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PMID: 15347581 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

A mathematical treatment of integrated Ca dynamics within the ventricular myocyte.

Biophysical journal ·Vol. 87 ·No. 5 ·2004-11-00 ·Pages 3351-71

Shannon TR, Wang F, Puglisi J, Weber C, Bers DM

Abstract

We have developed a detailed mathematical model for Ca2+ handling and ionic currents in the rabbit ventricular myocyte. The objective was to develop a model that: 1), accurately reflects Ca-dependent Ca release; 2), uses realistic parameters, particularly those that concern Ca transport from the cytosol; 3), comes to steady state; 4), simulates basic excitation-contraction coupling phenomena; and 5), runs on a normal desktop computer. The model includes the following novel features: 1), the addition of a subsarcolemmal compartment to the other two commonly formulated cytosolic compartments (junctional and bulk) because ion channels in the membrane sense ion concentrations that differ from bulk; 2), the use of realistic cytosolic Ca buffering parameters; 3), a reversible sarcoplasmic reticulum (SR) Ca pump; 4), a scheme for Na-Ca exchange transport that is [Na]i dependent and allosterically regulated by [Ca]i; and 5), a practical model of SR Ca release including both inactivation/adaptation and SR Ca load dependence. The data describe normal electrical activity and Ca handling characteristics of the cardiac myocyte and the SR Ca load dependence of these processes. The model includes a realistic balance of Ca removal mechanisms (e.g., SR Ca pump versus Na-Ca exchange), and the phenomena of rest decay and frequency-dependent inotropy. A particular emphasis is placed upon reproducing the nonlinear dependence of gain and fractional SR Ca release upon SR Ca load. We conclude that this model is more robust than many previously existing models and reproduces many experimental results using parameters based largely on experimental measurements in myocytes.

Keywords
NASA Discipline Cardiopulmonary Non-NASA Center
MeSH Terms
Action Potentials/physiology Animals Calcium/metabolism Calcium Signaling/physiology Cell Membrane/physiology Computer Simulation Humans Membrane Potentials/physiology Models, Cardiovascular Myocardial Contraction/physiology Myocytes, Cardiac/physiology Sarcoplasmic Reticulum/physiology Ventricular Function
Chemicals
Calcium
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Shannon Thomas R
Department of Molecular Biophysics and Physiology, Rush University, Chicago, Illinois, USA.
Wang Fei
Puglisi José
Weber Christopher
Bers Donald M
Investigators
1 investigators, click to expand
Bers D M
Loyola U, Chicago, IL
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Article Info
Journal
Biophysical journal
Abbr.
Biophys J
ISSN
0006-3495
Published
2004-11-00
Epub
2004-00-03
Pages
3351-71
Language
English
Region
United States
NLM ID
0370626
PMCID
PMC1304803
Subset
IM
Grants
NHLBI NIH HHS · HL64098 · United States
Corrections
ErratumIn
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