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女性生殖激素改变去卵巢大鼠的睡眠结构。

Female reproductive hormones alter sleep architecture in ovariectomized rats.

机构信息

Department of Anatomy & Neurobiology, Dalhousie University, Halifax, Nova Scotia, Canada.

出版信息

Sleep. 2011 Apr 1;34(4):519-30. doi: 10.1093/sleep/34.4.519.

DOI:10.1093/sleep/34.4.519
PMID:21461331
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3065263/
Abstract

STUDY OBJECTIVES

Treating ovariectomized rats with physiological levels of estradiol and/or progesterone affects aspects of both baseline (24 h) sleep and recovery (18 h) sleep after 6 h of sleep deprivation. We have extended the analysis of these effects by examining several additional parameters of sleep architecture using the same data set as in our previous study (Deurveilher et al. SLEEP 2009;32(7):865-877).

DESIGN

Sleep in ovariectomized rats implanted with oil, 17 β-estradiol and/or progesterone capsules was recorded using EEG and EMG before, during, and after 6 h of sleep deprivation during the light phase of a 12/12 h light/dark cycle.

MEASUREMENTS AND RESULTS

During the baseline dark, but not light, phase, treatments with estradiol alone or combined with progesterone decreased the mean duration of non-rapid eye movement sleep (NREMS) episodes and the number of REMS episodes, while also increasing brief awakenings, consistent with the previously reported lower baseline NREMS and REMS amounts. Following sleep deprivation, the hormonal treatments caused a larger percentage increase from baseline in the mean durations of NREMS and REMS episodes, and a larger percentage decrease in brief awakenings, consistent with the previously reported larger increase in recovery REMS amount. There were no hormonal effects on NREMS and REMS EEG power values, other than on recovery NREMS delta power, as previously reported.

CONCLUSIONS

Physiological levels of estradiol and/or progesterone in female rats modulate sleep architecture differently at baseline and after acute sleep loss, fragmenting baseline sleep while consolidating recovery sleep. These hormones also play a role in the diurnal pattern of NREMS maintenance.

摘要

研究目的

用生理水平的雌二醇和/或孕酮治疗去卵巢大鼠,会影响睡眠剥夺 6 小时后基线(24 小时)睡眠和恢复(18 小时)睡眠的各个方面。我们使用与之前研究相同的数据(Deurveilher 等人,SLEEP 2009;32(7):865-877),通过检查睡眠结构的几个其他参数,扩展了这些影响的分析。

设计

在 12/12 小时明暗循环的光相期间,使用 EEG 和 EMG 记录植入油、17β-雌二醇和/或孕酮胶囊的去卵巢大鼠的睡眠,在睡眠剥夺 6 小时之前、期间和之后。

测量和结果

在基线暗相期间,但不在光相期间,仅用雌二醇或与孕酮联合治疗会减少非快速眼动睡眠(NREMS)发作的平均持续时间和 REMS 发作的次数,同时增加短暂觉醒,这与之前报道的较低基线 NREMS 和 REMS 量一致。在睡眠剥夺后,激素治疗导致 NREMS 和 REMS 发作的平均持续时间从基线增加的百分比更大,短暂觉醒的百分比下降更大,这与之前报道的恢复 REMS 量的增加更大一致。除了先前报道的恢复 NREMS 德尔塔功率外,激素对 NREMS 和 REMS EEG 功率值没有影响。

结论

在雌性大鼠中,生理水平的雌二醇和/或孕酮在基线和急性睡眠剥夺后不同地调节睡眠结构,使基线睡眠碎片化,同时巩固恢复睡眠。这些激素在 NREMS 维持的昼夜模式中也发挥作用。

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