Modulation of NOX2 causes obesity-mediated atrial fibrillation

J Clin Invest. 2024 Aug 15;134(18):e175447. doi: 10.1172/JCI175447.

Abstract

Obesity is linked to an increased risk of atrial fibrillation (AF) via increased oxidative stress. While NADPH oxidase 2 (NOX2), a major source of oxidative stress and reactive oxygen species (ROS) in the heart, predisposes to AF, the underlying mechanisms remain unclear. Here, we studied NOX2-mediated ROS production in obesity-mediated AF using Nox2-knockout mice and mature human induced pluripotent stem cell-derived atrial cardiomyocytes (hiPSC-aCMs). Diet-induced obesity (DIO) mice and hiPSC-aCMs treated with palmitic acid (PA) were infused with a NOX blocker (apocynin) and a NOX2-specific inhibitor, respectively. We showed that NOX2 inhibition normalized atrial action potential duration and abrogated obesity-mediated ion channel remodeling with reduced AF burden. Unbiased transcriptomics analysis revealed that NOX2 mediates atrial remodeling in obesity-mediated AF in DIO mice, PA-treated hiPSC-aCMs, and human atrial tissue from obese individuals by upregulation of paired-like homeodomain transcription factor 2 (PITX2). Furthermore, hiPSC-aCMs treated with hydrogen peroxide, a NOX2 surrogate, displayed increased PITX2 expression, establishing a mechanistic link between increased NOX2-mediated ROS production and modulation of PITX2. Our findings offer insights into possible mechanisms through which obesity triggers AF and support NOX2 inhibition as a potential novel prophylactic or adjunctive therapy for patients with obesity-mediated AF.

Keywords: Arrhythmias; Cardiology.

MeSH terms

  • Animals
  • Atrial Fibrillation* / enzymology
  • Atrial Fibrillation* / etiology
  • Atrial Fibrillation* / genetics
  • Atrial Fibrillation* / metabolism
  • Atrial Fibrillation* / pathology
  • Atrial Remodeling
  • Homeodomain Proteins / genetics
  • Homeodomain Proteins / metabolism
  • Humans
  • Induced Pluripotent Stem Cells / metabolism
  • Male
  • Mice
  • Mice, Knockout*
  • Myocytes, Cardiac* / enzymology
  • Myocytes, Cardiac* / metabolism
  • Myocytes, Cardiac* / pathology
  • NADPH Oxidase 2* / genetics
  • NADPH Oxidase 2* / metabolism
  • Obesity* / genetics
  • Obesity* / metabolism
  • Obesity* / pathology
  • Oxidative Stress
  • Reactive Oxygen Species / metabolism
  • Transcription Factors / genetics
  • Transcription Factors / metabolism

Substances

  • NADPH Oxidase 2
  • Cybb protein, mouse
  • CYBB protein, human
  • Reactive Oxygen Species
  • Homeodomain Proteins
  • Transcription Factors