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腺苷与睡眠-觉醒调节。

Adenosine and sleep-wake regulation.

作者信息

Basheer Radhika, Strecker Robert E, Thakkar Mahesh M, McCarley Robert W

机构信息

Neuroscience Laboratory, Department of Psychiatry, Harvard Medical School and Boston VA Healthcare System, Brockton, MA 02301, USA.

出版信息

Prog Neurobiol. 2004 Aug;73(6):379-96. doi: 10.1016/j.pneurobio.2004.06.004.

Abstract

This review addresses three principal questions about adenosine and sleep-wake regulation: (1) Is adenosine an endogenous sleep factor? (2) Are there specific brain regions/neuroanatomical targets and receptor subtypes through which adenosine mediates sleepiness? (3) What are the molecular mechanisms by which adenosine may mediate the long-term effects of sleep loss? Data suggest that adenosine is indeed an important endogenous, homeostatic sleep factor, likely mediating the sleepiness that follows prolonged wakefulness. The cholinergic basal forebrain is reviewed in detail as an essential area for mediating the sleep-inducing effects of adenosine by inhibition of wake-promoting neurons via the A1 receptor. The A2A receptor in the subarachnoid space below the rostral forebrain may play a role in the prostaglandin D2-mediated somnogenic effects of adenosine. Recent evidence indicates that a cascade of signal transduction induced by basal forebrain adenosine A1 receptor activation in cholinergic neurons leads to increased transcription of the A1 receptor; this may play a role in mediating the longer-term effects of sleep deprivation, often called sleep debt.

摘要

本综述探讨了关于腺苷与睡眠-觉醒调节的三个主要问题:(1)腺苷是一种内源性睡眠因子吗?(2)是否存在特定的脑区/神经解剖靶点以及受体亚型,通过它们腺苷介导嗜睡?(3)腺苷可能介导睡眠剥夺长期影响的分子机制是什么?数据表明,腺苷确实是一种重要的内源性稳态睡眠因子,可能介导长时间清醒后的嗜睡。详细综述了胆碱能基底前脑,它是通过A1受体抑制促觉醒神经元来介导腺苷诱导睡眠作用的关键区域。在前脑嘴侧下方蛛网膜下腔中的A2A受体可能在腺苷的前列腺素D2介导的促眠作用中发挥作用。最近的证据表明,胆碱能神经元中基底前脑腺苷A1受体激活诱导的一系列信号转导导致A1受体转录增加;这可能在介导睡眠剥夺的长期影响(通常称为睡眠债)中发挥作用。

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