Ageing leads to selective type II myofibre deterioration and denervation independent of reinnervative capacity in human skeletal muscle DOI Creative Commons
Oscar Horwath, Marcus Moberg, Sebastian Edman

et al.

Experimental Physiology, Journal Year: 2024, Volume and Issue: 110(2), P. 277 - 292

Published: Oct. 28, 2024

Age-related loss of muscle mass and function is underpinned by changes at the myocellular level. However, our understanding aged phenotype might be confounded factors secondary to ageing per se, such as inactivity adiposity. Here, using healthy, lean, recreationally active, older men, we investigated impact on properties in skeletal muscle. Muscle biopsies were obtained from young men (22 ± 3 years, n = 10) (69 11) matched for health status, activity level body index. Immunofluorescence was used assess myofibre composition, morphology (size shape), capillarization, content satellite cells myonuclei, spatial relationship between capillaries, denervation grouping. Compared with muscle, contained 53% more type I myofibres, addition smaller (-32%) misshapen (3%) II myofibres (P < 0.05). Aged manifested fewer capillaries (-29%) (-38%) surrounding 0.05); however, these two remained intact. The proportion denervated ∼2.6-fold higher old than had grouped (∼18-fold), primarily driven increased size existing groups rather group frequency displayed selective deterioration alongside These data are key cellular basis age-related decline reveal a pressing need fine-tune strategies preserve innervation status populations.

Language: Английский

Muscle fibre size and myonuclear positioning in trained and aged humans DOI Creative Commons
Edmund Battey, Yotam Levy, Ross D. Pollock

et al.

Experimental Physiology, Journal Year: 2024, Volume and Issue: 109(4), P. 549 - 561

Published: March 10, 2024

Abstract Changes in myonuclear architecture and positioning are associated with exercise adaptations ageing. However, data on the number of myonuclei following inconsistent. Additionally, whether domains (MNDs; i.e., theoretical volume cytoplasm within which a myonucleus is responsible for transcribing DNA) altered age remains unclear. The aim this investigation was to investigate relationships between activity status positioning. Vastus lateralis muscle biopsies from younger endurance‐trained (YT) older (OT) individuals were compared age‐matched untrained counterparts (YU OU; OU samples acquired during surgical operation). Serial, optical z ‐slices throughout isolated fibres analysed give three‐dimensional coordinates fibre dimensions. mean cross‐sectional area (CSA) 33%–53% smaller other groups. nuclei relative CSA 90% greater YU fibres. scaling MND size individuals. arrangement, contrast, similar across Fibre most parameters significantly individuals, but not trained These indicate that regular endurance lifespan might better preserve maintain relationship volumes. Inactivity, however, result reduced parameters.

Language: Английский

Citations

2

Ageing leads to selective type II myofibre deterioration and denervation independent of reinnervative capacity in human skeletal muscle DOI Creative Commons
Oscar Horwath, Marcus Moberg, Sebastian Edman

et al.

Experimental Physiology, Journal Year: 2024, Volume and Issue: 110(2), P. 277 - 292

Published: Oct. 28, 2024

Age-related loss of muscle mass and function is underpinned by changes at the myocellular level. However, our understanding aged phenotype might be confounded factors secondary to ageing per se, such as inactivity adiposity. Here, using healthy, lean, recreationally active, older men, we investigated impact on properties in skeletal muscle. Muscle biopsies were obtained from young men (22 ± 3 years, n = 10) (69 11) matched for health status, activity level body index. Immunofluorescence was used assess myofibre composition, morphology (size shape), capillarization, content satellite cells myonuclei, spatial relationship between capillaries, denervation grouping. Compared with muscle, contained 53% more type I myofibres, addition smaller (-32%) misshapen (3%) II myofibres (P < 0.05). Aged manifested fewer capillaries (-29%) (-38%) surrounding 0.05); however, these two remained intact. The proportion denervated ∼2.6-fold higher old than had grouped (∼18-fold), primarily driven increased size existing groups rather group frequency displayed selective deterioration alongside These data are key cellular basis age-related decline reveal a pressing need fine-tune strategies preserve innervation status populations.

Language: Английский

Citations

1