Research Service (151A3), Veterans Affairs Greater Los Angeles Healthcare System, Sepulveda, CA, USA.
Research Service (151A3), Veterans Affairs Greater Los Angeles Healthcare System, Sepulveda, CA, USA; Department of Psychiatry, University of California, Los Angeles, CA, USA.
Neuroscience. 2020 Feb 10;427:29-42. doi: 10.1016/j.neuroscience.2019.11.046. Epub 2019 Dec 14.
Aging is a well-recognized risk factor for sleep disruption. The characteristics of sleep in aging include its disruption by frequent awakenings, a decline in both non-rapid eye movement (nonREM) and REM sleep amounts, and a weaker homeostatic response to sleep loss. Evidence also suggests that sleep in females is more sensitive to changes in the ovarian steroidal milieu. The Fischer-344 rats are commonly used experimental subjects in behavioral and physiological studies, including sleep and aging. Most sleep studies in Fischer-344 rats have used male subjects to avoid interactions between the estrus and sleep-waking cycles. The changes in the sleep-wake organization of female Fischer-344 rats, especially with advancing age, are not well-characterized. We determined sleep-waking features of cycling females across estrus stages. We also compared spontaneous and homeostatic sleep response profiles of young (3-4 months) and old (24-25 months) male and female Fischer-344 rats. The results suggest that: i) sleep-wake architectures across stages of estrus cycle in young females were largely comparable except for a significant suppression of REM sleep at proestrus night and an increase in REM sleep the following day; ii) despite hormonal differences, sleep-wake architecture in male and female rats of corresponding ages were comparable except for the suppression of REM sleep at proestrus night and higher nonREM delta power in recovery sleep; and iii) aging significantly affected sleep-wake amounts, sleep-wake stability, and homeostatic response to sleep loss in both male and female rats and that the adverse effects of aging were largely comparable in both sexes.
衰老是睡眠紊乱公认的危险因素。衰老相关的睡眠特点包括频繁觉醒、非快速动眼期(非 REM)和快速动眼期(REM)睡眠时间减少、对睡眠缺失的内稳态反应减弱。证据还表明,女性的睡眠对卵巢类固醇环境的变化更为敏感。Fischer-344 大鼠通常被用作行为和生理学研究(包括睡眠和衰老)的实验对象。大多数 Fischer-344 大鼠的睡眠研究都使用雄性实验对象,以避免发情和睡眠-觉醒周期之间的相互作用。然而,雌性 Fischer-344 大鼠的睡眠-觉醒组织变化,特别是随着年龄的增长,尚未得到很好的描述。我们确定了发情周期各个阶段循环雌性大鼠的睡眠-觉醒特征。我们还比较了年轻(3-4 个月)和年老(24-25 个月)雄性和雌性 Fischer-344 大鼠的自发性和内稳态睡眠反应特征。结果表明:i)年轻雌性大鼠发情周期各阶段的睡眠-觉醒结构基本相似,除了发情前期夜间 REM 睡眠显著抑制和第二天 REM 睡眠增加;ii)尽管存在激素差异,但同龄雄性和雌性大鼠的睡眠-觉醒结构相似,除了发情前期夜间 REM 睡眠抑制和恢复性睡眠中非 REM 德尔塔功率增加;iii)衰老显著影响了雄性和雌性大鼠的睡眠-觉醒量、睡眠-觉醒稳定性和对睡眠缺失的内稳态反应,而且衰老的不利影响在两性中基本相当。