非诺贝特
未折叠蛋白反应
XBP1型
非酒精性脂肪肝
内分泌学
内科学
内质网
医学
促炎细胞因子
甘油三酯
脂肪肝
炎症
胆固醇
化学
生物化学
疾病
核糖核酸
RNA剪接
基因
作者
Nan Zhang,Yunxia Lu,Xinru Shen,Yingying Bao,Jingjing Cheng,Li Chen,Li Bao,Qiu Zhang
出处
期刊:Pharmacology
[Karger Publishers]
日期:2015-01-01
卷期号:95 (3-4): 173-180
被引量:31
摘要
Fenofibrate is widely used in clinical practice, but its influence on chronic endoplasmic reticulum (ER) stress induced by feeding a high-calorie and high-cholesterol diet (HCD) has still not been studied. We thus investigated its effects on the liver of the nonalcoholic fatty liver disease (NAFLD) mouse model. Male C57BL/6 mice fed an HCD for 3 months were treated with fenofibrate (HCD + FF, 40 mg/kg, once daily) via gavage for 4 weeks. Insulin sensitivity, serum lipid and inflammatory cytokines were measured. Liver tissues were procured for histological examination as well as analysis of hepatic triglyceride levels, distribution of inflammatory cytokines and genes involved in ER stress. Our results showed that chronic feeding of an HCD successfully induced an NAFLD model accompanied by inflammatory activation, apoptosis and severe ER stress in the liver. Fenofibrate administration significantly improved symptoms of NAFLD and decreased apoptosis, expression of inflammatory cytokines and genes involved in ER stress, such as inositol-requiring enzyme 1α (IRE1α), X-box binding protein 1 (XBP1) and JNK phosphorylation. Thus, our study suggests that fenofibrate protected against inflammatory injury and apoptosis, maybe alleviating ER stress through the IRE1α-XBP1-JNK pathway in the liver of NAFLD mice.
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