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急性酒精摄入与单剂量苯二氮䓬类药物、三环和四环抗抑郁药之间的药代动力学相互作用——最新进展。

Pharmacokinetic interactions between acute alcohol ingestion and single doses of benzodiazepines, and tricyclic and tetracyclic antidepressants -- an update.

作者信息

Tanaka E, Misawa S

机构信息

Institute of Community Medicine, University of Tsukuba, Japan.

出版信息

J Clin Pharm Ther. 1998 Oct;23(5):331-6. doi: 10.1046/j.1365-2710.1998.00175.x.

Abstract

Recent reports of interactions between alcohol and benzodiazepines, tricyclic and tetracyclic antidepressants during their acute concomitant use are reviewed. Acute ingestion of alcohol (ethanol) with tranquilizers or hypnotics is responsible for several pharmacokinetic interactions that can have significant clinical implications. In general, metabolism of these drugs is delayed when combined with alcohol but some reports have suggested otherwise. The amount of alcohol consumed, the presence or absence of liver disease, and differences in the dosage and administration of these drugs may account for the observed discrepancies. In recent years, the cytochrome P450 (P450 or CYP) isoenzyme that catalyses the metabolism of these drugs has also been identified. However, since changes in the pharmacogenetic metabolism of benzodiazepines and tricyclic and tetracyclic antidepressants are mainly governed by CYP2C19 and CYP2D6, caution is needed when used together with alcohol.

摘要

本文综述了近期关于酒精与苯二氮䓬类药物、三环和四环抗抑郁药在急性同时使用期间相互作用的报告。酒精(乙醇)与镇静剂或催眠药的急性摄入会导致几种药代动力学相互作用,这些相互作用可能具有重大的临床意义。一般来说,这些药物与酒精合用时,其代谢会延迟,但也有一些报告提出了相反的观点。饮酒量、是否存在肝脏疾病以及这些药物在剂量和给药方式上的差异,可能是导致观察到的差异的原因。近年来,还确定了催化这些药物代谢的细胞色素P450(P450或CYP)同工酶。然而,由于苯二氮䓬类药物以及三环和四环抗抑郁药的药物遗传学代谢变化主要由CYP2C19和CYP2D6决定,因此与酒精同时使用时需要谨慎。

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