Effects of hypercapnia and hypoxemia on respiratory sinus arrhythmia in conscious humans during spontaneous respiration

Department of Surgery and Anesthesia, Wellington School of Medicine and Health Sciences, Wellington, New Zealand Submitted 30 July 2006 ; accepted in final form 11 January 2007 Normally, at rest, the amplitude of respiratory sinus arrhythmia (RSA) appears to correlate with cardiac vagal tone. Howeve...

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Veröffentlicht in:American journal of physiology. Heart and circulatory physiology 2007-05, Vol.292 (5), p.H2397-H2407
Hauptverfasser: Tzeng, Y. C, Larsen, P. D, Galletly, D. C
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Sprache:eng
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Zusammenfassung:Department of Surgery and Anesthesia, Wellington School of Medicine and Health Sciences, Wellington, New Zealand Submitted 30 July 2006 ; accepted in final form 11 January 2007 Normally, at rest, the amplitude of respiratory sinus arrhythmia (RSA) appears to correlate with cardiac vagal tone. However, recent studies showed that, under stress, RSA dissociates from vagal tone, indicating that separate mechanisms might regulate phasic and tonic vagal activity. This dissociation has been linked to the hypothesis that RSA improves pulmonary gas exchange through preferential distribution of heartbeats in inspiration. We examined the effects of hypercapnia and mild hypoxemia on RSA-vagal dissociation in relation to heartbeat distribution throughout the respiratory cycle in 12 volunteers. We found that hypercapnia, but not hypoxemia, was associated with significant increases in heart rate (HR), tidal volume, and RSA amplitude. The RSA amplitude increase remained statistically significant after adjustment for respiratory rate, tidal volume, and HR. Moreover, the RSA amplitude increase was associated with a paradoxical rise in HR and decrease in low-frequency-to-high-frequency mean amplitude ratio derived from spectral analysis, which is consistent with RSA-vagal dissociation. Although hypercapnia was associated with a significant increase in the percentage of heartbeats during inspiration, this association was largely secondary to increases in the inspiratory period-to-respiratory period ratio, rather than RSA amplitude. Additional model analyses of RSA were consistent with the experimental data. Heartbeat distribution did not change during hypoxemia. These results support the concept of RSA-vagal dissociation during hypercapnia; however, the putative role of RSA in optimizing pulmonary perfusion matching requires further experimental validation. ventilation-perfusion mismatch; heart rate variability Address for reprint requests and other correspondence: Y. C. Tzeng, Dept. of Surgery & Anaesthesia, Wellington School of Medicine & Health Sciences, Univ. of Otago, PO Box 7343, Wellington, New Zealand (e-mail: tzeng{at}slingshot.co.nz )
ISSN:0363-6135
1522-1539
DOI:10.1152/ajpheart.00817.2006