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eISSN: 1643-3750

Effects of Ivabradine on Cardiac Electrophysiology in Dogs with Age-Related Atrial Fibrillation

Yao-Dong Li, Yu-Tong Ji, Xian-Hui Zhou, Tao Jiang, Yi-fan Hong, Jin-Xin Li, Qiang Xing, Jian Xiong, Yueerguli Yusufuaji, Bao-Peng Tang

(Department of Pacing and Electrophysiology, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, Xinjiang, China (mainland))

Med Sci Monit 2015; 21:1414-1420

DOI: 10.12659/MSM.894320

Published: 2015-05-16


BACKGROUND: Ivabradine is an inhibitor of mixed Na+-K+ current that could combine with HCN channels to reduce the transmembrane velocity of funny current (If), heart rate, and cardiac efficiency, and thus be used for the treatment of cardiovascular diseases such as chronic heart failure. As an ion channel blocker, Ivabradine is also a potential antiarrhythmic agent.
MATERIAL AND METHODS: Twelve aging dogs (8–10 years old) underwent rapid atrial pacing for 2 months to induce age-related AF in this study. The dogs were randomly divided into the Ivabradine group and aging-AF group. The effects of Ivabradine on the electrophysiological parameters, including the effective refractory period (ERP) of the pulmonary veins and atrium, duration of AF, and inducing rate of AF, were investigated.
RESULTS: As compared to the aging-AF group, the ERPs of the left superior pulmonary vein (139.00±4.18 ms vs. 129.00±4.08 ms, P=0.005) and left auricle (135.00±3.53 ms vs. 122.00±4.47 ms, P=0.001) were significantly increased, while the duration of AF (46.60±5.07 s vs. 205.40±1.14 s, P=0.001) and inducing rate of AF (25% vs. 60%, P=0.001) were significantly decreased.
CONCLUSIONS: Ivabradine could effectively reduce the inducing rate of AF, and thus be used as an upstream drug for the prevention of age-related AF.

Keywords: Anti-Arrhythmia Agents - therapeutic use, Animals, Aging - physiology, Atrial Fibrillation - physiopathology, Benzazepines - therapeutic use, Cardiac Pacing, Artificial - adverse effects, Disease Models, Animal, Dogs, Drug Evaluation, Preclinical, Female, Heart Atria - physiopathology, Hyperpolarization-Activated Cyclic Nucleotide-Gated Channels - antagonists & inhibitors, Male, Pulmonary Veins - physiopathology, Refractory Period, Electrophysiological - drug effects, Sinoatrial Node - drug effects



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