Lazarus Michael, Chen Jiang-Fan, Huang Zhi-Li, Urade Yoshihiro, Fredholm Bertil B
International Institute for Integrative Sleep Medicine (WPI-IIIS), University of Tsukuba, Tsukuba, Ibaraki, 305-8575, Japan.
Department of Neurology, Boston University School of Medicine, Boston, MA, 02118, USA.
Handb Exp Pharmacol. 2019;253:359-381. doi: 10.1007/164_2017_36.
The classic endogenous somnogen adenosine promotes sleep via A and A receptors. In this chapter, we present an overview of the current knowledge regarding the regulation of adenosine levels, adenosine receptors, and available pharmacologic and genetic tools to manipulate the adenosine system. This is followed by a summary of current knowledge of the role of adenosine and its receptors in the regulation of sleep and wakefulness. Despite strong data implicating numerous brain areas, including the basal forebrain, the tuberomammillary nucleus, the lateral hypothalamus, and the nucleus accumbens, in the adenosinergic control of sleep, the complete neural circuitry in the brain involved in the sleep-promoting effects of adenosine remains unclear. Moreover, the popular demand for natural sleep aids has led to a search for natural compounds that can promote sleep via adenosine receptor activation. Finally, we discuss the effects of caffeine in man and the possible use of more selective adenosine receptor drugs for the treatment of sleep disorders.
经典的内源性促眠物质腺苷通过A1和A2受体促进睡眠。在本章中,我们概述了目前关于腺苷水平调节、腺苷受体以及用于操纵腺苷系统的现有药理学和遗传学工具的知识。接下来总结了目前关于腺苷及其受体在睡眠和觉醒调节中作用的知识。尽管有大量数据表明包括基底前脑、结节乳头体核、下丘脑外侧和伏隔核在内的许多脑区参与了腺苷能对睡眠的控制,但大脑中参与腺苷促眠作用的完整神经回路仍不清楚。此外,对天然助眠剂的普遍需求促使人们寻找能够通过激活腺苷受体来促进睡眠的天然化合物。最后,我们讨论了咖啡因对人的影响以及更具选择性的腺苷受体药物在治疗睡眠障碍方面的可能用途。