A newly developed transmural HF-OVVR computational model successfully replicated failing action potential properties, ionic dynamics, and arrhythmogenic mechanisms like early afterdepolarizations.
A newly developed transmural HF-OVVR computational model successfully replicates human heart failure cellular electrophysiology, providing a tool to study arrhythmogenic mechanisms like EADs and alternans.
During heart failure (HF) at the cellular level, the electrophysiological properties of single myocytes get remodeled, which can trigger the occurrence of ventricular arrhythmias that could be manifested in many forms such as early afterdepolarizations (EADs) and alternans (ALTs). In this paper, based on experimentally observed human HF data, specific ionic and exchanger current strengths are modified from a recently developed human ventricular cell model: the O'Hara-Virág-Varró-Rudy (OVVR) model. A new transmural HF-OVVR model is developed that incorporates HF changes and variability of the observed remodeling. This new heterogeneous HF-OVVR model is able to replicate many of the failing action potential (AP) properties and the dynamics of both Ca(2+)i and Na(+)i in accordance with experimental data. Moreover, it is able to generate EADs for different cell types and exhibits ALTs at modest pacing rate for transmural cell types. We have assessed the HF-OVVR model through the examination of the AP duration and the major ionic currents' rate dependence in single myocytes. The evaluation of the model comes from utilizing the steady-state (S-S) and S1-S2 restitution curves and from probing the accommodation of the HF-OVVR model to an abrupt change in cycle length. In addition, we have investigated the effect of chosen currents on the AP properties, such as blocking the slow sodium current to shorten the AP duration and suppress the EADs, and have found good agreement with experimental observations. This study should help elucidate arrhythmogenic mechanisms at the cellular level and predict unseen properties under HF conditions. In addition, this AP cell model might be useful for modeling and simulating HF at the tissue and organ levels.
Elshrif et al. (Wed,) conducted a other in Heart failure. Transmural HF-OVVR computational model was evaluated on Replication of failing action potential properties and ionic dynamics. A newly developed transmural HF-OVVR computational model successfully replicated failing action potential properties, ionic dynamics, and arrhythmogenic mechanisms like early afterdepolarizations.
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