Long-term diosbulbin B treatment induced liver fibrosis in mice

被引:15
|
作者
Zhang, Yi [1 ,2 ]
Miao, Hui [1 ,2 ]
Guan, Huida [1 ,2 ]
Wang, Changhong [1 ,2 ]
Wang, Zhengtao [1 ,2 ]
Ji, Lili [1 ,2 ]
机构
[1] Shanghai Univ Tradit Chinese Med, Inst Chinese Mat Med, Shanghai Key Lab Compound Chinese Med, MOE Key Lab Standardizat Chinese Med, 1200 Cailun Rd, Shanghai 201203, Peoples R China
[2] Shanghai Univ Tradit Chinese Med, Inst Chinese Mat Med, SATCM Key Lab New Resources & Qual Evaluat Chines, 1200 Cailun Rd, Shanghai 201203, Peoples R China
关键词
Diosbulbin B; Liver fibrosis; HSCs activation; EMT; NF kappa B; HEPATIC STELLATE CELLS; DIOSCOREA-BULBIFERA L; HEPATOTOXICITY; MECHANISMS; INSIGHTS; INJURY; FIBROGENESIS; ACTIVATION;
D O I
10.1016/j.cbi.2018.10.015
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Airpotato yam is a traditional Chinese medicine used for treating thyroid disease and cancer in China. Diosbulbin B (DB) is reported to be the main hepatotoxic compound isolated from Airpotato yam. A variety of reports have shown the acute liver injury induced by DB in vivo. However, whether long-term administration of DB will cause liver fibrosis in mice is unknown. This study aims to investigate the liver fibrosis induced by long-term DB treatment in mice. C57BL/6 mice were orally given with DB (25, 50 mg/kg) for 1 or 2 month, respectively. Liver hydroxyproline content, hepatic collagen deposition and immune cells infiltration were increased in mice treated with DB (50 mg/kg) for 2 months. Serum amounts of hyaluronic acid and laminin were increased in mice treated with DB for 1 or 2 months. DB (50 mg/kg) induced hepatic stellate cells (HSCs) activation when mice were treated with DB for 2 months. Liver mRNA expression of Col1a1, Col1a2, Col3a1, fibronectin (Fn1), vimentin (Vim) and fibroblast-specific protein 1 (FSP1) were all increased in DB-treated mice. Hepatic protein expression of Vim, FSP1 and collagen 1 (COL1) were increased in DB-treated mice. Additionally, DB induced nuclear factor KB (NF kappa B) activation and increased the expression of pro-inflammatory molecules including tumor necrosis factor (TNF)-alpha, interleukin (IL)-6, intercellular cell adhesion molecule-1 (ICAM-1) and inducible nitric oxide synthase (iNOS) in mice. In conclusion, long-term administration of DB induced liver fibrosis in mice. HSCs activation, epithelial-mesenchymal transition (EMT) and liver inflammation contributed to DB-induced liver fibrosis in mice.
引用
收藏
页码:15 / 23
页数:9
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