Naturally Occurring Stilbenoid TSG Reverses Non-Alcoholic Fatty Liver Diseases via Gut-Liver Axis

被引:39
|
作者
Lin, Pei [1 ]
Lu, Jianmei [1 ]
Wang, Yanfang [1 ]
Gu, Wen [1 ]
Yu, Jie [1 ]
Zhao, Ronghua [1 ]
机构
[1] Yunnan Univ Tradit Chinese Med, Dept Pharm, Kunming, Yunnan, Peoples R China
来源
PLOS ONE | 2015年 / 10卷 / 10期
基金
中国国家自然科学基金;
关键词
TOLL-LIKE RECEPTORS; TETRAHYDROXYSTILBENE GLUCOSIDE; METABOLIC-SYNDROME; CONTROLLED-TRIAL; VITAMIN-E; IN-VITRO; HEALTH; DIET; PIOGLITAZONE; ACTIVATION;
D O I
10.1371/journal.pone.0140346
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The gut-liver axis is largely involved in the development of non-alcoholic fatty liver disease (NAFLD). We investigated whether 2, 3, 5, 4'-tetrahydroxy-stilbene-2-O-beta-D-glucoside (TSG) could reverse NAFLD induced by a high-fat diet (HFD) and whether it did so via the gut-liver axis. Results showed that TSG could reduce the accumulation of FFA and it did so by reducing the expression of L-FABP and FATP4. TSG regulated gut microbiota balanced and increased the protein expression of ZO-1 and occludin, which could improve the function of the intestinal mucosal barrier and reduce serum LPS content by about 25%. TSG reduced TL4 levels by 56% and NF-kappa B expression by 23% relative to the NAFLD model group. This suggests that prevention of NAFLD by TSG in HFD-fed rats is mediated by modulation of the gut microbiota and TLR4/NF-kappa B pathway, which may alleviate chronic low-grade inflammation by reducing the exogenous antigen load on the host.
引用
收藏
页数:14
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