酒精性肝病
脂肪变性
肝硬化
内科学
流质饮食
肝损伤
乙醇
慢性肝病
医学
脂肪肝
内分泌学
肝细胞癌
炎症
肝病
狂饮
化学
酒
饮酒量
生物化学
疾病
作者
Adeline Bertola,Stephanie Mathews,Sung Hwan Ki,Hua Wang,Bin Gao
出处
期刊:Nature Protocols
[Springer Nature]
日期:2013-02-28
卷期号:8 (3): 627-637
被引量:864
标识
DOI:10.1038/nprot.2013.032
摘要
Chronic alcohol consumption is a leading cause of chronic liver disease worldwide, leading to cirrhosis and hepatocellular carcinoma. Currently, the most widely used model for alcoholic liver injury is ad libitum feeding with the Lieber-DeCarli liquid diet containing ethanol for 4–6 weeks; however, this model, without the addition of a secondary insult, only induces mild steatosis, slight elevation of serum alanine transaminase (ALT) and little or no inflammation. Here we describe a simple mouse model of alcoholic liver injury by chronic ethanol feeding (10-d ad libitum oral feeding with the Lieber-DeCarli ethanol liquid diet) plus a single binge ethanol feeding. This protocol for chronic-plus-single-binge ethanol feeding synergistically induces liver injury, inflammation and fatty liver, which mimics acute-on-chronic alcoholic liver injury in patients. This feeding protocol can also be extended to chronic feeding for longer periods of time up to 8 weeks plus single or multiple binges. Chronic-binge ethanol feeding leads to high blood alcohol levels; thus, this simple model will be very useful for the study of alcoholic liver disease (ALD) and of other organs damaged by alcohol consumption.
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