Molecular genetics and metabolism · 2013
Oxidative stress and Nrf2 signaling in McArdle disease.
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Kitaoka Yu, Ogborn Daniel I, Nilsson Mats I, Mocellin Nicholas J, MacNeil Lauren G, Tarnopolsky Mark A
Аннотация
McArdle disease (MD) is a metabolic myopathy due to myophosphorylase deficiency, which leads to a severe limitation in the rate of adenosine triphosphate (ATP) resynthesis. Compensatory flux through the myoadenylate deaminase > > xanthine oxidase pathway should result in higher oxidative stress in skeletal muscle; however, oxidative stress and nuclear factor erythroid 2-related factor 2 (Nrf2) mediated antioxidant response cascade in MD patients have not yet been examined. We show that MD patients have elevated muscle protein carbonyls and 4-hydroxynonenal (4-HNE) in comparison with healthy, age and activity matched controls (P < 0.05). Nuclear abundance of Nrf2 and Nrf2-antioxidant response element (ARE) binding was also higher in MD patients compared with controls (P < 0.05). The expressions of Nrf2 target genes were also higher in MD patients vs. controls. These observations suggest that MD patients experience elevated levels of oxidative stress, and that the Nrf2-mediated antioxidant response cascade is up-regulated in skeletal muscle to compensate.
Предметные рубрики MeSH
AldehydesFemaleGene Expression RegulationGlucosyltransferasesGlycogen Storage Disease Type VHeme Oxygenase-1HumansIntracellular Signaling Peptides and ProteinsKelch-Like ECH-Associated Protein 1MaleMiddle AgedMitochondriaNAD(P)H Dehydrogenase (Quinone)NF-E2-Related Factor 2Oxidative StressSignal TransductionTranscription, GeneticUric Acid