Impaired epicardial activation–repolarization coupling contributes to the proarrhythmic effects of hypokalaemia and dofetilide in guinea pig ventricles

Aim Activation–repolarization coupling refers to the inverse relationship between action potential duration and activation time in myocardial regions along the path of ventricular excitation. This study examined whether the activation–repolarization coupling plays a role in coordinating repolarization times between the right ventricular ( RV ) and left ventricular ( LV ) chambers, and if impaired coordination contributes to electrical instability produced by hypokalaemia or dofetilide, a blocker of the delayed rectifier K + current. Methods In Langendorff‐perfused, isolated guinea pig hearts, six monophasic action potential recording electrodes were attached to RV and LV epicardium. Local activation time and action potential duration ( APD 90 ) were determined during spontaneous beating, regular pacing and extrasystolic excitation. Results In regularly beating hearts, the RV epicardial sites had longer APD 90 , but exhibited earlier activation times, as compared to LV sites, which minimized the interventricular difference in repolarization time. Upon extrasystolic stimulation, the APD 90 was reduced to a greater extent in RV compared with LV , which translated to a reversed slope of APD 90 ‐to‐activation time relationship, and increased spatial repolarization gradients. Hypokalaemia and dofetilide prolonged APD 90 , with the effect being greater in LV compared with RV . In hypokalaemic hearts, LV activation was delayed. These changes contributed to increased asynchrony in repolarization times in the LV and RV in both regular and extrasystolic beats, and enhanced susceptibility to tachyarrhythmia. Conclusion Impaired RV ‐to‐ LV activation–repolarization coupling is an important determinant of electrical instability in the setting of non‐uniformly prolonged epicardial APD 90 or slowed interventricular conduction.