Preventive effect of α-linolenic acid-rich flaxseed oil against ethanol-induced liver injury is associated with ameliorating gut-derived endotoxin-mediated inflammation in mice

被引:26
|
作者
Wang, Meng [1 ]
Zhang, Xiao-Jing [1 ]
Yan, Chunyan [2 ]
He, Chengwei [1 ]
Li, Peng [1 ]
Chen, Meiwan [1 ]
Su, Huanxing [1 ]
Wan, Jian-Bo [1 ]
机构
[1] Univ Macau, Inst Chinese Med Sci, State Key Lab Qual Res Chinese Med, Room 6034,Bldg N22,Ave Univ, Taipa, Peoples R China
[2] Guangdong Pharmaceut Univ, Coll Pharm, Guangzhou, Guangdong, Peoples R China
关键词
alpha-linolenic acid; Flaxseed oil; Ethanol-induced liver injury; Intestinal barrier function; Endotoxin; FATTY LIVER; INTESTINAL MICROBIOME; DOCOSAHEXAENOIC ACID; DISEASE; BARRIER; PERMEABILITY; DYSFUNCTION; DEFICIENCY; INCREASES; MODEL;
D O I
10.1016/j.jff.2016.03.012
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
The effects of alpha-linolenic acid (ALA)-rich flaxseed oil (FDO) against ethanol-induced liver injury and the probable molecular mechanisms in a mouse model of chronic-plus-single binge ethanol feeding were evaluated. Mice were fed Lieber-DeCarli ethanol or control liquid diets with corn oil (CNO) or flaxseed oil for 10 days. On day 11, mice are gavaged with a single dose of ethanol or maltose dextrin. Ethanol exposure with CNO caused severe liver injury, inflammation and oxidative stress in liver, which were remarkably ameliorated by FDO. FDO supplementation decreased the elevation of plasma endotoxin level, which might be attributed to ameliorating ethanol-induced intestinal barrier dysfunction via upregulating the expressions of tight junction proteins. Additionally, FDO supplementation suppressed endotoxin-triggered inflammation via blocking TLR4/MyD88/NF-kappa B cascades in liver. These findings suggest that ALA -rich flaxseed oil may have potential to be developed as an effective agent for ethanol-induced liver injury. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:532 / 541
页数:10
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