Therapeutic effects of the endothelin receptor antagonist Ro 48-5695 in the TNBS/DNBS rat model of colitis

被引:22
作者
Padol, I [1 ]
Huang, JQ [1 ]
Hogaboam, CM [1 ]
Hunt, RH [1 ]
机构
[1] McMaster Univ, Hlth Sci Ctr, Dept Gastroenterol, Intestinal Dis Res Programme, Hamilton, ON L8N 3Z5, Canada
关键词
bosentan; colitis; endothelins; inflammatory bowel disease; therapy;
D O I
10.1097/00042737-200012030-00001
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Objective Endothelins can act as polyfunctional cytokines. It is therefore possible that endothelins could play an active role in gut inflammation. Elevated levels of endothelin-1 have been reported in ulcerative colitis and Crohn's disease. The aim of this study was to establish the therapeutic effect of a 'new' endothelin receptor antagonist Ro 48-5695 in an animal model of inflammatory bowel disease, This study compares the effect of Ro 48-5695 on colonic damage induced by two haptens: trinitrobenzenesulphonic (TNBS) or dinitrobenzenesulphonic acid (DNBS). Methods Colitis was induced by intra-rectal administration of TNBS or DNBS. After TNBS/DNBS injury, rats were treated with 10.0, 3.0, 1.0 or 0.3 mg/kg of Ro 48-5695 orally, daily for 5 days, On day 6 post-hapten treatment, colonic tissues were removed and examined in a blinded fashion for macroscopic damage (damage score) and myeloperoxidase (MPO) activity. Stool consistency and adhesions were also measured. Results Oral administration of Ro 48-5695 almost completely prevented TNBS-induced damage at a dose of 10 mg/kg. The same dose in this model also had a therapeutic effect as measured by MPO and incidence of diarrhoea and adhesions. In ONES-induced colonic damage, pc 48-5695 was more potent and at 1.0 and 3.0 mg/kg decreased the damage score by 50 and 60% respectively; also the incidence of adhesions and diarrhoea was significantly reduced. However, MPO activity in this model was affected only by the highest dose of Ro 48-5695 tested (3.0 mg/kg) where it was reduced by 48%. Conclusions These data provide evidence for the involvement of endothelins in the pathophysiology of inflammatory bowel disease and support the possibility of exploring a new therapeutic approach. Eur J Gastroenterol Hepatol 12:257-265 (C) 2000 Lippincott Williams & Wilkins.
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页码:257 / 265
页数:9
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