Abstract

Ca2+ waves underlying triggered propagated contractions (TPCs) are initiated in damaged regions in cardiac muscle and cause arrhythmias. We studied Ca2+ waves underlying TPCs in rat cardiac trabeculae under experimental conditions that simulate the functional nonuniformity caused by local mechanical or ischemic local damage of myocardium. A mechanical discontinuity along the trabeculae was created by exposing the preparation to a small jet of solution with a composition that reduces excitation-contraction coupling (ECC) in myocytes within that segment. The jet solution contained either caffeine (5 mmol/L), 2,3-butanedione monoxime (BDM; 20 mmol/L), or low Ca2+ concentration ([Ca2+]; 0.2 mmol/L). Force was measured with a silicon strain gauge and sarcomere length with laser diffraction techniques in 15 trabeculae. Simultaneously, [Ca2+]i was measured locally using epifluorescence of Fura-2. The jet of solution was applied perpendicularly to a small muscle region (200 to 300 microm) at constant flow. When the jet contained caffeine, BDM, or low [Ca2+], during the stimulated twitch, muscle-twitch force decreased and the sarcomeres in the exposed segment were stretched by shortening normal regions outside the jet. Typical protocols for TPC induction (7.5 s-2.5 Hz stimulus trains at 23 degrees C; [Ca2+]o=2.0 mmol/L) reproducibly generated Ca2+ waves that arose from the border between shortening and stretched regions. Such Ca2+ waves started during force-relaxation of the last stimulated twitch of the train and propagated (0.2 to 2.8 mm/sec) into segments both inside and outside of the jet. Arrhythmias, in the form of nondriven rhythmic activity, were induced when the amplitude of the Ca2+-wave was increased by raising [Ca2+]o. Arrhythmias disappeared rapidly when uniformity of ECC throughout the muscle was restored by turning the jet off. These results show, for the first time, that nonuniform ECC can cause Ca2+ waves underlying TPCs and suggest that Ca2+ dissociated from myofilaments plays an important role in the initiation of Ca2+ waves.

Highlights

  • Ca2ϩ waves underlying triggered propagated contractions (TPCs) are initiated in damaged regions in cardiac muscle and cause arrhythmias

  • I schemic and failing hearts are both prone to ventricular arrhythmias and commonly show regional differences in contractile strength caused by heterogeneous impairment of excitation– contraction coupling (ECC)

  • The initiation of arrhythmogenic Ca2ϩ waves can be explained by nonuniform ECC and Ca2ϩ-dissociation from the contractile filaments occurring during relaxation of nonuniform cardiac muscle

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Summary

Introduction

Ca2ϩ waves underlying triggered propagated contractions (TPCs) are initiated in damaged regions in cardiac muscle and cause arrhythmias. Typical protocols for TPC induction (7.5 s-2.5 Hz stimulus trains at 23°C; [Ca2ϩ]oϭ2.0 mmol/L) reproducibly generated Ca2ϩ waves that arose from the border between shortening and stretched regions Such Ca2ϩ waves started during force-relaxation of the last stimulated twitch of the train and propagated (0.2 to 2.8 mm/sec) into segments both inside and outside of the jet. We developed a novel model of controlled nonuniformity in rat trabeculae Using this model, we show that controlled initiation of Ca2ϩ waves underlying TPCs can trigger nondriven regular spontaneous contractions in cardiac muscle. The initiation of arrhythmogenic Ca2ϩ waves can be explained by nonuniform ECC and Ca2ϩ-dissociation from the contractile filaments occurring during relaxation of nonuniform cardiac muscle

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