Boutrel Benjamin, Koob George F
Department of Neuropharmacology, The Scripps Research Institute.
Sleep. 2004 Sep 15;27(6):1181-94. doi: 10.1093/sleep/27.6.1181.
Numerous studies dissecting the basic mechanisms that control sleep regulation have led to considerable improvement in our knowledge of sleep disorders. It is now well accepted that transitions between sleep and wakefulness are regulated by complex neurobiologic mechanisms, which, ultimately, can be delineated as oscillations between two opponent processes, one promoting sleep and the other promoting wakefulness. The role of several neurotransmitter or neuromodulator systems, including noradrenergic, serotonergic, cholinergic, adenosinergic, and histaminergic systems and, more recently, the hypocretin/orexin and dopamine systems, has been clearly established. Amphetamine-like stimulants are known to increase wakefulness by blocking dopamine reuptake, by stimulating dopamine release, or by both mechanisms. Modafinil may increase wakefulness through activation of noradrenergic and dopaminergic systems, possibly through interaction with the hypocretin/orexin system. Caffeine inhibits adenosinergic receptors, which in turn can produce activation via interaction with GABAergic and dopaminergic neurotransmission. Nicotine enhances acetylcholine neurotransmission in the basal forebrain and dopamine release. Understanding the exact role of the hypocretin/orexin and dopamine systems in the physiology and pharmacology of sleep-wake regulation may reveal new insights into current and future wakefulness-promoting drugs.
众多剖析控制睡眠调节基本机制的研究,使我们对睡眠障碍的认识有了显著提高。目前已普遍认为,睡眠与觉醒之间的转换由复杂的神经生物学机制调控,最终可描述为两个对立过程之间的振荡,一个促进睡眠,另一个促进觉醒。包括去甲肾上腺素能、血清素能、胆碱能、腺苷能和组胺能系统,以及最近发现的下丘脑分泌素/食欲素和多巴胺系统在内的几种神经递质或神经调质系统的作用已得到明确证实。已知苯丙胺类兴奋剂通过阻断多巴胺再摄取、刺激多巴胺释放或通过这两种机制来增加觉醒。莫达非尼可能通过激活去甲肾上腺素能和多巴胺能系统来增加觉醒,可能是通过与下丘脑分泌素/食欲素系统相互作用。咖啡因抑制腺苷能受体,进而可通过与γ-氨基丁酸能和多巴胺能神经传递相互作用产生激活作用。尼古丁增强基底前脑的乙酰胆碱神经传递和多巴胺释放。了解下丘脑分泌素/食欲素和多巴胺系统在睡眠-觉醒调节生理和药理学中的确切作用,可能会为当前及未来促进觉醒的药物带来新的见解。