Intestinal anti-inflammatory activity of UR-12746, a novel 5-ASA conjugate, on acute and chronic experimental colitis in the rat

被引:40
作者
Gálvez, J
Garrido, M
Merlos, M
Torres, MI
Zarzuelo, A
机构
[1] Univ Granada, Sch Pharm, Dept Pharmacol, E-18071 Granada, Spain
[2] J Uriach & Cia Res Ctr, Dept Pharmacol, Barcelona 08026, Spain
[3] Univ Granada, Sch Sci, Dept Cellular Biol, E-18071 Granada, Spain
关键词
UR-12746; 5-ASA; UR-12715; intestinal anti-inflammatory activity; TNBS-induced rat colitis; PAF antagonist;
D O I
10.1038/sj.bjp.0703505
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1 The present study was undertaken to investigate the intestinal anti-inflammatory effects of UR-12746 on the acute and chronic stages of a trinitrobenzene sulphonic acid (TNBS) experimental model of inflammatory bowel disease (IBD) in the rat. UR-12746 is a novel, locally-acting compound which combines, through an azo bond, 5-aminosalicylic (5-ASA) and UR-12715, a potent platelet activating factor (PAF)-antagonist. 2 UR-12746 oral pretreatment of colitic rats (50 and 100 mg kg(-1)) reduced acute colonic damage when evaluated 2 days after colonic insult. 3 Postreatment for 4 weeks with UR-12746 (50 and 100 mg kg(-1)) resulted in a faster recovery of the damaged colonic mucosa, which was macroscopically significant from the third week. 4 The intestinal anti-inflammatory effect of UR-12746 was associated with a decrease in leukocyte infiltration in the colonic mucosa, which was evidenced both biochemically, by a reduction in myeloperoxidase activity, and histologically, by a lower leukocyte count after morphometric analysis. This effect was higher than that seen with sulphasalazine, when assayed at the same doses and in the same experimental conditions. 5 Several mechanisms can be involved in the beneficial effects showed by UR-12746: inhibition of leukotriene Bq synthesis in the inflamed colon, improvement of the altered colonic oxidative status, and reduction of colonic interleukin-1 beta production. 6 The results suggest that the intestinal anti-inflammatory activity of UR-12746 can be attributed to the additive effects exerted by 5-ASA and UR-12715, the PAF antagonist compound, that are released in the colonic lumen after reduction of the azo bond by the intestinal bacteria.
引用
收藏
页码:1949 / 1959
页数:11
相关论文
共 41 条
[1]  
ANDERSON ME, 1985, METHOD ENZYMOL, V113, P548
[2]   Prolonged colonic epithelial hyporesponsiveness after colitis: role of inducible nitric oxide synthase [J].
Asfaha, S ;
Bell, CJ ;
Wallace, JL ;
MacNaughton, WK .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 1999, 276 (03) :G703-G710
[3]   THE EFFECTS OF PAF-ACETHER ON THE CARDIOVASCULAR-SYSTEM AND THEIR INHIBITION BY A NEW HIGHLY SPECIFIC PAF-ACETHER RECEPTOR ANTAGONIST BN 52021 [J].
BARANES, J ;
HELLEGOUARCH, A ;
LEHEGARAT, M ;
VIOSSAT, I ;
AUGUET, M ;
CHABRIER, PE ;
BRAQUET, P ;
BRAQUET, F .
PHARMACOLOGICAL RESEARCH COMMUNICATIONS, 1986, 18 (08) :717-737
[4]   DISRUPTION OF COLONIC ELECTROLYTE TRANSPORT IN EXPERIMENTAL COLITIS [J].
BELL, CJ ;
GALL, DG ;
WALLACE, JL .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 1995, 268 (04) :G622-G630
[5]  
CASALSSTENZEL J, 1987, J PHARMACOL EXP THER, V241, P974
[6]  
DeMedina FS, 1996, J PHARMACOL EXP THER, V278, P771
[7]   Drug therapy of inflammatory bowel disease [J].
Egan, LJ ;
Sandborn, WJ .
DRUGS OF TODAY, 1998, 34 (05) :431-446
[8]   ROLE OF PLATELET-ACTIVATING FACTOR IN ULCERATIVE-COLITIS - ENHANCED PRODUCTION DURING ACTIVE DISEASE AND INHIBITION BY SULFASALAZINE AND PREDNISOLONE [J].
ELIAKIM, R ;
KARMELI, F ;
RAZIN, E ;
RACHMILEWITZ, D .
GASTROENTEROLOGY, 1988, 95 (05) :1167-1172
[9]  
ESTERBAUER H, 1990, METHOD ENZYMOL, V186, P407
[10]   INTESTINAL EPITHELIAL-CELLS CONTRIBUTE TO THE ENHANCED GENERATION OF PLATELET-ACTIVATING-FACTOR IN ULCERATIVE-COLITIS [J].
FERRARIS, L ;
KARMELI, F ;
ELIAKIM, R ;
KLEIN, J ;
FIOCCHI, C ;
RACHMILEWITZ, D .
GUT, 1993, 34 (05) :665-668