Selective ablation of the ligament of Marshall attenuates atrial electrical remodeling in a short‐term rapid atrial pacing canine model

烧蚀 医学 内科学 心脏病学 心房颤动 有效耐火期 电生理学 房性心动过速 麻醉 导管消融
作者
Xiaomei Yu,Wenbo He,Zhiliang Qin,Shan Liu,Ruisong Ma,Da Luo,Huihui Hu,Jing Xie,Bo He,Zhibing Lu,Hong Jiang
出处
期刊:Journal of Cardiovascular Electrophysiology [Wiley]
卷期号:29 (9): 1299-1307 被引量:6
标识
DOI:10.1111/jce.13658
摘要

Abstract Introduction Cardiac sympathetic activation facilitates atrial electrical remodeling during atrial fibrillation (AF). Selective ablation of the distal part of the ligament of Marshall (LOM LSPV ) could decrease cardiac sympathetic innervation. This study aimed to investigate the effects of LOM LSPV ablation on atrial electrical remodeling in a short‐term rapid atrial pacing (RAP) model. Methods In 16 anesthetized dogs, 6 hours of RAP (20 Hz, 2 × threshold) was delivered before LOM LSPV ablation (group 1, N = 8) or after (group 2, N = 8). Heart rate variability (HRV), serum norepinephrine (NE), atrial electrophysiological indices were analyzed. Six times of burst pacing (20 Hz, 2 × threshold, lasting for 5 seconds, were performed to induce AF, the number of episodes and the duration of AF were compared. Results LOM LSPV ablation decreased sympathetic indices of HRV and serum NE. Atrial effective refractory period (ERP) was shortened during RAP in both groups with higher reduction degrees in group 1. In group 1, the shortening of atrial ERP, elevating of ERP dispersion and sum of window of vulnerability (ΣWOV), facilitating of AF induced by RAP were subsequently reversed by LOM LSPV ablation. In group 2, LOM LSPV ablation prolonged atrial ERP, decreased ΣWOV, eliminated AF induction. The subsequent RAP failed to alter these indices. Histological studies showed abundant sympathetic nerve fibers in LOM LSPV . Conclusion LOM LSPV ablation could inhibit atrial electrical remodeling during short‐term RAP by reducing the cardiac sympathetic activity. LOM LSPV may be a potential target in AF ablation, especially in patients with highly cardiac sympathetic activation or atrial electrical remodeling.

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