1. No sex differences in oxygen uptake or extraction kinetics in the moderate or heavy exercise intensity domains.
- Author
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Pons, Maria Solleiro, Bernert, Lina, Hume, Emily, Hughes, Luke, Williams, Zander J., Burnley, Mark, and Ansdell, Paul
- Abstract
The integrative response to exercise differs between sexes, with oxidative energy contribution purported as a potential mechanism. The present study investigated whether this difference was evident in the kinetics of oxygen uptake (V
O2 ) and extraction (HHb + Mb) during exercise. Sixteen adults (8 males, 8 females, age: 27 ± 5 yr) completed three experimental visits. Incremental exercise testing was performed to obtain lactate threshold and VO2 peak. Subsequent visits involved three 6-min cycling bouts at 80% of lactate threshold and one 30-min bout at a work rate of 30% between the lactate threshold and power at VO2 peak. Pulmonary gas exchange and near-infrared spectroscopy of the vastus lateralis were used to continuously sample VO2 and HHb + Mb, respectively. The phase II VO2 kinetics were quantified using monoexponential curves during moderate and heavy exercise. Slow component amplitudes were also quantified for the heavy-intensity domain. Relative VO2 peak values were not different between sexes (P = 0.111). Males achieved ~30% greater power outputs (P = 0.002). In the moderate- and heavy-intensity domains, the relative amplitude of the phase II transition was not different between sexes for VO2 (~24 and ~40% VO2 peak, P > 0.179) and HHb + Mb (~20 and ~32% ischemia, P > 0.193). Similarly, there were no sex differences in the time constants for VO2 (~28 s, P > 0.385) or HHb + Mb (~10 s, P > 0.274). In the heavy-intensity domain, neither VO2 (P > 0.686) or HHb + Mb (P > 0.432) slow component amplitudes were different between sexes. The oxidative response to moderate- and heavy-intensity exercises did not differ between males and females, suggesting similar dynamic responses of oxidative metabolism during intensity-matched exercise. [ABSTRACT FROM AUTHOR]- Published
- 2024
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