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
Link To Document :
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