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Phosphocreatine hydrolysis during submaximal exercise: the effect of F I O 2

1998; American Physiological Society; Volume: 85; Issue: 4 Linguagem: Inglês

10.1152/jappl.1998.85.4.1457

8750-7587

Luke J. Haseler, Russell S. Richardson, John S. Videen, Michael C. Hogan,

Muscle metabolism and nutrition

There is evidence that the concentration of the high-energy phosphate metabolites may be altered during steady-state submaximal exercise by the breathing of different fractions of inspired O 2 ([Formula: see text]). Whereas it has been suggested that these changes may be the result of differences in time taken to achieve steady-state O 2 uptake (V˙o 2 ) at different[Formula: see text] values, we postulated that they are due to a direct effect of O 2 tension. We used 31 P-magnetic resonance spectroscopy during constant-load, steady-state submaximal exercise to determine 1) whether changes in high-energy phosphates do occur at the sameV˙o 2 with varied[Formula: see text] and 2) that these changes are not due to differences in V˙o 2 onset kinetics. Six male subjects performed steady-state submaximal plantar flexion exercise [7.2 ± 0.6 (SE) W] for 10 min while lying supine in a 1.5-T clinical scanner. Magnetic resonance spectroscopy data were collected continuously for 2 min before exercise, 10 min during exercise, and 6 min during recovery. Subjects performed three different exercise bouts at constant load with the[Formula: see text] switched after 5 min of the 10-min exercise bout. The three exercise treatments were 1)[Formula: see text] of 0.1 switched to 0.21, 2)[Formula: see text] of 0.1 switched to 1.00, and 3)[Formula: see text] of 1.00 switched to 0.1. For all three treatments, the[Formula: see text] switch significantly ( P ≤ 0.05) altered phosphocreatine: 1) 55.5 ± 4.8 to 67.8 ± 4.9% (%rest); 2) 59.0 ± 4.3 to 72.3 ± 5.1%; and 3) 72.6 ± 3.1 to 64.2 ± 3.4%, respectively. There were no significant differences in intracellular pH for the three treatments. The results demonstrate that the differences in phosphocreatine concentration with varied [Formula: see text] are not the result of different V˙o 2 onset kinetics, as this was eliminated by the experimental design. These data also demonstrate that changes in intracellular oxygenation, at the same work intensity, result in significant changes in cell homeostasis and thereby suggest a role for metabolic control by O 2 even during submaximal exercise.