Chin Shui Hao, Allen Emily, Brack Kieran E, Ng G André
Cardiology group, Department of Cardiovascular Sciences, University of Leicester, UK.
University Hospitals of Leicester NHS Trust, Leicester, UK.
J Mol Cell Cardiol Plus. 2023 Sep;5:100044. doi: 10.1016/j.jmccpl.2023.100044.
Heart failure is a clinical syndrome typified by abnormal autonomic tone, impaired ventricular function, and increased arrhythmic vulnerability. This study aims to examine electrophysiological, structural and neuronal remodeling following myocardial infarction in a rabbit heart failure model to establish its neuro-cardiac profile.
Weight-matched adult male New Zealand White rabbits (3.2 ± 0.1 kg, = 25) were randomized to have coronary ligation surgeries (HF group, = 13) or sham procedures (SHM group, = 12). Transthoracic echocardiography was performed six weeks post-operatively. On week 8, dual-innervated Langendorff-perfused heart preparations were set up for terminal experiments. Seventeen hearts (HF group, = 10) underwent ex-vivo cardiac MRI. Twenty-two hearts (HF group, = 7) were examined histologically. Electrical remodeling and abnormal autonomic profile were evident in HF rabbits with exaggerated sympathetic and attenuated vagal effect on ventricular fibrillation threshold, ventricular refractoriness and restitution curves, in addition to increased spatial restitution dispersion. Histologically, there was significant neuronal enlargement at the heart hila and conus arteriosus in HF. Structural remodeling was characterized by quantifiable myocardial scarring, enlarged left ventricles, altered ventricular geometry and impaired contractility.
In an infarct-induced rabbit heart failure model, extensive structural, neuronal and electrophysiological remodeling in conjunction with abnormal autonomic profile provide substrates for ventricular arrhythmias.
心力衰竭是一种临床综合征,其特征为自主神经张力异常、心室功能受损以及心律失常易感性增加。本研究旨在检查兔心力衰竭模型心肌梗死后的电生理、结构和神经元重塑,以确定其神经心脏特征。
体重匹配的成年雄性新西兰白兔(3.2±0.1千克,n = 25)被随机分为接受冠状动脉结扎手术(心力衰竭组,n = 13)或假手术(假手术组,n = 12)。术后六周进行经胸超声心动图检查。在第8周,设置双神经支配的Langendorff灌注心脏标本用于终末实验。17颗心脏(心力衰竭组,n = 10)进行了离体心脏磁共振成像。22颗心脏(心力衰竭组,n = 7)进行了组织学检查。心力衰竭兔存在明显的电重塑和自主神经特征异常,对心室颤动阈值、心室不应期和恢复曲线的交感神经作用增强而迷走神经作用减弱,并伴有空间恢复离散度增加。组织学上,心力衰竭时心脏门和动脉圆锥处有明显的神经元肿大。结构重塑的特征为可量化的心肌瘢痕形成、左心室增大、心室几何形状改变和收缩力受损。
在梗死诱导的兔心力衰竭模型中,广泛的结构、神经元和电生理重塑以及自主神经特征异常为室性心律失常提供了基础。