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Am J Physiol Cell Physiol 288: C730-C738, 2005. First published November 10, 2004; doi:10.1152/ajpcell.00138.2004
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CELLULAR METABOLISM

Control of respiration and bioenergetics during muscle contraction

Youngran Chung,1 Paul A. Molé,2,{dagger} Napapon Sailasuta,3 Tuan Khanh Tran,1 Ralph Hurd,3 and Thomas Jue1

Departments of 1Biological Chemistry and 2Exercise Science, University of California, Davis; and 3GE Medical Systems, Fremont, California

Submitted 11 March 2004 ; accepted in final form 21 October 2004

1H-NMR experiments have determined intracellular O2 consumption (O2) with oxymyoglobin (MbO2) desaturation kinetics in human calf muscle during plantar flexion exercise at 0.75, 0.92, and 1.17 Hz with a constant load. At the onset of muscle contraction, myoglobin (Mb) desaturates rapidly. The desaturation rate constant of ~30 s reflects the intracellular O2. Although Mb desaturates quickly with a similar time constant at all workload levels, its final steady-state level differs. As work increases, the final steady-state cellular PO2 decreases progressively. After Mb desaturation has reached a steady state, however, O2 continues to rise. On the basis of current respiratory control models, the analysis in the present report reveals two distinct O2 phases: an ADP-independent phase at the onset of contraction and an ADP-dependent phase after Mb has reached a steady state. In contrast to the accepted view, the initial intracellular O2 shows that oxidative phosphorylation can support up to 36% of the energy cost, a significantly higher fraction than expected. Partitioning of the energy flux shows that a 31% nonoxidative component exists and responds to the dynamic energy utilization-restoration cycle (which lasts for only milliseconds) as postulated in the glycogen shunt theory. The present study offers perspectives on the regulation of respiration, bioenergetics, and Mb function during muscle contraction.

myoglobin; nuclear magnetic resonance; glycogen; oxygen; exercise



Address for reprint requests and other correspondence: T. Jue, Dept. of Biological Chemistry, Univ. of California, Davis, Davis, CA 95616-8635 (E-mail: TJue{at}ucdavis.edu)




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