• DocumentCode
    2515519
  • Title

    Oxyresveratrol from Ramulus mori Attenuates Alloxan-Induced Liver Damage in Mice

  • Author

    Zhang, Zuo-fa ; Lv, Guo-ying ; Shi, Lian-gen ; Pan, Hui-juan ; Wu, Yong-zhi ; Fan, Lei-fa

  • Author_Institution
    Inst. of Horticulture, Zhejiang Acad. of Agric. Sci., Hangzhou, China
  • fYear
    2009
  • fDate
    11-13 June 2009
  • Firstpage
    1
  • Lastpage
    4
  • Abstract
    The protective effect of oxyresveratrol from Ramulus mori against alloxan induced liver damage in mice was examined. In this study, the activities of serum aspartate aminotransferase, serum alanine aminotransferase and superoxide dismutase, catalase and the contents of malonyldialdehyde and reduced glutathione in liver were measured. Mice were divided into five groups as control, model control (only treated with alloxan), alloxan+25 mg/kg oxyresveratrol, alloxan+50 mg/kg oxyresveratrol and alloxan+30 mg/kg silymarin. The results revealed that alloxan could induce the liver damage through the elevation of transaminases activities and malondialdehyde accompanied by significant reductions in reduced glutathione level and superoxide dismutase and catalase activities. The treatment with oxyresveratrol can bring those changes to near normal level. The protective effect of oxyresveratrol was further supported by the histopathological observation and the expression of pro-inflammatory cytokines.
  • Keywords
    drugs; enzymes; liver; molecular biophysics; proteins; Ramulus mori; alloxan-induced liver damage; catalase; glutathione level reduction; histopathological observation; malonyldialdehyde; oxyresveratrol; proinflammatory cytokines; serum alanine aminotransferase; serum aspartate aminotransferase; superoxide dismutase; transaminases activity; Amino acids; Animals; Blood; Diabetes; Educational institutions; Liver; Mice; Pancreas; Protection; Stress;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Bioinformatics and Biomedical Engineering , 2009. ICBBE 2009. 3rd International Conference on
  • Conference_Location
    Beijing
  • Print_ISBN
    978-1-4244-2901-1
  • Electronic_ISBN
    978-1-4244-2902-8
  • Type

    conf

  • DOI
    10.1109/ICBBE.2009.5163163
  • Filename
    5163163