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Skeletal muscle mitochondrial correlates of critical power and W' in healthy active individuals

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posted on 2025-03-12, 09:03 authored by Donald Peden, Robert RogersRobert Rogers, Emma Mitchell, Suzanne M. Taylor, Stephen BaileyStephen Bailey, Richard FergusonRichard Ferguson

The asymptote (critical power; CP) and curvature constant (W') of the hyperbolic power–duration relationship can predict performance within the severe-intensity exercise domain. However, the extent to which these parameters relate to skeletal muscle mitochondrial content and respiratory function is not known. Fifteen males (peak O2 uptake, 52.2 ± 8.7 mL kg−1 min−1; peak work rate, 366 ± 40 W; and gas exchange threshold, 162 ± 41 W) performed three to five constant-load tests to task failure for the determination of CP (246 ± 44 W) and W' (18.6 ± 4.1 kJ). Skeletal muscle biopsies were obtained from the vastus lateralis to determine citrate synthase (CS) activity, as a marker of mitochondrial content, and the ADP-stimulated respiration (P) and maximal electron transfer (E) through mitochondrial complexes (C) I–IV. The CP was positively correlated with CS activity (absolute CP, r = 0.881, P < 0.001; relative CP, r = 0.751, P = 0.001). The W' was not correlated with CS activity (P > 0.05). Relative CP was positively correlated with mass-corrected CI + IIE (r = 0.659, P = 0.038), with absolute CP being inversely correlated with CS activity-corrected CIVE (r = −0.701, P = 0.024). Relative W' was positively correlated with CS activity-corrected CI + IIP (r = 0.713, P = 0.021) and the phosphorylation control ratio (r = 0.661, P = 0.038). There were no further correlations between CP or W' and mitochondrial respiratory variables. These findings support the assertion that skeletal muscle mitochondrial oxidative capacity is positively associated with CP and that this relationship is strongly determined by mitochondrial content.

Funding

NIHR | NIHR Leicester Biomedical Research Centre (Leicester BRC)

History

School

  • Sport, Exercise and Health Sciences

Published in

Experimental Physiology

Publisher

John Wiley & Sons Ltd on behalf of The Physiological Society

Version

  • VoR (Version of Record)

Rights holder

© The Authors

Publisher statement

This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

Acceptance date

2024-03-25

Publication date

2024-04-09

Copyright date

2024

ISSN

0958-0670

eISSN

1469-445X

Language

  • en

Depositor

Dr Stephen Bailey. Deposit date: 27 June 2024