Resistance to atrial fibrillation domestication and mitochondrial dysfunction in sheep: a potential key role of the TCA cycle and mitochondrial redox state
Year: 2026
Type: article
Abstract: Background Atrial fibrillation (AF) often progresses from paroxysmal to more stable forms. It is well-recognized that patients vary in their AF progression, but the underlying mechanisms remain unclear. This work, performed in a sheep AF-model, aimed to identify atrial redox and energetic status differences between animals developing stable AF (AF-S) versus those resistant to AF-stabilization (AF-R). Methods AF was induced with bursts of atrial tachystimulation, maintained whenever sinus rhythm resumed, and monitored with telemetry. Electrophysiological and structural remodeling were assessed via contact mapping, and histology, respectively. Proteomic, metabolomic, enzymatic, and bioenergetic remodeling were evaluated using left atrial appendage (LAA) tissues and isolated LAA mitochondria. Healthy rats were used to investigate whether a metabolic challenge stabilizes electrically induced AF episodes. Results AF-S (N = 12) sheep developed stable AF after 13 days on average, whereas AF-R (N = 8) sheep failed to develop self-sustained AF despite 120 days of tachypacing. Contact mapping and histological analysis revealed that AF-S animals presented reduced atrial conduction velocity, and increased endomysial fibrosis. Metabolic analysis showed significant differences in tricarboxylic acid cycle (TCA) enzymes activities and a 45% succinate content increase in AF-S LAA versus AF-R. AF-S mitochondria showed abnormal succinate oxidation, decreased ATP synthesis rate, and increased ROS emission. The ratios of ATP/ADP, NAD + /NADH, and Complex I/II activities were disturbed in AF-S compared to AF-R. Calculated mitochondrial NAD + /NADH ratios suggest an oxidized state in AF-S while AF-R showed a reduced state. Exogenous succinate was metabolized when incubated with rat atrial cardiomyocytes, while intravenous succinate injection stabilized atrial arrhythmias electrically-induced in vivo . Conclusions AF-S sheep showed TCA cycle, energetic and redox adaptations compared to AF-R. In this animal model, TCA cycle remodeling and associated redox and energetic responses determined the resistance to AF domestication, with potential relevance to identify new mechanistic determinants of AF progression in humans.
Source: Redox Biology
Authors: Guido Caluori, Stanley Nattel, Benoît Pinson, Patrice Naud, Bertrand Beauvoit, Stéphane Claverol, Fanny Vaillant, Sabine Charron, Florent Guilloteau, Virginie Loyer, Marion Constantin, Miruna Popa, Andrei Belykh, Anaïs Rogowsky, Andreas Haeberlin, Sylvain Ploux, Hassan Adam Mahamat, Rémi Dubois, Bastien Guillot, Philipp Krisai, Tsukasa Kamakura, Olivier Bernus, Pierre Jaïs, Pierre Dos Santos, Philippe Pasdois
Institutions: Inserm, Centre de Recherche Cardio-Thoracique de Bordeaux, Montreal Heart Institute, West German Heart and Vascular Center Essen, McGill University, University of Duisburg-Essen, Université de Montréal, Centre National de la Recherche Scientifique, Université de Bordeaux, Institut de Biochimie et Génétique Cellulaires, TBM-Core, Institut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement, Biologie du Fruit et Pathologie, Hôpital Maisonneuve-Rosemont, Centre Hospitalier Universitaire de Bordeaux
Language: English
Subfield: Cardiology and Cardiovascular Medicine
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $4,310
Funders: Abbott Laboratories, Heart and Stroke Foundation of Canada, Fondation Lefoulon Delalande, Deutsche Forschungsgemeinschaft, Agence Nationale de la Recherche, Institut National de la Santé et de la Recherche Médicale, Fédération Française de Cardiologie, Centre National de la Recherche Scientifique, Conseil Régional Aquitaine, Canadian Institutes of Health Research, Biosense Webster
Awards: G133457142, G1686619404, G3273634535, Understanding the remodeling processes during atrial fibrillation stabilization for improved therapeutics, G3825831990, G594818701, G6803667113, G7240651115, Die Rolle der Inflammation in der Pathogenese von Vorhofflimmern: Bedeutung für die Pathophysiologie des atrialen Remodelings und für Frührezidive atrialer Arrhythmien nach Radiofrequenzablation und Pulsed Field Ablation
OpenAlex ID: W7212192091
