Vericiguat suppresses ventricular tachyarrhythmias inducibility in a rabbit myocardial infarction model

PLoS One. 2024 Apr 16;19(4):e0301970. doi: 10.1371/journal.pone.0301970. eCollection 2024.

Abstract

Background: The VICTORIA trial demonstrated a significant decrease in cardiovascular events through vericiguat therapy. This study aimed to assess the potential mechanisms responsible for the reduction of cardiovascular events with vericiguat therapy in a rabbit model of myocardial infarction (MI).

Methods: A chronic MI rabbit model was created through coronary artery ligation. Following 4 weeks, the hearts were harvested and Langendorff perfused. Subsequently, electrophysiological examinations and dual voltage-calcium optical mapping studies were conducted at baseline and after administration of vericiguat at a dose of 5 μmol/L.

Results: Acute vericiguat therapy demonstrated a significant reduction in premature ventricular beat burden and effectively suppressed ventricular arrhythmic inducibility. The electrophysiological influences of vericiguat therapy included an increased ventricular effective refractory period, prolonged action potential duration, and accelerated intracellular calcium (Cai) homeostasis, leading to the suppression of action potential and Cai alternans. The pacing-induced ventricular arrhythmias exhibited a reentrant pattern, attributed to fixed or functional conduction block in the peri-infarct zone. Vericiguat therapy effectively mitigated the formation of cardiac alternans as well as the development of reentrant impulses, providing additional anti-arrhythmic benefits.

Conclusions: In the MI rabbit model, vericiguat therapy demonstrates anti-ventricular arrhythmia effects. The vericiguat therapy reduces ventricular ectopic beats, inhibiting the initiation of ventricular arrhythmias. Furthermore, the therapy successfully suppresses cardiac alternans, preventing conduction block and, consequently, the formation of reentry circuits.

MeSH terms

  • Animals
  • Anti-Arrhythmia Agents / therapeutic use
  • Arrhythmias, Cardiac / drug therapy
  • Calcium / therapeutic use
  • Heart Block
  • Heterocyclic Compounds, 2-Ring*
  • Myocardial Infarction* / complications
  • Myocardial Infarction* / drug therapy
  • Pyrimidines*
  • Rabbits
  • Tachycardia, Ventricular* / drug therapy
  • Ventricular Fibrillation

Substances

  • vericiguat
  • Calcium
  • Anti-Arrhythmia Agents
  • Heterocyclic Compounds, 2-Ring
  • Pyrimidines

Grants and funding

This study was supported by the Ministry of Science and Technology, Taiwan (110-2314-B-182A-119- to P.C. Chang) and Chang Gung Medical Foundation (CMRPG3L1202 to P.C. Chang). The funders contributed to the study design, data collection and analysis, and preparation of the manuscript in this study.