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首页> 外文期刊>BMC Complementary and Alternative Medicine >Yiguanjian decoction and its ingredients inhibit angiogenesis in carbon tetrachloride-induced cirrhosis mice
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Yiguanjian decoction and its ingredients inhibit angiogenesis in carbon tetrachloride-induced cirrhosis mice

机译:益冠健汤及其成分抑制四氯化碳致肝硬化小鼠血管新生

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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 (CCl 4 ) (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 α-smooth muscle actin (α-SMA), collagen I, CD31, vascular endothelial growth factor (VEGF), VEGF receptor (VEGFR) 2 and hypoxia-inducible factor (HIF)-1α. 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 CCl 4 treated animals, Hyp, α-SMA, collagen I, CD31, VEGF, VEGFR, and HIF-1α expression decreased in YGJ and iYGJ groups. Conclusions YGJ and iYGJ inhibited liver angiogenesis in cirrhotic mice treated with CCl 4 by inhibiting the HIF-1α/VEGF signaling pathway, suggesting that anti-angiogenic effects of YGJ and iYGJ are associated with improving the hepatic hypoxic microenvironment.
机译:背景技术肝硬化与血管生成和肝血管结构破坏有关。一贯煎汤(YGJ)是中药处方,被广泛用于治疗肝脏疾病。我们研究了YGJ或其成分(iYGJ)是否具有抗血管生成作用,并探讨了该过程的潜在机制。方法用四氯化碳(CCl 4 )(ip)诱导C57BL / 6小鼠肝硬化6周。从第4周到第6周,将肝硬化小鼠随机分为四组:索拉非尼治疗,YGJ治疗和iYGJ治疗的小鼠和安慰剂。测定血清生化指标,羟脯氨酸(Hyp)含量以及肝组织的病理学变化,包括α-平滑肌肌动蛋白(α-SMA),胶原蛋白I,CD31,血管内皮生长因子(VEGF),VEGF受体(VEGFR)2和低氧-诱导因子(HIF)-1α。结果YGJ和iYGJ均可改善血清生物化学。组织病理学改变表明,YGJ和iYGJ可以减轻肝硬化小鼠的肝组织坏死性炎症和胶原纤维沉积。与CCl 4 处理的动物相比,YGJ和iYGJ组的Hyp,α-SMA,胶原I,CD31,VEGF,VEGFR和HIF-1α表达降低。结论YGJ和iYGJ通过抑制HIF-1α/ VEGF信号通路抑制CCl 4 处理的肝硬化小鼠的肝血管生成,提示YGJ和iYGJ的抗血管生成作用与改善肝低氧微环境有关。 。

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