Loss of insulin signaling may contribute to atrial fibrillation and atrial electrical remodeling in type 1 diabetes.

Abstract

Atrial fibrillation (AF) is prevalent in diabetes mellitus (DM); however, the basis for this is unknown. This study investigated AF susceptibility and atrial electrophysiology in type 1 diabetic Akita mice using in vivo intracardiac electrophysiology, high-resolution optical mapping in atrial preparations, and patch clamping in isolated atrial myocytes. qPCR and western blotting were used to assess ion channel expression. Akita mice were highly susceptible to AF in association with increased P-wave duration and slowed atrial conduction velocity. In a second model of type 1 DM, mice treated with streptozotocin (STZ) showed a similar increase in susceptibility to AF. Chronic insulin treatment reduced susceptibility and duration of AF and shortened P-wave duration in Akita mice. Atrial action potential (AP) morphology was altered in Akita mice due to a reduction in upstroke velocity and increases in AP duration. In Akita mice, atrial Na⁺ current (I_Na) and repolarizing K⁺ current (I_K) carried by voltage gated K⁺ (K_v1.5) channels were reduced. The reduction in I_Na occurred in association with reduced expression of <i>SCN5a</i> and voltage gated Na⁺ (Na_V1.5) channels as well as a shift in I_Na activation kinetics. Insulin potently and selectively increased I_Na in Akita mice without affecting I_K Chronic insulin treatment increased I_Na in association with increased expression of Na_V1.5. Acute insulin also increased I_Na, although to a smaller extent, due to enhanced insulin signaling via phosphatidylinositol 3,4,5-triphosphate (PIP₃). Our study reveals a critical, selective role for insulin in regulating atrial I_Na, which impacts susceptibility to AF in type 1 DM.