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乙醇作为体外和体内微粒体巴比妥类药物羟基化的选择性抑制剂。

Ethanol as a selective inhibitor of microsomal barbiturate hydroxylation in vitro and in vivo.

作者信息

Schüppel R V, Kuthe C

出版信息

Adv Exp Med Biol. 1980;132:363-72. doi: 10.1007/978-1-4757-1419-7_36.

Abstract

Inhibition by ethanol of microsomal hydroxylation in vitro was studied for a series of barbiturates. Considerable variation was found both in the type and the degree of inhibition exerted by ethanol in this series. Degree of inhibition by ethanol, however, correlated well with both the increases in sleeping-time and the prolongation of half-life time of barbiturates found in rats acutely pretreated with a subnarcotic dose of ethanol. Results are interpreted to favour a distinct pharmacokinetic concept of barbiturate-ethanol interaction to occur in rats.

摘要

对一系列巴比妥酸盐进行了乙醇在体外对微粒体羟基化抑制作用的研究。发现乙醇在该系列中产生的抑制类型和程度都有相当大的差异。然而,乙醇的抑制程度与大鼠经亚麻醉剂量乙醇急性预处理后巴比妥酸盐睡眠时间的增加以及半衰期的延长均有很好的相关性。结果表明,大鼠体内巴比妥酸盐与乙醇相互作用存在明显的药代动力学概念。

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