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Angiogenic effect of saponin extract from Panax notoginseng on HUVECs in vitro and zebrafish in vivo

三七 血管生成 脐静脉 体内 PI3K/AKT/mTOR通路 药理学 斑马鱼 蛋白激酶B 血管内皮生长因子 生物 化学 体外 细胞生物学 信号转导 医学 生物化学 癌症研究 病理 血管内皮生长因子受体 替代医学 生物技术 基因
作者
Si‐Jia Hong,Jian‐Bo Wan,Yi Zhang,Guang Hu,Huichao Lin,Sai Wang Seto,Yiu Wa Kwan,Zhi‐Xiu Lin,Yitao Wang,Simon Ming‐Yuen Lee
出处
期刊:Phytotherapy Research [Wiley]
卷期号:23 (5): 677-686 被引量:93
标识
DOI:10.1002/ptr.2705
摘要

Abstract Angiogenesis plays an important role in a wide range of physiological processes such as wound healing and fetal development. In fact, many diseases are associated with imbalance in the regulation of angiogenesis in which there is either excessive or insufficient blood vessel formation. Panax notoginseng , a blood circulation invigorating herb, is commonly used in traditional Chinese medicine to treat circulation‐related diseases. However, the biological effects of saponin extract from Panax notoginseng (PNS) on angiogenesis and the underlying mechanisms are yet to be fully elucidated. This investigation describes the angiogenic effects of PNS on human umbilical vein endothelial cells (HUVECs) in vitro and zebrafish in vivo . The 2,3‐bis(2‐methoxy‐4‐nitro‐5‐sulfophenyl)5[(phenylamino)carbonyl]2H‐tetrazolium hydroxide (XTT) assay and microscopic cell counting demonstrated that the extract was able to stimulate the proliferation of HUVECs. Meanwhile, the numbers of invaded cells and tube branches were significantly increased in PNS treatment groups. PNS was also shown to promote changes in the subintestinal vessels, a feature of angiogenesis, in zebrafish. In addition, by using real‐time polymerase chain reaction (PCR), PNS was found to enhance vascular endothelial growth factor (VEGF) and kinase‐domain region/fetal liver kinase‐1 in mice (KDR/Flk‐1) mRNA expression, and the PNS‐induced HUVECs proliferation could be abolished by a KDR/Flk‐1 inhibitor. Furthermore, the proliferation of HUVECs induced by PNS was significantly attenuated by inhibitors of PI3K‐Akt‐eNOS. All the results suggest that PNS can promote angiogenesis, and that the proangiogenic effects involve the VEGF‐KDR/Flk‐1 and PI3K‐Akt‐eNOS signaling pathways. Copyright © 2008 John Wiley & Sons, Ltd.

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