Spengler C M, Czeisler C A, Shea S A
Circadian, Neuroendocrine and Sleep Disorders Section, Brigham and Women's Hospital, 221 Longwood Avenue, Boston, MA 02115-5817, USA.
J Physiol. 2000 Aug 1;526 Pt 3(Pt 3):683-94. doi: 10.1111/j.1469-7793.2000.00683.x.
Many physiological and behavioural functions have circadian rhythms - endogenous oscillations with a period of approximately 24 h that can occur even in the absence of sleep. We determined whether there is an endogenous circadian rhythm in breathing, metabolism and ventilatory chemosensitivity in humans. Ten healthy, adult males were studied throughout 4 days in a stable laboratory environment. After two initial baseline days (16 h wakefulness plus 8 h sleep) that served to achieve a steady state, subjects were studied under constant behavioural and environmental conditions throughout 41 h of wakefulness. Ventilation, metabolism and the magnitude of the hypercapnic ventilatory response (HCVR) were measured every 2 h. Individuals' data were aligned according to circadian phase (core body temperature minimum; CBTmin) and averaged. In the group average data, there was a significant and large amplitude circadian variation in HCVR slope (average of +/-0.4 l min-1 mmHg-1; corresponding to +/-12.1 % of 24 h mean), and a smaller amplitude rhythm in the HCVR x-axis intercept (average of +/-1.1 mmHg; +/-2.1 % of 24 h mean). Despite a significant circadian variation in metabolism (+/-3.2 % of 24 h mean), there were no detectable rhythms in tidal volume, respiratory frequency or ventilation. This small discrepancy between metabolism and ventilation led to a small but significant circadian variation in end-tidal PCO2 (PET,CO2; +/-0.6 mmHg; +/-1.5 % of 24 h mean). The circadian minima of the group-averaged respiratory variables occurred 6-8 h earlier than CBTmin, suggesting that endogenous changes in CBT across the circadian cycle have less of an effect on respiration than equivalent experimentally induced changes in CBT. Throughout these circadian changes, there were no correlations between HCVR parameters (slope or x-axis intercept) and either resting ventilation or resting PET,CO2. This suggests that ventilation and PET,CO2 are little influenced by central chemosensory respiratory control in awake humans even when at rest under constant environmental and behavioural conditions. The characteristic change in PET,CO2 during non-rapid eye movement sleep was shown to be independent of circadian variations in PET,CO2, and probably reflects a change from predominantly behavioural to predominantly chemosensory respiratory control. This study has documented the existence and magnitude of circadian variations in respiration and respiratory control in awake humans for the first time under constant behavioural and environmental conditions. These results provide unique insights into respiratory control in awake humans, and highlight the importance of considering the phase of the circadian cycle in studies of respiratory control.
许多生理和行为功能都有昼夜节律——即使在没有睡眠的情况下也会出现的、周期约为24小时的内源性振荡。我们确定了人类呼吸、代谢和通气化学敏感性是否存在内源性昼夜节律。在稳定的实验室环境中,对10名健康成年男性进行了为期4天的研究。在最初的两个基线日(16小时清醒加8小时睡眠)以达到稳定状态后,在持续41小时的清醒期间,让受试者处于恒定的行为和环境条件下进行研究。每2小时测量一次通气、代谢和高碳酸血症通气反应(HCVR)的幅度。根据昼夜节律阶段(核心体温最低值;CBTmin)对个体数据进行校准并求平均值。在组平均数据中,HCVR斜率存在显著且幅度较大的昼夜变化(平均±0.4升·分钟⁻¹·毫米汞柱⁻¹;相当于24小时平均值的±12.1%),HCVR x轴截距的节律幅度较小(平均±1.1毫米汞柱;24小时平均值的±2.1%)。尽管代谢存在显著的昼夜变化(24小时平均值的±3.2%),但潮气量、呼吸频率或通气量均未检测到节律。代谢与通气之间的这种微小差异导致呼气末二氧化碳分压(PET,CO₂)出现微小但显著的昼夜变化(±0.6毫米汞柱;24小时平均值的±1.5%)。组平均呼吸变量的昼夜最小值比CBTmin早出现6 - 8小时,这表明在昼夜周期中CBT的内源性变化对呼吸的影响小于等效的实验诱导的CBT变化。在这些昼夜变化过程中,HCVR参数(斜率或x轴截距)与静息通气或静息PET,CO₂之间均无相关性。这表明在清醒的人类中,即使在恒定的环境和行为条件下处于静息状态,通气和PET,CO₂也很少受中枢化学感受性呼吸控制的影响。非快速眼动睡眠期间PET,CO₂的特征性变化被证明与PET,CO₂的昼夜变化无关,可能反映了从主要是行为性呼吸控制到主要是化学感受性呼吸控制的转变。本研究首次在恒定的行为和环境条件下记录了清醒人类呼吸和呼吸控制的昼夜变化的存在及幅度。这些结果为清醒人类的呼吸控制提供了独特的见解,并强调了在呼吸控制研究中考虑昼夜周期阶段的重要性。