母体接触苯妥英对围产期肝氨基吡啶n -去甲基化酶的诱导作用。

B H Shapiro, R M Bardales, G M Lech
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引用次数: 0

摘要

苯妥英是妊娠癫痫妇女最常用的抗惊厥药之一。与此无关的是,该药也是肝脏药物代谢酶的诱导剂。我们在这里报道,母鼠用治疗样剂量的苯托英治疗大鼠,在坝的8日龄后代中,米切里斯常数和肝氨基吡啶n -去甲基化酶的最大速度显著升高。虽然这种药物对妊娠或新生儿的发育几乎没有任何不良影响,但母体给药的苯妥英似乎被转移到会阴处,在那里它诱导了肝脏药物代谢酶。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Perinatal induction of hepatic aminopyrine N-demethylase by maternal exposure to phenytoin.

Phenytoin is one of the most commonly used anticonvulsants in pregnant epileptic women. Unrelatedly, the drug is also an inducer of hepatic drug metabolizing enzymes. We report here that maternal treatment with therapeutic-like doses for the rat of phenytoin produces significant elevations in the Michaelis constants and maximal velocities of hepatic aminopyrine N-demethylase in the dams' 8-day-old offspring. Although the drug apparently had little, if any, adverse effects on the course of pregnancy or neonatal development, it appears that the maternally administered phenytoin was transferred to the perinates where it induced hepatic drug metabolizing enzymes.

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