Body position and cardiac dynamic and chronotropic responses to steady-state isocapnic hypoxaemia in humans

• Published in: Experimental physiology Vol. 85; no. 2; pp. 227 - 237
• Main Authors: Lucy, S. Deborah, Hughson, Richard L., Kowalchuk, John M., Paterson, Donald H., Cunningham, David A.
• Format: Journal Article
• Language: English
• Published: Cambridge, UK Cambridge University Press 01.03.2000; The Physiological Society; Blackwell Science Ltd
• Subjects: Adult; Carbon Dioxide; Female; Heart - physiology; Heart Rate - physiology; Homeostasis; Humans; Hypoxia - blood; Hypoxia - physiopathology; Male; Partial Pressure; Posture - physiology; Reference Values; Respiration
• ISSN: 0958-0670; 1469-445X
• DOI: 10.1111/j.1469-445X.2000.01932.x

Neural mediation of the human cardiac response to isocapnic (IC) steady-state hypoxaemia was investigated using coarse-graining spectral analysis of heart rate variability (HRV). Six young adults were exposed in random order to a hypoxia or control protocol, in supine and sitting postures, while end-tidal PCO2 (PET,CO2) was clamped at resting eucapnic levels. An initial 11 min period of euoxia (PET,O2 100 mmHg; 13.3 kPa) was followed by a 22 min exposure to hypoxia (PET,O2 55 mmHg; 7.3 kPa), or continued euoxia (control). Harmonic and fractal powers of HRV were determined for the terminal 400 heart beats in each time period. Ventilation was stimulated (P < 0.05) and cardiac dynamics altered only by exposure to hypoxia. The cardiac interpulse interval was shortened (P < 0.001) similarly during hypoxia in both body positions. Vagally mediated high-frequency harmonic power (Ph) of HRV was decreased by hypoxia only in the supine position, while the fractal dimension, also linked to cardiac vagal control, was decreased in the sitting position (P < 0.05). However, low-frequency harmonic power (Pl) and the HRV indicator of sympathetic activity (Pl/Ph) were not altered by hypoxia in either position. These results suggest that, in humans, tachycardia induced by moderate IC hypoxaemia (arterial O2 saturation Sa,O2 85 %) was mediated by vagal withdrawal, irrespective of body position and resting autonomic balance, while associated changes in HRV were positionally dependent.