» Articles » PMID: 24746049

Cardiorespiratory Coupling: Common Rhythms in Cardiac, Sympathetic, and Respiratory Activities

Overview
Journal Prog Brain Res
Publisher Elsevier
Specialty Neurology
Date 2014 Apr 22
PMID 24746049
Citations 74
Authors
Affiliations
Soon will be listed here.
Abstract

Cardiorespiratory coupling is an encompassing term describing more than the well-recognized influences of respiration on heart rate and blood pressure. Our data indicate that cardiorespiratory coupling reflects a reciprocal interaction between autonomic and respiratory control systems, and the cardiovascular system modulates the ventilatory pattern as well. For example, cardioventilatory coupling refers to the influence of heart beats and arterial pulse pressure on respiration and is the tendency for the next inspiration to start at a preferred latency after the last heart beat in expiration. Multiple complementary, well-described mechanisms mediate respiration's influence on cardiovascular function, whereas mechanisms mediating the cardiovascular system's influence on respiration may only be through the baroreceptors but are just being identified. Our review will describe a differential effect of conditioning rats with either chronic intermittent or sustained hypoxia on sympathetic nerve activity but also on ventilatory pattern variability. Both intermittent and sustained hypoxia increase sympathetic nerve activity after 2 weeks but affect sympatho-respiratory coupling differentially. Intermittent hypoxia enhances sympatho-respiratory coupling, which is associated with low variability in the ventilatory pattern. In contrast, after constant hypobaric hypoxia, 1-to-1 coupling between bursts of sympathetic and phrenic nerve activity is replaced by 2-to-3 coupling. This change in coupling pattern is associated with increased variability of the ventilatory pattern. After baro-denervating hypobaric hypoxic-conditioned rats, splanchnic sympathetic nerve activity becomes tonic (distinct bursts are absent) with decreases during phrenic nerve bursts and ventilatory pattern becomes regular. Thus, conditioning rats to either intermittent or sustained hypoxia accentuates the reciprocal nature of cardiorespiratory coupling. Finally, identifying a compelling physiologic purpose for cardiorespiratory coupling is the biggest barrier for recognizing its significance. Cardiorespiratory coupling has only a small effect on the efficiency of gas exchange; rather, we propose that cardiorespiratory control system may act as weakly coupled oscillator to maintain rhythms within a bounded variability.

Citing Articles

Peculiarities of cardio-respiratory relationships in qualified athletes with different types of heart rhythm regulation according to respiratory maneuver data.

Romanchuk O Front Sports Act Living. 2025; 6:1451643.

PMID: 39872494 PMC: 11769980. DOI: 10.3389/fspor.2024.1451643.


One-week test-retest recordings of resting cardiorespiratory data for reliability analysis.

Schumann A, Lukas F, Rieger K, Gupta Y, Bar K Sci Data. 2025; 12(1):12.

PMID: 39754019 PMC: 11698850. DOI: 10.1038/s41597-024-04303-y.


Photochemically Triggered, Transient, and Oscillatory Transcription Machineries Guide Temporal Modulation of Fibrinogenesis.

Dong J, Willner I J Am Chem Soc. 2024; 147(2):2216-2227.

PMID: 39740143 PMC: 11744759. DOI: 10.1021/jacs.4c16829.


Machine Learning Classification of Pediatric Health Status Based on Cardiorespiratory Signals with Causal and Information Domain Features Applied-An Exploratory Study.

Rosol M, Gasior J, Korzeniewski K, Laba J, Makuch R, Werner B J Clin Med. 2024; 13(23).

PMID: 39685811 PMC: 11642896. DOI: 10.3390/jcm13237353.


Exhaled Breath Analysis: From Laboratory Test to Wearable Sensing.

Heng W, Yin S, Chen Y, Gao W IEEE Rev Biomed Eng. 2024; 18:50-73.

PMID: 39412981 PMC: 11875904. DOI: 10.1109/RBME.2024.3481360.


References
1.
Larsen P, Galletly D . Cardioventilatory coupling in the anaesthetised rabbit, rat and guinea-pig. Pflugers Arch. 1999; 437(6):910-6. DOI: 10.1007/s004240050862. View

2.
Zhu Y, Hsieh Y, Dhingra R, Dick T, Jacono F, Galan R . Quantifying interactions between real oscillators with information theory and phase models: application to cardiorespiratory coupling. Phys Rev E Stat Nonlin Soft Matter Phys. 2013; 87(2):022709. PMC: 3767161. DOI: 10.1103/PhysRevE.87.022709. View

3.
Baekey D, Dick T, Paton J . Pontomedullary transection attenuates central respiratory modulation of sympathetic discharge, heart rate and the baroreceptor reflex in the in situ rat preparation. Exp Physiol. 2008; 93(7):803-16. DOI: 10.1113/expphysiol.2007.041400. View

4.
Limberg J, Morgan B, Schrage W, Dempsey J . Respiratory influences on muscle sympathetic nerve activity and vascular conductance in the steady state. Am J Physiol Heart Circ Physiol. 2013; 304(12):H1615-23. PMC: 3680774. DOI: 10.1152/ajpheart.00112.2013. View

5.
Guyenet P, Bayliss D, Stornetta R, Fortuna M, Abbott S, DePuy S . Retrotrapezoid nucleus, respiratory chemosensitivity and breathing automaticity. Respir Physiol Neurobiol. 2009; 168(1-2):59-68. PMC: 2734912. DOI: 10.1016/j.resp.2009.02.001. View