Elucidation of the mechanisms underlying the angiogenic effects of ginsenoside Rg1 in vivo and in vitro

被引:32
|
作者
Yue P.Y.K. [1 ]
Wong D.Y.L. [1 ]
Ha W.Y. [1 ]
Fung M.C. [2 ]
Mak N.K. [3 ]
Yeung H.W. [1 ]
Leung H.W. [1 ]
Chan K. [1 ]
Liu L. [1 ]
Fan T.P.D. [4 ]
Wong R.N.S. [1 ,3 ,5 ]
机构
[1] Hung Lai Ching Laboratory of Biomedical Science, School of Chinese Medicine, Hong Kong Baptist University, Kowloon
[2] Department of Biology, Science Faculty, Chinese University of Hong Kong, Shatin
[3] Department of Biology, Hong Kong Baptist University, Kowloon Tong, Kowloon
[4] Angiogenesis and TCM Laboratory, Department of Pharmacology, University of Cambridge, Cambridge
[5] Department of Biology, Hong Kong Baptist University, Science Building, Kowloon Tong, Kowloon
关键词
Angiogenesis; Gene expression profiling; Ginsenosides; HUVEC; Microarray; Rg[!sub]1[!/sub;
D O I
10.1007/s10456-005-9000-2
中图分类号
学科分类号
摘要
The major active constituents of ginseng are ginsenosides, and Rg 1 is a predominant compound of the total extract. Recent studies have demonstrated that Rg1 can promote angiogenesis in vivo and in vitro. In this study, we used a DNA microarray technology to elucidate the mechanisms of action of Rg1. We report that Rg1 induces the proliferation of HUVECs, monitored using [3H]-thymidine incorporation and Trypan blue exclusion assays. Furthermore, Rg1 (150-600 nM) also showed an enhanced tube forming inducing effect on the HUVEC. Rg1 was also demonstrated to promote angiogenesis in an in vivo Matrigel plug assay, and increase endothelial sprouting in the ex vivo rat aorta ring assay. Differential gene expression profile of HUVEC following treatment with Rg 1 revealed the expression of genes related to cell adhesion, migration and cytoskeleton, including RhoA, RhoB, IQGAP1, CALM2, Vav2 and LAMA4. Our results suggest that Rg1 can promote angiogenesis in multiple models, and this effect is partly due to the modulation of genes that are involved in the cytoskeletal dynamics, cell-cell adhesion and migration. © Springer 2005.
引用
收藏
页码:205 / 216
页数:11
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