Borbély A A, Achermann P
Institute of Pharmacology, University of Zürich, Switzerland.
Eur J Pharmacol. 1991 Mar 19;195(1):11-8. doi: 10.1016/0014-2999(91)90376-2.
A single bedtime dose of the benzodiazepine hypnotics, flunitrazepam (2 mg), triazolam (0.5 mg) or flurazepam (30 mg), was administered to young, healthy subjects. Abortive first rapid eye movement sleep (REMS) episodes, characterized by a low level of EEG slow-wave activity (spectral power density in the 0.75-4.5 Hz band) without rapid eye movements and/or muscle atonia, were more frequent in the drug night than in the placebo night or in the drug-free night following upon the drug night. The benzodiazepine hypnotics depressed slow-wave activity in non-REM sleep (NREMS) in the drug night and the subsequent drug-free night. However, the typical declining trend of slow-wave activity over the first three NREMS-REMS cycles, and the cyclic ultradian pattern of slow-wave activity were little affected by the hypnotics. The results indicate that benzodiazepine hypnotics depress the generation of slow EEG waves without disrupting the homeostatic and ultradian processes of sleep regulation.
给年轻健康受试者睡前单次服用苯二氮䓬类催眠药氟硝西泮(2毫克)、三唑仑(0.5毫克)或氟西泮(30毫克)。以低水平脑电图慢波活动(0.75 - 4.5赫兹频段的频谱功率密度)为特征且无快速眼动和/或肌肉弛缓的首次快速眼动睡眠(REMS)发作中止现象,在用药当晚比安慰剂当晚或用药当晚后的无药当晚更频繁。苯二氮䓬类催眠药在用药当晚和随后的无药当晚均抑制非快速眼动睡眠(NREMS)中的慢波活动。然而,在前三个NREMS - REMS周期中慢波活动的典型下降趋势以及慢波活动的周期性超日节律模式受催眠药影响较小。结果表明,苯二氮䓬类催眠药抑制脑电图慢波的产生,但不干扰睡眠调节的稳态和超日节律过程。