内分泌学
睡眠剥夺
内科学
淀粉样β
医学
认知功能衰退
阿尔茨海默病
τ蛋白
心理学
神经科学
认知
睡眠(系统调用)
疾病
痴呆
计算机科学
操作系统
作者
Jerrah K. Holth,Sarah K. Fritschi,Chanung Wang,Nigel P. Pedersen,John R. Cirrito,Thomas E. Mahan,Mary Beth Finn,Melissa Manis,Joel C. Geerling,Patrick M. Fuller,Brendan P. Lucey,David M. Holtzman
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2019-01-24
卷期号:363 (6429): 880-884
被引量:786
标识
DOI:10.1126/science.aav2546
摘要
The sleep-wake cycle regulates interstitial fluid (ISF) and cerebrospinal fluid (CSF) levels of β-amyloid (Aβ) that accumulates in Alzheimer's disease (AD). Furthermore, chronic sleep deprivation (SD) increases Aβ plaques. However, tau, not Aβ, accumulation appears to drive AD neurodegeneration. We tested whether ISF/CSF tau and tau seeding and spreading were influenced by the sleep-wake cycle and SD. Mouse ISF tau was increased ~90% during normal wakefulness versus sleep and ~100% during SD. Human CSF tau also increased more than 50% during SD. In a tau seeding-and-spreading model, chronic SD increased tau pathology spreading. Chemogenetically driven wakefulness in mice also significantly increased both ISF Aβ and tau. Thus, the sleep-wake cycle regulates ISF tau, and SD increases ISF and CSF tau as well as tau pathology spreading.
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