Aging Impairs Reverse Remodeling and Recovery of Ventricular Function after Isoproterenol-Induced Cardiomyopathy

Information about heart failure with reduced ejection fraction (HFrEF) in women and the potential effects of aging in the female heart is scarce. We investigated the vulnerability to develop HFrEF in female elderly mice compared to young animals, as well as potential differences in reverse remodelin...

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Detalles Bibliográficos
Autores: Yáñez-Bisbe, Laia|||0000-0001-9084-7296, Garcia-Elias, Anna|||0000-0002-6609-6119, Tajes, Marta, Almendros, Isaac|||0000-0002-1998-9379, Rodríguez Sinovas, Antonio|||0000-0003-2930-8773, Inserte, Javier|||0000-0003-2283-3591, Ruiz Meana, Marisol|||0000-0002-4067-4638, Farré, Ramon|||0000-0002-9084-7824, Farré, Núria|||0000-0003-3110-6572, Benito Villabriga, Begoña|||0000-0002-8668-1251
Tipo de recurso: artículo
Fecha de publicación:2021
País:España
Institución:Universitat Autònoma de Barcelona
Repositorio:Dipòsit Digital de Documents de la UAB
Idioma:inglés
OAI Identifier:oai:ddd.uab.cat:252170
Acceso en línea:https://ddd.uab.cat/record/252170
https://dx.doi.org/urn:doi:10.3390/ijms23010174
Access Level:acceso abierto
Palabra clave:Heart failure
HFrEF
Ageing
Cardiac remodeling
Ventricular dysfunction
Reverse remodeling
Female animals
Descripción
Sumario:Information about heart failure with reduced ejection fraction (HFrEF) in women and the potential effects of aging in the female heart is scarce. We investigated the vulnerability to develop HFrEF in female elderly mice compared to young animals, as well as potential differences in reverse remodeling. First, HF was induced by isoproterenol infusion (30 mg/kg/day, 28 days) in young (10-week-old) and elderly (22-month-old) female mice. In a second set of animals, mice underwent isoproterenol infusion followed by no treatment during 28 additional days. Cardiac remodeling was assessed by echocardiography, histology and gene expression of collagen-I and collagen-III. Following isoproterenol infusion, elderly mice developed similar HFrEF features compared to young animals, except for greater cell hypertrophy and tissue fibrosis. After beta-adrenergic withdrawal, young female mice experienced complete reversal of the HFrEF phenotype. Conversely, reversed remodeling was impaired in elderly animals, with no significant recovery of LV ejection fraction, cardiomyocyte hypertrophy and collagen deposition. In conclusion, chronic isoproterenol infusion is a valid HF model for elderly and young female mice and induces a similar HF phenotype in both. Elderly animals, unlike young, show impaired reverse remodeling, with persistent tissue fibrosis and cardiac dysfunction even after beta-adrenergic withdrawal.