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一种新型丁酰苯衍生物(溴氮卓)对正常男性夜间睡眠的影响。

Effects of a new butyrophenone derivate (Buronil) on nocturnal sleep in normal man.

作者信息

Risberg A M, Henricson S, Elmqvist D, Ingvar D H

出版信息

Psychopharmacologia. 1975 Jul 23;43(1):95-9. doi: 10.1007/BF00437622.

Abstract

Nocturnal sleep was studied in eight young normal volunteers (3 female and 5 male students) with polygraphic technique during 2 periods of 10 night each. After 2 adaptation and 2 baseline nights with placebo, they were given methylperone (Buronil) 10 or 50 mg per night during three nights and then again placebo for three withdrawal nights. The study was made double blind. The scoring of the records was done according to the manual by Rechtschaffen and Kales (1968). No changes of sleep stages were seen during the drug periods. The lower dose gave an increase of sleep latency but a decrease of number of awakenings during the night. An increase of REM-periods was shown after 50 mg and also a decrease of REM-latency and REM-density. The only significant change during withdrawal periods was a decrease of REM-sleep after methylperone 50 mg, so there was no "barbiturate type" of withdrawal. The change was also different from that of chloropromazine, which has no clear rebound effect.

摘要

采用多导记录技术,对8名年轻正常志愿者(3名女学生和5名男学生)的夜间睡眠进行了研究,研究分两个阶段进行,每个阶段持续10个夜晚。在经过2个适应期夜晚和2个服用安慰剂的基线夜晚后,他们在三个夜晚每晚服用10毫克或50毫克美哌隆(溴哌利多),然后在三个撤药夜晚再次服用安慰剂。该研究采用双盲法。根据Rechtschaffen和Kales(1968年)的手册对记录进行评分。在用药期间未观察到睡眠阶段的变化。较低剂量使睡眠潜伏期延长,但夜间觉醒次数减少。50毫克剂量后快速眼动睡眠期增加,快速眼动潜伏期和快速眼动密度也降低。撤药期间唯一显著的变化是50毫克美哌隆后快速眼动睡眠减少,因此不存在“巴比妥类药物型”撤药反应。这种变化也与氯丙嗪不同,氯丙嗪没有明显的反跳效应。

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