Department of Pharmacology, University of Virginia, Charlottesville, VA 22908, United States.
Respir Physiol Neurobiol. 2013 Sep 15;188(3):333-43. doi: 10.1016/j.resp.2013.04.011. Epub 2013 Apr 19.
Arousal protects against the adverse and potentially fatal effects of asphyxia during sleep. Asphyxia stimulates the carotid bodies and central chemoreceptors but the sequence of events leading to arousal is uncertain. In this review, the theoretical mechanisms leading to arousal from sleep are briefly summarized and the issue of whether central respiratory chemoreceptors (CRCs) or other types of CO2-responsive CNS neurons contribute to asphyxia-induced arousal is discussed. We focus on the role of the retrotrapezoid nucleus, the raphe and the locus coeruleus and emphasize the anatomical and neurophysiological evidence which suggests that these putative central chemoreceptors could contribute to arousal independently of their effects on breathing. Finally, we describe recent attempts to test the contribution of specific brainstem pathways to asphyxia-induced arousal using optogenetic and other tools and the possible contribution of a group of hypoxia-sensitive brainstem neurons (the C1 cells) to breathing and arousal.
觉醒可防止睡眠中窒息的不良和潜在致命影响。窒息刺激颈动脉体和中枢化学感受器,但导致觉醒的事件顺序尚不确定。在这篇综述中,简要总结了导致睡眠觉醒的理论机制,并讨论了中枢呼吸化学感受器(CRC)或其他类型的 CO2 反应性中枢神经系统神经元是否有助于窒息引起的觉醒。我们专注于后梯形核、中缝核和蓝斑的作用,并强调了这些假定的中枢化学感受器可能独立于其对呼吸的影响而有助于觉醒的解剖学和神经生理学证据。最后,我们描述了最近使用光遗传学和其他工具测试特定脑干通路对窒息引起的觉醒的贡献的尝试,以及一组对缺氧敏感的脑干神经元(C1 细胞)对呼吸和觉醒的可能贡献。