A newly developed ionic model of cardiac myocytes successfully recreated action potential duration alternans at cycle lengths of 150-210 ms, with a maximum amplitude of 39 ms.
This computational model establishes an ionic basis for APD alternans, providing a framework for developing pharmacological approaches to eliminate alternans.
Although alternans of action potential duration (APD) is a robust feature of the rapidly paced canine ventricle, currently available ionic models of cardiac myocytes do not recreate this phenomenon. To address this problem, we developed a new ionic model using formulations of currents based on previous models and recent experimental data. Compared with existing models, the inward rectifier K + current ( I K1 ) was decreased at depolarized potentials, the maximum conductance and rectification of the rapid component of the delayed rectifier K + current ( I Kr ) were increased, and I Kr activation kinetics were slowed. The slow component of the delayed rectifier K + current ( I Ks ) was increased in magnitude and activation shifted to less positive voltages, and the L-type Ca 2+ current ( I Ca ) was modified to produce a smaller, more rapidly inactivating current. Finally, a simplified form of intracellular calcium dynamics was adopted. In this model, APD alternans occurred at cycle lengths = 150–210 ms, with a maximum alternans amplitude of 39 ms. APD alternans was suppressed by decreasing I Ca magnitude or calcium-induced inactivation and by increasing the magnitude of I K1 , I Kr , or I Ks . These results establish an ionic basis for APD alternans, which should facilitate the development of pharmacological approaches to eliminating alternans.
Fox et al. (Fri,) conducted a other in Electrical alternans. New ionic model vs. Existing models was evaluated on Action potential duration (APD) alternans. A newly developed ionic model of cardiac myocytes successfully recreated action potential duration alternans at cycle lengths of 150-210 ms, with a maximum amplitude of 39 ms.