4.4 Article

Electrical and structural remodeling contribute to atrial fibrillation in type 2 diabetic db/db mice

Journal

HEART RHYTHM
Volume 18, Issue 1, Pages 118-129

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.hrthm.2020.08.019

Keywords

Action potential; Atrial fibrillation; Atrial remodeling; Diabetes mellitus; Fibrosis; K+ current

Funding

  1. Canadian Institutes of Health Research [MOP 142486, PJT 1666105]
  2. Killam Postdoctoral Fellowship
  3. Libin Cardiovascular Institute Postdoctoral Fellowship

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The study revealed that AF susceptibility in db/db mice is linked to impaired electrical conduction, along with electrical and structural remodeling of the atria.
BACKGROUND Atrial fibrillation (AF) is highly prevalent in diabetes mellitus (DM), yet the basis for this finding is poorly understood. Type 2 DM may be associated with unique patterns of atrial electrical and structural remodeling; however, this has not been investigated in detail. OBJECTIVE The purpose of this study was to investigate AF susceptibility and atrial electrical and structural remodeling in type 2 diabetic db/db mice. METHODS AF susceptibility and atrial function were assessed in male and female db/db mice and age-matched wildtype littermates. Electrophysiological studies were conducted in vivo using intracardiac electrophysiology and programmed stimulation. Atrial electrophysiology was also investigated in isolated atrial preparations using high-resolution optical mapping and in isolated atrial myocytes using patch-damping. Molecular biology studies were performed using quantitative polymerase chain reaction and western blotting. Atrial fibrosis was assessed using histology. RESULTS db/db mice were highly susceptible to AF in association with reduced atrial conduction velocity, action potential duration prolongation, and increased heterogeneity in repolarization in left and right atria. In db/db mice, atrial K+ currents, including the transient outward current (I-to) and the ultrarapid delayed rectifier current (I-Kur), were reduced. The reduction in I to occurred in association with reductions in Kcnd2 mRNA expression and K(v)4.2 protein levels. The reduction in I-Kur was not related to gene or protein expression changes. Interstitial atrial fibrosis was increased in db/db mice. CONCLUSION Our study demonstrates that increased susceptibility to AF in db/db mice occurs in association with impaired electrical conduction as well as electrical and structural remodeling of the atria.

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