Mechanisms underlying extremely fast muscle V˙O on-kinetics in humans.

Physiol Rep

Department of Muscle Physiology, Chair of Physiology and Biochemistry, Faculty of Rehabilitation, University School of Physical Education, Kraków, Poland.

Published: August 2018

The time constant of the primary phase of pulmonary V˙O on-kinetics (τ ), which reflects muscle V˙O kinetics during moderate-intensity exercise, is about 30 s in young healthy untrained individuals, while it can be as low as 8 s in endurance-trained athletes. We aimed to determine the intramuscular factors that enable very low values of t to be achieved (analogous to τ , t is the time to reach 63% of the V˙O amplitude). A computer model of oxidative phosphorylation (OXPHOS) in skeletal muscle was used. Muscle t was near-linearly proportional to the difference in phosphocreatine (PCr) concentration between rest and work (ΔPCr). Of the two main factors that determine t , a huge increase in either OXPHOS activity (six- to eightfold) or each-step activation (ESA) of OXPHOS intensity (>3-fold) was needed to reduce muscle t from the reference value of 29 s (selected to represent young untrained subjects) to below 10 s (observed in athletes) when altered separately. On the other hand, the effect of a simultaneous increase of both OXPHOS activity and ESA intensity required only a twofold elevation of each to decrease t below 10 s. Of note, the dependence of t on OXPHOS activity and ESA intensity is hyperbolic, meaning that in trained individuals a large increase in OXPHOS activity and ESA intensity are required to elicit a small reduction in τ . In summary, we postulate that the synergistic action of elevated OXPHOS activity and ESA intensity is responsible for extremely low τ (t ) observed in highly endurance-trained athletes.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6113137PMC
http://dx.doi.org/10.14814/phy2.13808DOI Listing

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