Aim To parse out the impact of advanced ageing and disuse on skeletal muscle function, we utilized both in vivo and in vitro techniques to comprehensively assess upper- and lower-limb muscle contractile properties in 8 young (YG; 25±6yrs) and 8 oldest-old mobile (OM; 87±5yrs) and 8 immobile (OI; 88±4yrs) women. Methods In vivo, maximal voluntary contraction (MVC), electrically evoked resting twitch force (RT), and physiological cross sectional area (PCSA) of the quadriceps and elbow flexors was assessed. Muscle biopsies of the vastus lateralis and biceps brachii facilitated the in vitro assessment of single fibre specific tension (Po). Results In vivo, compared to the young, both the OM and OI exhibited a more pronounced loss of MVC in the lower-limb (OM (-60%) and OI (-75%)) than the upper-limb (OM=-51%; OI=-47%). Taking into account the reduction in muscle PCSA (OM=-10%; OI=-18%), only evident in the lower-limb, by calculating voluntary muscle specific force, the lower-limb of the OI (-40%) was more compromised than the OM (-13%). However, in vivo, RT in both upper- and lower-limbs (~9.8 N∙m∙cm−2) and Po (~123 mN∙mm−2), assessed in vitro, implies preserved intrinsic contractile function in all muscles of the oldest-old and were well correlated (r=0.81). Conclusion These findings suggest that in the oldest-old neither advanced ageing nor disuse, per se, impact intrinsic skeletal muscle function, as assessed in vitro. However, in vivo, muscle function is attenuated by age and exacerbated by disuse, implicating factors other than skeletal muscle, such as neuromuscular control, in this diminution of function.

In vivo and in vitro evidence that in oldest-old humans intrinsic upper- and lower-limb skeletal muscle function is unaffected by ageing and disuse in oldest-old humans / M. Venturelli, P. Saggin, E. Muti, F. Naro, L. Cancellara, L. Toniolo, C. Tarperi, E. Calabria, R.S. Richardson, C. Reggiani, F. Schena. - In: ACTA PHYSIOLOGICA. - ISSN 1748-1708. - 215:1(2015 Sep), pp. 58-71. [10.1111/apha.12524]

In vivo and in vitro evidence that in oldest-old humans intrinsic upper- and lower-limb skeletal muscle function is unaffected by ageing and disuse in oldest-old humans

M. Venturelli
Primo
;
2015

Abstract

Aim To parse out the impact of advanced ageing and disuse on skeletal muscle function, we utilized both in vivo and in vitro techniques to comprehensively assess upper- and lower-limb muscle contractile properties in 8 young (YG; 25±6yrs) and 8 oldest-old mobile (OM; 87±5yrs) and 8 immobile (OI; 88±4yrs) women. Methods In vivo, maximal voluntary contraction (MVC), electrically evoked resting twitch force (RT), and physiological cross sectional area (PCSA) of the quadriceps and elbow flexors was assessed. Muscle biopsies of the vastus lateralis and biceps brachii facilitated the in vitro assessment of single fibre specific tension (Po). Results In vivo, compared to the young, both the OM and OI exhibited a more pronounced loss of MVC in the lower-limb (OM (-60%) and OI (-75%)) than the upper-limb (OM=-51%; OI=-47%). Taking into account the reduction in muscle PCSA (OM=-10%; OI=-18%), only evident in the lower-limb, by calculating voluntary muscle specific force, the lower-limb of the OI (-40%) was more compromised than the OM (-13%). However, in vivo, RT in both upper- and lower-limbs (~9.8 N∙m∙cm−2) and Po (~123 mN∙mm−2), assessed in vitro, implies preserved intrinsic contractile function in all muscles of the oldest-old and were well correlated (r=0.81). Conclusion These findings suggest that in the oldest-old neither advanced ageing nor disuse, per se, impact intrinsic skeletal muscle function, as assessed in vitro. However, in vivo, muscle function is attenuated by age and exacerbated by disuse, implicating factors other than skeletal muscle, such as neuromuscular control, in this diminution of function.
oldest-old; sarcopenia; in vivo; in vitro
Settore M-EDF/02 - Metodi e Didattiche delle Attivita' Sportive
set-2015
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/276208
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