Nicholson A N, Stone B M
Int Pharmacopsychiatry. 1982;17 Suppl 2:92-7.
Effects of 2.5, 5.0, 7.5, and 10.0 mg zopiclone on sleep and on performance the next day were studied in 6 healthy adult males aged between 21 and 33 years. The experiment was double-blind and placebo controlled. 5.0 and 10.0 mg zopiclone decreased the amount of awake activity and drowsy (stage 1) sleep over the first 6 h of sleep, but this effect was only present for the whole sleep period with the 10.0-mg dose. The duration and percentage of stage 3 sleep were increased with 7.5 mg. The 7.5- and 10.0-mg doses increased the combined duration of stages 2, 3, and 4 sleep over the first 6 h and over the whole night. The first period of rapid eye movement sleep was delayed with 7.5 mg, and with 10.0 mg the time spent in rapid eye movement sleep was reduced during the first 6 h of sleep, but not over the whole night. The number of substitutions in the digit symbol substitution test was decreased 9 h after ingestion of 7.5 and 10.0 mg, and the number of symbols copied reduced after 10.0 mg. The clinical dose range of zopiclone is likely to be up to 7.5 mg. The latter dose provides a useful hypnotic effect with minimal residual effects the next day, whilst 5.0 mg is appropriate for those involved in skilled tasks where even the most minor changes in performance during the early part of the next day must be avoided.
在6名年龄在21至33岁之间的健康成年男性中,研究了2.5毫克、5.0毫克、7.5毫克和10.0毫克佐匹克隆对睡眠及次日表现的影响。该实验为双盲且有安慰剂对照。5.0毫克和10.0毫克佐匹克隆在睡眠的前6小时减少了清醒活动量和困倦(第1阶段)睡眠时间,但这种效果仅在10.0毫克剂量的整个睡眠期间出现。7.5毫克增加了第3阶段睡眠的时长和百分比。7.5毫克和10.0毫克剂量在睡眠的前6小时及整个夜间增加了第2、3和4阶段睡眠的总时长。7.5毫克使快速眼动睡眠的首个时段延迟,10.0毫克使睡眠前6小时内快速眼动睡眠的时长减少,但在整个夜间并非如此。摄入7.5毫克和10.0毫克后9小时,数字符号替换测试中的替换次数减少,摄入10.0毫克后复制的符号数量减少。佐匹克隆的临床剂量范围可能高达7.5毫克。后一剂量具有有效的催眠作用,且次日残留效应最小,而5.0毫克适用于那些从事需要避免次日早期表现出现哪怕最微小变化的熟练任务的人群。