The effect of isolation stress on some hepatic drug and carcinogen metabolising enzymes in rats.

I D Capel, M Jenner, M H Pinnock, H M Dorrell, D C Williams
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Abstract

Rats were subjected to stress by isolation for periods of up to eight days, which produced an elevation in plasma cortisol. In vivo drug metabolism as estimated by the plasma elimination rate of orally-administered antipyrine was not significantly affected by this treatment although there was an apparent decrease in the absorption rate of the drug. In vitro experiments on hepatic microsomal preparations derived from stressed animals indicate that this stress increased in the activity of some enzyme systems concerned with benzo(a)pyrene activation and this correlated with an increased binding of the carcinogen to DNA. The activity of conjugating enzyme which could catalyze the excretion of such carcinogens was not significantly altered. The results indicated that stress could have an important bearing on carcinogenesis by enhancing to a greater extent enzyme systems responsible for activation than those involved in the excretion of polycyclic aromatic hydrocarbons.

分离应激对大鼠肝脏某些药物和致癌物代谢酶的影响。
大鼠受到长达8天的隔离压力,这导致血浆皮质醇升高。口服安替比林的血浆消除率对体内药物代谢的影响不明显,但药物的吸收率明显降低。对应激动物肝微粒体制剂的体外实验表明,应激增加了与苯并(a)芘活化有关的一些酶系统的活性,这与致癌物质与DNA结合的增加有关。催化这些致癌物排出的偶联酶活性没有明显变化。结果表明,与参与多环芳烃排泄的酶系统相比,应激在更大程度上增强了负责活化的酶系统,从而可能对癌变产生重要影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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