AZD7009 delays repolarization and increases refractoriness in atrial tissue through synergistic inhibition of IKr, Ito, IKur and INa, while inhibiting late sodium current to prevent proarrhythmia.
Does AZD7009 inhibit specific cardiac ion currents and modulate action potential duration in mammalian cells and rabbit cardiac tissue?
AZD7009 exhibits a mixed ion channel blockade that delays repolarization in atrial tissue while inhibiting late sodium current to counteract excessive APD prolongation in susceptible ventricular cells, explaining its high antiarrhythmic efficacy and low proarrhythmic potential.
Atrial fibrillation (AF) is the most common tachyarrhythmia in the adult population and is a major cause of morbidity and mortality. AF can be terminated and sinus rhythm restored by prolonging the action potential duration (APD) and the refractory period. Unfortunately, antiarrhythmic agents that prolong the APD and increase the refractory period via selective inhibition of the rapid delayed rectifier potassium current (IKr), i. e. class III antiarrhythmic drugs, are associated with an increased risk of the ventricular tachycardia Torsades de Pointes. AZD7009 is an antiarrhythmic agent with predominant actions on atrial electrophysiology that shows high antiarrhythmic efficacy and low proarrhythmic potential in animals and man. The aim of the current studies was to characterize the effect of AZD7009 on cardiac ion currents and APD in order to provide a mechanistic explanation for its predominant atrial effects and low proarrhythmic potential. human cardiac ion channels hERG (IKr), Kv1. 5 (IKur), Kv4. 3/KChIP2. 2 (Ito), KvLQT1/minK (IKs), Kir3. 1/Kir3. 4 (IKACh) and Nav1. 5 (INa) were expressed in mammalian cells. Whole-cell currents were inhibited by AZD7009 with the following IC50 values: hERG 0. 6 μM, Nav1. 5 8 μM, Kv4. 3/KChIP2. 2 24 μM, Kv1. 5 27 μM, Kir3. 1/Kir3. 4 166 μM and KvLQT1/minK 193 μM. Whole-cell sodium and calcium currents were recorded in isolated rabbit atrial and ventricular myocytes using amphotericin B perforated patch. The late sodium current in rabbit atrial and ventricular myocytes was inhibited by AZD7009 in a concentration dependent way, with approximately 50% inhibition at 10 μM AZD7009. The L type Ca2+ current (ICaL) in rabbit ventricular myocytes was inhibited with an IC50 of 90 μM. Transmembrane action potentials were recorded in tissue pieces from rabbit atrium, ventricle and Purkinje fibre in control, during exposure to the selective IKr blocker E 4031 and to E 4031 in combination with AZD7009. In Purkinje fibres, but not in ventricular tissue, AZD7009 attenuated the E 4031-induced APD prolongation. In contrast, in atrial cells, AZD7009 further prolonged the APD. In addition, AZD7009 was able to suppress early afterdepolarisations (EADs) induced by E 4031 in Purkinje fibre preparations. conclusion, AZD7009 delays repolarisation and increases refractoriness in atrial tissue through synergistic inhibition of IKr, Ito, IKur and INa, a mixed ion channel blockade that may underlie its high antiarrhythmic efficacy. Inhibition of the late sodium current, counteracting excessive APD prolongation and EADs in susceptible cells (midmyocardial and Purkinje cells), may explain the low proarrhythmic potential of AZD7009.
Frida Persson (Fri,) conducted a other in Atrial fibrillation. AZD7009 vs. Control / E 4031 was evaluated on Effect on cardiac ion currents and action potential duration. AZD7009 delays repolarization and increases refractoriness in atrial tissue through synergistic inhibition of IKr, Ito, IKur and INa, while inhibiting late sodium current to prevent proarrhythmia.