Centre for Biological Timing and Cognition, Department of Cell and Systems Biology, University of Toronto, Toronto, ON M5S 3G5, Canada.
Centre for Biological Timing and Cognition, Department of Cell and Systems Biology, University of Toronto, Toronto, ON M5S 3G5, Canada; Centre for Biological Timing and Cognition, Department of Physiology, University of Toronto, Toronto, ON M5S 3G5, Canada.
Curr Opin Neurobiol. 2017 Jun;44:50-58. doi: 10.1016/j.conb.2017.02.010. Epub 2017 Mar 23.
Narcolepsy is a debilitating sleep disorder caused by loss of orexin neurons in the lateral hypothalamus. Excessive daytime sleepiness and cataplexy are the major complaints in narcolepsy, and are associated with impaired quality of life. Although it is unclear how orexin loss causes sleepiness and cataplexy, animal models have been instrumental in identifying the neurobiological underpinnings of narcolepsy because they reliably recapitulate disease symptoms. Current evidence indicates that orexin cell loss causes sleepiness and cataplexy by destabilizing the ability of the circuits that initiate and sustain normal levels of arousal and motor activity. This review highlights the latest research concerning the normal function of the orexin system and how its dysfunction causes narcolepsy symptoms.
发作性睡病是一种由外侧下丘脑的食欲素神经元丧失引起的使人虚弱的睡眠障碍。白天过度嗜睡和猝倒症是发作性睡病的主要症状,它们与生活质量受损有关。尽管目前尚不清楚食欲素的丧失如何导致嗜睡和猝倒症,但动物模型在确定发作性睡病的神经生物学基础方面发挥了重要作用,因为它们可靠地再现了疾病症状。目前的证据表明,食欲素细胞的丧失导致嗜睡和猝倒症,是通过破坏启动和维持正常觉醒和运动活动水平的回路的稳定性。这篇综述强调了关于食欲素系统正常功能以及其功能障碍如何导致发作性睡病症状的最新研究。