van Hunnik Arne, Sobota Vladimír, Zeemering Stef, Opacic Dragan, Scaf Billy, D'Alessandro Elisa, Oyaert Karel, Kuiper Marion, Diness Jonas G, Sørensen Ulrik S, Milnes James T, van der Heyden Marcel A G, Jespersen Thomas, Schotten Ulrich, Verheule Sander
Department of Physiology, Cardiovascular Research Institute Maastricht, Maastricht, Netherlands.
IHU-LIRYC, Electrophysiology and Heart Modeling Institute, Fondation Bordeaux Université, Bordeaux, France.
Front Physiol. 2024 Jul 18;15:1399037. doi: 10.3389/fphys.2024.1399037. eCollection 2024.
The mechanisms leading to the conversion of atrial fibrillation (AF) to sinus rhythm are poorly understood. This study describes the dynamic behavior of electrophysiological parameters and conduction patterns leading to spontaneous and pharmacological AF termination.
Five independent groups of goats were investigated: (1) spontaneous termination of AF, and drug-induced terminations of AF by various potassium channel inhibitors: (2) AP14145, (3) PA-6, (4) XAF-1407, and (5) vernakalant. Bi-atrial contact mapping was performed during an open chest surgery and intervals with continuous and discrete atrial activity were determined. AF cycle length (AFCL), conduction velocity and path length were calculated for each interval, and the final conduction pattern preceding AF termination was evaluated.
AF termination was preceded by a sudden episode of discrete activity both in the presence and absence of an antiarrhythmic drug. This episode was accompanied by substantial increases in AFCL and conduction velocity, resulting in prolongation of path length. In 77% ± 4% of all terminations the conduction pattern preceding AF termination involved medial to lateral conduction along Bachmann's bundle into both atria, followed by anterior to posterior conduction. This finding suggests conduction block in the interatrial septum and/or pulmonary vein area as final step of AF termination.
AF termination is preceded by an increased organization of fibrillatory conduction. The termination itself is a sudden process with a critical role for the interplay between spatiotemporal organization and anatomical structure.
导致心房颤动(AF)转复为窦性心律的机制尚不清楚。本研究描述了导致AF自发终止和药物终止的电生理参数及传导模式的动态行为。
对五组独立的山羊进行研究:(1)AF的自发终止,以及各种钾通道抑制剂导致的AF药物性终止:(2)AP14145,(3)PA - 6,(4)XAF - 1407,和(5)维纳卡兰。在开胸手术期间进行双心房接触标测,并确定连续和离散心房活动的间期。计算每个间期的AF周期长度(AFCL)、传导速度和路径长度,并评估AF终止前的最终传导模式。
无论是否存在抗心律失常药物,AF终止之前均会突然出现离散活动。这一过程伴随着AFCL和传导速度的显著增加,导致路径长度延长。在所有终止情况的77%±4%中,AF终止前的传导模式涉及沿巴赫曼束从内侧到外侧传导至双心房,随后从前向后传导。这一发现提示房间隔和/或肺静脉区域的传导阻滞是AF终止的最后一步。
AF终止之前颤动传导的组织化增强。终止本身是一个突然的过程,时空组织与解剖结构之间的相互作用起关键作用。