4.6 Article

Atrophy Resistant vs. Atrophy Susceptible Skeletal Muscles: aRaS as a Novel Experimental Paradigm to Study the Mechanisms of Human Disuse Atrophy

Journal

FRONTIERS IN PHYSIOLOGY
Volume 12, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fphys.2021.653060

Keywords

skeletal muscle atrophy; aRaS; disuse atrophy; tibialis anterior muscle; medial gastrocnemius muscle

Categories

Funding

  1. BBSRC [BB/R010358/1]
  2. Medical Research Council, United Kingdom as part of the MRCVersus Arthritis Centre for Musculoskeletal Ageing Research [MR/P021220/1]
  3. National Institute for Health Research, United Kingdom, Nottingham Biomedical Research Centre
  4. BBSRC [BB/R010358/1] Funding Source: UKRI

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This study aimed to develop an experimental paradigm to investigate muscles with different susceptibility to atrophy, with the hope of uncovering central mechanisms. Results showed that after immobilization, there were differences in muscle volume and thickness between the tibialis anterior (TA) and medial gastrocnemius (MG) muscles, providing valuable insights into mechanisms of disuse atrophy.
Objective Disuse atrophy (DA) describes inactivity-induced skeletal muscle loss, through incompletely defined mechanisms. An intriguing observation is that individual muscles exhibit differing degrees of atrophy, despite exhibiting similar anatomical function/locations. We aimed to develop an innovative experimental paradigm to investigate Atrophy Resistant tibialis anterior (TA) and Atrophy Susceptible medial gastrocnemius (MG) muscles (aRaS) with a future view of uncovering central mechanisms. Method Seven healthy young men (22 +/- 1 year) underwent 15 days unilateral leg immobilisation (ULI). Participants had a single leg immobilised using a knee brace and air-boot to fix the leg (75 degrees knee flexion) and ankle in place. Dual-energy X-ray absorptiometry (DXA), MRI and ultrasound scans of the lower leg were taken before and after the immobilisation period to determine changes in muscle mass. Techniques were developed for conchotome and microneedle TA/MG muscle biopsies following immobilisation (both limbs), and preliminary fibre typing analyses was conducted. Results TA/MG muscles displayed comparable fibre type distribution of predominantly type I fibres (TA 67 +/- 7%, MG 63 +/- 5%). Following 15 days immobilisation, MG muscle volume (-2.8 +/- 1.4%, p < 0.05) and muscle thickness decreased (-12.9 +/- 1.6%, p < 0.01), with a positive correlation between changes in muscle volume and thickness (R-2 = 0.31, p = 0.038). Importantly, both TA muscle volume and thickness remained unchanged. Conclusion The use of this unique aRaS paradigm provides an effective and convenient means by which to study the mechanistic basis of divergent DA susceptibility in humans, which may facilitate new mechanistic insights, and by extension, mitigation of skeletal muscle atrophy during human DA.

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