Hepatic anti-inflammatory effect of hexane extracts of Dioscorea batatas Decne: Possible suppression of toll-like receptor 4-mediated signaling

被引:6
作者
Koo, Hyun Jung [1 ]
Lee, SungRyul [2 ]
Chang, Kwang Jin [1 ]
Sohn, Eunsoo [3 ]
Sohn, Eun-Hwa [4 ]
Kang, Se Chan [5 ]
Pyo, Suhkneung [6 ]
机构
[1] Korea Natl Coll Agr & Fisheries, Dept Med & Ind Crops, Jeonju 54874, South Korea
[2] Inje Univ, Coll Med, Cardiovasc & Metab Dis Ctr, Dept Integrated Biomed Sci, Busan 47392, South Korea
[3] Korea Inst Sci & Technol Informat, Dept Scientometr Res, Seoul, South Korea
[4] Kangwon Natl Univ, Dept Herbal Med Resources, Samcheok 25913, South Korea
[5] Kyung Hee Univ, Coll Life Sci, Dept Oriental Med Biotechnol, Yongin 17104, South Korea
[6] Sungkyunkwan Univ, Sch Pharm, Suwon 16419, South Korea
基金
新加坡国家研究基金会;
关键词
ApoE; Dioscorea batatas Decne; Inflammation; Toll-like receptor 4; Activator protein 1; HepG2; FATTY LIVER-DISEASE; APOLIPOPROTEIN-E; BETA-SITOSTEROL; NONALCOHOLIC STEATOHEPATITIS; METABOLIC SYNDROME; KNOCKOUT MICE; INFLAMMATION; EXPRESSION; FIBROSIS; ACTIVATION;
D O I
10.1016/j.biopha.2017.05.036
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The hepatic anti-inflammatory potential of hexane extracts of Dioscorea batatas Decne edible part (EDH-1e) and bark (EDH-2b) were investigated in Western-type diet-fed apolipoprotein E null [ApoE (-/-)] mice and HepG2 cells. EDH-1e and EDH-2b suppressed the increased levels of tumor necrosis factor alpha (TNF-alpha), interleukin (IL)-6, transforming growth factor beta 1 (TGF-beta 1), vascular cell adhesion protein 1 (VCAM-1), and monocyte chemoattractant protein-1 (MCP-1), and reduced infiltration of monocytes into liver tissue. The protein levels of Toll-like receptor 4 (TLR4) were also downregulated by EDH-1e and EDH-2b treatment as were the levels of activator protein 1 (AP-1), c-fos, and c-jun in the livers from Western-type diet-fed ApoE (-/-) mice and in lipopolysaccharide-stimulated HepG2 cells. Taken together, EDH-1e and EDH-2b attenuated hepatic inflammation and fibrosis via suppression of the TLR4-AP1-mediated signaling pathway. (C) 2017 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:157 / 167
页数:11
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