男性单次口服阿米替林50和75 mg后的消除和药理作用。

P Schulz, A E Balant-Gorgia, A Kubli, C Gertsch-Genet, G Garrone
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引用次数: 1

摘要

在另一篇论文中,我们描述了75毫克单剂量阿米替林在正常志愿者中的配置,这些志愿者表现为对德异喹和丁胺醇的广泛或不良代谢,并且口服抗抑郁药的清除率有四倍的范围,50毫克阿米替林也被给予相同的志愿者。本文比较了两种剂量后的结果,表明阿米替林的处置即使在口服清除率低的受试者中也是线性的。药代动力学数据与镇静强度或精神运动障碍之间无相关性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Elimination and pharmacological effects following single oral doses of 50 and 75 mg of amitriptyline in man.

In a companion paper we described the disposition of a 75 mg single dose of amitriptyline in normal volunteers who were phenotyped as extensive or poor metabolizers of debrisoquine and bufuralol, and had a four-fold range in the oral clearance of the antidepressant, 50 mg of amitriptyline was also administered to the same volunteers. This paper compares the results after both doses and suggests that the disposition of amitriptyline is linear even in subjects with a low oral clearance. There was no relation between the pharmacokinetic data and the intensity of sedation or of psychomotor impairment.

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