Ilia State University, Tbilisi 0162, Georgia.
Int Rev Neurobiol. 2010;93:1-21. doi: 10.1016/S0074-7742(10)93001-8.
Daily cycles of wakefulness and sleep are regulated by coordinated interactions between wakefulness- and sleep-regulating neural circuitry. Wakefulness is associated with neuronal activity in cholinergic neurons in the brainstem and basal forebrain, monoaminergic neurons in the brainstem and posterior hypothalamus, and hypocretin (orexin) neurons in the lateral hypothalamus that act in a coordinated manner to stimulate cortical activation on the one hand and behavioral arousal on the other hand. Each of these neuronal groups subserves distinct aspects of wakefulness-related functions of the brain. Normal transitions from wakefulness to sleep involve sleep-related inhibition and/or disfacilitation of the multiple arousal systems. The cell groups that shut off the network of arousal systems, at sleep onset, occur with high density in the ventral lateral preoptic area (VLPO) and the median preoptic nucleus (MnPN) of the hypothalamus. Preoptic neurons are activated during sleep and exhibit sleep-wake state-dependent discharge patterns that are reciprocal of that observed in several arousal systems. Neurons in the VLPO contain the inhibitory neuromodulator, galanin, and the inhibitory neurotransmitter, gamma-aminobutyric acid (GABA). The majority of MnPN sleep-active neurons synthesize GABA. VLPO and MnPN neurons are sources of projections to arousal-regulatory systems in the posterior and lateral hypothalamus and the rostral brainstem. Mechanisms of sleep induction by these nuclei are hypothesized to involve GABA-mediated inhibition of multiple arousal systems. Normal cycling between discrete behavioral states is mediated by the combined influence of a sleep need that increases with continued wakefulness and an intrinsic circadian oscillation. This chapter will review anatomical and functional properties of populations of sleep-/wake-regulating neurons, focusing on recent findings supporting functional significance of the VLPO and MnPN in the regulation of sleep--wake homeostasis. Evidence indicating that MnPN and VLPO neurons have different, but complementary sleep regulatory functions will be summarized. Potential mechanisms that function to couple activity in these two sleep-regulatory neurons will be discussed.
昼夜节律的觉醒和睡眠是由觉醒和睡眠调节神经回路之间的协调相互作用来调节的。觉醒与脑桥和基底前脑的胆碱能神经元、脑桥和下丘脑后部的单胺能神经元以及外侧下丘脑的食欲素(orexin)神经元的神经元活动有关,这些神经元以协调的方式作用,一方面刺激皮质激活,另一方面刺激行为觉醒。这些神经元群中的每一个都为大脑与觉醒相关的功能的不同方面提供服务。从觉醒到睡眠的正常过渡涉及与睡眠相关的多个觉醒系统的抑制和/或去活化。在睡眠开始时关闭觉醒系统网络的细胞群,在丘脑腹外侧视前区(VLPO)和中视前核(MnPN)中高密度发生。视前神经元在睡眠期间被激活,并表现出与几种觉醒系统观察到的相反的睡眠-觉醒状态依赖性放电模式。VLPO 中的神经元包含抑制性神经调质甘丙肽和抑制性神经递质γ-氨基丁酸(GABA)。大多数 MnPN 睡眠活性神经元合成 GABA。VLPO 和 MnPN 神经元是向下丘脑后部和外侧以及脑干前部的觉醒调节系统投射的来源。这些核诱导睡眠的机制被假设涉及 GABA 介导的对多个觉醒系统的抑制。通过这些核的正常离散行为状态之间的循环是由持续觉醒时增加的睡眠需求和内在的昼夜节律振荡的综合影响介导的。这一章将回顾睡眠/觉醒调节神经元群体的解剖和功能特性,重点介绍支持 VLPO 和 MnPN 在调节睡眠-觉醒平衡中的功能意义的最新发现。将总结表明 MnPN 和 VLPO 神经元具有不同但互补的睡眠调节功能的证据。将讨论有助于这两个睡眠调节神经元活动偶联的潜在机制。