Roehrs T A, Zorick F J, Wittig R M, Roth T
Br J Clin Pharmacol. 1986 Aug;22(2):143-7. doi: 10.1111/j.1365-2125.1986.tb05241.x.
A polysomnographic assessment in healthy normal sleepers of possible dose relations for rebound insomnia was conducted. As an additional measure of rebound the study included a direct test of sleep/wake tendency during the night of drug discontinuation. Twelve, healthy men (21-30 years) each received placebo, 0.25 mg and 0.50 mg triazolam for 6 consecutive nights followed by a discontinuation night and 14 nights of recovery at home. The three conditions were presented, double-blind, in a latin square design. On night 6 of drug administration both doses increased total sleep time compared to placebo, but 0.50 mg did not improve sleep beyond 0.25 mg. On drug discontinuation (night 7) wake time over the 8 h recording and sleep latency after an experimental awakening (02.30 h) were increased with 0.50 mg compared to placebo and 0.25 mg. On these measures of rebound 0.25 mg did not differ from placebo. Thus rebound insomnia occurred only at a dose (0.50 mg) which produced no additional hypnotic efficacy in these normal sleepers. Whether tests of sleep/wake tendency make a useful measure of rebound insomnia needs further clarification.
对健康正常睡眠者进行了多导睡眠图评估,以探究反弹性失眠可能的剂量关系。作为反弹性的一项额外测量指标,该研究纳入了在停药当晚对睡眠/觉醒倾向的直接测试。12名健康男性(年龄在21至30岁之间)每人连续6晚分别服用安慰剂、0.25毫克和0.50毫克三唑仑,随后是停药一晚以及在家中恢复14晚。这三种情况采用双盲拉丁方设计呈现。在给药的第6晚,与安慰剂相比,两种剂量均增加了总睡眠时间,但0.50毫克的效果并未超过0.25毫克。在停药当晚(第7晚),与安慰剂和0.25毫克相比,0.50毫克组在8小时记录期间的觉醒时间以及实验性觉醒(02:30)后的睡眠潜伏期均增加。在这些反弹性测量指标上,0.25毫克组与安慰剂组无差异。因此,反弹性失眠仅在一个剂量(0.50毫克)下出现,而该剂量在这些正常睡眠者中并未产生额外的催眠效果。睡眠/觉醒倾向测试是否能作为反弹性失眠的有效测量指标,还需要进一步阐明。