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AICAR, an AMPK Activator, Has Protective Effects on Alcohol‐Induced Fatty Liver in Rats
Author(s) -
Tomita Kengo,
Tamiya Gen,
Ando Satoshi,
Kitamura Naoto,
Koizumi Haruna,
Kato Shinzo,
Horie Yoshinori,
Kaneko Takehiko,
Azuma Toshifumi,
Nagata Hiroshi,
Ishii Hiromasa,
Hibi Toshifumi
Publication year - 2005
Publication title -
alcoholism: clinical and experimental research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.267
H-Index - 153
eISSN - 1530-0277
pISSN - 0145-6008
DOI - 10.1097/01.alc.0000191126.11479.69
Subject(s) - ampk , medicine , endocrinology , metformin , steatosis , amp activated protein kinase , liquid diet , fatty liver , fatty acid synthase , chemistry , activator (genetics) , alcoholic fatty liver , triglyceride , protein kinase a , lipid metabolism , ethanol , cholesterol , kinase , biochemistry , diabetes mellitus , receptor , disease
A bstract : Background: Previous work with metformin has shown that this antidiabetic agent improves nonalcoholic fatty liver in ob/ob mice. AMP‐activated protein kinase (AMPK) is one of the major cellular regulators of lipid and glucose metabolism, and reportedly mediates the beneficial metabolic effects of metformin. In this study, we examined the effects of 5‐aminoimidazole‐4‐carboxamide‐1‐β‐D‐ribofuranoside (AICAR), an AMPK activator, on an experimental model of ethanol‐induced hepatic steatosis. Methods: Rats were randomly divided into three groups: (A) rats fed ethanol‐containing liquid diet for six weeks; (B) rats pair‐fed ethanol‐containing liquid diet for six weeks, during the last three weeks of which they were subcutaneously injected with 0.5 mg AICAR/g body weight per day; (C) rats pair‐fed isocaloric liquid diet without ethanol for six weeks. At the end of the six‐week period, the animals were sacrificed. Serum and liver specimens were analyzed using biochemical and histologic methods, as well as real‐time PCR. Results: Chronic ethanol feeding resulted in fatty liver both histologically and biochemically, whereas AICAR administration attenuated the degree of change in the liver. AICAR also decreased the hepatic sterol regulatory factor binding protein‐1c (SREBP‐1c) and reduced fatty acid synthase (FAS) expression; these changes led to reduced triglyceride synthesis in rat livers. Furthermore, detection of 4‐hydroxy‐2‐nonenal (4‐HNE)‐protein adducts showed that the AICAR treatment also decreased the products of lipid peroxidation. Conclusion: In this preclinical rat model, AICAR, an AMPK activator, appears to protect the liver from fatty changes associated with chronic alcohol use. As such, AICAR may have a role in the treatment and prevention of alcohol‐induced fatty liver.