1979 Sep 28;27(1):27-46. doi: 10.1007/BF00849277.

DOI:10.1007/BF00849277
PMID:229404
Abstract

All organisms possess a number of genetically regulated mechanisms in order to cope with rapid adverse changes in the environment. The two systems which appear to respond to a seemingly endless array of chemical specificities are the immune response and the induction of drug-metabolizing enzymes. Similarities and differences between the immunoglobulin and the cytochrome P-450-mediated monooxygenase systems are described. DNA insertion sequences, plasmid "transposons," maize "controlling elements," gene duplication, intervening sequences, and high-frequency intergenic recombination are all discussed as possible methods by which organisms can "adapt" quickly to a new selective pressure. If the regulation of P-450 induction resembles in any way the other methods by which pro- and eukaryotes cope genetically with numerous forms of environmental adversity, therefore, it is very likely that mammalian tissues contain hundreds, if not thousands, of inducible forms of P-450.

摘要

所有生物体都拥有一些基因调控机制,以便应对环境中迅速出现的不利变化。似乎能对一系列看似无穷无尽的化学特异性做出反应的两个系统是免疫反应和药物代谢酶的诱导。文中描述了免疫球蛋白和细胞色素P - 450介导的单加氧酶系统之间的异同。DNA插入序列、质粒“转座子”、玉米“控制元件”、基因复制、间隔序列和高频基因间重组都被作为生物体能够快速“适应”新选择压力的可能方式进行了讨论。因此,如果P - 450诱导的调控在任何方面类似于原核生物和真核生物在基因上应对多种形式环境逆境的其他方式,那么哺乳动物组织很可能含有数百种(即便不是数千种)可诱导形式的P - 450。

相似文献

1
Multiple forms of inducible drug-metabolizing enzymes: a reasonable mechanism by which any organism can cope with adversity.多种形式的诱导性药物代谢酶:一种任何生物体都能应对逆境的合理机制。
Mol Cell Biochem. 1979 Sep 28;27(1):27-46. doi: 10.1007/BF00849277.
2
Genetic mechanisms controlling the induction of polysubstrate monooxygenase (P-450) activities.控制多底物单加氧酶(P-450)活性诱导的遗传机制。
Annu Rev Pharmacol Toxicol. 1981;21:431-62. doi: 10.1146/annurev.pa.21.040181.002243.
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[The role of drug metabolizing enzymes in the effect and side-effect of the drugs].[药物代谢酶在药物疗效及副作用中的作用]
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Induction of drug metabolism: species differences and toxicological relevance.药物代谢的诱导:种属差异及毒理学相关性
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Impact of dioxin-type induction of drug-metabolizing enzymes on the metabolism of endo- and xenobiotics.二噁英类诱导药物代谢酶对内源性和外源性物质代谢的影响。
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Induction of the drug-metabolizing enzymes.药物代谢酶的诱导
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7
[The effect of foreign-substance-metabolizing enzymes on skin diseases].[外来物质代谢酶对皮肤疾病的影响]
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Characterization of human cytochrome P450 enzymes.人类细胞色素P450酶的特性分析。
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Important role of proinflammatory cytokines/other endogenous substances in drug-induced hepatotoxicity: depression of drug metabolism during infections/inflammation states, and genetic polymorphisms of drug-metabolizing enzymes/cytokines may markedly contribute to this pathology.促炎细胞因子/其他内源性物质在药物性肝毒性中的重要作用:感染/炎症状态下药物代谢的抑制,以及药物代谢酶/细胞因子的基因多态性可能对这种病理状况有显著影响。
Am J Ther. 2005 May-Jun;12(3):254-61.

引用本文的文献

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Gene expression of Dnmt1 isoforms in porcine oocytes, embryos, and somatic cells.猪卵母细胞、胚胎和体细胞中Dnmt1亚型的基因表达。
Cell Reprogram. 2013 Aug;15(4):309-21. doi: 10.1089/cell.2012.0088. Epub 2013 Jun 28.
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The evolving role of drug metabolism in drug discovery and development.药物代谢在药物发现与开发中不断演变的作用。
Pharm Res. 2007 May;24(5):842-58. doi: 10.1007/s11095-006-9217-9. Epub 2007 Mar 1.
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Molecular genetics of cytochrome P450 IID. Anomalies of drug metabolism.细胞色素P450 IID的分子遗传学。药物代谢异常。

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Partial purification and characterization of two enzymes from guinea-pig liver microsomes that hydrolyze carcinogenic amides 2-acetylaminofluorene and N-hydroxy-2-acetylaminofluorene.从豚鼠肝脏微粒体中部分纯化和鉴定两种水解致癌酰胺2-乙酰氨基芴和N-羟基-2-乙酰氨基芴的酶。
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