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Inhibition of voltage-gated Na(+) currents by eleclazine in rat atrial and ventricular myocytes

BACKGROUND: Atrial-ventricular differences in voltage-gated Na(+) currents might be exploited for atrial-selective antiarrhythmic drug action for the suppression of atrial fibrillation without risk of ventricular tachyarrhythmia. Eleclazine (GS-6615) is a putative antiarrhythmic drug with properties...

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Detalles Bibliográficos
Autores principales: Caves, Rachel E., Carpenter, Alexander, Choisy, Stéphanie C., Clennell, Ben, Cheng, Hongwei, McNiff, Cameron, Mann, Brendan, Milnes, James T., Hancox, Jules C., James, Andrew F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7442036/
https://www.ncbi.nlm.nih.gov/pubmed/32864638
http://dx.doi.org/10.1016/j.hroo.2020.05.006
Descripción
Sumario:BACKGROUND: Atrial-ventricular differences in voltage-gated Na(+) currents might be exploited for atrial-selective antiarrhythmic drug action for the suppression of atrial fibrillation without risk of ventricular tachyarrhythmia. Eleclazine (GS-6615) is a putative antiarrhythmic drug with properties similar to the prototypical atrial-selective Na(+) channel blocker ranolazine that has been shown to be safe and well tolerated in patients. OBJECTIVE: The present study investigated atrial-ventricular differences in the biophysical properties and inhibition by eleclazine of voltage-gated Na(+) currents. METHODS: The fast and late components of whole-cell voltage-gated Na(+) currents (respectively, I(Na) and I(NaL)) were recorded at room temperature (∼22°C) from rat isolated atrial and ventricular myocytes. RESULTS: Atrial I(Na) activated at command potentials ∼5.5 mV more negative and inactivated at conditioning potentials ∼7 mV more negative than ventricular I(Na). There was no difference between atrial and ventricular myocytes in the eleclazine inhibition of I(NaL) activated by 3 nM ATX-II (IC(50)s ∼200 nM). Eleclazine (10 μM) inhibited I(Na) in atrial and ventricular myocytes in a use-dependent manner consistent with preferential activated state block. Eleclazine produced voltage-dependent instantaneous inhibition in atrial and ventricular myocytes; it caused a negative shift in voltage of half-maximal inactivation and slowed the recovery of I(Na) from inactivation in both cell types. CONCLUSIONS: Differences exist between rat atrial and ventricular myocytes in the biophysical properties of I(Na). The more negative voltage dependence of I(Na) activation/inactivation in atrial myocytes underlies differences between the 2 cell types in the voltage dependence of instantaneous inhibition by eleclazine. Eleclazine warrants further investigation as an atrial-selective antiarrhythmic drug.