Why the study?
Does virtual transient outward K current (Ito) injection promote early afterdepolarizations in rabbit ventricular myocytes with reduced repolarization reserve?
Does virtual transient outward K current (Ito) injection promote early afterdepolarizations in rabbit ventricular myocytes with reduced repolarization reserve?
The finding that Ito can dynamically reduce late repolarization reserve and paradoxically promote early afterdepolarizations raises caution regarding the development of Ito-targeted antiarrhythmic therapies.
Ito modulation may promote EADs under reduced repolarization reserve; leaves open arrhythmia risk of Ito-targeted therapies in vivo.
BACKGROUND: Transient outward K currents (Ito) have been reported both to suppress and to facilitate early afterdepolarizations (EADs) when repolarization reserve is reduced. Here, we used the dynamic clamp technique to analyze how Ito accounts for these paradoxical effects on EADs by influencing the dynamic evolution of repolarization reserve during the action potential. METHODS AND RESULTS: Isolated patch-clamped rabbit ventricular myocytes were exposed to either oxidative stress (H2O2) or hypokalemia to induce bradycardia-dependent EADs at a long pacing cycle length of 6 s, when native rabbit Ito is substantial. EADs disappeared when the pacing cycle length was shortened to 1 s, when Ito becomes negligible because of incomplete recovery from inactivation. During 6-s pacing cycle length, EADs were blocked by the Ito blocker 4-aminopyridine, but reappeared when a virtual current with appropriate Ito-like properties was reintroduced using the dynamic clamp (n=141 trials). During 1-s pacing cycle length in the absence of 4-aminopyridine, adding a virtual Ito-like current (n=1113 trials) caused EADs to reappear over a wide range of Ito conductance (0.005-0.15 nS/pF), particularly when inactivation kinetics were slow (τinact≥20 ms) and the pedestal (noninactivating component) was small (<25% of peak Ito). Faster inactivation or larger pedestals tended to suppress EADs. CONCLUSIONS: Repolarization reserve evolves dynamically during the cardiac action potential. Whereas sufficiently large Ito can suppress EADs, a wide range of intermediate Ito properties can promote EADs by influencing the temporal evolution of other currents affecting late repolarization reserve. These findings raise caution in targeting Ito as an antiarrhythmic strategy.
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Nguyen et al. (2015) studied Early afterdepolarizations (EADs) in isolated ventricular myocytes (n=131). Virtual transient outward K current (Ito) injection vs. Baseline without virtual Ito (1-s pacing cycle length) was evaluated on Reappearance of early afterdepolarizations (EADs).
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