Endogenous n-3 Fatty Acids Alleviate Carbon-Tetrachloride-Induced Acute Liver Injury in Fat-1 Transgenic Mice

被引:19
|
作者
Feng, Ruibing [1 ]
Wang, Meng [1 ]
Yan, Chunyan [2 ]
Li, Peng [1 ]
Chen, Meiwan [1 ]
He, Chengwei [1 ]
Wan, Jian-Bo [1 ]
机构
[1] Univ Macau, Inst Chinese Med Sci, State Key Lab Qual Res Chinese Med, Macau, Peoples R China
[2] Guangdong Pharmaceut Univ, Coll Pharm, Guangzhou 510006, Guangdong, Peoples R China
关键词
INDUCED OXIDATIVE STRESS; RICH FLAXSEED OIL; HEPATIC STEATOSIS; APOPTOSIS; SUPPRESSION; GLUTATHIONE; HOMEOSTASIS; MECHANISMS; PREVENTS; PATHWAY;
D O I
10.1155/2016/7962948
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
n-3 polyunsaturated fatty acids (PUFAs) are beneficial for numerous models of liver diseases. The probable protective effects of n-3 PUFA against carbon-tetrachloride-(CCl4-) induced acute liver injury were evaluated in a fat-1 transgenic mouse that synthesizes endogenous n-3 from n-6 PUFA. Fat-1 mice and their WT littermates were fed a modified AIN93 diet containing 10% corn oil and were injected intraperitoneally with a single dose of CCl4 or vehicle. CCl4 challenge caused severe liver injury in WT mice, as indicated by serum parameters and histopathological changes, which were remarkably ameliorated in fat-1 mice. Endogenous n-3 PUFA decreased the elevation of oxidative stress induced by CCl4 challenge, which might be attributed to the activation of Nrf2/keap1 pathway. Additionally, endogenous n-3 PUFA reduces hepatocyte apoptosis via suppressing MAPK pathway. These findings indicate that n-3 PUFA has potent protective effects against acute liver injury induced by CCl4 in mice, suggesting that n-3 PUFA can be used for the prevention and treatment of liver injury.
引用
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页数:12
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