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性别差异以及加巴喷丁和唑吡坦对非快速眼动和快速眼动睡眠 EEG 功率谱的影响。

Sex differences and the effect of gaboxadol and zolpidem on EEG power spectra in NREM and REM sleep.

机构信息

Surrey Sleep Research Centre, University of Surrey, Guildford, UK.

出版信息

J Psychopharmacol. 2010 Nov;24(11):1613-8. doi: 10.1177/0269881109105788. Epub 2009 Jun 1.

Abstract

Hypnotics that interact with the GABA(A) receptor have marked effects on the electroencephalogram (EEG) during sleep. It is not known whether the effects of hypnotics on EEG power spectra differ between the sexes. The effects of 5, 10 and 15 mg of gaboxadol (GBX) and 10 mg of zolpidem (ZOL) on EEG power spectra were assessed in a randomized, double-blind, placebo-controlled, 5-way cross-over design study using a phase-advance model of transient insomnia. Sleep stage specific EEG power spectra were computed in 36 men and 45 women. GBX enhanced power density in delta and theta activity in non-rapid eye movement (NREM) and rapid eye movement (REM) sleep, and suppressed sleep spindle activity in NREM sleep. The increase of delta and theta activity in NREM and REM sleep was significantly larger for women than for men but the suppression of spindle activity did not differ between the sexes. After ZOL administration, no sex differences were observed in the reduction of delta and theta activity in NREM sleep, but the increase in sleep spindle activity in NREM sleep was greater in women than in men. These sex dependent and differential effects of GBX and ZOL may be related to their differential affinity for GABA(A) receptor subtypes and their modulation by neurosteroids.

摘要

与 GABA(A) 受体相互作用的催眠药在睡眠期间对脑电图 (EEG) 有明显影响。目前尚不清楚催眠药对 EEG 功率谱的影响是否存在性别差异。在一项使用短暂性失眠的相移模型的随机、双盲、安慰剂对照、5 向交叉设计研究中,评估了 5、10 和 15mg 加巴喷丁 (GBX) 和 10mg 唑吡坦 (ZOL) 对 EEG 功率谱的影响。在 36 名男性和 45 名女性中计算了睡眠阶段特异性 EEG 功率谱。GBX 增强了非快速眼动 (NREM) 和快速眼动 (REM) 睡眠中的 delta 和 theta 活动的功率密度,并抑制了 NREM 睡眠中的睡眠纺锤波活动。女性 NREM 和 REM 睡眠中 delta 和 theta 活动的增加明显大于男性,但纺锤波活动的抑制在性别之间没有差异。在给予 ZOL 后,在 NREM 睡眠中 delta 和 theta 活动减少方面未观察到性别差异,但女性 NREM 睡眠中睡眠纺锤波活动的增加大于男性。GBX 和 ZOL 的这些性别依赖性和差异作用可能与其对 GABA(A) 受体亚型的不同亲和力以及神经甾体的调制有关。

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