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- W2111087016 endingPage "258" @default.
- W2111087016 startingPage "249" @default.
- W2111087016 abstract "Abstract Reactive oxygen intermediates (ROI) and nitric oxide (NO · ) are produced in abundance in the inflammatory muscle diseases of autoimmune origin polymyositis (PM), dermatomyositis (DM), and inclusion body myositis (IBM). However, their role in the pathogenesis of these diseases is so far not clear. In contrast to demyelinating neuropathies, there is no convincing evidence for oxide‐induced apoptosis either in myocytes or in lymphocytes and phagocytes in inflammatory myopathies. On the contrary, NO · released at low concentrations at target sites may even have cell‐protective effects. A major mechanism of protection from apoptosis in both myocytes and inflammatory cells seems to be the upregulation of anti‐apoptotic proteins like Bcl‐2. Caution is warranted to apply antioxidative and anti‐apoptotic agents to patients with inflammatory myopathies as long as the pathogenic role of oxides and apoptosis in the individual case is not resolved. Microsc. Res. Tech. 55:249–258, 2001. © 2001 Wiley‐Liss, Inc." @default.
- W2111087016 created "2016-06-24" @default.
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- W2111087016 creator A5062220148 @default.
- W2111087016 creator A5071871570 @default.
- W2111087016 date "2001-11-15" @default.
- W2111087016 modified "2023-10-16" @default.
- W2111087016 title "Oxides and apoptosis in inflammatory myopathies" @default.
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