The selective INaL blocker GS967 reduced ventricular fibrillation induction (7.1% vs 50.0% in control) and suppressed polymorphic ventricular tachycardia in a long QT syndrome type 2 rabbit model.
Does GS967 prevent early afterdepolarizations and polymorphic ventricular tachycardia in a transgenic rabbit model of long QT syndrome type 2?
Selective INaL blockade by GS967 prevents early afterdepolarizations and abolishes polymorphic ventricular tachycardia in a transgenic rabbit model of long QT syndrome type 2.
Tasa de eventos absoluta: 7.1% vs 50%
Background: Long QT syndrome has been associated with sudden cardiac death likely caused by early afterdepolarizations (EADs) and polymorphic ventricular tachycardias (PVTs). Suppressing the late sodium current (I NaL ) may counterbalance the reduced repolarization reserve in long QT syndrome and prevent EADs and PVTs. Methods: We tested the effects of the selective I NaL blocker GS967 on PVT induction in a transgenic rabbit model of long QT syndrome type 2 using intact heart optical mapping, cellular electrophysiology and confocal Ca 2+ imaging, and computer modeling. Results: GS967 reduced ventricular fibrillation induction under a rapid pacing protocol (n=7/14 hearts in control versus 1/14 hearts at 100 nmol/L) without altering action potential duration or restitution and dispersion. GS967 suppressed PVT incidences by reducing Ca 2+ -mediated EADs and focal activity during isoproterenol perfusion (at 30 nmol/L, n=7/12 and 100 nmol/L n=8/12 hearts without EADs and PVTs). Confocal Ca 2+ imaging of long QT syndrome type 2 myocytes revealed that GS967 shortened Ca 2+ transient duration via accelerating Na + /Ca 2+ exchanger (I NCX )-mediated Ca 2+ efflux from cytosol, thereby reducing EADs. Computer modeling revealed that I NaL potentiates EADs in the long QT syndrome type 2 setting through (1) providing additional depolarizing currents during action potential plateau phase, (2) increasing intracellular Na + (Na i ) that decreases the depolarizing I NCX thereby suppressing the action potential plateau and delaying the activation of slowly activating delayed rectifier K + channels (I Ks ), suggesting important roles of I NaL in regulating Na i . Conclusions: Selective I NaL blockade by GS967 prevents EADs and abolishes PVT in long QT syndrome type 2 rabbits by counterbalancing the reduced repolarization reserve and normalizing Na i . Graphic Abstract: A graphic abstract is available for this article.
Hwang et al. (Mon,) conducted a other in Long QT syndrome type 2 (n=14). GS967 vs. Control was evaluated on Ventricular fibrillation induction under a rapid pacing protocol. The selective INaL blocker GS967 reduced ventricular fibrillation induction (7.1% vs 50.0% in control) and suppressed polymorphic ventricular tachycardia in a long QT syndrome type 2 rabbit model.
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