Brief Article
Copyright ©2012 Baishideng Publishing Group Co., Limited. All rights reserved.
World J Gastroenterol. Dec 21, 2012; 18(47): 7063-7069
Published online Dec 21, 2012. doi: 10.3748/wjg.v18.i47.7063
Protective role of metalloproteinase inhibitor (AE-941) on ulcerative colitis in rats
Jing-Wei Mao, Xiao-Mei He, Hai-Ying Tang, Ying-De Wang
Jing-Wei Mao, Xiao-Mei He, Ying-De Wang, Department of Gastroenterology, the First Affiliated Hospital of Dalian Medical University, Dalian 116011, Liaoning Province, China
Hai-Ying Tang, Department of Respiratory Medicine, the First Affiliated Hospital of Dalian Medical University, Dalian 116011, Liaoning Province, China
Author contributions: Wang YD initiated the study, participated in its design, reviewed the article and gave the final approval; Mao JW and He XM performed the majority of experiments; Mao JW and Tang HY wrote the paper and did the statistical analysis.
Supported by Grants from Fund of the Education Department, Liaoning Province
Correspondence to: Ying-De Wang, Professor, Department of Gastroenterology, the First Affiliated Hospital of Dalian Medical University, 222 Zhongshan Road, Dalian 116011, Liaoning Province, China. albertwyd@yahoo.com.cn
Telephone: +86-411-83635963 Fax: +86-411-83632844
Received: March 13, 2012
Revised: June 12, 2012
Accepted: July 9, 2012
Published online: December 21, 2012
Abstract

AIM: To evaluate the protective role of AE-941, a matrix metalloproteinase (MMP) inhibitor, on ulcerative colitis (UC) in rats.

METHODS: Sprague Dawley (SD) rats were randomly divided into three groups: a control group, an AE-941 treatment group, and an UC model group. Rats were sacrificed on days 7, 21, or 56 following administration of treatment by enema and the disease activity index (DAI), colonic mucosa damage index (CMDI) and colonic expression of MMP-2 and MMP-9 were assessed.

RESULTS: DAI and CDMI scores in the UC model group increased significantly compared to the control group at all timepoints (P < 0.001), and also increased significantly at the 21- and 56-d timepoints compared to the AE-941-treated group (DAI: 21- and 56-d = 2.09 ± 0.25, 1.52 ± 0.30 vs 1.55 ± 0.28, 0.59 ± 0.19, respectively, P = 0.040 and 0.007, CMDI: 21- and 56-d = 3.03 ± 0.42, 1.60 ± 0.35 vs 2.08 ± 0.46, 0.86 ± 0.37, respectively, P = 0.040 and 0.005). Furthermore, the colonic expression of MMP-2 and MMP-9 in the UC model group increased significantly compared to the control group (P < 0.001), and also increased compared to the AE-941-treated group on the 21- and 56-d timepoints (MMP-2: 21- and 56-d = 0.6048 ± 0.0522, 0.4163 ± 0.0330 vs 0.3983 ± 0.0218, 0.1093 ± 0.0072, respectively, P = 0.010; MMP-9: 21- and 56-d = 0.6873 ± 0.0472, 0.4328 ± 0.0257 vs 0.5179 ± 0.0305, 0.2673 ± 0.0210, respectively, P = 0.010 and 0.040).

CONCLUSION: Expression of MMP-2 and MMP-9 increased significantly in rats with UC. AE-941 can reduce colonic mucosal damage by downregulating the expression of MMP-2 and MMP-9.

Keywords: AE-941, Extracellular matrix, Matrix metalloproteinase-2, Matrix metalloproteinase-9, Ulcerative colitis