Department of Molecular and Biomedical Pharmacology, University of Kentucky College of Medicine, Lexington, Kentucky, United States of America.
PLoS One. 2011 Apr 4;6(4):e18387. doi: 10.1371/journal.pone.0018387.
Age-related cognitive deficits negatively affect quality of life and can presage serious neurodegenerative disorders. Despite sleep disruption's well-recognized negative influence on cognition, and its prevalence with age, surprisingly few studies have tested sleep's relationship to cognitive aging.
We measured sleep stages in young adult and aged F344 rats during inactive (enhanced sleep) and active (enhanced wake) periods. Animals were behaviorally characterized on the Morris water maze and gene expression profiles of their parietal cortices were taken.
Water maze performance was impaired, and inactive period deep sleep was decreased with age. However, increased deep sleep during the active period was most strongly correlated to maze performance. Transcriptional profiles were strongly associated with behavior and age, and were validated against prior studies. Bioinformatic analysis revealed increased translation and decreased myelin/neuronal pathways.
The F344 rat appears to serve as a reasonable model for some common sleep architecture and cognitive changes seen with age in humans, including the cognitively disrupting influence of active period deep sleep. Microarray analysis suggests that the processes engaged by this sleep are consistent with its function. Thus, active period deep sleep appears temporally misaligned but mechanistically intact, leading to the following: first, aged brain tissue appears capable of generating the slow waves necessary for deep sleep, albeit at a weaker intensity than in young. Second, this activity, presented during the active period, seems disruptive rather than beneficial to cognition. Third, this active period deep sleep may be a cognitively pathologic attempt to recover age-related loss of inactive period deep sleep. Finally, therapeutic strategies aimed at reducing active period deep sleep (e.g., by promoting active period wakefulness and/or inactive period deep sleep) may be highly relevant to cognitive function in the aging community.
与年龄相关的认知能力下降会降低生活质量,并可能预示着严重的神经退行性疾病。尽管睡眠中断对认知能力有明显的负面影响,而且随着年龄的增长而普遍存在,但令人惊讶的是,很少有研究测试过睡眠与认知衰老的关系。
我们在年轻成年和老年 F344 大鼠的非活动期(增强睡眠)和活动期(增强觉醒)期间测量睡眠阶段。对动物进行 Morris 水迷宫行为特征测试,并对其顶叶皮层的基因表达谱进行检测。
水迷宫表现受损,随着年龄的增长,非活动期深度睡眠减少。然而,活动期深度睡眠增加与迷宫表现相关性最强。转录谱与行为和年龄密切相关,并与之前的研究相验证。生物信息学分析显示翻译增加和少突胶质细胞/神经元通路减少。
F344 大鼠似乎是一种合理的模型,可用于研究人类常见的一些睡眠结构和认知变化,包括活动期深度睡眠对认知的干扰影响。微阵列分析表明,这种睡眠所涉及的过程与其功能一致。因此,活动期深度睡眠似乎在时间上错位,但在机制上完整,导致以下结果:第一,老年脑组织似乎能够产生深度睡眠所需的慢波,但强度比年轻脑组织弱。第二,这种活动在活动期出现,似乎对认知有干扰作用,而不是有益的。第三,这种活动期深度睡眠可能是一种认知病理性尝试,以弥补与年龄相关的非活动期深度睡眠的丧失。最后,旨在减少活动期深度睡眠的治疗策略(例如,通过促进活动期觉醒和/或非活动期深度睡眠)可能与老龄化人群的认知功能高度相关。