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J Appl Physiol 97: 1077-1081, 2004. First published May 7, 2004; doi:10.1152/japplphysiol.01321.2003
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Skeletal muscle oxidative metabolism in sedentary humans: 31P-MRS assessment of O2 supply and demand limitations

Luke J. Haseler,1 Alexander P. Lin,2 and Russell S. Richardson1

1Department of Medicine, University of California, San Diego, La Jolla 92093-0623; and 2Huntington Medical Research Institutes, Pasadena, California 91105

Submitted 10 December 2003 ; accepted in final form 4 May 2004

Previously, it was demonstrated in exercise-trained humans that phosphocreatine (PCr) recovery is significantly altered by fraction of inspired O2 (FIO2), suggesting that in this population under normoxic conditions, O2 availability limits maximal oxidative rate. Haseler LJ, Hogan ML, and Richardson RS. J Appl Physiol 86: 2013–2018, 1999. To further elucidate these population-specific limitations to metabolic rate, we used 31P-magnetic resonance spectroscopy to study the exercising human gastrocnemius muscle under conditions of varied FIO2 in sedentary subjects. To test the hypothesis that PCr recovery from submaximal exercise in sedentary subjects is not limited by O2 availability, but rather by their mitochondrial capacity, six sedentary subjects performed three bouts of 6-min steady-state submaximal plantar flexion exercise followed by 5 min of recovery while breathing three different FIO2 (0.10, 0.21, and 1.00). PCr recovery time constants were significantly longer in hypoxia (47.0 ± 3.2 s), but there was no difference between hyperoxia (31.8 ± 1.9 s) and normoxia (30.0 ± 2.1 s) (mean ± SE). End-exercise pH was not significantly different across treatments. These results suggest that the maximal muscle oxidative rate of these sedentary subjects, unlike their exercise-trained counterparts, is limited by mitochondrial capacity and not O2 availability in normoxia. Additionally, the significant elongation of PCr recovery in these subjects in hypoxia illustrates the reliance on O2 supply at the other end of the O2 availability spectrum in both sedentary and active populations.

oxidative capacity; mitochondria; exercise; intracellular oxygenation; 31-phosphorous-magnetic resonance spectroscopy



Address for reprint requests and other correspondence: L. J. Haseler, Gold Coast Campus Griffith University, PMB 50 Gold Coast Mail Centre, Queensland 9726, Australia (E-mail: L.Haseler{at}griffith.edu.au).




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