A human skeletal muscle cross-bridge model to characterize the role of metabolite accumulation in muscle fatigue.

Abstract

Skeletal muscle fatigue is accompanied by the accumulation of metabolites, such as adenosine diphosphate (ADP), inorganic phosphate (P_i), and protons (H⁺). However, we lack a comprehensive understanding of the contribution of these metabolic changes to the development of muscle fatigue during intense exercise and the underlying mechanisms. To address this gap, we collected data from young adults performing a dynamic (0.75 Hz) plantar flexion exercise to task failure (642 ± 104 s), including in vivo concentrations of metabolites and H⁺ measured by ³¹P magnetic resonance spectroscopy as well as muscle activation signals obtained via electromyography. Using these data, we developed and validated a human skeletal muscle model. Our model-based simulations suggested that to continue the plantar flexion exercise at the required power output, muscle activation should progressively increase. In the absence of this increased activation, we observed a reduction in force-generating capacity due to metabolite-mediated inhibition of actin-myosin cross-bridge cycling. Our simulations also showed that P_i reduced force production by 30% when we increased it 50% above the concentrations measured experimentally. A parameter sensitivity analysis suggested that force generation is strongly dependent on the rate of P_i release from the actin-myosin complex, and P_i inhibits force by increasing the rate of actin-myosin detachment. In addition, we proposed an alternative mechanism through which H⁺ might reduce muscle force generation during exercise. In contrast, elevated ADP levels did not significantly affect force generation. This study provides insight into the impact of metabolite accumulation on force generation and muscle fatigue development.