Markers of Mitochondrial Function and DNA Repair Associated with Physical Function in Centenarians

Mitochondrial dysfunction and genomic instability are key hallmarks of aging. The aim of this study was to evaluate whether maintenance of physical capacities at very old age is associated with key hallmarks of aging. To investigate this, we measured mitochondrial bioenergetics, mitochondrial DNA (m...

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Detalles Bibliográficos
Autores: Sánchez-Román Rojas, Inés, Ferrando, Beatriz, Myrup Holst, Camilla, Mengel-From, Jonas, Hoei Rasmussen, Signe, Thinggaard, Mikael, Bohr, Vilhelm A., Christensen, Kaare, Stevnsner, Tinna
Tipo de recurso: artículo
Fecha de publicación:2024
País:España
Institución:Universidad Complutense de Madrid (UCM)
Repositorio:Docta Complutense
Idioma:inglés
OAI Identifier:oai:docta.ucm.es:20.500.14352/115374
Acceso en línea:https://hdl.handle.net/20.500.14352/115374
Access Level:acceso abierto
Palabra clave:612.82
577.24
159.95
612.67
796:612
Centenarians
Mitochondria
DNA repair
Grip strength
Physical function
Fisiología
Neurociencias (Biológicas)
Ancianos
2411 Fisiología Humana
2411.11 Neurofisiología
2410.07 Genética Humana
6104.01 Procesos Cognitivos
2411.06 Fisiología del Ejercicio
Descripción
Sumario:Mitochondrial dysfunction and genomic instability are key hallmarks of aging. The aim of this study was to evaluate whether maintenance of physical capacities at very old age is associated with key hallmarks of aging. To investigate this, we measured mitochondrial bioenergetics, mitochondrial DNA (mtDNA) copy number and DNA repair capacity in peripheral blood mononuclear cells from centenarians. In addition, circulating levels of NAD+/NADH, brain-derived neurotrophic factor (BDNF) and carbonylated proteins were measured in plasma and these parameters were correlated to physical capacities. Centenarians without physical disabilities had lower mitochondrial respiration values including ATP production, reserve capacity, maximal respiration and non-mitochondrial oxygen-consumption rate and had higher mtDNA copy number than centenarians with moderate and severe disabilities (p < 0.05). In centenarian females, grip strength had a positive association with mtDNA copy number (p < 0.05), and a borderline positive trend for activity of the central DNA repair enzyme, APE 1 (p = 0.075), while a negative trend was found with circulating protein carbonylation (p = 0.07) in the entire cohort. Lastly, a trend was observed for a negative association between BDNF and activity of daily living disability score (p = 0.06). Our results suggest that mechanisms involved in maintaining mitochondrial function and genomic stability may be associated with maintenance of physical function in centenarians.