Liu Jing, Zhuang Zhen-Jie, Bian Dong-Xue, Ma Xiao-Jie, Xun Yun-Hao, Yang Wen-Jun, Luo Yan, Liu Yin-Lan, Jia Ling, Wang Yan, Zhu Ming-Li, Ye De-Wei, Zhou Gang, Lou Guo-Qiang, Shi Jun-Ping
Second Clinical Medical College, Zhejiang Chinese Medical University, Hangzhou, China.
Clin Exp Pharmacol Physiol. 2014 Jul;41(7):482-8. doi: 10.1111/1440-1681.12241.
The aim of the present study was to investigate Toll-like receptor-4 (TLR4) signalling at different stages of non-alcoholic fatty liver disease (NAFLD) induced by a high-fat, high-fructose (HFHFr) diet in mice. Both TLR4 wild-type (WT) and mutant (TLR4(mut) ) mice were fed either standard chow (SC) or the HFHFr diet for different periods of time from 4 to 16 weeks. Pathological characteristics and function of the liver were assessed. Simple steatosis, steatohepatitis and hepatic fibrosis occurred sequentially in Week 4, 8 and 16 in WT mice fed with the HFHFr. Expression of TLR4, myeloid differentiation factor 88 (MyD88), interferon regulatory factor (IRF) 3 and IRF7 started to increase at Week 4, peaked at Week 8 and then declined to basal levels at Week 16. This pattern was consistent with changes in inflammation in the liver revealed by haematoxylin and eosin staining. However, lipid accumulation, inflammation and fibrosis in livers of TLR4(mut) mice fed the HFHFr diet were significantly alleviated. In addition, the expression of activin A in WT mice fed the HFHFr diet increased at Week 16. The data suggest that TLR4 signalling mediates non-alcoholic steatohepatitis before fibrosis and that activin A is subsequently involved in NAFLD.
本研究旨在探讨高脂高果糖(HFHFr)饮食诱导的小鼠非酒精性脂肪性肝病(NAFLD)不同阶段的Toll样受体4(TLR4)信号传导。TLR4野生型(WT)小鼠和突变型(TLR4(mut))小鼠从4周龄到16周龄的不同时间段内分别喂食标准饲料(SC)或HFHFr饮食。评估肝脏的病理特征和功能。喂食HFHFr的WT小鼠在第4周、第8周和第16周依次出现单纯性脂肪变性、脂肪性肝炎和肝纤维化。TLR4、髓样分化因子88(MyD88)、干扰素调节因子(IRF)3和IRF7的表达在第4周开始增加,在第8周达到峰值,然后在第16周降至基础水平。这种模式与苏木精和伊红染色显示的肝脏炎症变化一致。然而,喂食HFHFr饮食的TLR4(mut)小鼠肝脏中的脂质积累、炎症和纤维化明显减轻。此外,喂食HFHFr饮食的WT小鼠在第16周时激活素A的表达增加。数据表明,TLR4信号传导在纤维化之前介导非酒精性脂肪性肝炎,并且激活素A随后参与NAFLD。