Beneficial effects of Batimastat (BB-94), a matrix metalloproteinase inhibitor, in rat experimental colitis

被引:64
作者
Di Sebastiano, P [1 ]
di Mola, FF
Artese, L
Rossi, C
Mascetta, G
Pernthaler, H
Innocenti, P
机构
[1] Bolzano Gen Hosp, Dept Surg 1, I-39100 Bolzano, Italy
[2] Lega Tumori, Oncol Mol Lab, Pescara, Italy
[3] Univ G DAnnunzio, Unit Gen & Laparoscop Surg, Chieti, Italy
[4] Univ G DAnnunzio, Dept Pathol, Chieti, Italy
[5] Mario Negri Sud Res Inst, S Maria Imbaro, Italy
关键词
IBD (inflammatory bower diseases); inflammation; metalloproteinases; experimental colitis; Batimastat (BB-94);
D O I
10.1159/000051895
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background and Aims: Matrix metalloproteinases (MMPs) represent a group of enzymes that regulate cell-matrix com position playing a major role in the inflammatory response. In the present study we evaluated the ability of the MMP inhibitor Batimastat (BB-94) to modify the course of experimental colitis induced in the rat by trinitrobenzensulfonic acid (TNB). Methods: Colitis was induced in 40 rats by intracolonic administration of TNB. Animals were divided into four groups of ten rats each: group 1 received only intracolonic TNB, group 2 received TNB+5 mg/kg intraperitoneal BB-94, group 3 TNB+10 mg/kg BB-94 and group 4 TNB+20 mg/kg BB-94. The MMP inhibitor was administered 30 min before induction of colitis and twice daily until death. Ten rats receiving only intracolonic 0.9% saline served as controls. Animals were killed after seven days; segments of colon were removed and used for histological score of inflammation and myeloperoxidase (MPO) activity. Results: Rats receiving only intracolonic 0.9% saline showed no evidence of colitis. The inflammation score was 0.9, MPO activity 0.235 U/mg. Group 1 (TNB-treated rats) exhibited a high inflammation score (12.4) and MPO activity (0.715 U/mg). Conversely, BE-94-treated rats showed, compared to the TNB group, a significantly lower inflammation score and MPO activity in a dose-dependent fashion. Group 2: inflammatory score 10.1, MPO activity 0.474 (p < 0.05 vs. TNB); group 3: inflammatory score 8.3, MPO activity 0.287 (p < 0.01 vs. TNB); group 4: inflammatory score 5.0, MPO activity 0.256 (p < 0.01 vs. TNB). Conclusions: Treatment with BB-94 has dose-dependent beneficial effects on the inflammatory alterations in rat experimental colitis. Thus, the inhibition of MMPs may represent a novel therapeutic approach for treatment of intestinal inflammation. Copyright (C) 2001 S. Karger AG, Basel.
引用
收藏
页码:234 / 239
页数:6
相关论文
共 33 条
[1]   DISTRIBUTION OF THE MATRIX METALLOPROTEINASES STROMELYSIN, GELATINASE-A AND GELATINASE-B, AND COLLAGENASE IN CROHNS-DISEASE AND NORMAL INTESTINE [J].
BAILEY, CJ ;
HEMBRY, RM ;
ALEXANDER, A ;
IRVING, MH ;
GRANT, ME ;
SHUTTLEWORTH, CA .
JOURNAL OF CLINICAL PATHOLOGY, 1994, 47 (02) :113-116
[2]  
Beattie GJ, 1998, CLIN CANCER RES, V4, P1899
[3]   Synergistic upregulation of metalloproteinase-9 by growth factors and inflammatory cytokines:: an absolute requirement for transcription factor NF-κB [J].
Bond, M ;
Fabunmi, RP ;
Baker, AH ;
Newby, AC .
FEBS LETTERS, 1998, 435 (01) :29-34
[4]  
Bramhall SR, 1997, INT J PANCREATOL, V21, P1
[5]  
Di Girolamo N, 1998, EUR J IMMUNOL, V28, P1773, DOI 10.1002/(SICI)1521-4141(199806)28:06<1773::AID-IMMU1773>3.0.CO
[6]  
2-B
[7]   SR140333, a substance P receptor antagonist, influences morphological and motor changes in rat experimental colitis [J].
Di Sebastiano, P ;
Grossi, L ;
Di Mola, FF ;
Angelucci, D ;
Friess, H ;
Marzio, L ;
Innocenti, P ;
Büchler, MW .
DIGESTIVE DISEASES AND SCIENCES, 1999, 44 (02) :439-444
[8]   EXPERIMENTAL-MODELS OF INFLAMMATORY BOWEL-DISEASE [J].
ELSON, CO ;
SARTOR, RB ;
TENNYSON, GS ;
RIDDELL, RH .
GASTROENTEROLOGY, 1995, 109 (04) :1344-1367
[9]  
Goss KJH, 1998, INT J CANCER, V78, P629
[10]   ON THE SPECIFICITY OF ALTERED MUSCLE FUNCTION IN EXPERIMENTAL COLITIS IN RATS [J].
GROSSI, L ;
MCHUGH, K ;
COLLINS, SM .
GASTROENTEROLOGY, 1993, 104 (04) :1049-1056