Effect of Icatibant, a bradykinin B2 receptor antagonist, on the development of experimental ulcerative colitis in mice

被引:28
作者
Arai, Y
Takanashi, H
Kitagawa, H
Wirth, KJ
Okayasu, I
机构
[1] Hoechst Marion Roussel Ltd, Lab Pharmacol Lead Optimization Drug Innovat & Ap, Kawagoe, Saitama 3501165, Japan
[2] Hoechst Marion Roussel Ltd, Project Management & Planning Dept, Kawagoe, Saitama 3501165, Japan
[3] Hoechst Marion Roussel Ltd, TA Cardiovasc Agents, Frankfurt, Germany
[4] Kitasato Univ, Fac Med, Dept Pathol, Kanagawa, Japan
关键词
ulcerative colitis; dextran sulfate sodium; mice; Icatibant; bradykinin;
D O I
10.1023/A:1026694732602
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Dextran sulfate sodium-induced colitis in mice has been recognized as a model for human ulcerative colitis. Using this model, we carried out a study on the preventive effect of Icatibant, a bradykinin B-2 receptor antagonist previously called HOE 140, on the development of colitis. Subcutaneous administration of Icatibant (0.3 or 1.5 mg/kg) significantly suppressed shortening of the large intestine and worsening of the general health. Oral administration of Icatibant (50 mg/kg) significantly suppressed shortening of the large intestine, the onset of diarrhea, and worsening of the general health. In addition, the oral treatment significantly inhibited the development of colitis that was observed histopathologically. These results indicate a role of BK in the development of dextran sulfate sodium-induced colitis in mice, and suggest that BK could be important in human ulcerative colitis.
引用
收藏
页码:845 / 851
页数:7
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