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嘌呤分子作为催眠因子——腺苷、三磷酸腺苷和咖啡因的作用

Purine molecules as hypnogenic factors role of adenosine, ATP, and caffeine.

作者信息

Díaz-Muñoz M, Salín-Pascual R

机构信息

Departamento de Neurobiología Celular y Molecular, Instituto de Neurobiología, Campus UNAM-Juriquilla, Querétaro, México.

出版信息

Cent Nerv Syst Agents Med Chem. 2010 Dec 1;10(4):259-68. doi: 10.2174/187152410793429692.

Abstract

Purines are ubiquitous molecules with important roles in the regulation of metabolic networks and signal transduction events. In the central nervous system, adenosine and ATP modulate the sleep-wake cycle, acting as ligands of specific transmembrane receptors and as allosteric effectors of key intracellular enzymes for brain energy expenditure. Two types of adenosine receptors seem to be relevant to the sleep function, A1 and A2A. Caffeine, an antagonist of adenosine receptors, has been used as a tool in some of the studies reviewed in the present chapter. Possible changes in adenosine functioning due to the aging process have been observed in animal models and abnormalities in the adenosine system could also explain primary insomnia or the reduced amount of delta sleep and increased sensitivity to caffeine in some subjects with sleep deficits. Caffeine is a methylated-derivate of xanthine with profound effects on the onset and quality of sleep episodes. This purine acts principally as an antagonist of the A2A receptors. Adenosine and ATP in the nervous system are the bridge between metabolic activity, recovery function, and purinergic transmission that underlies the daily wake-sleep cycle in mammals. Modulators of purine actions have the potential to alleviate insomnia and other sleep disorders based on their physiopathological role during the sleep process.

摘要

嘌呤是普遍存在的分子,在代谢网络调节和信号转导事件中发挥着重要作用。在中枢神经系统中,腺苷和三磷酸腺苷(ATP)调节睡眠-觉醒周期,作为特定跨膜受体的配体以及大脑能量消耗关键细胞内酶的变构效应物。两种类型的腺苷受体似乎与睡眠功能相关,即A1和A2A。咖啡因作为腺苷受体的拮抗剂,在本章所综述的一些研究中被用作工具。在动物模型中已观察到衰老过程导致的腺苷功能可能变化,腺苷系统异常也可解释原发性失眠,或在一些有睡眠缺陷的受试者中慢波睡眠量减少以及对咖啡因敏感性增加的现象。咖啡因是黄嘌呤的甲基化衍生物,对睡眠发作的起始和质量有深远影响。这种嘌呤主要作为A2A受体的拮抗剂发挥作用。神经系统中的腺苷和ATP是代谢活动、恢复功能以及嘌呤能传递之间的桥梁,而嘌呤能传递是哺乳动物日常睡眠-觉醒周期的基础。基于嘌呤作用在睡眠过程中的生理病理作用,嘌呤作用调节剂有减轻失眠和其他睡眠障碍的潜力。

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