Berry R B, Gleeson K
Department of Medicine, Long Beach VA Medical Center, CA, 90822, USA.
Sleep. 1997 Aug;20(8):654-75. doi: 10.1093/sleep/20.8.654.
The mechanisms by which respiratory stimuli induce arousal from sleep and the clinical significance of these arousals have been explored by numerous studies in the last two decades. Evidence to date suggests that the arousal stimulus in nonrapid eye movement sleep (NREM) is related to the level of inspiratory effort rather than the individual stimuli that contribute to ventilatory drive. A component of the arousal stimulus proportional to the level of inspiratory effort may originate in mechanoreceptors either in the upper airway or respiratory pump. Medullary centers responsible for ventilatory drive may also send a signal proportionate to the level of drive to higher centers in the brain which are responsible for arousal. Thus, the arousal stimulus may consist of multiple components, each increasing as inspiratory effort increases. The level of effort triggering arousal is an index of the arousability of the brain (arousal threshold). A deeper stage of sleep, central nervous system depressants, prior sleep fragmentation, and the presence of obstructive sleep apnea (OSA) have been observed to increase the arousal threshold to airway occlusion. Less information is available concerning the mechanisms of arousal from rapid eye movement (REM) sleep. While REM sleep is associated with the longest obstructive apneas in patients with OSA, normal human subjects appear to have a similar or lower arousal threshold to respiratory stimuli in REM compared to NREM sleep. Recent studies have challenged the assumption that the termination of all obstructive apnea is dependent on arousal from sleep. Improvements in methods to detect and quantitate changes in the cortical electroencephalogram (EEG) may better define the relationship between arousal and apnea termination. This may result in improved criteria for identifying EEG changes of clinical significance. While little is known concerning the mechanisms of arousal in central sleep apnea, arousal may play an important role in inducing this type of apnea in some patients.
在过去二十年中,众多研究探讨了呼吸刺激引发睡眠觉醒的机制以及这些觉醒的临床意义。迄今为止的证据表明,非快速眼动睡眠(NREM)中的觉醒刺激与吸气努力程度相关,而非与构成通气驱动的个体刺激相关。与吸气努力程度成比例的觉醒刺激成分可能起源于上气道或呼吸泵中的机械感受器。负责通气驱动的延髓中枢也可能向大脑中负责觉醒的更高中枢发送与驱动水平成比例的信号。因此,觉醒刺激可能由多个成分组成,每个成分都随着吸气努力的增加而增加。触发觉醒的努力程度是大脑觉醒能力(觉醒阈值)的一个指标。已观察到睡眠更深阶段、中枢神经系统抑制剂、先前的睡眠片段化以及阻塞性睡眠呼吸暂停(OSA)的存在会增加气道阻塞的觉醒阈值。关于快速眼动(REM)睡眠觉醒机制的信息较少。虽然REM睡眠与OSA患者最长的阻塞性呼吸暂停相关,但与NREM睡眠相比,正常人类受试者在REM睡眠中对呼吸刺激的觉醒阈值似乎相似或更低。最近的研究对所有阻塞性呼吸暂停的终止都依赖于睡眠觉醒这一假设提出了挑战。检测和量化皮质脑电图(EEG)变化方法的改进可能会更好地定义觉醒与呼吸暂停终止之间的关系。这可能会导致确定具有临床意义的EEG变化的标准得到改进。虽然对中枢性睡眠呼吸暂停的觉醒机制知之甚少,但觉醒可能在某些患者诱发这种类型的呼吸暂停中起重要作用。