Centre d'Investigació de Medicaments, Institut d'Investigacions Biomèdiques Sant Pau (IIB-Sant Pau), Barcelona, Spain.
Neuropsychobiology. 2011;63(4):252-60. doi: 10.1159/000321806. Epub 2011 Apr 13.
BACKGROUND/AIMS: The correlation between theta activity during wakefulness and slow-wave activity (SWA) during sleep observed after sleep deprivation suggests such patterns can be used as electroencephalogram (EEG) biomarkers of the sleep homeostasis process. Since these EEG components would be very useful objective measures to assess CNS drug effects, we investigated whether the relationship between sleep homeostatic EEG biomarkers could be reproduced after an experimental pharmacological intervention.
Seventeen healthy volunteers took part in a phase I randomized, double-blind, crossover design study. To increase sleep propensity, all participants received a single morning oral dose of olanzapine (5 mg) and placebo. Quantitative EEG analysis was done by power spectra calculations: theta activity (3.5-7.5 Hz) during wakefulness and SWA (0.5-4.0 Hz) during sleep. The relationship between the 2 EEG parameters was assessed by correlating the rise rate (percent/hour) of theta activity in wakefulness and the increase (percent) of SWA in the first non-REM sleep episode.
Following olanzapine administration we observed increases in theta activity during wakefulness, and increases in total sleep time, sleep efficiency and slow-wave sleep time during sleep. However, a weak and unreliable correlation was observed between the increases in theta activity and changes in sleep SWA.
From these results, we cannot affirm that these waking and sleep EEG variables behave as biomarkers of human sleep homeostasis after drug administration. It is possible that these EEG biomarkers reflect different physiological mechanisms if they are assessed during drug CNS effects.
背景/目的:睡眠剥夺后观察到的清醒时θ活动与睡眠慢波活动(SWA)之间的相关性表明,这些模式可以用作睡眠稳态过程的脑电图(EEG)生物标志物。由于这些 EEG 成分将是评估中枢神经系统药物效应的非常有用的客观措施,因此我们研究了在实验药理学干预后睡眠稳态 EEG 生物标志物之间的关系是否可以重现。
17 名健康志愿者参加了一项 I 期随机、双盲、交叉设计研究。为了增加睡眠倾向,所有参与者均接受了一次早晨口服奥氮平(5 毫克)和安慰剂。通过功率谱计算进行定量脑电图分析:清醒时的θ活动(3.5-7.5 Hz)和睡眠时的 SWA(0.5-4.0 Hz)。通过将清醒时θ活动的上升率(每小时百分比)与第一个非快速眼动睡眠期 SWA 的增加(百分比)相关联,评估了这 2 个 EEG 参数之间的关系。
在奥氮平给药后,我们观察到清醒时θ活动增加,睡眠总时间、睡眠效率和慢波睡眠时间增加。然而,在θ活动增加和睡眠 SWA 变化之间观察到的相关性较弱且不可靠。
从这些结果来看,我们不能肯定这些清醒和睡眠 EEG 变量在给药后作为人类睡眠稳态的生物标志物。如果在药物对中枢神经系统的影响期间评估这些 EEG 生物标志物,则它们可能反映了不同的生理机制。