It remains uncertain whether the delayed onset of mitochondrial respiration
on initiation of muscle contractions is related to O-2 availability. The p
urpose of this research was to measure the kinetics of the fall in intracel
lular PO2 at the onset of a contractile work period in rested and previousl
y worked single skeletal muscle fibers. Intact single skeletal muscle fiber
s (n = 11) from Xenopus laevis were dissected from the lumbrical muscle, in
jected with an O-2-sensitive probe, mounted in a glass chamber, and perfuse
d with Ringer solution (PO2 = 32 +/- 4 Torr and pH = 7.0) at 20 degreesC. I
ntracellular PO2 was measured in each fiber during a protocol consisting se
quentially of 1-min rest; 3 min of tetanic contractions (1 contraction/2 s)
; 5-min rest; and, finally, a second 3-min contractile period identical to
the first. Maximal force development and the fall in force (to 83 +/- 2 vs.
86 +/- 3% of maximal force development) in contractile periods 1 and 2, re
spectively, were not significantly different. The time delay (time before i
ntracellular PO2 began to decrease after the onset of contractions) was sig
nificantly greater (P < 0.01) in the first contractile period (13 +/- 3 s)
compared with the second (5 +/- 2 s), as was the time to reach 50% of the c
ontractile steady-state intracellular PO2 (28 +/- 5 vs. 18 +/- 4 s, respect
ively). In Xenopus single skeletal muscle fibers, 1) the lengthy response t
ime for the fall in intracellular PO2 at the onset of contractions suggests
that intracellular factors other than O-2 availability determine the on-ki
netics of oxidative phosphorylation and 2) a prior contractile period resul
ts in more rapid on-kinetics.