Basic Research
Copyright ©The Author(s) 2004. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Dec 15, 2004; 10(24): 3621-3627
Published online Dec 15, 2004. doi: 10.3748/wjg.v10.i24.3621
Dynamic changes in the expression of matrix metalloproteinases and their inhibitors, TIMPs, during hepatic fibrosis induced by alcohol in rats
Guang-Fu Xu, Peng-Tao Li, Xin-Yue Wang, Xu Jia, De-Lu Tian, Liang-Duo Jiang, Jin-Xiang Yang
Guang-Fu Xu, Department of infectious Diseases, 1st Affiliated Dongzhimen Hospital, Beijing University of Traditional Chinese Medicine, Beijing 100700, China
Xin-Yue Wang, De-Lu Tian, Liang-Duo Jiang, Jin-Xiang Yang, Department of Digestive Diseases, 1st Affiliated Dongzhimen Hospital, Beijing University of Traditional Chinese Medicine, Beijing 100700, China
Peng-Tao Li, Xu Jia, Basic Medicine College of Beijing University of Traditional Chinese Medicine, Beijing 100029, China
Author contributions: All authors contributed equally to the work.
Correspondence to: Director. Guang-Fu Xu, Department of Infectious Diseases, 1st Affiliated Dongzhimen Hospital, Beijing University of Tradi-tional Chinese Medicine, Beijing 100700, China. guangfuxu@hotmail.com
Telephone: +86-10-84290755
Received: September 7, 2003
Revised: October 28, 2003
Accepted: November 6, 2003
Published online: December 15, 2004
Abstract

AIM: To determine the dynamic changes in the expression of matrix metalloproteinases (MMPs) and the endogenous tissue inhibitors of MMPs inhibitors (TIMPs) during hepatic fibrosis induced by alcohol.

METHODS: Male Sprague-Dawley rats were randomly divided into normal, 4 d, 2 wk, 4 wk, 9 wk and 11 wk groups, and the model rats were fed with a mixture of alcohol by gastric infusion at the designed time, respectively, then decollated and their livers were harvested for the examination of MMP-2, MMP-3, MMP-9, MMP-13, TIMP-1 and TIMP-2 by immunoh-istochemistry, zymograghy and Western blotting, respectively.

RESULTS: Normal rats had moderate expression of MMP-2, which was decreased in the model rats except in the 11 wk group, where MMP-2 expression slightly increased. MMP-3 had the similar changing pattern to MMP-2 despite weaker expression. MMP-9 expression decreased in the 4 d and 2 wk groups, rose in the 4 wk group, decreased again in the 9 wk group and returned to normal levels in the 11 wk group. MMP-13 expression decreased in the 4 d and 2 wk groups, and returned to normal levels in the 4 wk, 9 wk and 11 wk groups. TIMP-1 expression decreased in the 4 d and 2 wk groups, but sharply increased in the 4 wk group and sustained at a high level even after modeling was stopped for 2 wk. In normal rats TIMP-2 expression was strong. However, it decreased as soon as modeling began, and then gradually rose, but remained to a level lower than that in normal rats even after modeling was stopped for 2 wk.

CONCLUSION: MMP-2 may not always expresses at a high level during hepatic fibrosis. MMP-13 and MMP-3 are acutely affected by TIMP-1. In this model TIMP-1 is the most powerful factor imposed on capillarization and peri-sinusoidal fibrosis. TIMP-2 is the most effective regulator on the metabolism of type IV collagen located in the basement of sinus.

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