Induction of CYP2E1 in non-alcoholic fatty liver diseases

被引:73
作者
Aljomah, Ghanim [1 ]
Baker, Susan S. [1 ]
Liu, Wensheng [1 ]
Kozielski, Rafal [2 ]
Oluwole, Janet [1 ]
Lupu, Benita [1 ]
Baker, Robert D. [1 ]
Zhu, Lixin [1 ]
机构
[1] SUNY Buffalo, Digest Dis & Nutr Ctr, Women & Childrens Hosp Buffalo, Dept Pediat, Buffalo, NY 14214 USA
[2] SUNY Buffalo, Dept Pathol, Women & Childrens Hosp Buffalo, Buffalo, NY 14214 USA
基金
美国国家卫生研究院;
关键词
CYP2E1; NASH; NAFLD; Simple steatosis; HEPATIC CYTOCHROME-P450 2E1; HUMAN HEPATOCYTES; ETHANOL; STEATOHEPATITIS; PATHOGENESIS; INFLAMMATION; STEATOSIS; ALCOHOL; SYSTEM; HITS;
D O I
10.1016/j.yexmp.2015.11.008
中图分类号
R36 [病理学];
学科分类号
100103 [病原生物学];
摘要
Mounting evidence supports a contribution of endogenous alcohol metabolism in the pathogenesis of nonalcoholic steatohepatitis (NASH). However, it is not known whether the expression of alcohol metabolism genes is altered in the livers of simple steatosis. There is also a current debate on whether fatty acids induce CYP2E1 in fatty livers. In this study, expression of alcohol metabolizing genes in the liver biopsies of simple steatosis patients was examined by quantitative real-time PCR (gRT-PCR), in comparison to biopsies of NASH livers and normal controls. Induction of alcohol metabolizing genes was also examined in cultured HepG2 cells treated with ethanol or oleic acid, by gRT-PCR and Western blots. We found that the mRNA expression of alcohol metabolizing genes including ADH1C, ADH4, ADH6, catalase and CYP2E1 was elevated in the livers of simple steatosis, to similar levels found in NASH livers. In cultured HepG2 cells, ethanol induced the expression of CYP2E1 mRNA and protein, but not ADH4 or ADH6; oleic acid did not induce any of these genes. These results suggest that elevated alcohol metabolism may contribute to the pathogenesis of NAFLD at the stage of simple steatosis as well as more severe stages. Our in vitro data support that CYP2E1 is induced by endogenous alcohol but not by fatty acids. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:677 / 681
页数:5
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