Chamber oxygen concentration impacts mitochondrial function and hydrogen peroxide appearance in permeabilized human skeletal muscle fibers
Skeletal muscle mitochondrial respiration is commonly assessed ex vivo using permeabilized fibers in media with high oxygen (O<sub>2</sub>) concentrations to ensure that O<sub>2</sub> availability does not limit respiration. However, high O<sub>2</sub> concentrations also increase the production of reactive O<sub>2</sub> species that can negatively affect respiration. In this study, we tested the hypotheses that permeabilized fiber mitochondria in a high, compared to low, O<sub>2</sub> concentration would (i) not be different at maximal state 3 respiration rate (V<sub>max</sub>), (ii) have lower submaximal respiration rates at submaximal O<sub>2</sub> concentrations, and (iii) have greater total cumulative hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>) appearance. We continuously monitored mitochondrial state 3 respiration and H<sub>2</sub>O<sub>2</sub> appearance rates using high-resolution respirometry in permeabilized skeletal muscle fibers (12 untrained participants; 22 ± 4 yrs) with either control (~127 mmHg; CON) or high (~327 mmHg; HIGH) partial pressures of O<sub>2</sub> (PO<sub>2</sub>). V<sub>max</sub> was not different between conditions (HIGH: 80.7 ± 16.7 vs. CON: 82.3 ± 18.7 pmol/s/mg, p = 0.695). The PO<sub>2</sub> at 80 % V<sub>max</sub> (P<sub>80</sub>) was greater in HIGH (73.9 ± 25.5 vs. 28.0 ± 7.1 mmHg, p < 0.001) and respiration rates at 5-60 mmHg PO<sub>2</sub> were lower for HIGH than CON (all p < 0.001). Additionally, the total cumulative H<sub>2</sub>O<sub>2</sub> appearance was greater in HIGH than CON (n = 11; 51.5 ± 23.2 vs. 18.3 ± 10.3 pmol/mg, p < 0.001), and this difference was directly correlated with the difference in P<sub>80</sub> (r = 0.655, p = 0.029). The current findings support that a high O<sub>2</sub> concentration, by itself, does not appear to affect V<sub>max</sub> in the permeabilized skeletal muscle fiber preparation, but the corollary increase in H<sub>2</sub>O<sub>2</sub> exposure may diminish mitochondrial state 3 respiratory function.
Authors
- Matthew T. Lewis (ORCID: https://orcid.org/0000-0003-0580-6866)
- Ryan M. Broxterman (ORCID: https://orcid.org/0000-0002-7388-2214)
- Russell S. Richardson (ORCID: https://orcid.org/0000-0003-0233-5923)
- Bradley A. Ruple (ORCID: https://orcid.org/0009-0001-7277-0771)
- Joel D. Trinity (ORCID: https://orcid.org/0000-0001-8271-6536)
- Soung Hun Park (ORCID: https://orcid.org/0000-0002-1423-0929)
- Jesse C. Craig (ORCID: https://orcid.org/0000-0001-5959-4139)
Institutions
- University of Utah (US)
- George E. Wahlen Department of VA Medical Center (US)
Publication Details
- Journal
- Biochimica et Biophysica Acta (BBA) - Bioenergetics
- Published
- 2025-08-11
- DOI
- https://doi.org/10.1016/j.bbabio.2025.149568
- Citations
- 1
- Primary Topic
- Mitochondrial Function and Pathology
- Type
- article
- Field-Weighted Citation Impact
- 0.81
Funders
- U.S. Department of Veterans Affairs
- National Institutes of Health
- Rehabilitation Research and Development Service
- Clinical Science Research and Development
- National Heart, Lung, and Blood Institute