Halperin J M, Miller D, Iorio L C
Pharmacol Biochem Behav. 1981 Jun;14(6):811-4. doi: 10.1016/0091-3057(81)90365-8.
Sleep-inducing effects of hypnotic drugs are difficult to demonstrate in rats because of high baseline sleep times. Most increases in slow wave sleep (SWS) following the administration of hypnotics have been found to be at the expense of REM sleep rather than waking. In the first experiment we found that rats chronically implanted with electrodes for recording ECoG and EMG slept significantly less during the first two hours of the dark period when housed under 16-hr light 8-hr dark (16L/8D) than when housed under 12L/12D conditions. The second experiment examined the effects of flurazepam, phenobarbital and thalidomide administered orally at the onset of the two-hour period of increased waking resulting from the 16L/8D lighting. All three drugs caused dose-dependent reductions in waking and increases in SWS with no alterations in REM% of total sleep time. Sleep onset latency was also significantly was also significantly reduced by all three drugs. As in man, flurazepam was the most potent, and thalidomide was the least potent of the hypnotics in rats.
由于大鼠的基线睡眠时间较长,催眠药物的助眠效果很难在大鼠身上得到证实。多数催眠药物给药后慢波睡眠(SWS)的增加是以快速眼动睡眠(REM)为代价,而非清醒时间。在第一个实验中,我们发现,长期植入电极用于记录皮层脑电图(ECoG)和肌电图(EMG)的大鼠,在16小时光照/8小时黑暗(16L/8D)条件下饲养时,在黑暗期的前两小时睡眠明显少于在12L/12D条件下饲养时。第二个实验研究了在16L/8D光照导致清醒增加的两小时开始时口服氟西泮、苯巴比妥和沙利度胺的效果。所有三种药物都导致清醒时间呈剂量依赖性减少以及SWS增加,总睡眠时间中REM%无变化。三种药物还均显著缩短了入睡潜伏期。与人类一样,在大鼠中,氟西泮是最有效的催眠药,而沙利度胺是最无效的催眠药。