Bayer AG, Research and Development, Pharmaceuticals, Wuppertal, Germany.
Bayer AG, Research and Development, Pharmaceuticals, Wuppertal, Germany.
Heart Rhythm. 2021 Apr;18(4):632-640. doi: 10.1016/j.hrthm.2020.12.015. Epub 2020 Dec 17.
Atrial fibrillation (AF) is the most common arrhythmia occurring in humans, and new treatment strategies are critically needed. The lack of reliable preclinical animal models of AF is a major limitation to drug development of novel antiarrhythmic compounds.
The purpose of this study was to provide a comprehensive head-to-head assessment of 5 canine AF models.
Five canine models were evaluated for the efficacy of AF induction and AF duration. We tested 2 acute models: short-term atrial tachypacing (AT) for 6 hours with analysis of AF at hourly increments, and carbachol injection into a cardiac fat pad followed by short-term AT. We also tested 3 chronic models: pacemaker implantation followed by either 4 weeks of AT and subsequent atrial burst pacing or intermittent long-term AT for up to 4-5 months to generate AF ≥4.5 hours, and finally ventricular tachypacing to induce heart failure followed by atrial burst pacing to induce AF.
Careful evaluation showed that acute AT, AT for 4 weeks, and the heart failure model all were unsuccessful in generating reproducible AF episodes of sufficient duration to study antiarrhythmic drugs. In contrast, intermittent long-term AT generated AF lasting ≥4.5 hours in ∼30% of animals. The acute model using carbachol and short-term AT resulted in AF induction of ≥15 minutes in ≥75% of animals, thus enabling testing of antiarrhythmic drugs.
Intermittent long-term AT and the combination of local carbachol injection with successive short-term AT may contribute to future drug development efforts for AF treatment.
心房颤动(AF)是人类最常见的心律失常,迫切需要新的治疗策略。缺乏可靠的 AF 临床前动物模型是新型抗心律失常化合物药物开发的主要限制。
本研究旨在全面比较 5 种犬 AF 模型。
评估了 5 种犬 AF 模型的诱导成功率和 AF 持续时间。我们测试了 2 种急性模型:持续 6 小时的短期心房快速起搏(AT),每隔 1 小时分析 AF,以及注射乙酰胆碱到心脏脂肪垫后进行短期 AT。我们还测试了 3 种慢性模型:植入起搏器后进行 4 周 AT,然后进行心房突发起搏,或间歇性长期 AT 长达 4-5 个月以产生≥4.5 小时的 AF,最后进行心室快速起搏诱导心力衰竭,然后进行心房突发起搏诱导 AF。
仔细评估显示,急性 AT、4 周 AT 和心力衰竭模型均未能产生足够持续时间的可重复 AF 发作,不足以研究抗心律失常药物。相比之下,间歇性长期 AT 在约 30%的动物中产生持续时间≥4.5 小时的 AF。使用乙酰胆碱和短期 AT 的急性模型在≥75%的动物中诱导 AF 发作≥15 分钟,从而能够测试抗心律失常药物。
间歇性长期 AT 和局部乙酰胆碱注射与连续短期 AT 的组合可能有助于未来的 AF 治疗药物开发工作。