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Название: The inter-chamber differences in the contractile function between left and right atrial cardiomyocytes in atrial fibrillation in rats
Авторы: Butova, X.
Myachina, T.
Simonova, R.
Kochurova, A.
Mukhlynina, E.
Kopylova, G.
Shchepkin, D.
Khokhlova, A.
Дата публикации: 2023
Издатель: Frontiers Media SA
Библиографическое описание: Butova, X, Myachina, T, Simonova, R, Kochurova, A, Mukhlynina, E, Kopylova, G, Shchepkin, D & Khokhlova, A 2023, 'The inter-chamber differences in the contractile function between left and right atrial cardiomyocytes in atrial fibrillation in rats', Frontiers in Cardiovascular Medicine, Том. 10, 1203093. https://doi.org/10.3389/fcvm.2023.1203093
Butova, X., Myachina, T., Simonova, R., Kochurova, A., Mukhlynina, E., Kopylova, G., Shchepkin, D., & Khokhlova, A. (2023). The inter-chamber differences in the contractile function between left and right atrial cardiomyocytes in atrial fibrillation in rats. Frontiers in Cardiovascular Medicine, 10, [1203093]. https://doi.org/10.3389/fcvm.2023.1203093
Аннотация: Introduction: The left and right atria (LA, RA) work under different mechanical and metabolic environments that may cause an intrinsic inter-chamber diversity in structure and functional properties between atrial cardiomyocytes (CM) in norm and provoke their different responsiveness to pathological conditions. In this study, we assessed a LA vs. RA difference in CM contractility in paroxysmal atrial fibrillation (AF) and underlying mechanisms. Methods: We investigated the contractile function of single isolated CM from LA and RA using a 7-day acetylcholine (ACh)-CaCl2 AF model in rats. We compared auxotonic force, sarcomere length dynamics, cytosolic calcium ([Ca2+]i) transients, intracellular ROS and NO production in LA and RA CM, and analyzed the phosphorylation levels of contractile proteins and actin-myosin interaction using an in vitro motility assay. Results: AF resulted in more prominent structural and functional changes in LA myocardium, reducing sarcomere shortening amplitude, and velocity of sarcomere relengthening in mechanically non-loaded LA CM, which was associated with the increased ROS production, decreased NO production, reduced myofibrillar content, and decreased phosphorylation of cardiac myosin binding protein C and troponin I. However, in mechanically loaded CM, AF depressed the auxotonic force amplitude and kinetics in RA CM, while force characteristics were preserved in LA CM. Discussion: Thus, inter-atrial differences are increased in paroxysmal AF and affected by the mechanical load that may contribute to the maintenance and progression of AF. 2023 Butova, Myachina, Simonova, Kochurova, Mukhlynina, Kopylova, Shchepkin and Khokhlova.
Ключевые слова: ([CA2+]I) TRANSIENTS
ACTIN-MYOSIN INTERACTION
ATRIAL FIBRILLATION
AUXOTONIC FORCE
LEFT AND RIGHT ATRIA
PROTEIN PHOSPHORYLATION
SARCOMERE SHORTENING
SINGLE CARDIOMYOCYTES
ACETYLCHOLINE
ACTIN
CALCIUM ION
CARBON FIBER
CARDIAC MYOSIN
CONTRACTILE PROTEIN
GLYCOGEN
MYOSIN BINDING PROTEIN C
NITRIC OXIDE
REACTIVE OXYGEN METABOLITE
TROPONIN I
TROPONIN T
ACTIN MYOSIN INTERACTION
ANIMAL EXPERIMENT
ANIMAL MODEL
ANIMAL TISSUE
ARTICLE
ATRIAL FIBRILLATION
CELL VIABILITY
CONFOCAL LASER SCANNING MICROSCOPY
CONTROLLED STUDY
DEPRESSION
ELECTROCARDIOGRAPHY
ELECTROPHYSIOLOGY
GENE EXPRESSION
HEART ATRIUM CONTRACTILITY
HEART DEVELOPMENT
HEART MUSCLE CONTRACTILITY
HISTOLOGY
MORPHOLOGY
NONHUMAN
OXIDATIVE PHOSPHORYLATION
PAROXYSMAL ATRIAL FIBRILLATION
PROTEIN PHOSPHORYLATION
RAT
SARCOMERE
SARCOMERE LENGTH
SARCOPLASMIC RETICULUM
SINUS RHYTHM
TACHYCARDIA
URI: http://elar.urfu.ru/handle/10995/130723
Условия доступа: info:eu-repo/semantics/openAccess
cc-by
Текст лицензии: https://creativecommons.org/licenses/by/4.0/
Идентификатор SCOPUS: 85168382468
Идентификатор WOS: 001051362400001
Идентификатор PURE: 43602414
ISSN: 2297-055X
DOI: 10.3389/fcvm.2023.1203093
Сведения о поддержке: Russian Science Foundation, RSF: 22-75-10134
This research was supported by the Russian Science Foundation #22-75-10134. The work was performed using the equipment of the Shared Research Center of Scientific Equipment of Institute of Immunology and Physiology. The funders had no role in study design, data collection and analysis, decision to publish or preparation of the manuscript.
This research was supported by the Russian Science Foundation #22-75-10134. The work was performed using the equipment of the Shared Research Center of Scientific Equipment of Institute of Immunology and Physiology. The funders had no role in study design, data collection and analysis, decision to publish or preparation of the manuscript.
Карточка проекта РНФ: 22-75-10134
Располагается в коллекциях:Научные публикации ученых УрФУ, проиндексированные в SCOPUS и WoS CC

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