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Biophys. J. BioFAST: First Published October 7, 2005. doi:10.1529/biophysj.105.065169
© 2005 by the Biophysical Society.


A more recent version of this article appeared on January 1, 2006.
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BIOPHYSICAL THEORY AND MODELING

Mechanisms of excitation-contraction coupling in an integrative model of the cardiac ventricular myocyte

Joseph L Greenstein 1*, Robert Hinch 2 and Raimond L Winslow 1

1 The Johns Hopkins University, Center for Computational Bioinformatics and Modeling
2 Oxford University

* To whom correspondence should be addressed. E-mail: jgreenst{at}jhu.edu.

Submitted on April 22, 2005
Revised on June 10, 2005
Accepted on 23 September 2005


   Abstract
It is now well established that characteristic properties of excitation-contraction (EC) coupling in cardiac myocytes, such as high gain and graded Ca2+ release, arise from the interactions that occur between L-type Ca2+ channels (LCCs) and nearby ryanodine-sensitive Ca2+ release channels (RyRs) in localized microdomains. Descriptions of Ca2+-induced Ca2+ release (CICR) that account for these local mechanisms are lacking from many previous models of the cardiac action potential (AP), and those that do include local control of CICR are able to reconstruct properties of EC coupling, but require computationally demanding stochastic simulations of ~ 105 individual ion channels. In this study we generalize a recently developed analytical approach for deriving simplified mechanistic models of CICR in order to formulate an integrative model of the canine cardiac myocyte which is computationally efficient. The resulting model faithfully reproduces experimentally measured properties of EC coupling and whole cell phenomena. The model is used to study the role of local redundancy in L-type Ca2+ channel gating and the role of dyad configuration on EC coupling. Simulations suggest that the characteristic steep rise in EC coupling gain observed at hyperpolarized potentials is a result of increased functional coupling between LCCs and RyRs. We also demonstrate mechanisms by which alterations in the early repolarization phase of the AP, resulting from reduction of the transient outward potassium current, alters properties of EC coupling.

Key Words: action potential, calcium transient, cardiac myocyte, excitation-contraction coupling, local control, multi-scale model




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Copyright © 2005 by the Biophysical Society.