Muscle metabolism and activation heterogeneity by combined31P chemical shift and T2imaging, and pulmonary O2uptake during incremental knee-extensor exercise

Author:

Cannon Daniel T.12,Howe Franklyn A.34,Whipp Brian J.56,Ward Susan A.67,McIntyre Dominick J.38,Ladroue Christophe39,Griffiths John R.38,Kemp Graham J.10,Rossiter Harry B.125

Affiliation:

1. Rehabilitation Clinical Trials Center, Division of Respiratory & Critical Care Physiology & Medicine, Los Angeles Biomedical Research Institute at Harbor-UCLA Medical Center, Torrance, California;

2. School of Biomedical Sciences, University of Leeds, Leeds, United Kingdom;

3. Department of Biochemistry, St George's, University of London, London, United Kingdom;

4. Division of Clinical Sciences, St George's, University of London, London, United Kingdom;

5. Department of Physiology, St George's, University of London, London, United Kingdom;

6. Human Bio-Energetics Research Centre, Crickhowell, Powys, United Kingdom;

7. Centre for Exercise Science and Medicine, University of Glasgow, Glasgow, United Kingdom;

8. Cancer Research UK Cambridge Research Institute, Li Ka Shing Centre, Cambridge, United Kingdom;

9. Department of Computer Science, University of Warwick, Coventry, United Kingdom; and

10. Department of Musculoskeletal Biology and Magnetic Resonance & Image Analysis Research Centre, University of Liverpool, Liverpool, United Kingdom

Abstract

The integration of skeletal muscle substrate depletion, metabolite accumulation, and fatigue during large muscle-mass exercise is not well understood. Measurement of intramuscular energy store degradation and metabolite accumulation is confounded by muscle heterogeneity. Therefore, to characterize regional metabolic distribution in the locomotor muscles, we combined31P magnetic resonance spectroscopy, chemical shift imaging, and T2-weighted imaging with pulmonary oxygen uptake during bilateral knee-extension exercise to intolerance. Six men completed incremental tests for the following: 1) unlocalized31P magnetic resonance spectroscopy; and 2) spatial determination of31P metabolism and activation. The relationship of pulmonary oxygen uptake to whole quadriceps phosphocreatine concentration ([PCr]) was inversely linear, and three of four knee-extensor muscles showed activation as assessed by change in T2. The largest changes in [PCr], [inorganic phosphate] ([Pi]) and pH occurred in rectus femoris, but no voxel (72 cm3) showed complete PCr depletion at exercise cessation. The most metabolically active voxel reached 11 ± 9 mM [PCr] (resting, 29 ± 1 mM), 23 ± 11 mM [Pi] (resting, 7 ± 1 mM), and a pH of 6.64 ± 0.29 (resting, 7.08 ± 0.03). However, the distribution of31P metabolites and pH varied widely between voxels, and the intervoxel coefficient of variation increased between rest (∼10%) and exercise intolerance (∼30–60%). Therefore, the limit of tolerance was attained with wide heterogeneity in substrate depletion and fatigue-related metabolite accumulation, with extreme metabolic perturbation isolated to only a small volume of active muscle (<5%). Regional intramuscular disturbances are thus likely an important requisite for exercise intolerance. How these signals integrate to limit muscle power production, while regional “recruitable muscle” energy stores are presumably still available, remains uncertain.

Publisher

American Physiological Society

Subject

Physiology (medical),Physiology

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