Journal
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY
Volume 302, Issue 4, Pages H934-H952Publisher
AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajpheart.00493.2011
Keywords
cardiac myocytes; action potential; computer modeling; alternans; reentry
Funding
- National Heart, Lung, and Blood Institute [R01HL-66096, R01HL-59614, R01HL-70722, R01HL-59526]
- National Science Foundation [DBI9873173]
- American Heart Association [10GRNT4720012]
- Georgia State University
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Petkova-Kirova PS, London B, Salama G, Rasmusson RL, Bondarenko VE. Mathematical modeling mechanisms of arrhythmias in transgenic mouse heart overexpressing TNF-alpha. Am J Physiol Heart Circ Physiol 302: H934-H952, 2012. First published November 11, 2011; doi:10.1152/ajpheart.00493.2011.-Transgenic mice overexpressing tumor necrosis factor-alpha (TNF-alpha mice) possess many of the features of human heart failure, such as dilated cardiomyopathy, impaired Ca2+ handling, arrhythmias, and decreased survival. Although TNF-alpha mice have been studied extensively with a number of experimental methods, the mechanisms of heart failure are not completely understood. We created a mathematical model that reproduced experimentally observed changes in the action potential (AP) and Ca2+ handling of isolated TNF-alpha mice ventricular myocytes. To study the contribution of the differences in ion currents, AP, Ca2+ handling, and intercellular coupling to the development of arrhythmias in TNF-alpha mice, we further created several multicellular model tissues with combinations of wild-type (WT)/reduced gap junction conductance, WT/prolonged AP, and WT/decreased Na+ current (I-Na) amplitude. All model tissues were examined for susceptibility to Ca2+ alternans, AP propagation block, and reentry. Our modeling results demonstrated that, similar to experimental data in TNF-alpha mice, Ca2+ alternans in TNF-alpha tissues developed at longer basic cycle lengths. The greater susceptibility to Ca2+ alternans was attributed to the prolonged AP, resulting in larger inactivation of INa, and to the decreased SR Ca2+ uptake and corresponding smaller SR Ca2+ load. Simulations demonstrated that AP prolongation induces an increased susceptibility to AP propagation block. Programmed stimulation of the model tissues with a premature impulse showed that reduced gap junction conduction increased the vulnerable window for initiation reentry, supporting the idea that reduced intercellular coupling is the major factor for reentrant arrhythmias in TNF-alpha mice.
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