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西咪替丁与三唑并苯二氮䓬类药物阿普唑仑和三唑仑的相互作用。

Interaction of cimetidine with the triazolobenzodiazepines alprazolam and triazolam.

作者信息

Abernethy D R, Greenblatt D J, Divoll M, Moschitto L J, Harmatz J S, Shader R I

出版信息

Psychopharmacology (Berl). 1983;80(3):275-8. doi: 10.1007/BF00436169.

Abstract

The influence of cimetidine on the pharmacokinetics of alprazolam and triazolam, two triazolobenzodiazepines metabolized by hepatic microsomal oxidation, was evaluated in a series of healthy volunteers. Subjects ingested single 1.0 mg dose of alprazolam or 0.5 mg doses of triazolam on two occasions, with and without concurrent administration of cimetidine (300 mg) every 6 h. For alprazolam, which has a low hepatic clearance and low extraction ratio, cimetidine significantly impaired total metabolic clearance (1.05 versus 1.66 ml/min/kg, P less than 0.005), resulting in significantly prolonged elimination half-life (16.6 versus 12.4 h, P less than 0.005). For triazolam, which has higher hepatic clearance and an intermediate extraction ratio, total clearance was reduced by cimetidine (3.9 versus 5.9 ml/min/kg), causing a significant increase in total area under the plasma concentration curve (25 versus 38 ng/ml X h, P less than 0.02). However, elimination half-life of triazolam was not influenced by cimetidine (3.3 versus 3.2 h), indicating that the reduction in clearance was manifested as increased systemic availability. Thus, cimetidine impairs the clearance of both alprazolam and triazolam, but the consequences of the kinetic change are different because of the differing hepatic extraction profiles of the two drugs.

摘要

在一系列健康志愿者中评估了西咪替丁对阿普唑仑和三唑仑这两种经肝微粒体氧化代谢的三氮唑苯二氮䓬类药物药代动力学的影响。受试者在两个不同时段分别单次服用1.0毫克阿普唑仑或0.5毫克三唑仑,一次是在未同时服用西咪替丁(每6小时300毫克)的情况下,另一次是在同时服用西咪替丁的情况下。对于肝清除率低且提取率低的阿普唑仑,西咪替丁显著损害了总代谢清除率(分别为1.05对1.66毫升/分钟/千克,P小于0.005),导致消除半衰期显著延长(分别为16.6对12.4小时,P小于0.005)。对于肝清除率较高且提取率中等的三唑仑,西咪替丁降低了总清除率(分别为3.9对5.9毫升/分钟/千克),导致血浆浓度曲线下总面积显著增加(分别为25对38纳克/毫升×小时,P小于0.02)。然而,三唑仑的消除半衰期不受西咪替丁影响(分别为3.3对3.2小时),这表明清除率的降低表现为全身可用性增加。因此,西咪替丁损害了阿普唑仑和三唑仑的清除率,但由于两种药物不同的肝提取特性,动力学变化的后果有所不同。

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