4.1 Article

Respiratory and heart rate dynamics during peripheral chemoreceptor deactivation compared to targeted sympathetic and sympathetic/ parasympathetic (co-)activation

Journal

AUTONOMIC NEUROSCIENCE-BASIC & CLINICAL
Volume 241, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.autneu.2022.103009

Keywords

Hyperoxia; Peripheral chemoreceptors; Respiratory rate; Autonomic nervous system; Heart rate variability

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Funding

  1. European Commission [FP7-216695]
  2. Die Hans und Gertie Fischer-Stiftung

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This study investigated the effects of different testing methods (hyperoxic cardiac chemoreflex sensitivity testing, cold face test, and cold pressor test) on heart rate dynamics, hemodynamics, and respiratory rate. The results showed that changes in heart rate characteristics during the deactivation of peripheral chemoreceptors were related to a decrease in respiratory rate. This highlights the importance of assessing respiratory rate when evaluating adaptations of cardiorespiratory chemoreceptor control.
Background: The importance of peripheral chemoreceptors for cardiorespiratory neural control is known for decades. Pure oxygen inhalation deactivates chemoreceptors and increases parasympathetic outflow. However, the relationship between autonomic nervous system (ANS) activation and resulting respiratory as well as heart rate (HR) dynamics is still not fully understood. Methods: In young adults the impact of (1) 100 % pure oxygen inhalation (hyperoxic cardiac chemoreflex sensitivity (CHRS) testing), (2) the cold face test (CFT) and (3) the cold pressor test (CPT) on heart rate variability (HRV), hemodynamics and respiratory rate was investigated in randomized order. Baseline ANS outflow was determined assessing respiratory sinus arrhythmia via deep breathing, baroreflex sensitivity and HRV. Results: Baseline ANS outflow was normal in all participants (23 +/- 1 years, 7 females, 3 males). Hyperoxic CHRS testing decreased HR (after 60 +/- 3 vs before 63 +/- 3 min(-1), p = 0.004), while increasing total peripheral resistance (1053 +/- 87 vs 988 +/- 76 dyne*s + m(2)/cm5, p = 0.02) and mean arterial blood pressure (93 +/- 4 vs 91 +/- 4 mm Hg, p = 0.02). HRV indicated increased parasympathetic outflow after hyperoxic CHRS testing accompanied by a decrease in respiratory rate (15 +/- 1vs 19 +/- 1 min-1, p = 0.001). In contrast, neither CFT nor CPT altered the respiratory rate (18 +/- 1 vs 18 +/- 2 min(-1), p = 0.38 and 18 +/- 1 vs 18 +/- 1 min(-1), p = 0.84, respectively). Conclusion: Changes in HR characteristics during deactivation of peripheral chemoreceptors but not during the CFT and CPT are related with a decrease in respiratory rate. This highlights the need of respiratory rate assessment when evaluating adaptations of cardiorespiratory chemoreceptor control.

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