Physiological Reports (Aug 2021)

Individual physiological and mitochondrial responses during 12 weeks of intensified exercise

  • Macsue Jacques,
  • Shanie Landen,
  • Javier Alvarez Romero,
  • Xu Yan,
  • Andrew Garnham,
  • Danielle Hiam,
  • Mélina Siegwald,
  • Emma Mercier,
  • Anne Hecksteden,
  • Nir Eynon,
  • Sarah Voisin

DOI
https://doi.org/10.14814/phy2.14962
Journal volume & issue
Vol. 9, no. 15
pp. n/a – n/a

Abstract

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Abstract Aim Observed effects of exercise are highly variable between individuals, and subject‐by‐training interaction (i.e., individual response variability) is often not estimated. Here, we measured mitochondrial (citrate synthetase, cytochrome‐c oxidase, succinate dehydrogenase, and mitochondrial copy‐number), performance markers (Wpeak, lactate threshold [LT], and VO2peak), and fiber type proportions/expression (type I, type IIa, and type IIx) in multiple time points during 12‐week of high‐intensity interval training (HIIT) to investigate effects of exercise at the individual level. Methods Sixteen young (age: 33.1 ± 9.0 years), healthy men (VO2peak 35–60 ml/min/kg and BMI: 26.4 ± 4.2) from the Gene SMART study completed 12‐week of progressive HIIT. Performance markers and muscle biopsies were collected every 4 weeks. We used mixed‐models and bivariate growth models to quantify individual response and to estimate correlations between variables. Results All performance markers exhibited significant (Wpeak 0.56 ± 0.33 p = 0.003, LT 0.37 ± 0.35 p = 0.007, VO2peak 3.81 ± 6.13 p = 0.02) increases overtime, with subject‐by‐training interaction being present (95% CI: Wpeak 0.09–0.24, LT 0.06–0.18, VO2peak 0.27–2.32). All other measurements did not exhibit significant changes. Fiber type IIa proportions at baseline was significantly associated with all physiological variables (p < 0.05), and citrate synthetase and cytochrome‐c oxidase levels at baseline and overtime (i.e., intercept and slope) presented significant covariance (p < 0.05). Finally, low correlations between performance and mitochondrial markers were observed. Conclusion We identified a significant subject‐by‐training interaction for the performance markers. While for all other measures within‐subject variability was too large and interindividual differences in training efficacy could not be verified. Changes in measurements in response to exercise were not correlated, and such disconnection should be further investigated by future studies.

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