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来自石斛的联苄抑制血管生成及其潜在机制

[Bibenzyl from Dendrobium inhibits angiogenesis and its underlying mechanism].

作者信息

Gong Chen-Yuan, Lu Bin, Yang Li, Wang Lei, Ji Li-Li

机构信息

The MOE Key Laboratory for Standardization of Chinese Medicines, SATCM Key Laboratory for New Resources and Quality Evaluation of Chinese Medicines, Institute of Chinese Materia Medica, Shanghai University of Traditional Chinese Medicine, Shanghai 201210, China.

出版信息

Yao Xue Xue Bao. 2013 Mar;48(3):337-42.

Abstract

Bibenzyl is a type of active compounds abundant in Dendrobium. In the present study, we investigated the inhibitory effects of six bibenzyls isolated from Dendrobium species on vascular endothelial growth factor (VEGF)-induced tube formation in human umbilical vascular endothelial cells (HUVECs). All those bibenzyls inhibited VEGF-induced tube formation at 10 micromol x L(-1) except tristin, and of which moscatilin was found to have the strongest activity at the same concentration. The lowest effective concentration of moscatilin was 1 micromol x L(-1). Further results showed that moscatilin inhibited VEGF-induced capillary-like tube formation on HUVECs in a concentration-dependent manner. Western blotting results showed that moscatilin also inhibited VEGF-induced phosphorylation of VEGFR2 (Flk-1/KDR) and extracellular signal-regulated kinase 1/2 (ERK1/2). Further results showed that moscatilin inhibited VEGF-induced activation of c-Raf and MEK1/2, which are both upstream signals of ERK1/2. Taken together, results presented here demonstrated that moscatilin inhibited angiogenesis via blocking the activation of VEGFR2 (Flk-1/KDR) and c-Raf-MEK1/2-ERK1/2 signals.

摘要

联苄是石斛属植物中富含的一类活性化合物。在本研究中,我们研究了从石斛属植物中分离得到的六种联苄对人脐静脉血管内皮细胞(HUVECs)中血管内皮生长因子(VEGF)诱导的管腔形成的抑制作用。除了曲菌素外,所有这些联苄在10微摩尔×L⁻¹时均抑制VEGF诱导的管腔形成,并且发现在相同浓度下,毛兰素具有最强的活性。毛兰素的最低有效浓度为1微摩尔×L⁻¹。进一步的结果表明,毛兰素以浓度依赖的方式抑制VEGF诱导的HUVECs上毛细血管样管腔的形成。蛋白质印迹结果表明,毛兰素还抑制VEGF诱导的VEGFR2(Flk-1/KDR)和细胞外信号调节激酶1/2(ERK1/2)的磷酸化。进一步的结果表明,毛兰素抑制VEGF诱导的c-Raf和MEK1/2的激活,而这两者都是ERK1/2的上游信号。综上所述,此处呈现的结果表明,毛兰素通过阻断VEGFR2(Flk-1/KDR)和c-Raf-MEK1/2-ERK1/2信号的激活来抑制血管生成。

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