Gillin J C, Jernajczyk W, Valladares-Neto D C, Golshan S, Lardon M, Stahl S M
University of California, San Diego.
Psychopharmacology (Berl). 1994 Dec;116(4):433-6. doi: 10.1007/BF02247474.
In order to test the hypothesis that serotonergic mechanisms inhibit REM sleep via a 5HT1A receptor, we administered placebo and ipsapirone (10 and 20 mg by mouth 15 min before bedtime) to ten normal volunteers in a double blind fashion. Ipsapirone is a relatively selective 5HT1A receptor agonist. As predicted, ipsapirone prolonged REM latency and Mean Latency to Eye Movements (M-LEM), a measure of time between onset of REM sleep and the first eye movement of the REM period, and REM% at both doses compared with placebo. It also reduced sleep efficiency and total REM sleep time at the highest dose. These results support the hypothesis that systemic stimulation of 5HT1A receptors prolong REM latency and inhibit REM sleep.
为了验证血清素能机制通过5HT1A受体抑制快速眼动睡眠这一假说,我们以双盲方式给10名正常志愿者服用安慰剂和伊沙匹隆(睡前15分钟口服10毫克和20毫克)。伊沙匹隆是一种相对选择性的5HT1A受体激动剂。正如所预测的那样,与安慰剂相比,两种剂量的伊沙匹隆均延长了快速眼动潜伏期和平均眼动潜伏期(M-LEM,即快速眼动睡眠开始至快速眼动期首次眼动之间的时间测量值)以及快速眼动睡眠占比。在最高剂量时,它还降低了睡眠效率和总的快速眼动睡眠时间。这些结果支持了全身刺激5HT1A受体会延长快速眼动潜伏期并抑制快速眼动睡眠这一假说。