TY - JOUR
T1 - Mathematical model of cellular basis for the respiratory sinus arrhythmia
AU - Dexter, Franklin
AU - Rudy, Yoram
AU - Levy, Matthew N.
AU - Bruce, Eugene N.
N1 - Funding Information:
The authors thank Jehuda Reich for help in designing the simulations. This research was supported by grants HL-10951 and HL-33343 from the National Institutes of Health, and the Research Initiative Award from the American Heart Association, North East Ohio Affiliate. Franklin Dexter was supported by the Medical Scientist Training Program (GMO-7250).
PY - 1991/5/21
Y1 - 1991/5/21
N2 - The respiratory sinus arrhythmia (RSA) is a vagally mediated oscillation in cardiac cycle length at the frequency of breathing. We developed a mathematical model that predicted the temporal and frequency dependence of the RSA. We used the mathematical model to examine the underlying cellular basis for the RSA at the level of the sinus node. We alternated efferent vagal activity between a low and a high frequency at the frequency of breathing. This oscillation caused the rate of acetylcholine (ACh) release to oscillate between a low and a high rate at the frequency of breathing. ACh degradation followed linear pharmacokinetics for physiological concentrations of ACh. Therefore, the concentration of ACh in neuroeffector junctions of the sinus node oscillated at the frequency of breathing. Membrane potential responded rapidly to changes in the concentration of ACh relative to the rate of ACh degradation. Thus, the time course of the RSA depended on the rate of ACh degradation. Membrane potential oscillated at several integer multiples of frequency of breathing and at various higher frequencies, which were integer multiples of the frequency of breathing and the frequencies of firing of the sinus node. However, computing cardiac cycle length from membrane potential eliminated the higher frequencies. Therefore, cardiac cycle length oscillated at several integer multiples of the frequency of breathing, but not at these higher frequencies.
AB - The respiratory sinus arrhythmia (RSA) is a vagally mediated oscillation in cardiac cycle length at the frequency of breathing. We developed a mathematical model that predicted the temporal and frequency dependence of the RSA. We used the mathematical model to examine the underlying cellular basis for the RSA at the level of the sinus node. We alternated efferent vagal activity between a low and a high frequency at the frequency of breathing. This oscillation caused the rate of acetylcholine (ACh) release to oscillate between a low and a high rate at the frequency of breathing. ACh degradation followed linear pharmacokinetics for physiological concentrations of ACh. Therefore, the concentration of ACh in neuroeffector junctions of the sinus node oscillated at the frequency of breathing. Membrane potential responded rapidly to changes in the concentration of ACh relative to the rate of ACh degradation. Thus, the time course of the RSA depended on the rate of ACh degradation. Membrane potential oscillated at several integer multiples of frequency of breathing and at various higher frequencies, which were integer multiples of the frequency of breathing and the frequencies of firing of the sinus node. However, computing cardiac cycle length from membrane potential eliminated the higher frequencies. Therefore, cardiac cycle length oscillated at several integer multiples of the frequency of breathing, but not at these higher frequencies.
UR - https://www.scopus.com/pages/publications/0025809989
U2 - 10.1016/S0022-5193(05)80329-7
DO - 10.1016/S0022-5193(05)80329-7
M3 - Article
C2 - 1890853
AN - SCOPUS:0025809989
SN - 0022-5193
VL - 150
SP - 157
EP - 173
JO - Journal of Theoretical Biology
JF - Journal of Theoretical Biology
IS - 2
ER -