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

Joseph L. Greenstein, Robert Hinch, Raimond L. Winslow

Research output: Contribution to journalArticlepeer-review

95 Scopus citations


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, 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 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 action potential, resulting from reduction of the transient outward potassium current, alters properties of EC coupling.

Original languageEnglish (US)
Pages (from-to)77-91
Number of pages15
JournalBiophysical journal
Issue number1
StatePublished - Jan 2006

ASJC Scopus subject areas

  • Biophysics


Dive into the research topics of 'Mechanisms of excitation-contraction coupling in an integrative model of the cardiac ventricular myocyte'. Together they form a unique fingerprint.

Cite this