Basic Research
Copyright ©The Author(s) 2004. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. May 1, 2004; 10(9): 1329-1332
Published online May 1, 2004. doi: 10.3748/wjg.v10.i9.1329
Peroxisome proliferator activated receptor-γ in pathogenesis of experimental fatty liver disease
Cai-Yan Zhao, Ling-Ling Jiang, Li Li, Zhuo-Jun Deng, Bao-Li Liang, Jian-Mei Li
Cai-Yan Zhao, Ling-Ling Jiang, Department of Biochemistry, Hebei Medical University, Shijiazhuang 050017, Hebei Province, China
Li Li, Zhuo-Jun Deng, Bao-Li Liang, Jian-Mei Li, Department of Liver Disease, Third Affiliated Hospital of Hebei Medical University, Shijiazhuang 050051, Hebei Province, China
Author contributions: All authors contributed equally to the work.
Correspondence to: Ling-Ling Jiang, Department of Biochemistry, Hebei Medical University, Shijiazhuang 050017, Hebei Province, China. zhaoyy63811@sohu.com
Telephone: +86-13313012898
Received: October 29, 2003
Revised: December 20, 2003
Accepted: February 8, 2004
Published online: May 1, 2004
Abstract

AIM: To study the expression of peroxisome proliferator activated receptor-γ (PPARγ) in the liver of rats with fatty liver disease (FLD) and to explore the role of PPARγ in the pathogenesis of FLD to provide the basis for using PPARγ ligand to treat patients with FLD.

METHODS: Forty Wistar rats were divided into 4 groups of ten rats each randomly: normal group (group A), alcohol group (group B), fat-rich diet group (group C), alcohol and fat-rich diet group (group D). The rats were sacrificed at the end of the 16th week from the feeding day. Alanine aminotransferase (ALT), tumor necrosis factor-alfa (TNFα) in serum and malondialdehyde (MDA) in liver homogenate were determined; livers were collected for observing pathologic changes by HE, Sudan IV, Masson stain under microscope. The morphologic results were analyzed by picture quantitative analysis technique. The changes of ultrastructure were also examined under electron microscope. The expression of PPARγ in liver was detected by immunoh-istochemistry and RT-PCR. The correlations between the expression of PPARγ and biochemical indexes, and liver histology were analyzed.

RESULTS: The steatosis, inflammation, necrosis and fibrosis were present in livers of different experimental groups, especially in livers of alcohol and fat-rich diet group. The content of immunodetectable PPARγ was decreased remarkably in the livers of model rats (group B-D); the level in alcohol and fat-rich diet group (3.43 ± 1.48) was significantly lower than that in normal group (18.34 ± 3.73), alcohol group (8.82 ± 2.52) and fat-rich diet group (11.73 ± 2.51) (all P < 0.01). The level of PPARγ mRNA was also lower in the livers of model rats (group B-D) than in livers of controls. The expression of PPARγ in rat liver correlated negatively with the degree of its inflammation, necrosis and fibrosis, as well as the level of serum TNFα and the content of MDA in liver homogenates, but not with steatosis or serum ALT.

CONCLUSION: Decreased expression of PPARγ may play an important role in the development of hepatocellular inflammation, necrosis and fibrosis of rats with FLD. Thus, activating PPARγ by its ligand can be anticipated to provide a therapy target for FLD.

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