An endogenous circadian rhythm of respiratory control in humans

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...

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Veröffentlicht in:The Journal of physiology 2000-08, Vol.526 (3), p.683-694
Hauptverfasser: Spengler, Christina M., Czeisler, Charles A., Shea, Steven A.
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Czeisler, Charles A.
Shea, Steven A.
description 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; CBT min ) 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 P CO 2 ( P ET,CO 2 ; ±0.6 mmHg; ±1.5 % of 24 h mean). The circadian minima of the group-averaged respiratory variables occurred 6-8 h earlier than CBT min , 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 P ET,CO 2 . This suggests that ventilation and P ET,CO 2 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 P ET,CO 2 during non-rapid eye movement sleep was shown to be independent of circadian variations in P ET,CO 2 , 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
doi_str_mv 10.1111/j.1469-7793.2000.00683.x
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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 P CO 2 ( P ET,CO 2 ; ±0.6 mmHg; ±1.5 % of 24 h mean). The circadian minima of the group-averaged respiratory variables occurred 6-8 h earlier than CBT min , 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 P ET,CO 2 . This suggests that ventilation and P ET,CO 2 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 P ET,CO 2 during non-rapid eye movement sleep was shown to be independent of circadian variations in P ET,CO 2 , 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. 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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 P CO 2 ( P ET,CO 2 ; ±0.6 mmHg; ±1.5 % of 24 h mean). The circadian minima of the group-averaged respiratory variables occurred 6-8 h earlier than CBT min , 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 P ET,CO 2 . This suggests that ventilation and P ET,CO 2 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 P ET,CO 2 during non-rapid eye movement sleep was shown to be independent of circadian variations in P ET,CO 2 , 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. 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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; CBT min ) 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). 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subjects Adult
Blood Gas Analysis
Body Temperature - physiology
Carbon Dioxide - metabolism
Circadian Rhythm - physiology
Humans
Hypercapnia - metabolism
Male
Monitoring, Ambulatory
Original
Pulmonary Gas Exchange - physiology
Pulmonary Ventilation - physiology
Sleep - physiology
Wakefulness - physiology
title An endogenous circadian rhythm of respiratory control in humans
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