Basic Research
Copyright ©2005 Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Nov 7, 2005; 11(41): 6483-6488
Published online Nov 7, 2005. doi: 10.3748/wjg.v11.i41.6483
Pathological mechanisms of alcohol-induced hepatic portal hypertension in early stage fibrosis rat model
Jian Li, Jian-Zhao Niu, Ji-Feng Wang, Yu Li, Xiao-Hua Tao
Jian Li, Jian-Zhao Niu, Ji-Feng Wang, Yu Li, Xiao-Hua Tao, Cell Biochemistry Laboratory, Basic Medicine College, Beijing University of Traditional Chinese Medicine, Beijing 100029, China
Author contributions: All authors contributed equally to the work.
Supported by National Natural Science Foundation of China, No. 30130220 and Program for Changjiang Scholars and Innovative Research Team in University (2004)
Correspondence to: Jian-Zhao Niu, Basic Medicine College, Beijing University of Traditional Chinese Medicine, Beijing 100029, China. niujjzz@263.net
Telephone: +86-10-64287538 Fax: +86-10-64286716
Received: May 9, 2005
Revised: June 21, 2005
Accepted: June 24, 2005
Published online: November 7, 2005
Abstract

AIM: To study the role of hepatic sinusoidal capillarization and perisinusoidal fibrosis in rats with alcohol-induced portal hypertension and to discuss the pathological mechanisms of alcohol-induced hepatic portal hypertension.

METHODS: Fifty SD rats were divided into control group (n=20) and model group (n=30). Alcoholic liver fibrosis rat model was induced by intragastric infusion of a mixture containing alcohol, corn oil and pyrazole (1 000:250:3). Fifteen rats in each group were killed at wk 16. The diameter and pressure of portal vein were measured. Plasma hyaluronic acid (HA), type IV collagen (CoIV) and laminin (LN) were determined by radioimmunoassay. Liver tissue was fixed in formalin (10%) and 6-μm thick sections were routinely stained with Mallory and Sirius Red. Liver tissue was treated with rabbit polyclonal antibody against LN and ColIV. Hepatic non-parenchymal cells were isolated, total protein was extracted and separated by SDS-PAGE. MMP-2 and TIMP-1 protein expression was estimated by Western blotting.

RESULTS: The diameter (2.207 ± 0.096 vs 1.528 ± 0.054 mm, P<0.01) and pressure (11.014±0.395 vs 8.533±0.274 mmHg, P<0.01) of portal vein were significantly higher in model group than those in the control group. Plasma HA (129.97±16.10 vs 73.09±2.38 ng/mL, P<0.01), ColIV (210.49±4.36 vs 89.65±4.42 ng/mL, P<0.01) and LN (105.00±7.29 vs 55.70±4.32 ng/mL, P<0.01) were upregulated in model group. Abundant collagen deposited around the central vein of lobules, hepatic sinusoids and hepatocytes in model group. ColI and ColIII increased remarkably and perisinusoids were almost surrounded by ColIII. Immunohistochemical staining showed that ColIV protein level (0.130±0.007 vs 0.032±0.004, P<0.01) and LN protein level (0.152±0.005 vs 0.029±0.005, P<0.01) were up-regulated remarkably in model group. MMP-2 protein expression (2.306±1.089 vs 0.612±0.081, P<0.01) and TIMP-1 protein expression (3.015±1.364 vs 0.446±0.009, P<0.01) in freshly isolated hepatic non-parenchymal cells were up-regulated in model group and TIMP-1 protein expression was evidently higher than MMP-2 protein expression (2.669±0.170 vs 1.695±0.008, P<0.05).

CONCLUSION: Hepatic sinusoidal capillarization and peri-sinusoidal fibrosis are responsible for alcohol-induced portal hypertension in rats.

Keywords: Alcoholic liver fibrosis, Portal hypertension, Hepatic sinusoidal capillarization, Perisinusoidal fibrosis