Journal Article

American ginseng suppresses inflammation and DNA damage associated with mouse colitis

Yu Jin, Venkata S. Kotakadi, Lei Ying, Anne B. Hofseth, Xiangli Cui, Patricia A. Wood, Anthony Windust, Lydia E. Matesic, Edsel A. Pena, Codruta Chiuzan, Narendra P. Singh, Mitzi Nagarkatti, Prakash S. Nagarkatti, Michael J. Wargovich and Lorne J. Hofseth

in Carcinogenesis

Volume 29, issue 12, pages 2351-2359
Published in print December 2008 | ISSN: 0143-3334
Published online September 2008 | e-ISSN: 1460-2180 | DOI: http://dx.doi.org/10.1093/carcin/bgn211

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Ulcerative colitis (UC) is a dynamic, idiopathic, chronic inflammatory condition associated with a high colon cancer risk. American ginseng has antioxidant properties and targets many of the players in inflammation. The aim of this study was to test whether American ginseng extract prevents and treats colitis. Colitis in mice was induced by the presence of 1% dextran sulfate sodium (DSS) in the drinking water or by 1% oxazolone rectally. American ginseng extract was mixed in the chow at levels consistent with that currently consumed by humans as a supplement (75 p.p.m., equivalent to 58 mg daily). To test prevention of colitis, American ginseng extract was given prior to colitis induction. To test treatment of colitis, American ginseng extract was given after the onset of colitis. In vitro studies were performed to examine mechanisms. Results indicate that American ginseng extract not only prevents but it also treats colitis. Inducible nitric oxide synthase and cyclooxygenase-2 (markers of inflammation) and p53 (induced by inflammatory stress) are also downregulated by American ginseng. Mucosal and DNA damage associated with colitis is at least in part a result of an oxidative burst from overactive leukocytes. We therefore tested the hypothesis that American ginseng extract can inhibit leukocyte activation and subsequent epithelial cell DNA damage in vitro and in vivo. Results are consistent with this hypothesis. The use of American ginseng extract represents a novel therapeutic approach for the prevention and treatment of UC.

Journal Article.  7437 words.  Illustrated.

Subjects: Clinical Cytogenetics and Molecular Genetics

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