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J Physiol Volume 564, Number 1, 189-199, April 1, 2005 DOI: 10.1113/jphysiol.2005.083519
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Reactive oxygen species reduce myofibrillar Ca2+ sensitivity in fatiguing mouse skeletal muscle at 37°C

Terence R Moopanar1 and David G Allen1

1 Institute for Biomedical Sciences, School of Medical Sciences, University of Sydney F13, NSW 2006, Australia

The mechanisms of muscle fatigue were studied in small muscle bundles and single fibres isolated from the flexor digitorum brevis of the mouse. Fatigue caused by repeated isometric tetani was accelerated at body temperature (37°C) when compared to room temperature (22°C). The membrane-permeant reactive oxygen species (ROS) scavenger, Tiron (5 mM), had no effect on the rate of fatigue at 22°C but slowed the rate of fatigue at 37°C to that observed at 22°C. Single fibres were microinjected with indo-1 to measure intracellular calcium. In the accelerated fatigue at 37°C the tetanic [Ca2+]i did not change significantly and the decline of maximum Ca2+-activated force was similar to that observed at 22°C. The cause of the greater rate of fatigue at 37°C was a large fall in myofibrillar Ca2+ sensitivity. In the presence of Tiron, the large fall in Ca2+ sensitivity was abolished and the usual decline in tetanic [Ca2+]i was observed. This study confirms the importance of ROS in fatigue at 37°C and shows that the mechanism of action of ROS is a decline in myofibrillar Ca2+ sensitivity.

(Received 19 January 2005; accepted after revision 16 February 2005; first published online 17 February 2005)
Corresponding author D. G. Allen: Institute for Biomedical Sciences, School of Medical Sciences, University of Sydney F13, NSW 2006, Australia. Email: davida{at}physiol.usyd.edu.au




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