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| Research article summary (published 14 May 2008): |
Dietary resveratrol administration increases MnSOD expression and activity in mouse brain.
Full Abstract
trans-Resveratrol (3,4',5-trihydroxystilbene; RES) is of interest for its reported protective effects in a variety of pathologies, including neurodegeneration. Many of these protective properties have been attributed to the ability of RES to reduce oxidative stress. In vitro studies have shown an increase in antioxidant enzyme activities following exposure to RES, including upregulation of mitochondrial superoxide dismutase, an enzyme that is capable of reducing both oxidative stress and cell death. We sought to determine if a similar increase in endogenous antioxidant enzymes is observed with RES treatment in vivo. Three separate modes of RES delivery were utilized; in a standard diet, a high fat diet and through a subcutaneous osmotic minipump. RES given in a high fat diet proved to be effective in elevating antioxidant capacity in brain resulting in an increase in both MnSOD protein level (140%) and activity (75%). The increase in MnSOD was not due to a substantial proliferation of mitochondria, as RES treatment induced a 10% increase in mitochondrial abundance (Citrate Synthase activity). The potential neuroprotective properties of MnSOD have been well established, and we demonstrate that a dietary delivery of RES is able to increase the expression and activity of this enzyme in vivo.
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Author information
Author/s: Robb, Ellen L (EL); Winkelmolen, Lieke (L); Visanji, Naomi (N); Brotchie, Jonathan (J); Stuart, Jeffrey A (JA);
Affiliation: Department of Biological Sciences, Brock University, 500 Glenridge Road, St. Catharines, Ont., Canada.
Journal and publication information
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal: Biochemical and biophysical research communications (Biochem Biophys Res Commun), published in United States. (Language: eng)
Reference: 2008-Jul; vol 372 (issue 1) : pp 254-9
Dates: Created 2008/06/09; Completed 2008/06/20;
PMID: 18486604, status: MEDLINE (last retrieval date: 11/6/2008)
Sourced from the National Library of Medicine. Abstract text and other information may be subject to copyright.
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