Skeletal muscle biochemical origin of exercise intensity domains and their relation to whole-body V̇O2 kinetics

Biosci Rep. 2022 Aug 31;42(8):BSR20220798. doi: 10.1042/BSR20220798.

Abstract

This article presents the biochemical intra-skeletal-muscle basis of exercise intensity domains: moderate (M), heavy (H), very heavy (VH) and severe (S). Threshold origins are mediated by a 'Pi double-threshold' mechanism of muscle fatigue, which assumes (1) additional ATP usage, underlying muscle V̇O2 and metabolite slow components, is initiated when inorganic phosphate (Pi) exceeds a critical value (Picrit); (2) exercise is terminated because of fatigue, when Pi reaches a peak value (Pipeak); and (3) the Pi increase and additional ATP usage increase mutually stimulate each other forming a positive feedback. M/H and H/VH borders are defined by Pi on-kinetics in relation to Picrit and Pipeak. The values of the ATP usage activity, proportional to power output (PO), for the M/H, H/VH and VH/S borders are lowest in untrained muscle and highest in well-trained muscle. The metabolic range between the M/H and H/VH border (or 'H space') decreases with muscle training, while the difference between the H/VH and VH/S border (or 'VH space') is only weakly dependent on training status. The absolute magnitude of the muscle V̇O2 slow-component, absent in M exercise, rises gradually with PO to a maximal value in H exercise, and then decreases with PO in VH and S exercise. Simulations of untrained, physically active and well-trained muscle demonstrate that the muscle M/H border need not be identical to the whole-body M/H border determined from pulmonary V̇O2 on-kinetics and blood lactate, while suggesting that the biochemical origins of the H/VH border reside within skeletal muscle and correspond to whole-body critical power.

Keywords: blood lactate; exercise intensity; inorganic phosphate; muscle fatigue; oxygen consumption; skeletal muscle.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, N.I.H., Extramural

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Kinetics
  • Muscle Fatigue
  • Muscle, Skeletal* / metabolism
  • Oxygen / metabolism
  • Oxygen Consumption* / physiology

Substances

  • Adenosine Triphosphate
  • Oxygen