保留射血分数的心力衰竭小鼠模型的心房颤动、窦房结和房室结功能障碍。

IF 2.8 4区 医学 Q2 PHYSIOLOGY
Bernadin Ndongson-Dongmo, Reinhard Bauer, Finn Olav Levy
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引用次数: 0

摘要

数以百万计的人受到房颤(AF)和心力衰竭并保留射血分数(HFpEF)的影响,这两种疾病经常同时发现。然而,这些相互交织的疾病之间的相互关系知之甚少,部分原因是缺乏临床前模型。我们的目的是评估最近开发的HFpEF小鼠模型是否也可以用作AF模型,并有可能研究这两种情况之间的共发生和相互关系。采用高脂肪饮食和饮水中添加n ω-硝基-l-精氨酸甲酯的饮食方案诱导小鼠HFpEF。通过遥测获得的24小时心电图记录分析自主神经失衡。记录24 h心电图后,给予异丙肾上腺素,再记录1 h,评估变时功能不全、心房心律失常易感性和传导障碍。通过经颈动脉导管和对心脏进行组织学分析来评估舒张功能。静息心率在饮食方案3周后显著增加,早在1周就观察到这种趋势。提前心房收缩、窦性暂停和房室传导阻滞在饮食方案3周后显著发生。在饮食方案的第6周,HFpEF组在异丙肾上腺素刺激后观察到明显的舒张功能障碍、变时功能不全和房颤发生率较高。我们的研究表明,窦房结和心房功能障碍先于房颤、舒张功能障碍和变时功能不全同时发生。该小鼠HFpEF模型可能有助于研究AF与HFpEF之间的相互依赖性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Atrial fibrillation, sinoatrial and atrioventricular node dysfunction in a mouse model of heart failure with preserved ejection fraction.

Millions of people are affected by atrial fibrillation (AF) and heart failure with preserved ejection fraction (HFpEF), two disorders frequently found simultaneously. However, the interrelationship between these intertwined disorders is poorly understood, partly owing to the lack of preclinical models. We aimed to evaluate whether a recently developed mouse model of HFpEF could also be used as a model of AF and, potentially, to study the co-occurrence and interrelationship between the two conditions. Mice were fed a dietary regimen of high-fat diet and Nω-nitro-l-arginine methyl ester in the drinking water to induce HFpEF. Twenty-four-hour ECG recordings acquired by telemetry were analysed for autonomic imbalance. After 24 h ECG recording, mice received isoprenaline, and a further 1 h of recording was assessed for chronotropic incompetence, susceptibility to atrial arrhythmia and conduction impairment. Evaluation of diastolic function was achieved by transcarotid catheterization and histological analysis performed on the hearts. Resting heart rate was significantly increased after 3 weeks of the dietary regimen, with a trend observed as early as 1 week. Premature atrial contractions, sinus pauses and atrioventricular blocks occurred significantly after 3 weeks of the dietary regimen. Significant diastolic dysfunction, chronotropic incompetence and higher occurrence of AF after isoprenaline stimulation were observed in the HFpEF group at 6 weeks of the dietary regimen. Our study revealed that sinoatrial node and atrial dysfunction precede the simultaneous occurrence of AF, diastolic dysfunction and chronotropic incompetence. This mouse HFpEF model might be helpful for studying the interdependence between AF and HFpEF.

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来源期刊
Experimental Physiology
Experimental Physiology 医学-生理学
CiteScore
5.10
自引率
3.70%
发文量
262
审稿时长
1 months
期刊介绍: Experimental Physiology publishes research papers that report novel insights into homeostatic and adaptive responses in health, as well as those that further our understanding of pathophysiological mechanisms in disease. We encourage papers that embrace the journal’s orientation of translation and integration, including studies of the adaptive responses to exercise, acute and chronic environmental stressors, growth and aging, and diseases where integrative homeostatic mechanisms play a key role in the response to and evolution of the disease process. Examples of such diseases include hypertension, heart failure, hypoxic lung disease, endocrine and neurological disorders. We are also keen to publish research that has a translational aspect or clinical application. Comparative physiology work that can be applied to aid the understanding human physiology is also encouraged. Manuscripts that report the use of bioinformatic, genomic, molecular, proteomic and cellular techniques to provide novel insights into integrative physiological and pathophysiological mechanisms are welcomed.
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