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催眠药的镇静、记忆及行为效应。

Sedative, memory, and performance effects of hypnotics.

作者信息

Roehrs T, Merlotti L, Zorick F, Roth T

机构信息

Henry Ford Hospital, Sleep Disorders and Research Center, Detroit, MI 48202.

出版信息

Psychopharmacology (Berl). 1994 Oct;116(2):130-4. doi: 10.1007/BF02245054.

Abstract

The sedative, amnestic, and performance disruptive effects of benzodiazepine (Bz) receptor selective and non-selective hypnotics were studied in 23 healthy, normal subjects, aged 26.8 +/- 1.0 years. Triazolam (0.25 and 0.50 mg), zolpidem (10 and 20 mg) and placebo were administered, double-blind, at bedtime in a repeated measures design. During an awakening 90 min later (at approximate peak concentration of each drug) a 30-min performance battery which included memory, vigilance, and psychomotor tasks was completed. Each drug and dose impaired memory (both immediate and delayed), vigilance, and psychomotor performance relative to placebo. Among active drugs impairment was greatest with zolpidem 20 mg, next triazolam 0.50 mg, then zolpidem 10 mg, and finally triazolam 0.25 mg. Next morning delayed recall was also impaired by all drugs and doses (i.e. anterograde amnesia). The amnestic and performance-disruptive effects paralleled the relative hypnotic effects of the drugs and doses. No receptor selectivity in these pharmacodynamic effects was observed.

摘要

在23名年龄为26.8±1.0岁的健康正常受试者中,研究了苯二氮䓬(Bz)受体选择性和非选择性催眠药的镇静、遗忘和对行为表现的干扰作用。采用重复测量设计,在睡前双盲给予三唑仑(0.25毫克和0.50毫克)、唑吡坦(10毫克和20毫克)和安慰剂。90分钟后觉醒时(每种药物的浓度接近峰值),完成了一个包括记忆、警觉性和精神运动任务的30分钟行为测试。与安慰剂相比,每种药物及其剂量均损害了记忆(即时和延迟)、警觉性和精神运动表现。在活性药物中,20毫克唑吡坦的损害最大,其次是0.50毫克三唑仑,然后是10毫克唑吡坦,最后是0.25毫克三唑仑。第二天早上,所有药物及其剂量也损害了延迟回忆(即顺行性遗忘)。遗忘和对行为表现的干扰作用与药物及其剂量的相对催眠作用平行。在这些药效学作用中未观察到受体选择性。

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