Establishment of an alcoholic fatty liver disease model in mice

ABSTRACT

Background: Alcoholic fatty liver disease (AFLD) defines an important stage in the progression of alcoholic liver disease (ALD), which is a major cause of morbidity and mortality worldwide. Objective: To establish a mouse model of AFLD. Methods: Male C57BL/6 mice were divided into the following two groups: (i) a control group, which was allowed free access to food and water and (ii) an alcohol-treated group, which was administered a 15% (v/v) alcohol solution instead of water. After 8–9 months of treatment, serum biochemical indexes, histopathological changes, liver triglyceride content, iron storage, and ferritin light chain protein expression were measured using an automatic biochemical analyzer, hematoxylin–eosin (HE) staining, a commercially available kit, Prussian blue staining, and Western blot analysis, respectively. Results: Compared with the control group, the alcohol-treated group displayed increased levels of serum LDH, ALT, and AST, decreased levels of ALB, and no significant change in levels of TP. Additionally, increased levels of serum TG, T-CHO, and LDL and decreased levels of serum GLU and HDL were observed in the alcohol-treated mice. HE staining showed that lipid vacuolization occurred in the livers of alcohol-treated mice. The alcohol-treated mice also exhibited increased liver triglyceride content. Moreover, Prussian blue staining and Western blot analysis demonstrated that chronic alcohol administration caused iron overloading of the liver. Conclusions: Chronic administration of 15% (v/v) alcohol in the drinking water over 8–9 months caused AFLD in mice. Our results establish an AFLD model that represents a promising tool for the future study of the progression of ALD.

KEYWORDS:

• Alcoholic fatty liver disease (AFLD)
• alcoholic liver disease (ALD)
• serum biochemical indexes
• triglyceride
• iron

Declaration of interest

This work was supported by the National Natural Science Foundation of China (81200406), the Scientific Research Foundation for the Returned Overseas Chinese Scholars of Heilongjiang Province (C140202), and the Graduate Innovation Foundation of Harbin Medical University (YJSCX2015-1HYD). Dr. Ying Liu was supported by the Scientific Research Foundation of Heilongjiang Province (ZD201419).

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Notes on contributors

Peizhu Tan

Peizhu Tan and Huan Liang contributed equally to this work.