ATP synthesis and proton handling in muscle during short periods of exercise and subsequent recovery

Author:

Bendahan David1,Kemp Graham J.2,Roussel Magali1,Fur Yann Le1,Cozzone Patrick J.1

Affiliation:

1. Faculté de Médecine, Centre de Resonance Magnetique Biologique et Medicale, Unité Mixte de Recherche 6612 Centre National de la Recherche Scientifique, Marseille 13005, France; and

2. Department of Musculoskeletal Science, University of Liverpool, Liverpool L69 3GA, United Kingdom

Abstract

We used31P-magnetic resonance spectroscopy to study proton buffering in finger flexor muscles of eight healthy men (25–45 yr), during brief (18-s) voluntary finger flexion exercise (0.67-Hz contraction at 10% maximum voluntary contraction; 50/50 duty cycle) and 180-s recovery. Phosphocreatine (PCr) concentration fell 19 ± 2% during exercise and then recovered with half time = 0.24 ± 0.01 min. Cell pH rose by 0.058 ± 0.003 units during exercise as a result of H+ consumption by PCr splitting, which (assuming no lactate production or H+ efflux) implies a plausible non-Pi buffer capacity of 20 ± 3 mmol · l intracellular water−1 · pH unit−1. There was thus no evidence of significant glycogenolysis to lactate during exercise. Analysis of PCr kinetics as a classic linear response suggests that oxidative ATP synthesis reached 48 ± 2% of ATP demand by the end of exercise; the rest was met by PCr splitting. Postexercise pH recovery was faster than predicted, suggesting “excess proton” production, with a peak value of 0.6 ± 0.2 mmol/l intracellular water at 0.45 min of recovery, which might be due to, e.g., proton influx driven by cellular alkalinization, or a small glycolytic contribution to PCr resynthesis in recovery.

Publisher

American Physiological Society

Subject

Physiology (medical),Physiology

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