首页> 美国卫生研究院文献>The Journal of Neuroscience >Interactions between GABAergic and Cholinergic Processes in the Nucleus Pontis Oralis: Neuronal Mechanisms Controlling Active (Rapid Eye Movement) Sleep and Wakefulness
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Interactions between GABAergic and Cholinergic Processes in the Nucleus Pontis Oralis: Neuronal Mechanisms Controlling Active (Rapid Eye Movement) Sleep and Wakefulness

机译:之间的相互作用GABA能过程和胆碱能过程之间的相互作用:主动(快速眼动)睡眠和觉醒的神经元机制。

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摘要

The cholinergic system within the nucleus pontis oralis (NPO) of the pontine tegmentum is critically involved in the generation of active (rapid eye movement) sleep. Previously, we demonstrated that a GABAergic system in the NPO also plays an important role in the control of the behavioral states of wakefulness as well as active sleep. The present study examined interactions between these two neuronal systems vis-à-vis the occurrence of these behavioral states. Accordingly, cholinergic and GABAergic agonists and antagonists were injected into the NPO, and their combined effects on sleep and waking states of chronic, unanesthetized cats were examined. Microinjections of carbachol into the NPO elicited active sleep with a short latency. However, a preinjection of muscimol (a GABAA agonist) completely blocked the active sleep-inducing effects of carbachol. The induction of active sleep by carbachol was also suppressed by a subsequent injection of muscimol. On the other hand, the microinjection of scopolamine (a muscarinic receptor antagonist) did not block the induction of active sleep by bicuculline (a GABAA antagonist). We conclude that the excitatory cholinergic control of NPO neurons that are involved in the generation of active sleep is gated by a pontine GABAergic system that exerts its effects postsynaptically by inhibiting NPO neurons, resulting in the suppression of active sleep and the generation of wakefulness. In the absence of the activation of this GABAergic gating mechanism, active sleep occurs. These results reveal that specific interactions between cholinergic and GABAergic processes in the NPO play a critical role in the generation of active sleep and wakefulness.
机译:桥脑桥盖的脑桥核内的胆碱能系统主要参与主动(快速眼动)睡眠的产生。以前,我们证明了NPO中的GABA能系统在控制清醒和积极睡眠的行为状态中也起着重要作用。本研究检查了相对于这些行为状态的发生这两个神经元系统之间的相互作用。因此,将胆碱能和GABA能激动剂和拮抗剂注入NPO中,并检查它们对慢性,非麻醉猫的睡眠和苏醒状态的综合影响。向NPO微量注射卡巴胆碱可引起短暂的睡眠时间。但是,预先注射麝香酚(一种GABAA激动剂)完全阻断了卡巴胆碱的主动睡眠诱导作用。随后注射麝香酚也抑制了卡巴胆碱对主动睡眠的诱导。另一方面,东pol碱(毒蕈碱受体拮抗剂)的显微注射并没有阻止双瓜氨酸(GABAA拮抗剂)诱导主动睡眠。我们得出的结论是,参与主动睡眠产生的NPO神经元的兴奋性胆碱能控制是由桥脑GABA能系统控制的,该系统通过抑制NPO神经元在突触后发挥其作用,从而抑制主动睡眠和产生清醒。在没有激活这种GABA能门控机制的情况下,会发生活跃的睡眠。这些结果表明,NPO中胆碱能和GABA能过程之间的特定相互作用在活跃睡眠和清醒的产生中起着关键作用。

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