Inhibition of NF-κB Activation by 4-Hydroxynonenal Contributes to Liver Injury in a Mouse Model of Alcoholic Liver Disease

被引:42
作者
Dou, Xiaobing [1 ,3 ]
Li, Songtao [1 ]
Wang, Zhigang [1 ,4 ]
Gu, Dongfang [1 ,4 ]
Shen, Chen [1 ]
Yao, Tong [1 ]
Song, Zhenyuan [1 ,2 ]
机构
[1] Univ Illinois, Dept Kinesiol & Nutr, Chicago, IL 60612 USA
[2] Univ Illinois, Med Ctr, Dept Pathol, Chicago, IL 60612 USA
[3] Zhejiang Chinese Med Univ, Coll Life Sci, Dept Mol Biol, Hangzhou, Zhejiang, Peoples R China
[4] Harbin Med Univ, Coll Pharm, Dept Biochem Pharmacol, Harbin, Peoples R China
关键词
TUMOR-NECROSIS-FACTOR; DIETARY SATURATED FAT; LIPID-PEROXIDATION; FACTOR-ALPHA; OXIDATIVE STRESS; ETHANOL; MICE; RATS; INDUCTION; IRON;
D O I
10.1016/j.ajpath.2012.08.004
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Long-term alcohol exposure sensitizes hepatocytes to tumor necrosis factor-alpha (TNF) cytotoxicity. 4-Hydroxynonenal (4-HNE) is one of the most abundant and reactive lipid peroxides. Increased hepatic 4-HNE contents present in both human alcoholics and alcohol-fed animals. In the present study, we investigated the effects of intracellular 4-HNE accumulation on TNF-induced hepatotoxicity and its potential implication in the pathogenesis of alcoholic liver disease. Male C578L/6 mice were fed an ethanol-containing or a control diet for 5 weeks. Long-term alcohol exposure increased hepatic 4-HNE and TNF levels. Cell culture studies revealed that 4-HNE, at nontoxic concentrations, sensitized hepatocytes to TNF killing, which was associated with suppressed NF-kappa B transactivity. Further investigation demonstrated that 4-HNE prevented TNF-induced inhibitor of KB alpha phosphorylation without affecting upstream I kappa B kinase activity. An immunoprecipitation assay revealed that increased 4-HNE content was associated with increased formation of 4-HNE inhibitor of KBa adduction in both 4-HNE treated hepatocytes and in the livers of alcohol-fed mice. Prevention of intracellular 4-HNE accumulation by bezafibrate, a peroxisome proliferator-activated receptor-alpha agonist, protected hepatocytes from TNF killing via NF-kappa B activation. Supplementation of N-acetylcysteine, a glutathione precursor, conferred a protective effect on alcohol-induced liver injury in mice, was associated with decreased hepatic 4-HNE formation, and improved hepatic NF-kappa B activity. In conclusion, increased 4-HNE accumulation represents a potent and clinically relevant sensitizer to TNF-induced hepatotoxicity. These data support the notion that removal of intracellular 4-HNE can serve as a potential therapeutic option for alcoholic liver disease. (Am J Pathol 2012, 181:1702-1710; http://dx.doi.org/10.1016/j.ajpath.2012.08.004)
引用
收藏
页码:1702 / 1710
页数:9
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