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β-肾上腺素能阻滞剂的中枢神经系统效应:辅助特性的作用

Central nervous system effects of beta-adrenergic-blocking drugs: the role of ancillary properties.

作者信息

Kostis J B, Rosen R C

出版信息

Circulation. 1987 Jan;75(1):204-12. doi: 10.1161/01.cir.75.1.204.

Abstract

Among the side effects commonly reported with the use of beta-blockers are symptoms related to the central nervous system (CNS). In this study we compared the effects of four beta-blockers with different ancillary properties (atenolol, metoprolol, propranolol, and pindolol) and placebo on objective and subjective measures of CNS function in 30 healthy male subjects. All subjects were randomly assigned to a double-blind, placebo controlled, Latin-square design study in which five 1 week periods of drug or placebo administration were separated by 2 week washout periods. Laboratory evaluations were conducted at the end of each treatment period, and included multistage exercise stress testing; questionnaire assessments of mood state, sexual function, and sleep habits; tests of psychomotor function; and overnight polysomnographic measures of sleep. Significant effects on sleep continuity were observed for each of the lipophilic drugs, as reflected in the number of awakenings (pindolol = 6.4 +/- 5.0; propranolol = 6.3 +/- 3.2; metoprolol = 7.2 +/- 4.7; atenolol = 3.6 +/- 2.9; placebo = 3.9 +/- 2.7) and time of wakefulness (pindolol = 20.6 +/- 27.0 min; propranolol = 15.5 +/- 23.0 min; metoprolol = 19.5 +/- 24.3 min; atenolol = 10.2 +/- 11.6 min; placebo = 9.2 +/- 74.5 min). Only pindolol significantly affected rapid eye movement (REM) sleep time (pindolol = 54.5 +/- 21.9 min; placebo = 74.5 +/- 74.5 min) and REM latency (pindolol = 175.0 +/- 60.7 min; placebo = 95.4 +/- 43.8 min). Subjective reports of sleep similarly indicated increased wakefulness and greater restlessness with lipophilic beta-blockers.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

使用β受体阻滞剂时常见的副作用包括与中枢神经系统(CNS)相关的症状。在本研究中,我们比较了四种具有不同辅助特性的β受体阻滞剂(阿替洛尔、美托洛尔、普萘洛尔和吲哚洛尔)以及安慰剂对30名健康男性受试者中枢神经系统功能的客观和主观测量指标的影响。所有受试者均被随机分配至一项双盲、安慰剂对照、拉丁方设计研究中,其中五个为期1周的药物或安慰剂给药期被2周的洗脱期隔开。在每个治疗期结束时进行实验室评估,包括多级运动应激测试;情绪状态、性功能和睡眠习惯的问卷调查评估;精神运动功能测试;以及睡眠的夜间多导睡眠图测量。亲脂性药物均对睡眠连续性有显著影响,这体现在觉醒次数(吲哚洛尔 = 6.4 ± 5.0;普萘洛尔 = 6.3 ± 3.2;美托洛尔 = 7.2 ± 4.7;阿替洛尔 = 3.6 ± 2.9;安慰剂 = 3.9 ± 2.7)和清醒时间(吲哚洛尔 = 20.6 ± 27.0分钟;普萘洛尔 = 15.5 ± 23.0分钟;美托洛尔 = 19.5 ± 24.3分钟;阿替洛尔 = 10.2 ± 11.6分钟;安慰剂 = 9.2 ± 74.5分钟)上。只有吲哚洛尔显著影响快速眼动(REM)睡眠时间(吲哚洛尔 = 54.5 ± 21.9分钟;安慰剂 = 74.5 ± 74.5分钟)和REM潜伏期(吲哚洛尔 = 175.0 ± 60.7分钟;安慰剂 = 95.4 ± 43.8分钟)。关于睡眠的主观报告同样表明,亲脂性β受体阻滞剂会增加清醒感和不安感。(摘要截短于250字)

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