Yiguanjian decoction and its ingredients inhibit angiogenesis in carbon tetrachloride-induced cirrhosis mice

被引:25
作者
Zhou, Ya-Ning [1 ]
Mu, Yong-Ping [1 ]
Fu, Wen-Wei [1 ]
Ning, Bing-Bing [1 ]
Du, Guang-Li [2 ]
Chen, Jia-Mei [1 ]
Sun, Ming-Yu [1 ]
Zhang, Hua [1 ]
Hu, Yi-Yang [1 ,3 ]
Liu, Cheng-Hai [1 ,3 ]
Xu, Lie-Ming [1 ]
Liu, Ping [1 ,3 ]
机构
[1] Shanghai Univ Tradit Chinese Med, Inst Liver Dis, Shuguang Hosp, Shanghai 201203, Peoples R China
[2] Shanghai Univ Tradit Chinese Med, Shanghai 201203, Peoples R China
[3] Shanghai Municipal Educ Commiss, E Inst, Shanghai 201203, Peoples R China
来源
BMC COMPLEMENTARY AND ALTERNATIVE MEDICINE | 2015年 / 15卷
关键词
Cirrhosis; Angiogenesis; Yiguanjian; ENDOTHELIAL GROWTH-FACTOR; YI GUAN JIAN; HYPOXIA; FIBROSIS; FIBROGENESIS; RATS; CCL4;
D O I
10.1186/s12906-015-0862-6
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Background: Cirrhosis is associated with angiogenesis and disruption of hepatic vascular architecture. Yiguanjian (YGJ) decoction, a prescription from traditional Chinese medicine, is widely used for treating liver diseases. We studied whether YGJ or its ingredients (iYGJ) had an anti-angiogenic effect and explored possible mechanisms underlying this process. Methods: Cirrhosis was induced with carbon tetrachloride (CCl4) (ip) in C57BL/6 mice for 6 weeks. From week 4 to week 6, cirrhotic mice were randomly divided into four groups: sorafenib-treated, YGJ-treated and iYGJ-treated mice and placebo. Serum biochemistries, hydroxyproline (Hyp) content and histopathological changes of hepatic tissues were measured as were alpha-smooth muscle actin (alpha-SMA), collagen I, CD31, vascular endothelial growth factor (VEGF), VEGF receptor (VEGFR) 2 and hypoxia-inducible factor (HIF)-1 alpha. Results: Both YGJ and iYGJ improved serum biochemistries. Changes of histopathology showed that YGJ and iYGJ reduced hepatic tissue necroinflammatory and collagen fiber deposition in cirrhosis mice. Compared to the CCl4 treated animals, Hyp, alpha-SMA, collagen I, CD31, VEGF, VEGFR, and HIF-1 alpha expression decreased in YGJ and iYGJ groups. Conclusions: YGJ and iYGJ inhibited liver angiogenesis in cirrhotic mice treated with CCl4 by inhibiting the HIF-1 alpha/VEGF signaling pathway, suggesting that anti-angiogenic effects of YGJ and iYGJ are associated with improving the hepatic hypoxic microenvironment.
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页数:9
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