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药物代谢酶的诱导:机制与后果

Induction of drug-metabolizing enzymes: mechanisms and consequences.

作者信息

Okey A B, Roberts E A, Harper P A, Denison M S

出版信息

Clin Biochem. 1986 Apr;19(2):132-41. doi: 10.1016/s0009-9120(86)80060-1.

Abstract

The activity of many enzymes that carry out biotransformation of drugs and environmental chemicals can be substantially increased by prior exposure of humans or animals to a wide variety of foreign chemicals. Increased enzyme activity is due to true enzyme induction mediated by increased synthesis of mRNAs which code for specific drug-metabolizing enzymes. Several species of cytochrome P-450 are inducible as are certain conjugating enzymes such as glutathione S-transferases, glucuronosyl transferases, and epoxide hydrolases. Induction of drug-metabolizing enzymes has been shown in several instances to alter the efficacy of some therapeutic agents. Induction of various species of cytochrome P-450 also is known to increase the rate at which potentially toxic reactive metabolic intermediates are formed from drugs or environmental chemicals. Overall, however, induction of drug-metabolizing enzymes appears to be a beneficial adaptive response for organisms living in a "chemically-hostile" world.

摘要

人类或动物预先接触多种外来化学物质后,许多参与药物和环境化学物质生物转化的酶的活性会大幅提高。酶活性的增加是由于真正的酶诱导作用,这种诱导由编码特定药物代谢酶的mRNA合成增加介导。几种细胞色素P-450以及某些结合酶,如谷胱甘肽S-转移酶、葡糖醛酸转移酶和环氧化物水解酶都是可诱导的。在一些情况下,药物代谢酶的诱导已被证明会改变某些治疗药物的疗效。还已知各种细胞色素P-450的诱导会增加药物或环境化学物质形成潜在毒性反应性代谢中间体的速率。然而,总体而言,药物代谢酶的诱导对于生活在“化学恶劣”环境中的生物体似乎是一种有益的适应性反应。

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