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三唑仑和唑吡坦:健康志愿者中它们对精神运动、认知及主观影响的比较

Triazolam and zolpidem: a comparison of their psychomotor, cognitive, and subjective effects in healthy volunteers.

作者信息

Mintzer M Z, Frey J M, Yingling J E, Griffiths R R

机构信息

Department of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, Baltimore, MD 21224, USA.

出版信息

Behav Pharmacol. 1997 Nov;8(6-7):561-74. doi: 10.1097/00008877-199711000-00014.

Abstract

The psychomotor/cognitive performance, subject-rated, and observer-rated effects of single oral doses of the benzodiazepine hypnotic triazolam (0.125, 0.25, and 0.5 mg/70 kg) and the imidazopyridine hypnotic zolpidem (5, 10, and 20 mg/70 kg) were compared in 11 volunteers, in a double-blind, placebo-controlled, crossover design. Triazolam and zolpidem produced similar dose-related decrements on several performance measures, and similar dose-related increases on most observer-rated and several subject-rated measures. The drugs differed in the time course of their effects on these measures; the effects of zolpidem typically peaked 30 min earlier (1-1.5 h postdrug) than the effects of triazolam (1.5-2 h postdrug). Triazolam and zolpidem produced a different profile of effects on other performance measures which could not be attributed to time course differences. Triazolam produced significantly more impairment than zolpidem in time estimation. Triazolam, but not zolpidem, produced significant impairment on a short-term memory task. Zolpidem produced significantly more impairment than triazolam on several novel measures of performance on a computerized trail-making test. The observed differences between triazolam and zolpidem may be related to zolpidem's reported binding selectivity for the omega 1 receptor subtype.

摘要

采用双盲、安慰剂对照、交叉设计,在11名志愿者中比较了单次口服苯二氮䓬类催眠药三唑仑(0.125、0.25和0.5mg/70kg)和咪唑吡啶类催眠药唑吡坦(5、10和20mg/70kg)对精神运动/认知表现、受试者自评及观察者评定的影响。三唑仑和唑吡坦在多项表现指标上产生了相似的剂量相关下降,在大多数观察者评定及多项受试者评定指标上产生了相似的剂量相关增加。这两种药物对这些指标的作用时间过程有所不同;唑吡坦的作用通常比三唑仑(用药后1.5 - 2小时)提前30分钟达到峰值(用药后1 - 1.5小时)。三唑仑和唑吡坦对其他表现指标产生了不同的作用模式,这不能归因于时间过程差异。在时间估计方面,三唑仑产生的损害明显多于唑吡坦。三唑仑对一项短期记忆任务产生了显著损害,而唑吡坦未产生。在计算机化连线测试的多项新表现指标上,唑吡坦产生的损害明显多于三唑仑。三唑仑和唑吡坦之间观察到的差异可能与唑吡坦报道的对ω1受体亚型的结合选择性有关。

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