Ursodeoxycholic acid ameliorates experimental ileitis counteracting intestinal barrier dysfunction and oxidative stress

被引:36
作者
Bernardes-Silva, CF
Damiao, AOMC
Sipahi, AM
Laurindo, FRM
Iriya, K
Lopasso, FP
Buchpiguel, CA
Lordello, MLL
Agostinho, CLO
Laudanna, AA
机构
[1] Univ Sao Paulo, Sch Med, Dept Gastroenterol, Lab Invest Med 07, BR-05403900 Sao Paulo, Brazil
[2] Univ Sao Paulo, Sch Med, Dept Pathol, BR-05403900 Sao Paulo, Brazil
[3] Univ Sao Paulo, Sch Med, Dept Radiol, BR-05403900 Sao Paulo, Brazil
[4] Univ Sao Paulo, Sch Med, Heart Inst InCor, BR-05403900 Sao Paulo, Brazil
基金
巴西圣保罗研究基金会;
关键词
ursodeoxycholic acid; indomethacin; intestinal permeability; oxidative stress;
D O I
10.1023/B:DDAS.0000043365.39251.6e
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The aim of this study was to evaluate the effect of ursodeoxycholic acid ( UDCA) on intestinal permeability (IP) and reactive oxygen species (ROS) generation in indomethacin-induced enteropathy, a well-known experimental model of Crohn's disease. Seventy-eight male Wistar rats were randomly assigned to receive indomethacin, indomethacin C UDCA, or vehicles. Indomethacin induced a significant increase in the fraction of urinary excretion of Cr-51-EDTA following oral administration (7.9 +/- 1.3 vs 2.3 +/- 0.2%; P < 0.05) and lucigenin-amplified chemiluminescence in intestinal fragments ex vivo (10.1 +/- 1.9 vs 2.6 +/- 0.4 cpm x 10(3)/mg; P < 0.05) compared to controls. UDCA significantly reversed these effects (P < 0.05), without being incorporated in biliary bile acid composition (HPLC analysis). These findings support a local protective effect of UDCA in experimental ileitis by the modulation of intestinal barrier dysfunction and oxidative stress. In short, they provide insights into mechanisms of action of UDCA in intestinal inflammation and a new perspective on the treatment of Crohn's disease.
引用
收藏
页码:1569 / 1574
页数:6
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