右美沙芬细胞色素p450依赖性代谢:胎儿和成人研究。

Evelyne Jacqz-Aigrain, Thierry Cresteil
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引用次数: 47

摘要

右美沙芬经过o -去甲基化转化为右美沙芬,n -去甲基化转化为3-甲氧基morphinan。3-羟基吗啡酮,一种二甲基化化合物,是次生形成的。右旋孤儿的o -去甲基化途径是多态性的,受CYP2D6遗传控制。对成人和胎儿进行了研究,以确定参与右美沙芬代谢及其个体发生的细胞色素P450家族的特征。在成人志愿者体内和体外研究表明,o -去甲基化途径到右旋孤儿依赖于CYP2D6,主要是在广泛代谢的药物和缺陷的低代谢的药物。3-甲氧基morphinan的n -去甲基化途径是辅助的,依赖于CYP3A亚家族。在人类胎儿微粒体中,CYP2D6蛋白和活性直到出生前才可检测到,而CYP2D6 RNA在出生前就已大量存在。CYP3A活性早在妊娠第17周就可大量检测到。免疫抑制研究表明,胎儿和成人的CYP3A亚家族成员虽然不同,但性质相近。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cytochrome P450-dependent metabolism of dextromethorphan: fetal and adult studies.
Dextromethorphan undergoes O-demethylation to dextrorphan and N-demethylation to 3-methoxymorphinan. 3-Hydroxymorphinan, a didemethylated compound, is secondarily formed. The O-demethylation pathway to dextrorphan is polymorphic and under CYP2D6 genetic control. Adult and fetal studies were performed to characterize the cytochrome P450 families involved in dextromethorphan metabolism and their ontogeny. In adult volunteers in vivo and in vitro studies demonstrate that the O-demethylation pathway to dextrorphan is dependent on CYP2D6 and is predominant in extensive metabolizers and defective in poor metabolizers of the drug. The N-demethylation pathway to 3-methoxymorphinan is accessory and is dependent on the CYP3A subfamily. In human fetal microsomes, CYP2D6 protein and activity are not detectable until birth, while CYP2D6 RNA is present in significant amounts before birth. CYP3A activity is detectable in large amounts as early as the 17th week of gestation. Fetal and adult members of the CYP3A subfamily have close, although different, properties, as demonstrated by immunoinhibition studies.
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