Increased activity and expression of matrix metalloproteinase-9 in a rat model of distal colitis

被引:76
作者
Medina, C
Videla, S
Radomski, A
Radomski, MW
Antolín, M
Guarner, F
Vilaseca, J
Salas, A
Malagelada, JR
机构
[1] Univ Alberta, Dept Pharmacol, Edmonton, AB T6G 2H7, Canada
[2] Hosp Mutua Terrassa, Dept Pathol, Barcelona 08221, Spain
[3] Hosp Gen Valle Hebron, Digest Dis Res Unit, Barcelona 08035, Spain
来源
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY | 2003年 / 284卷 / 01期
关键词
gelatinases; inflammatory bowel disease; matrix metalloproteinase inhibitors; dextran sulphate sodium;
D O I
10.1152/ajpheart.00036.2002
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Matrix metalloproteinases may play a role in tissue remodelling and destruction associated with inflammation. We investigated activity and expression of matrix metalloproteinases in a rat model of colitis and tested the therapeutic potential of a synthetic inhibitor (CGS-27023-A). Colitis was induced by dextran sulphate sodium (at 5% in drinking water for 5 days) in a group of eight rats, whereas a matched control group received plain water. Activity and expression of matrix metalloproteinases were measured in colonic tissue homogenates using zymography and Western blot on days 3 and 5 after induction of colitis. In another set of experiments, two groups of colitic rats (20 per group) were treated with CGS-27023-A (20 mg/kg) or vehicle, respectively. On days 5 and 14, colonic mucosal lesions were blindly scored by microscopic examination. Induction of colitis led to a significant upregulation of matrix metalloproteinase-9 protein and its activity, but no change in matrix metalloproteinase-2 activity was observed. Treatment with CGS-27023-A significantly decreased the extent and severity of epithelial injury but did not influence mucosal repair. We conclude that increased activity of matrix metalloproteinases may contribute to epithelial damage in this model of colitis.
引用
收藏
页码:G116 / G122
页数:7
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