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The cardiac Na+/K+ ATPase: An updated, thermodynamically consistent model
Open Access
Reproducible Model
Retrospective Article

Published: 2020-08-27
Last edited: 2020-08-27

The cardiac Na+/K+ ATPase: An updated, thermodynamically consistent model

Pan, M. ORCID logo , Gawthrop, P. J. ORCID logo , Cursons, J. ORCID logo , Tran, K. ORCID logo , Crampin, E. J.

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To cite this Physiome article, cite the whole collection at the DOI: 10.36903/physiome.12871070, and the Primary Publication at the DOI: https://doi.org/10.1152/ajpheart.00771.2007.

All Physiome articles are published as a collection containing the manuscript as a PDF file and the model implementation as an OMEX file.

Primary Publication: The balance between inactivation and activation of the Na+-K+ pump underlies the triphasic accumulation of extracellular K+ during myocardial ischemia. 2007, Jonna R. Terkildsen, Edmund J. Crampin, and Nicolas P. Smith

Abstract: The Na+/K+ATPase is an essential component of cardiac electrophysiology, maintaining physiological Na+ and K+ concentrations over successive heart beats. Terkildsen et al. (2007) developed a model of the ventricular myocyte Na+/K+ ATPase to study extracellular potassium accumulation during ischaemia, demonstrating the ability to recapitulate a wide range of experimental data, but unfortunately there was no archived code associated with the original manuscript. Here we detail an updated version of the model and provide CellML and MATLAB code to ensure reproducibility and reusability. We note some errors within the original formulation which have been corrected to ensure that the model is thermodynamically consistent, and although this required some reparameterisation, the resulting model still provides a good fit to experimental measurements that demonstrate the dependence of Na+/K+ ATPase pumping rate upon membrane voltage and metabolite concentrations. To demonstrate thermodynamic consistency we also developed a bond graph version of the model. We hope that these models will be useful for community efforts to assemble a whole-cell cardiomyocyte model which facilitates the investigation of cellular energetics.


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