腺苷A2A受体与睡眠。

International review of neurobiology Pub Date : 2023-01-01 Epub Date: 2023-04-29 DOI:10.1016/bs.irn.2023.04.007
Mustafa Korkutata, Michael Lazarus
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引用次数: 0

摘要

腺苷是一种已知的内源性睡眠原,通过A1和A2A受体诱导睡眠。在本章中,我们回顾了目前关于腺苷A2A受体及其激动剂、拮抗剂和变构调节剂在睡眠-觉醒调节中的作用的知识。尽管已经鉴定出许多腺苷A2A受体激动剂、拮抗剂和变构调节剂,但只有少数经过测试,看看它们是否能促进睡眠或清醒。此外,随着天然助眠剂的日益普及,人们对可以通过激活腺苷A2A受体来改善睡眠的天然化合物进行了研究。最后,我们讨论了腺苷A2A受体变构调节剂相对于经典激动剂和拮抗剂在治疗睡眠和神经系统疾病方面的潜在治疗优势。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Adenosine A2A receptors and sleep.

Adenosine, a known endogenous somnogen, induces sleep via A1 and A2A receptors. In this chapter, we review the current knowledge regarding the role of the adenosine A2A receptor and its agonists, antagonists, and allosteric modulators in sleep-wake regulation. Although many adenosine A2A receptor agonists, antagonists, and allosteric modulators have been identified, only a few have been tested to see if they can promote sleep or wakefulness. In addition, the growing popularity of natural sleep aids has led to an investigation of natural compounds that may improve sleep by activating the adenosine A2A receptor. Finally, we discuss the potential therapeutic advantage of allosteric modulators of adenosine A2A receptors over classic agonists and antagonists for treating sleep and neurologic disorders.

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