Abstract

BackgroundThe activation of stretch-activated channels (SACs) in cardiac myocytes, which changes the phases of action potential repolarization, is proven to be highly efficient for the conversion of atrial fibrillation. The expression of Na+ current in myofibroblasts (Mfbs) regenerates myocytes’ action potentials, suggesting that Mfbs play an active role in triggering cardiac rhythm disturbances. Moreover, the excitation of mechano-gated channels (MGCs) in Mfbs depolarizes their membrane potential and contributes to the increased risk of post-infarct arrhythmia. Although these electrophysiological mechanisms have been largely known, the roles of these currents in cardiac mechanics are still debated. In this study, we aimed to investigate the mechanical influence of these currents via mathematical modeling. A novel mathematical model was developed by integrating models of human atrial myocyte (including the stretch-activated current, Ca2+–force relation, and mechanical behavior of a single segment) and Mfb (including our formulation of Na+ current and mechano-gated channels’ current). The effects of the changes in basic cycle length, number of coupled Mfbs and intercellular coupling conductance on myocyte mechanical properties were compared.ResultsOur results indicated that these three currents significantly regulated myocyte mechanical parameters. In isosarcometric contraction, these currents increased segment force by 13.8–36.6% and dropped element length by 12.1–31.5%. In isotonic contraction, there are 2.7–5.9% growth and 0.9–24% reduction. Effects of these currents on the extremum of myocyte mechanical parameters become more significant with the increase of basic cycle length, number of coupled Mfbs and intercellular coupling conductance.ConclusionsThe results demonstrated that stretch-activated current in myocytes and Na+ current and mechano-gated channels’ current in Mfbs significantly influenced myocyte mechanical behavior and should be considered in future cardiac mechanical mathematical modeling.

Highlights

  • The activation of stretch-activated channels (SACs) in cardiac myocytes, which changes the phases of action potential repolarization, is proven to be highly efficient for the conversion of atrial fibrillation

  • Effects of ISAC, INa_Mfb, and IMGC_Mfb on atrial myocyte action potential (AP), ­[Ca2+]i, and the normalized force Figure 1 shows the combinational effects in five groups of ISAC, INa_Mfb, and IMGC_Mfb on the membrane potential, intracellular C­ a2+ concentration and the normalized force (Fnorm) of myocytes with a Ggap of 3 nS and a basic cycle length (BCL) of 1 s

  • This study demonstrated the combinational effects of ISAC in myocytes and INa_Mfb and IMGC_Mfb in Mfbs on myocyte mechanical properties

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Summary

Introduction

The activation of stretch-activated channels (SACs) in cardiac myocytes, which changes the phases of action potential repolarization, is proven to be highly efficient for the conversion of atrial fibrillation. The excitation of mechano-gated channels (MGCs) in Mfbs depolarizes their membrane potential and contributes to the increased risk of post-infarct arrhythmia. These electrophysiological mechanisms have been largely known, the roles of these currents in cardiac mechanics are still debated. A novel mathematical model was developed by integrating models of human atrial myocyte (including the stretch-activated current, ­Ca2+–force relation, and mechanical behavior of a single segment) and Mfb (including our formulation of ­Na+ current and mechano-gated channels’ current). Several cellular experimental and modeling studies have examined the impact of SACs on cardiac electrophysiology [8,9,10,11]

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