101. A mathematical model of the murine ventricular myocyte: a data-driven biophysically based approach applied to mice overexpressing the canine NCX isoform.
- Author
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Li, L., Niederer, S. A., Idigo, W., Zhang, V. H., Swietach, P., Casadei, B., and Smith, N. P.
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MATHEMATICAL models , *MUSCLE cells , *VENTRICULAR remodeling , *ELECTROPHYSIOLOGY , *ALLOSTERIC regulation , *PHYSIOLOGY - Abstract
Mathematical modeling of Ca2+ dynamics in the heart has the potential to provide an integrated understanding of Ca2+ handling mechanisms. However, many previous published models use heterogeneous experimental data sources from a variety of animals and temperatures to characterize model parameters and motivate model equations. This methodology limits the direct comparison of these models to any particular experimental data set. To directly address this issue, in this study, we present a biophysically-based model of Ca2+ dynamics, directly fitted to experimental data collected in left ventricular (LV) myocytes isolated from the C57BL/6 mouse, the most commonly used genetic background for genetically modified mice in studies of heart diseases. This Ca2+ dynamics model is then integrated into an existing mouse cardiac electrophysiology model which has been re-parameterized using experimental data recorded at consistent and physiological temperatures. The model is validated against experimentally observed frequency response of Ca2+ dynamics, action potential shape, the dependence of action potential duration on cycle length and electrical restitution. Using this framework, the implications of cardiac NCX over-expression in transgenic mice were investigated. These simulations show that heterozygous over-expression of the canine cardiac NCX increases [Ca2+]i transient magnitude and SR Ca2+ loading in agreement with experimental observations, while acute over-expression of murine cardiac NCX results in a significant loss of Ca2+ from the cell and hence depressed SR Ca2+ load and intracellular Ca2+concentration transient magnitude. From this analysis we conclude these differences are primarily due to the presence of allosteric regulation in canine cardiac NCX which has not been observed experimentally in wild-type mouse heart. [ABSTRACT FROM AUTHOR]
- Published
- 2010
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