犬CAVB模型诱发心律失常的关键因素分析。

IF 3.7 3区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS
Cardiovascular Toxicology Pub Date : 2025-09-01 Epub Date: 2025-06-24 DOI:10.1007/s12012-025-10033-3
Joanne J A van Bavel, Henriëtte D M Beekman, Marien J C Houtman, Marc A Vos, Marcel A G van der Heyden
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引用次数: 0

摘要

患有慢性房室传导阻滞(CAVB)的犬合并了与点扭转型心律失常(TdP)相关的许多危险因素。然而,大约33%的动物对多非利特诱发的TdP心律失常有抵抗力。在78只实验相同的CAVB狗中,我们比较了TdP诱导和非诱导动物的一组基本参数,以及心脏电和机械参数。体重,而不是性别或年龄,与TdP的诱发性有关。在心脏参数中,更长的心室复极持续时间和基线时收缩力增加与多非利特诱发的TdP心律失常有关。多非利特输注后,心脏参数的差异消失。我们讨论了复极延长和收缩力增加可能是钙介导的去极化后早期可能发展为TdP心律失常的早期指征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Arrhythmia Inducibility in the CAVB Dog Model, A Critical Analysis on Underlying Factors.

The dog with chronic atrioventricular block (CAVB) combines a number of risk factors associated with Torsade de Pointes (TdP) arrhythmias. Nevertheless, approximately 33% of the animals are resistant to dofetilide-induced TdP arrhythmia. Of a group of 78 experimentally identical CAVB dogs, we compared TdP inducible vs. non-inducible animals for a set of basic, and cardiac electrical and mechanical parameters. Body weight, but not sex or age, is associated with TdP inducibility. Of the cardiac parameters, longer ventricular repolarization duration and increased contractility at baseline are associated with dofetilide-induced TdP arrhythmias. Differences in cardiac parameters disappeared upon dofetilide infusion. We discuss that prolonged repolarization and increased contractility may be early indications of calcium-mediated early after depolarization that may develop into TdP arrhythmias.

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来源期刊
Cardiovascular Toxicology
Cardiovascular Toxicology 医学-毒理学
CiteScore
6.60
自引率
3.10%
发文量
61
审稿时长
>12 weeks
期刊介绍: Cardiovascular Toxicology is the only journal dedicated to publishing contemporary issues, timely reviews, and experimental and clinical data on toxicological aspects of cardiovascular disease. CT publishes papers that will elucidate the effects, molecular mechanisms, and signaling pathways of environmental toxicants on the cardiovascular system. Also covered are the detrimental effects of new cardiovascular drugs, and cardiovascular effects of non-cardiovascular drugs, anti-cancer chemotherapy, and gene therapy. In addition, Cardiovascular Toxicology reports safety and toxicological data on new cardiovascular and non-cardiovascular drugs.
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