Autor según el artículo: Odria, R; Cardús, A; Gomis-Coloma, C; Balanyà-Segura, M; Mercado-Amarilla, A; Maestre-Mora, P; Poveda-Sabuco, A; Domingo, JC; Nogales-Gadea, G; Gomez-Sanchez, JA; Hurtado, E; Suelves, M
Departamento: Ciències Mèdiques Bàsiques
e-ISSN: 2509-2723
Autor/es de la URV: Balanya Segura, Marta / Hurtado Caballero, Erica
Palabras clave: Strength; Skeletal-muscle; Skeletal muscle regeneration; Sarcopenia; Omega-6/omega-3 fatty acid ratio; Omega-6/omega-3 fatty acid rati; Muscle atrophy; Mas; Histone deacetylase 11; Hdac11; Fish-oil supplementation; Fatty acid oxidation; Breakdown; Acid
Resumen: Sarcopenia, defined as the progressive loss of skeletal muscle mass and function associated with ageing, has devastating effects in terms of reducing the quality of life of older people. Muscle ageing is characterised by muscle atrophy and decreased capacity for muscle repair, including a reduction in the muscle stem cell pool that impedes recovery after injury. Histone deacetylase 11 (HDAC11) is the newest member of the HDAC family and it is highly expressed in skeletal muscle. Our group recently showed that genetic deficiency in HDAC11 increases skeletal muscle regeneration, mitochondrial function and globally improves muscle performance in young mice. Here, we explore for the first time the functional consequences of HDAC11 deficiency in old mice, in homeostasis and during muscle regeneration. Aged mice lacking HDAC11 show attenuated muscle atrophy and postsynaptic fragmentation of the neuromuscular junction, but no significant differences in the number or diameter of myelinated axons of peripheral nerves. Maintenance of the muscle stem cell reservoir and advanced skeletal muscle regeneration after injury are also observed. HDAC11 depletion enhances mitochondrial fatty acid oxidation and attenuates age-associated alterations in skeletal muscle fatty acid composition, reducing drastically the omega-6/omega-3 fatty acid ratio and improving significantly the omega-3 index, providing an explanation for improved muscle strength and fatigue resistance and decreased mortality. Taken together, our results point to HDAC11 as a new target for the treatment of sarcopenia. Importantly, selective HDAC11 inhibitors have recently been developed that could offer a new therapeutic approach to slow the ageing process.
Grupo de investigación: Unitat d'Histologia i Neurobiologia
Áreas temáticas: Veterinary (miscellaneous); Geriatrics and gerontology; Geriatrics & gerontology; Complementary and alternative medicine; Cardiology and cardiovascular medicine; Aging
Acceso a la licencia de uso: https://creativecommons.org/licenses/by/3.0/es/
ISSN: 2509-2715
Direcció de correo del autor: erica.hurtado@urv.cat; marta.balanya@urv.cat
Fecha de alta del registro: 2026-03-02
Versión del articulo depositado: info:eu-repo/semantics/publishedVersion
URL Documento de licencia: https://repositori.urv.cat/ca/proteccio-de-dades/
Referencia al articulo segun fuente origial: Geroscience. 47 (4): 5843-5868
Referencia de l'ítem segons les normes APA: Odria, R; Cardús, A; Gomis-Coloma, C; Balanyà-Segura, M; Mercado-Amarilla, A; Maestre-Mora, P; Poveda-Sabuco, A; Domingo, JC; Nogales-Gadea, G; Gomez- (2025). HDAC11 deficiency regulates age-related muscle decline and sarcopenia. Geroscience, 47(4), 5843-5868. DOI: 10.1007/s11357-025-01611-y
DOI del artículo: 10.1007/s11357-025-01611-y
Entidad: Universitat Rovira i Virgili
Año de publicación de la revista: 2025-04-12
DOI del conjunto de datos relacionado: 10.1007/s11357-025-01611-y
Tipo de publicación: Journal Publications