Journal
JOURNAL OF APPLIED PHYSIOLOGY
Volume 97, Issue 2, Pages 661-668Publisher
AMER PHYSIOLOGICAL SOC
DOI: 10.1152/japplphysiol.00096.2004
Keywords
manoalide; hydroethidine; arachidonic acid; cytochrome c; heat stress
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Funding
- NHLBI NIH HHS [HL-53333] Funding Source: Medline
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Superoxide anion radical (O-2(.-)) is released from skeletal muscle at rest and is particularly elevated during conditions of heat stress (42degreesC). Previous studies have shown that in isolated rat diaphragm O-2(.-) release is not dependent on mitochondrial electron transport, reduced NADP oxidase activity, or the integrity of membrane anion channels. This study hypothesized that O-2(.-) release, as measured by cytochrome c reduction, is linked to metabolism of arachidonic acid. Phospholipase A(2) inhibition with manoalide significantly decreased O-2(.-) release. In downstream pathways, neither the blockage of cyclooxygenase with indomethacin nor the inhibition of cytochrome P-450-dependent monooxygenase with SKF-525A decreased O-2(.-) - release. However, lipoxygenase (LOX) inhibition with general LOX blockers 5,8,11,14-eicosatetraynoic acid and cinnamyl-3,4-dihydroxy-alpha-cyanocinnamate greatly attenuated the signal. Furthermore, the specific 5-LOX inhibitor diethylcarbamazine also significantly decreased O-2(.-) release. Immunohistochemistry localized 5- and 12-LOX to the cytosol and sarcolemma of muscle cells. Confocal studies, using the O-2(.-)-sensitive fluorescent indicator hydroethidine, demonstrated that LOX inhibition had no significant influence on intracellular 0;- formation. When compared with the cytochrome c results, this indicates that intra- and extracellular O-2(.-) must arise from different sources. These data show for the first time that arachidonic acid metabolism through LOX activity, is a major source of extracellular O-2(.-) release in skeletal muscle.
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