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首页> 外文期刊>Basic & clinical pharmacology & toxicology. >Natural antioxidant pedicularioside G inhibits angiogenesis and tumourigenesis in vitro and in vivo.
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Natural antioxidant pedicularioside G inhibits angiogenesis and tumourigenesis in vitro and in vivo.

机译:天然抗氧化剂叶梗苷G在体外和体内均可抑制血管生成和肿瘤生成。

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摘要

Pedicularioside G is a new compound of phenylpropanoid glycosides, isolated from Pedicularis striata in our laboratory. Pedicularioside G inhibited two major angiogenic responses, human umbilical vein endothelial cell proliferation and migration, as well as neovascularization in a chicken embryo chorioallantoic membrane model. In addition, pedicularioside G inhibited human hepatoma cells proliferation and migration in vitro along with transplanting tumour formation and growth in a chicken embryo chorioallantoic membrane model. So pedicularioside G has anti-angiogenic, antitumour growth, antimetastatic and antitumoural effects. Pedicularioside G also remarkably reduced reactive oxygen species level in both vein endothelial cells and hepatoma cells in a concentration-dependent manner. These results suggest that the anti-angiogenic and antitumoural effects of pedicularioside G might partially attribute to its antioxidative activity.
机译:蛇床苷G是一种新的苯基丙烷类糖苷化合物,在我们的实验室中从蛇床菌中分离出来。在鸡胚绒膜尿囊膜模型中,Pedicularioside G抑制了两个主要的血管生成反应,即人脐静脉内皮细胞的增殖和迁移以及新血管形成。此外,在鸡胚绒膜尿囊膜模型中,黄柏甙G在体外抑制人肝癌细胞的增殖和迁移以及移植肿瘤的形成和生长。因此,黄柏苷G具有抗血管生成,抗肿瘤生长,抗转移和抗肿瘤作用。鹅膏苷G还以浓度依赖性方式显着降低静脉内皮细胞和肝癌细胞中的活性氧水平。这些结果表明,黄柏苷G的抗血管生成和抗肿瘤作用可能部分归因于其抗氧化活性。

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