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American Ginseng Suppresses Colitis through p53-Mediated Apoptosis of …

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American Ginseng Suppresses Colitis through p53-Mediated Apoptosis of Inflammatory Cells

  1. Yu Jin1
  2. Anne B. Hofseth1
  3. Xiangli Cui1
  4. Anthony J. Windust4
  5. Deepak Poudyal1,
  6. Alex A. Chumanevich1
  7. Lydia E. Matesic2
  8. Narendra P. Singh3
  9. Mitzi Nagarkatti3,
  10. Prakash S. Nagarkatti3, and 
  11. Lorne J. Hofseth1

+Author Affiliations

  1. Authors' Affiliations: 1Department of Pharmaceutical and Biomedical Sciences, South Carolina College of Pharmacy, 2Department of Biological Sciences, and 3Department of Pathology and Microbiology, School of Medicine, University of South Carolina, Columbia, South Carolina and 4Institute for National Measurement Standards, National Research Council, Ottawa, Ontario, Canada
  1. Corresponding Author:
    Lorne J. Hofseth, Department of Biomedical and Pharmaceutical Sciences, South Carolina College of Pharmacy, 770 Sumter Street, Coker Life Sciences, Room 513C, University of South Carolina, Columbia, SC 29208. Phone: 803-777-6627/2080; Fax: 803-777-8356; E-mail: hofseth@cop.sc.edu.

Abstract

Ulcerative colitis is a dynamic, chronic inflammatory condition associated with an increased colon cancer risk. Inflammatory cell apoptosis is a key mechanism regulating ulcerative colitis. American ginseng (AG) is a putative antioxidant that can suppress hyperactive immune cells. We have recently shown that AG can prevent and treat mouse colitis. Because p53 levels are elevated in inflammatory cells in both mouse and human colitis, we tested the hypothesis that AG protects from colitis by driving inflammatory cell apoptosis through a p53 mechanism. We used isogenic p53+/+ and p53−/− inflammatory cell lines as well as primary CD4+/CD25 effector T cells from p53+/+ and p53−/− mice to show that AG drives apoptosis in a p53-dependent manner. Moreover, we used a dextran sulfate sodium (DSS) model of colitis in C57BL/6 p53+/+ and p53−/− mice to test whether the protective effect of AG against colitis is p53 dependent. Data indicate that AG induces apoptosis in p53+/+ but not in isogenic p53−/− cells in vitro. In vivo, C57BL/6 p53+/+ mice are responsive to the protective effects of AG against DSS-induced colitis, whereas AG fails to protect from colitis in p53−/− mice. Furthermore, terminal deoxynucleotidyl transferase–mediated dUTP nick end labeling of inflammatory cells within the colonic mesenteric lymph nodes is elevated in p53+/+ mice consuming DSS + AG but not in p53−/− mice consuming DSS + AG. Results are consistent with our in vitro data and with the hypothesis that AG drives inflammatory cell apoptosis in vivo, providing a mechanism by which AG protects from colitis in this DSS mouse model. Cancer Prev Res; 3(3); 339–47 

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