Abstract Fri089: Effect of Empagliflozin on Cardiac Arrhythmia by Attenuating Cardiac Fibrosis via Na V 1.5 Regulation in β-Adrenergic Stimulated KK/HIJ Mice

Introduction: The progression of cardiac fibrosis leads to increased myocardial stiffness and disruption of the cardiac conduction system as well as impaired contractile function. Empagliflozin is a drug for type 2 diabetes mellitus patients and lowers glucose reabsorption by inhibiting sodium-glucose co-transporter 2 (SGLT2). Recent studies reported that empagliflozin can produce off-target effects that improve cardiac function independently of diabetes. Although empagliflozin has shown to attenuate cardiac fibrosis, the underlying regulatory mechanisms remain to be elucidated. Methods: The mouse model with cardiac fibrosis was established by inducing β-adrenergic stimulation through osmotic pump in KK/HIJ mouse. Echocardiographic, histological and electrophysiological experiments were conducted in saline or isoproterenol (30 mg/kg)-induced C57BL/6 mouse and KK/HIJ mouse following intraperitoneally injection of vehicle (DMSO) vs. empagliflozin (10 mg/kg). Results: In the KK/HIJ mice following isoproterenol infusion, i) cardiac hypertrophy and fibrosis were induced (p<0.001); ii) left ventricular ejection fraction and fractional shortening were decreased, but not significantly; iii) QRS width and QTc interval were prolonged ( p <0.001); iv) AF inducibility was increased, but not significantly; v) action potential duration was prolonged ( p <0.05); vi) I Na,Peak (-16.07±1.76 vs. -7.06±0.77, p<0.01) and I Na,Late (0.98±0.15 vs. 0.56±0.05, p<0.01) were increased, and vii) spontaneous Ca 2+ release was increased (47.33±9 vs. 4.72±3.02, p<0.001), compared to C57BL/6 mice. After empagliflozin injection, isoproterenol-induced KK/HIJ mice showed that the histological, echocardiographic and electrophysiological properties significantly improved compared to the vehicle group. Both inducibility and duration of AF were also significantly reduced in the empagliflozin group than in vehicle group. Conclusion: This study demonstrated that empagliflozin, a SGLT2i, improved cardiac fibrosis and reduced AF inducibility/duration through modulation of electrophysiological remodeling, suggesting that empagliflozin can be considered a potential new antiarrhythmic drug for atrial fibrillation.