Lipoxygenase-dependent superoxide release in skeletal muscle

J Appl Physiol (1985). 2004 Aug;97(2):661-8. doi: 10.1152/japplphysiol.00096.2004. Epub 2004 Apr 23.

Abstract

Superoxide anion radical (O(2)(*-)) is released from skeletal muscle at rest and is particularly elevated during conditions of heat stress (42 degrees C). 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 O(2)(*-) 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.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • 5,8,11,14-Eicosatetraynoic Acid / pharmacology
  • Animals
  • Arachidonate 12-Lipoxygenase / metabolism*
  • Arachidonate 5-Lipoxygenase / metabolism*
  • Arachidonic Acid / metabolism
  • Caffeic Acids / pharmacology
  • Cyclooxygenase Inhibitors / pharmacology
  • Enzyme Inhibitors / pharmacology
  • Indomethacin / pharmacology
  • Lipoxygenase Inhibitors
  • Male
  • Muscle, Skeletal / enzymology*
  • Proadifen / pharmacology
  • Rats
  • Rats, Sprague-Dawley
  • Superoxides / metabolism*

Substances

  • Caffeic Acids
  • Cyclooxygenase Inhibitors
  • Enzyme Inhibitors
  • Lipoxygenase Inhibitors
  • cinnamyl-3,4-dihydroxycyanocinnamate
  • Superoxides
  • 5,8,11,14-Eicosatetraynoic Acid
  • Arachidonic Acid
  • Proadifen
  • Arachidonate 12-Lipoxygenase
  • Arachidonate 5-Lipoxygenase
  • Indomethacin