TY - JOUR
T1 - Spatiotemporal control of heart rate in a rabbit heart
AU - Lang, Di
AU - Petrov, Valentin
AU - Lou, Qing
AU - Osipov, Grigory
AU - Efimov, Igor R.
PY - 2011/11
Y1 - 2011/11
N2 - Sinoatrial node is responsible for the origin of the wave of excitation, which spreads throughout the heart and orchestrates cardiac contraction via calcium-mediated excitation-contraction coupling. P wave represents the spread of excitation in the atria. It is well known that the autonomic nervous system controls the heart rate by dynamically altering both cellular ionic fluxes and the anatomical location of the leading pacemaker. In this study, we used isolated rabbit right atria and mathematical model of the pacemaker region of the rabbit heart. Application of isoproterenol resulted in dose-dependent acceleration of the heart rate and superior shift of the leading pacemaker. In the mathematical model, such behavior could be reproduced by a gradient of expression in β1-adrenergic receptors along the superior-inferior axis. Application of acetylcholine resulted in preferentially inferior shift of pacemaker and slowing of the heart rate. The mathematical model reproduced this behavior with imposing a gradient of expression of acetylcholine-sensitive potassium channel. We conclude that anatomical shift of the leading pacemaker in the rabbit heart could be achieved through gradient of expression of β1-adrenergic receptors and I K,ACh.
AB - Sinoatrial node is responsible for the origin of the wave of excitation, which spreads throughout the heart and orchestrates cardiac contraction via calcium-mediated excitation-contraction coupling. P wave represents the spread of excitation in the atria. It is well known that the autonomic nervous system controls the heart rate by dynamically altering both cellular ionic fluxes and the anatomical location of the leading pacemaker. In this study, we used isolated rabbit right atria and mathematical model of the pacemaker region of the rabbit heart. Application of isoproterenol resulted in dose-dependent acceleration of the heart rate and superior shift of the leading pacemaker. In the mathematical model, such behavior could be reproduced by a gradient of expression in β1-adrenergic receptors along the superior-inferior axis. Application of acetylcholine resulted in preferentially inferior shift of pacemaker and slowing of the heart rate. The mathematical model reproduced this behavior with imposing a gradient of expression of acetylcholine-sensitive potassium channel. We conclude that anatomical shift of the leading pacemaker in the rabbit heart could be achieved through gradient of expression of β1-adrenergic receptors and I K,ACh.
UR - http://www.scopus.com/inward/record.url?scp=80054932960&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=80054932960&partnerID=8YFLogxK
U2 - 10.1016/j.jelectrocard.2011.08.010
DO - 10.1016/j.jelectrocard.2011.08.010
M3 - Article
C2 - 21937057
AN - SCOPUS:80054932960
SN - 0022-0736
VL - 44
SP - 626
EP - 634
JO - Journal of Electrocardiology
JF - Journal of Electrocardiology
IS - 6
ER -