4.0 Article

No effect of five days of bed rest or short-term resistance exercise prehabilitation on markers of skeletal muscle mitochondrial content and dynamics in older adults

Journal

PHYSIOLOGICAL REPORTS
Volume 10, Issue 13, Pages -

Publisher

WILEY
DOI: 10.14814/phy2.15345

Keywords

ageing; bed rest; disuse; mitochondria; skeletal muscle

Categories

Funding

  1. Biotechnology and Biological Sciences Research Council [BB/N018214/1]
  2. NIHR Clinical Research Facility in University Hospitals Birmingham NHS Foundation Trust, Birmingham
  3. MRC-Versus Arthritis, Centre for Musculoskeletal Ageing Research

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In healthy older adults, a 5-day period of bed rest did not result in significant perturbation in muscle mitochondrial protein signaling, and short-term resistance exercise prehabilitation did not affect this situation. Therefore, muscle atrophy induced by disuse may precede alterations in mitochondrial content.
Bed rest (BR) results in significant impairments in skeletal muscle metabolism. Mitochondrial metabolism is reportedly highly sensitive to disuse, with dysregulated fission-fusion events and impaired oxidative function previously reported. The effects of clinically relevant short-term BR ('' 5 days) on mitochondrial protein expression are presently unclear, as are the effects of exercise prehabilitation as a potential counteractive intervention. The present study examined the effects of a 5-day period of BR and short-term resistance exercise prehabilitation (ST-REP) on mitochondrial-protein content. Ten older men (71 +/- 4 years) underwent 5 days of BR, completing four sessions of high-volume unilateral resistance exercise prehabilitation over 7 days beforehand. Muscle biopsies were obtained from the vastus lateralis in the non-exercised control and exercised legs, both pre-and post-prehabilitation and pre- and post-BR, to determine changes in citrate synthase enzyme activity and the expression of key proteins in the mitochondrial electron transport chain and molecular regulators of fission-fusion dynamics, biosynthesis, and mitophagy. We observed no significant effect of either BR or ST-REP on citrate synthase protein content, enzyme activity, or ETC complex I-V protein content. Moreover, we observed no significant changes in markers of mitochondrial fission and fusion (p-DRP1(S616), p-DRP1(S637), p-DRP1(S616/S637) ratio, p-MFFS146, Mitofillin, OPA1, or MFN2 (p > 0.05 for all). Finally, we observed no differences in markers of biosynthesis (p-AMPK(T172), p-ACC(S)(79), PGC1a, TPAM) or mitophagy-related signaling (ULK-1, BNIP3/NIX, LC3B I/II) (p > 0.05 for all). In contrast to previous longer-term periods of musculoskeletal disuse (i.e., 7-14 days), a clinically relevant, 5-day period of BR resulted in no significant perturbation in muscle mitochondria' protein signaling in healthy older adults, with no effect of ST-REP in the week prior to BR. Accordingly, disuse-induced muscle atrophy may precede alterations in mitochondria' content.

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