Hydroxyl Radical Formation in Skeletal Muscle of Rats with Glucocorticoid-Induced Myopathy |
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Authors: | Shingo?Konno mailto:d@oha.toho-u.ac.jp" title=" d@oha.toho-u.ac.jp" itemprop=" email" data-track=" click" data-track-action=" Email author" data-track-label=" " >Email author |
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Affiliation: | (1) Department of Neurology, Toho University School of Medicine, Oohashi Hospital, 2-17-6 Oohashi, 153-8515 Meguro-ku, Tokyo, Japan |
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Abstract: | ![]() Steroid myopathy is a well-known adverse effect of glucocorticoids that causes muscle weakness and atrophy; however, its pathogenic mechanism is still unclear. Recently, oxidative stress was reported to contribute to steroid myopathy, but there is no report that actually attempts to measure hydroxyl radical. I developed an animal model of steroid myopathy in rat with dexamethasone (9-Fluoro−11β,17, 21-trihydroxy−16α-methylpregna−1,4-diene−3,20-dione), and measured hydroxyl radical using the salicylate trapping method. There was significant dose-dependent relation between both 2,5- and 2,3-dihydroxybenzoic acids and dexamethasone in the treated group, compared to the control group. These results suggest that hydroxyl radical plays a role in the pathogenesis of steroid myopathy. |
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Keywords: | 2,3-DHBA dexamethasone glucocorticoid-induced myopathy hydroxyl radical 2,5-DHBA |
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