Key result
High (400-ms) contraction duration did not alter the mean response time for the fall in intracellular PO2 compared to low (200-ms) duration in single frog skeletal myocytes.
Why the study?
Does contraction duration affect intracellular PO2 kinetics in Xenopus single skeletal myocytes?
Does contraction duration affect intracellular PO2 kinetics in Xenopus single skeletal myocytes?
Intracellular PO2 dynamics in isolated skeletal myocytes are invariant despite differing contraction durations, suggesting mitochondria respond more rapidly at the onset of contractions when challenged with an augmented metabolic stimulus.
Answers are grounded in this paper and cite their sources.
PO2 kinetics independent of contraction duration in isolated myocytes; leaves open mitochondrial scaling with metabolic demand in vivo.
It has been suggested that skeletal muscle O(2) uptake (Vo(2)) kinetics follow a first-order control model. Consistent with that, Vo(2) should show both 1) similar onset kinetics and 2) an on-off symmetry across submaximal work intensities regardless of the metabolic perturbation. To date, consensus on this issue has not been reached in whole body studies due to numerous confounding factors associated with O(2) availability and fiber-type recruitment. To test whether single myocytes demonstrate similar intracellular Po(2) (Pi(O(2))) on- and off-transient kinetics at varying work intensities, we studied Xenopus laevis single myocyte (n = 8) Pi(O(2)) via phosphorescence quenching during two bouts of electrically induced isometric muscle contractions of 200 (low)- and 400 (high)-ms contraction duration (1 contraction every 4 s, 15 min between trials, order randomized). The fall in Pi(O(2)), which is inversely proportional to the net increase in Vo(2), was significantly greater (P < 0.05) during the high (24.1 +/- 3.2 Torr) vs. low (17.4 +/- 1.6 Torr) contraction bout. However, the mean response time (MRT; time to 63% of the overall change) for the fall in Pi(O(2)) from resting baseline to end contractions was not different (high, 77.8 +/- 11.5 vs. low, 76.1 +/- 13.6 s; P > 0.05) between trials. The initial rate of change at contraction onset, defined as DeltaPi(O(2))/MRT, was significantly greater (P < 0.05) in high compared with low. Pi(O(2)) off-transient MRT from the end of the contraction bout to initial baseline was unchanged (high, 83.3 +/- 18.3 vs. low, 80.4 +/- 21.6 s; P > 0.05) between high and low trials. These data revealed that Pi(O(2)) dynamics in frog isolated skeletal myocytes were invariant despite differing contraction durations and, by inference, metabolic demands. Thus these findings demonstrate that mitochondria can respond more rapidly at the initial onset of contractions when challenged with an augmented metabolic stimulus in accordance with an apparent first-order rate law.
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Kindig et al. (2005) studied this question. High (400-ms) contraction duration vs. Low (200-ms) contraction duration was evaluated on Mean response time (MRT) for the fall in intracellular PO2 from resting baseline to end contractions (p=>0.05). High (400-ms) contraction duration did not alter the mean response time for the fall in intracellular PO2 compared to low (200-ms) duration in single frog skeletal myocytes.
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