In rabbit and porcine ventricular cardiomyocytes, IKr and INaL are counterbalancing currents whose integrals covary, and targeting their balance can restore action potential duration and stability.
Does pharmacological modulation of IKr and INaL affect action potential duration and repolarization stability in rabbit and porcine ventricular cardiomyocytes?
IKr and INaL act as counterbalancing currents during physiological ventricular action potentials, and targeting their balance may offer therapeutic potential for repolarization abnormalities.
Background: Rapid delayed rectifier K + current (I Kr ) and late Na + current (I NaL ) significantly shape the cardiac action potential (AP). Changes in their magnitudes can cause either long or short QT syndromes associated with malignant ventricular arrhythmias and sudden cardiac death. Methods: Physiological self AP-clamp was used to measure I NaL and I Kr during the AP in rabbit and porcine ventricular cardiomyocytes to test our hypothesis that the balance between I Kr and I NaL affects repolarization stability in health and disease conditions. Results: We found comparable amount of net charge carried by I Kr and I NaL during the physiological AP, suggesting that outward K + current via I Kr and inward Na + current via I NaL are in balance during physiological repolarization. Remarkably, I Kr and I NaL integrals in each control myocyte were highly correlated in both healthy rabbit and pig myocytes, despite high overall cell-to-cell variability. This close correlation was lost in heart failure myocytes from both species. Pretreatment with E-4031 to block I Kr (mimicking long QT syndrome 2) or with sea anemone toxin II to impair Na + channel inactivation (mimicking long QT syndrome 3) prolonged AP duration (APD); however, using GS-967 to inhibit I NaL sufficiently restored APD to control in both cases. Importantly, I NaL inhibition significantly reduced the beat-to-beat and short-term variabilities of APD. Moreover, I NaL inhibition also restored APD and repolarization stability in heart failure. Conversely, pretreatment with GS-967 shortened APD (mimicking short QT syndrome), and E-4031 reverted APD shortening. Furthermore, the amplitude of AP alternans occurring at high pacing frequency was decreased by I NaL inhibition, increased by I Kr inhibition, and restored by combined I NaL and I Kr inhibitions. Conclusions: Our data demonstrate that I Kr and I NaL are counterbalancing currents during the physiological ventricular AP and their integrals covary in individual myocytes. Targeting these ionic currents to normalize their balance may have significant therapeutic potential in heart diseases with repolarization abnormalities. Visual Overview: A visual overview is available for this article.
Hegyi et al. (Mon,) conducted a other in Ventricular repolarization abnormalities and heart failure. Ion channel inhibitors (E-4031, sea anemone toxin II, GS-967) vs. Control myocytes was evaluated on Action potential duration (APD) and repolarization stability. In rabbit and porcine ventricular cardiomyocytes, IKr and INaL are counterbalancing currents whose integrals covary, and targeting their balance can restore action potential duration and stability.
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