Key result
Mathematical modeling reveals aerobic metabolism in most skeletal muscle fibers is reaction-controlled rather than diffusion-limited.
Why the study?
The study aimed to analyze the effects of intracellular diffusion of oxygen and high-energy phosphate metabolites on aerobic energy metabolism in skeletal muscle and test hypotheses about diffusion limitation across muscle fibers from different species.
Does not support diffusion as primary limit in most fibers; leaves open in vivo validation and clinical translation.
A mathematical model was developed to analyze the effects of intracellular diffusion of O(2) and high-energy phosphate metabolites on aerobic energy metabolism in skeletal muscle. We tested the hypotheses that in a range of muscle fibers from different species (1) aerobic metabolism was not diffusion limited and (2) that fibers had a combination of rate and fiber size that placed them at the brink of substantial diffusion limitation. A simplified chemical reaction rate law for mitochondrial oxidative phosphorylation was developed utilizing a published detailed model of isolated mitochondrial function. This rate law was then used as a boundary condition in a reaction-diffusion model that was further simplified using the volume averaging method and solved to determine the rates of oxidative phosphorylation as functions of the volume fraction of mitochondria, the size of the muscle cell, and the amount of oxygen delivered by the capillaries. The effectiveness factor, which is the ratio of reaction rate in the system with finite rates of diffusion to those in the absence of any diffusion limitations, defined the regions where intracellular diffusion of metabolites and O(2) may limit aerobic metabolism in both very small, highly oxidative fibers as well as in larger fibers with lower aerobic capacity. Comparison of model analysis with experimental data revealed that none of the fibers was strongly limited by diffusion, as expected. However, while some fibers were near substantial diffusion limitation, most were well within the domain of reaction control of aerobic metabolic rate. This may constitute a safety factor in muscle that provides a level of protection from diffusion constraints under conditions such as hypoxia.
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Dasika et al. (2010) studied aerobic energy metabolism in skeletal muscle. Mathematical model of intracellular diffusion of O(2) and high-energy phosphate metabolites was evaluated on rates of oxidative phosphorylation as functions of the volume fraction of mitochondria, the size of the muscle cell, and the amount of oxygen delivered by the capillaries. Mathematical modeling revealed that while some skeletal muscle fibers were near substantial diffusion limitation, most were well within the domain of reaction control of aerobic metabolic rate.
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