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J Appl Physiol 88: 1743-1748, 2000;
8750-7587/00 $5.00
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Vol. 88, Issue 5, 1743-1748, May 2000

Impairment of Ca2+ release in single Xenopus muscle fibers fatigued at varied extracellular PO2

Creed M. Stary and Michael C. Hogan

Department of Medicine, University of California, San Diego, La Jolla, California 92093-0623

We tested the hypothesis that the mechanisms involved in the more rapid onset of fatigue when O2 availability is reduced in contracting skeletal muscle are similar to those when O2 availability is more sufficient. Two series of experiments were performed in isolated, single skeletal muscle fibers from Xenopus laevis. First, relative force and free cytosolic Ca2+ concentrations ([Ca2+]c) were measured simultaneously in single fibers (n = 6) stimulated at increasing frequencies (0.25, 0.33, 0.5, and 1 Hz) at an extracellular PO2 of either 22 or 159 Torr. Muscle fatigue (force = 50% of initial peak tension) occurred significantly sooner (P < 0.05) during the low- (237 ± 40 s) vs. high-PO2 treatments (280 ± 38 s). Relative [Ca2+]c was significantly decreased from maximal values at the fatigue time point during both the high- (72 ± 4%) and low-PO2 conditions (78 ± 4%), but no significant difference was observed between the treatments. In the second series of experiments, using the same stimulation regime as the first, fibers (n = 6) exposed to 5 mM caffeine immediately after fatigue demonstrated an immediate but incomplete relative force recovery during both the low- (89 ± 4%) and high-PO2 treatments (82 ± 3%), with no significant difference between treatments. Additionally, there was no significant difference in relative [Ca2+]c between the high- (100 ± 12% of prefatigue values) and low-PO2 treatments (108 ± 12%) on application of caffeine. These results suggest that in isolated, single skeletal muscle fibers, the earlier onset of fatigue that occurred during the low-extracellular PO2 condition was modulated through similar pathways as the fatigue process during the high and involved a decrease in relative peak [Ca2+]c.

oxidative phosphorylation; exercise; contractions; caffeine; relaxation; excitation-contraction coupling


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