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First published online June 29, 2006
Journal of Experimental Biology 209, 2628-2636 (2006)
Published by The Company of Biologists 2006
doi: 10.1242/jeb.02278

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Evidence for a respiratory component, similar to mammalian respiratory sinus arrhythmia, in the heart rate variability signal from the rattlesnake, Crotalus durissus terrificus

Hamish A. Campbell^1,2,*, Cleo A. C. Leite^1,3, Tobias Wang^1,4, Marianne Skals^1,4, Augusto S. Abe¹, Stuart Egginton², F. Tadeu Rantin³, Charles M. Bishop⁵ and Edwin W. Taylor^1,2

¹ UNESP, Rio Claro, SP, Brazil
² Department of Physiology, University of Birmingham, Birmingham, UK
³ Universidade Federal, Sao Carlos, SP, Brazil
⁴ Aarhus University, Denmark
⁵ University of Wales, Bangor, UK

^* Author for correspondence (e-mail: h.a.campbell{at}bham.ac.uk)

Accepted 18 April 2006

Autonomic control of heart rate variability and the central location of vagal preganglionic neurones (VPN) were examined in the rattlesnake (Crotalus durissus terrificus), in order to determine whether respiratory sinus arrhythmia (RSA) occurred in a similar manner to that described for mammals. Resting ECG signals were recorded in undisturbed snakes using miniature datalogging devices, and the presence of oscillations in heart rate (fH) was assessed by power spectral analysis (PSA). This mathematical technique provides a graphical output that enables the estimation of cardiac autonomic control by measuring periodic changes in the heart beat interval. At fH above 19 min^-1 spectra were mainly characterised by low frequency components, reflecting mainly adrenergic tonus on the heart. By contrast, at fH below 19 min^-1 spectra typically contained high frequency components, demonstrated to be cholinergic in origin. Snakes with a fH >19 min^-1 may therefore have insufficient cholinergic tonus and/or too high an adrenergic tonus acting upon the heart for respiratory sinus arrhythmia (RSA) to develop. A parallel study monitored fH simultaneously with the intraperitoneal pressures associated with lung inflation. Snakes with a fH<19 min^-1 exhibited a high frequency (HF) peak in the power spectrum, which correlated with ventilation rate (fV). Adrenergic blockade by propranolol infusion increased the variability of the ventilation cycle, and the oscillatory component of the fH spectrum broadened accordingly. Infusion of atropine to effect cholinergic blockade abolished this HF component, confirming a role for vagal control of the heart in matching fH and fV in the rattlesnake. A neuroanatomical study of the brainstem revealed two locations for vagal preganglionic neurones (VPN). This is consistent with the suggestion that generation of ventilatory components in the heart rate variability (HRV) signal are dependent on spatially distinct loci for cardiac VPN. Therefore, this study has demonstrated the presence of RSA in the HRV signal and a dual location for VPN in the rattlesnake. We suggest there to be a causal relationship between these two observations.

Key words: heart rate, power spectral analysis, vagal preganglionic neurones

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