|Anti-oxidant Effects of Resveratrol on Mice with DSS-induced Ulcerative Colitis|
|Yao, Jun1; Wang, Jian-Yao2; Liu, Lei2; Li, Ying-Xue1; Xun, An-Ying3; Zeng, Wei-Sen4; Jia, Chun-Hong4; Wei, Xiao-Xia1; Feng, Ju-Ling1; Zhao, Li4; Wang, Li-Sheng1|
|关键词||Resveratrol Oxidative damage Cytokines Ulcerative colitis|
|刊名||ARCHIVES OF MEDICAL RESEARCH|
|WOS标题词||Science & Technology|
|类目[WOS]||Medicine, Research & Experimental|
|研究领域[WOS]||Research & Experimental Medicine|
|关键词[WOS]||INFLAMMATORY-BOWEL-DISEASE ; OXIDATIVE STRESS ; VITAMIN-E ; MURINE COLITIS ; CANCER-CELLS ; THERAPY ; RATS ; INFLIXIMAB ; DAMAGE ; PATHOGENESIS|
Background and Aims. Oxidant/antioxidant balance is suggested to be an important factor for the recurrence and progression of ulcerative colitis (UC). The aim of the study is to investigate the potential protective role of resveratrol (Res) against dextran sodium sulfate (DSS)-induced oxidative damage in colon of mice with UC.
Methods. UC was induced in mice by oral administration of synthetic DSS (molecular weight 5000) for 7 days. Mice were divided into normal group, colitis control group, low-dose Res-treated group (RLD-treated group), and high-dose Res-treated group (RHD-treated group). Inhibitory effects of concomitant treatment with Res were assessed daily using a Disease Activity Index (DAI) and severity of histological changes. MDA, MPO, SOD and GSH-PX activity of colonic tissue were determined in colon samples by chemical colorimetry. TNF-alpha, IL-8, IFN-gamma, p22(phox) and gp91(phox) expression levels were detected using quantitative reverse-transcriptase polymerase chain reaction (qRT-PCR), ELISA, and Western blot analysis.
Result. Administration of Res significantly inhibited the severity of UC compared to the colitis control group. Colonic tissue MDA and MPO activities decreased significantly in Res-treated groups compared to colitis control groups. Furthermore, colonic tissue SOD and GSH-Px activities increased significantly in Res-treated groups compared to colitis control groups. The expression levels of TNF-alpha, IL-8, IFN-gamma, p22(phox), and gp91(phox) also decreased significantly in the Res-treated group compared to the colitis control group.
Conclusions. Oral administration of Res exerts marked inhibitory effects on UC in mice. Resveratrol may play an important role in preventing DSS-induced oxidative damage. (C) 2010 IMSS. Published by Elsevier Inc.
|资助机构||Natural Science Foundation of Guangdong Province, China|
|作者单位||1.Jinan Univ Med Sci, Shenzhen Municipal Peoples Hosp, Dept Gastroenterol, Shenzhen 518020, Guangdong, Peoples R China|
2.Jinan Univ Med Sci, Shenzhen Municipal Peoples Hosp, Dept Gen Surg, Shenzhen 518020, Guangdong, Peoples R China
3.Peking Univ, Shenzhen Hosp, Dept Gastroenterol, Shenzhen, Guangdong, Peoples R China
4.So Med Univ, Dept Cell Biol, Guangzhou, Guangdong, Peoples R China
|Yao, Jun,Wang, Jian-Yao,Liu, Lei,et al. Anti-oxidant Effects of Resveratrol on Mice with DSS-induced Ulcerative Colitis[J]. ARCHIVES OF MEDICAL RESEARCH,2010,41(4):288-294.|
|APA||Yao, Jun.,Wang, Jian-Yao.,Liu, Lei.,Li, Ying-Xue.,Xun, An-Ying.,...&Wang, Li-Sheng.(2010).Anti-oxidant Effects of Resveratrol on Mice with DSS-induced Ulcerative Colitis.ARCHIVES OF MEDICAL RESEARCH,41(4),288-294.|
|MLA||Yao, Jun,et al."Anti-oxidant Effects of Resveratrol on Mice with DSS-induced Ulcerative Colitis".ARCHIVES OF MEDICAL RESEARCH 41.4(2010):288-294.|