Phosphocreatine hydrolysis during submaximal exercise: the effect of FIO2

Division of Physiology, Department of Medicine, University of California, San Diego, La Jolla, California 92093 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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of applied physiology (1985) 1998-10, Vol.85 (4), p.1457-1463
Hauptverfasser: Haseler, Luke J, Richardson, Russell S, Videen, John S, Hogan, Michael C
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Division of Physiology, Department of Medicine, University of California, San Diego, La Jolla, California 92093 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 (F I O 2 ). Whereas it has been suggested that these changes may be the result of differences in time taken to achieve steady-state O 2 uptake ( O 2 ) at different F I O 2 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 same O 2 with varied F I O 2 and 2 ) that these changes are not due to differences in 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 F I O 2 switched after 5 min of the 10-min exercise bout. The three exercise treatments were 1 ) F I O 2 of 0.1 switched to 0.21,  2 ) F I O 2 of 0.1 switched to 1.00, and 3 ) F I O 2 of 1.00 switched to 0.1. For all three treatments, the F I O 2 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 F I O 2 are not the result of different 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. fraction of inspired oxygen; skeletal muscle; intracellular oxygenation
ISSN:8750-7587
1522-1601
DOI:10.1152/jappl.1998.85.4.1457