Pentoxifylline attenuates steatohepatitis induced by the methionine choline deficient diet

被引:111
作者
Koppe, SWP
Sahai, A
Malladi, P
Whitington, PF
Green, RM
机构
[1] Northwestern Univ, Feinberg Sch Med, Dept Med, Div Hepatol, Chicago, IL 60611 USA
[2] Northwestern Univ, Feinberg Sch Med, Dept Pediat, Chicago, IL USA
关键词
steatohepatitis; pentoxifylline; TNF-alpha; oxidative stress; methionine choline deficient (MCD) diet;
D O I
10.1016/j.jhep.2004.06.030
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/Aims: Feeding mice a methionine choline deficient (MCD) diet serves as a nutritional model of nonalcoholic steatohepatitis (NASH). NASH and alcohol-induced steatohepatitis are histologically similar, suggesting a similar pathogenesis. Pentoxifylline (PTX) attenuates TNF-alpha production, acts as an antioxidant and decreases mortality in alcoholic steatohepatitis. The aim of our study is to determine if PTX attenuates MCD diet induced steatohepatitis and determine the mechanism of this effect. Methods: Mice were placed on an MCD or control diet for 2 weeks and were treated with or without PTX. Serum ALT, liver histology, and inflammatory mechanisms were evaluated. Results: PTX attenuates MCD diet induced steatohepatitis, decreasing both serum ALT levels and hepatic inflammation. Serum ALT levels were reduced approximately 50% in the MCD+PTX group compared to the MCD group. Hepatic glutathione levels were significantly higher in the MCD+PTX group compared to the MCD group. There was also a reduction in TNF-alpha mRNA in female mice treated with PTX. MCD+PTX mice had increased hepatic triglyceride content compared to the MCD mice, but less histologic evidence of inflammation despite the increased steatosis. Serum lipid and bile salt levels also were similar in PTX and vehicle control treated mice. Conclusions: PTX decreases serum ALT levels and hepatic inflammation in the MCD model of steatohepatitis, likely via increasing glutathione levels or reducing TNF-alpha expression. (C) 2004 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
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收藏
页码:592 / 598
页数:7
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