The Journal of Physiology · 2005 · 469 citations · 25 references
Life SciencesCell BiologyPhysiologyCell SignalingExercise PhysiologySignal TransductionAerobic ExerciseMetabolic Adaptation To ExerciseMetabolic Responses To ExerciseOxidative StressOxidative Stress PhysiologyStress Signaling PathwaysDefence MechanismsEnzymesNuclear Factor Kappa B ActivationNuclear Factor Kappa B InhibitionNuclear Factor Kappa B ModulationOxidative Stress InjuryOxidative Stress Signaling PathwaysTissue Damage Mechanisms
Reactive oxygen or nitrogen species (RONS) are produced during exercise due, at least in part, to the activation of xanthine oxidase. When exercise is exhaustive they cause tissue damage; however, they may also act as signals inducing specific cellular adaptations to exercise. We have tested this hypothesis by studying the effects of allopurinol-induced inhibition of RONS production on cell signalling pathways in rats submitted to exhaustive exercise. Exercise caused an activation of mitogen-activated protein kinases (MAPKs: p38, ERK 1 and ERK 2), which in turn activated nuclear factor kappaB (NF-kappaB) in rat gastrocnemius muscle. This up-regulated the expression of important enzymes associated with cell defence (superoxide dismutase) and adaptation to exercise (eNOS and iNOS). All these changes were abolished when RONS production was prevented by allopurinol. Thus we report, for the first time, evidence that decreasing RONS formation prevents activation of important signalling pathways, predominantly the MAPK-NF-kappaB pathway; consequently the practice of taking antioxidants before exercise may have to be re-evaluated.
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Allopurinol and oxypurinol are hydroxyl radical scavengers
P.Christopher Moorhouse, Martin Grootveld, Barry Halliwell et al. · FEBS Letters · 1987 · 393 citations · Full text
Reactive oxygen in skeletal muscle. II. Extracellular release of free radicals
Margaret Reid, T Shoji, Melanie R. Moody et al. · Journal of Applied Physiology · 1992 · 304 citations