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正常志愿者口服给药后去甲安定的效应及血药浓度

Effects and plasma levels of N-desmethyldiazepam after oral administration in normal volunteers.

作者信息

Dasberg H H

出版信息

Psychopharmacologia. 1975 Aug 21;43(2):191-8. doi: 10.1007/BF00421024.

Abstract

In the course of a previous study on the pharmaco-kinetics and effects of diazepam in anxiety patients, it was hypothesized that the N-desmethyl derivative is a disturbing agent causing side effects. The present study served to test the validity of this assumption. Diazepam and N-desmethyl-diazepam, the latter as a separate drug, were orally administered to 6 subjects, each drug during 7 days, 15 mg daily in divided doses. Using a randomized, placebo controlled, double-blind design, subjective and observer ratings of a wide range of clinical effects were made. Plasma levels of the benzodiazepine compounds were determined by the G.L.C. method. Results showed that steady state plasma levels were reached on the 5th day; the N-desmethyldiazepam, considering its lower clearance rates, is a longer acting drug than diazepam; that both substances induce hypnosedative effects, mood changes, and somatic disturbances and facilitate sexual behaviour in normals; that desmethyldiazepam is a more effective hypnosedative and mood-lowering substance as compared to equal doses of diazepam. Further comparisons in anxiety patients are recommended in order to find out if the specific desmethyldiazepma effects are therapeutically favourable or disturbing.

摘要

在之前一项关于地西泮在焦虑症患者中的药代动力学及效应的研究过程中,曾有假设认为N -去甲基衍生物是一种会引发副作用的干扰剂。本研究旨在检验这一假设的正确性。将地西泮和N -去甲基地西泮(后者作为一种独立药物)口服给予6名受试者,每种药物给药7天,每日15毫克,分剂量服用。采用随机、安慰剂对照、双盲设计,对一系列临床效应进行主观和观察者评分。通过气相色谱法测定苯二氮䓬类化合物的血浆水平。结果显示,第5天达到稳态血浆水平;考虑到其较低的清除率,N -去甲基地西泮比地西泮作用时间更长;两种物质均能诱导催眠镇静作用、情绪变化和躯体不适,并促进正常人的性行为;与等量的地西泮相比,去甲基地西泮是一种更有效的催眠镇静和降低情绪的物质。建议在焦虑症患者中进行进一步比较,以确定去甲基地西泮的特定效应在治疗上是有益还是有干扰。

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