Greene Robert W, Bjorness Theresa E, Suzuki Ayako
UT Southwestern Medical Center, Dallas, TX, United States; International Institute of Integrative Sleep Medicine, University of Tsukuba, Japan; VAMC, Dallas, TX, United States.
UT Southwestern Medical Center, Dallas, TX, United States; VAMC, Dallas, TX, United States.
Curr Opin Neurobiol. 2017 Jun;44:236-242. doi: 10.1016/j.conb.2017.05.015. Epub 2017 Jun 19.
Slow wave activity (SWA) during slow wave sleep (SWS) is the best indicator of the sleep homeostasis. The intensity of the SWA observed during SWS that follows prolonged waking is directly correlated with the duration of prior waking and its intensity decays during SWS suggesting a buildup and a resolution of sleep need. This sleep-homeostasis related SWA results from a buildup and decay of extracellular adenosine that acts at neuronal adenosine A1 receptors to facilitate SWA and is metabolized by adenosine kinase found in glia. This local neuronal-glial circuit for homeostatic SWA is primarily under the requisite control of two genes, the Adora1 and Adk, encoding the responsible adenosine receptor and adenosine's highest affinity metabolizing enzyme.
慢波睡眠(SWS)期间的慢波活动(SWA)是睡眠稳态的最佳指标。长时间清醒后出现的慢波睡眠期间观察到的慢波活动强度与先前清醒的持续时间直接相关,并且在慢波睡眠期间其强度会衰减,这表明睡眠需求的积累和解决。这种与睡眠稳态相关的慢波活动是由细胞外腺苷的积累和衰减引起的,腺苷作用于神经元腺苷A1受体以促进慢波活动,并被神经胶质细胞中发现的腺苷激酶代谢。这种用于稳态慢波活动的局部神经元-神经胶质细胞回路主要受两个基因Adora1和Adk的必要控制,这两个基因分别编码负责的腺苷受体和腺苷的最高亲和力代谢酶。