Discipline of Physiology, School of Medical Sciences, University of Adelaide, Adelaide, South Australia, Australia;
Adelaide Institute for Sleep Health: A Flinders Centre of Research Excellence, Repatriation General Hospital, Daw Park, South Australia, Australia; and.
J Appl Physiol (1985). 2017 Sep 1;123(3):534-543. doi: 10.1152/japplphysiol.01005.2016. Epub 2017 Jun 15.
Intermittent hypoxia-induced ventilatory neuroplasticity is likely important in obstructive sleep apnea pathophysiology. Although concomitant CO levels and arousal state critically influence neuroplastic effects of intermittent hypoxia, no studies have investigated intermittent hypercapnic hypoxia effects during sleep in humans. Thus the purpose of this study was to investigate if intermittent hypercapnic hypoxia during sleep induces neuroplasticity (ventilatory long-term facilitation and increased chemoreflex responsiveness) in humans. Twelve healthy males were exposed to intermittent hypercapnic hypoxia (24 × 30 s episodes of 3% CO and 3.0 ± 0.2% O) and intermittent medical air during sleep after 2 wk washout period in a randomized crossover study design. Minute ventilation, end-tidal CO, O saturation, breath timing, upper airway resistance, and genioglossal and diaphragm electromyograms were examined during 10 min of stable stage 2 sleep preceding gas exposure, during gas and intervening room air periods, and throughout 1 h of room air recovery. There were no significant differences between conditions across time to indicate long-term facilitation of ventilation, genioglossal or diaphragm electromyogram activity, and no change in ventilatory response from the first to last gas exposure to suggest any change in chemoreflex responsiveness. These findings contrast with previous intermittent hypoxia studies without intermittent hypercapnia and suggest that the more relevant gas disturbance stimulus of concomitant intermittent hypercapnia frequently occurring in sleep apnea influences acute neuroplastic effects of intermittent hypoxia. These findings highlight the need for further studies of intermittent hypercapnic hypoxia during sleep to clarify the role of ventilatory neuroplasticity in the pathophysiology of sleep apnea. Both arousal state and concomitant CO levels are known modulators of the effects of intermittent hypoxia on ventilatory neuroplasticity. This is the first study to investigate the effects of combined intermittent hypercapnic hypoxia during sleep in humans. The lack of neuroplastic effects suggests a need for further studies more closely replicating obstructive sleep apnea to determine the pathophysiological relevance of intermittent hypoxia-induced ventilatory neuroplasticity.
间歇性低氧诱导的通气神经重塑在阻塞性睡眠呼吸暂停病理生理学中可能很重要。尽管同时存在的 CO 水平和觉醒状态严重影响间歇性低氧的神经重塑效应,但尚无研究调查人类睡眠期间间歇性高碳酸缺氧的影响。因此,本研究的目的是调查睡眠期间间歇性高碳酸缺氧是否会引起人类通气的神经重塑(通气的长期易化和化学感受反射敏感性增加)。12 名健康男性在 2 周洗脱期后,以随机交叉研究设计在睡眠期间接受间歇性高碳酸缺氧(24×30 s 期,3%CO 和 3.0±0.2%O)和间歇性医用空气暴露。分钟通气量、呼气末 CO、O 饱和度、呼吸计时、上气道阻力以及颏舌肌和膈肌肌电图在气体暴露前的稳定 2 期睡眠 10 分钟内、气体和中间室内空气期间以及整个 1 小时室内空气恢复期间进行检查。结果表明,在通气、颏舌肌或膈肌肌电图活动的长期易化方面,各条件之间在整个时间内均无显著差异,且从第一次到最后一次气体暴露的通气反应没有变化,提示化学感受反射敏感性没有变化。这些发现与以前没有间歇性高碳酸血症的间歇性低氧研究结果相反,表明睡眠中经常发生的同时存在的间歇性高碳酸血症更相关的气体干扰刺激影响间歇性低氧的急性神经重塑效应。这些发现强调需要进一步研究睡眠期间的间歇性高碳酸缺氧,以阐明通气神经重塑在睡眠呼吸暂停病理生理学中的作用。觉醒状态和同时存在的 CO 水平是间歇性低氧对通气神经重塑影响的已知调节剂。这是第一项研究人类睡眠期间联合间歇性高碳酸缺氧的影响的研究。缺乏神经重塑效应表明,需要进一步的研究更密切地模拟阻塞性睡眠呼吸暂停,以确定间歇性低氧诱导的通气神经重塑的病理生理学相关性。