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从中药猕猴桃中分离得到的抗血管生成三萜

Antiangiogenic triterpenes isolated from Chinese herbal medicine Actinidia chinensis Planch.

机构信息

Department of Traditional Chinese Medicine, Shanghai Institute of Pharmaceutical Industry, Shanghai 200040, China.

出版信息

Anticancer Agents Med Chem. 2013 Feb;13(2):195-8. doi: 10.2174/1871520611313020002.

DOI:10.2174/1871520611313020002
PMID:22934692
Abstract

Actinidia chinensis Planch. is a famous Chinese herbal medicine to treat many diseases such as cancers. Triterpenes, polyphenols and anthraquinones are normally considered as the main constituents for its effects. In this study, eleven known triterpenes were isolated from the root of Actinidia chinensis., and were examined for its antiangiogenic activities. Their structures were elucidated by comprehensive spectroscopic methods, including IR, UV, HR-ESI-MS, and 1D and 2D NMR techniques. The eleven compounds are following: 2α,3α,19-trihydroxyurs-12-en-28-oic acid (1), 2α,3β-dihydroxyurs-12-en-28-oic acid (2), 2α,3α,23-trihydroxyurs-12-en-28-oic acid (3), asiatic acid (4), ursolic acid (5), 2α,3β,19,24-tetrahydroxyurs-12-en-28-oic acid (6), 2α,3β,19-trihydroxyolean-12-en-28-oic acid (7), 2α,3α,24-trihydroxyolean-12-en-28-oic acid (8), oleanolic acid (9), 3β-O-acetyloleanolic acid (10), 2α,23-dihydroxylmicromeric acid (11). All these compounds were evaluated with respect to their antiangiogenic activities utilizing the assays of human umbilical vein endothelial cells (HUVEC) proliferation and tube formation and Ursolic acid (used as control) and compounds 2, 3, 4, and 8 exhibited significant, dose-dependently, antiangiogenic activity in the tested concentration range. Our findings suggest that antitumor action of Actinidia chinensis Planch. is partly via inhibiting tumor angiogenesis by triterpenes, and compounds 2, 3, 4, and 8 as the novel potential antiangiogenic agents are worthy of further translational research.

摘要

中华猕猴桃是一种著名的中草药,可用于治疗多种疾病,如癌症。三萜、多酚和蒽醌类化合物通常被认为是其作用的主要成分。在这项研究中,从中华猕猴桃的根部分离出 11 种已知的三萜类化合物,并对其抗血管生成活性进行了研究。通过综合光谱方法,包括 IR、UV、HR-ESI-MS 以及 1D 和 2D NMR 技术,阐明了它们的结构。这 11 种化合物如下:2α,3α,19-三羟基乌苏-12-烯-28-酸(1)、2α,3β-二羟基乌苏-12-烯-28-酸(2)、2α,3α,23-三羟基乌苏-12-烯-28-酸(3)、齐墩果酸(4)、熊果酸(5)、2α,3β,19,24-四羟基乌苏-12-烯-28-酸(6)、2α,3β,19-三羟基齐墩果酸(7)、2α,3α,24-三羟基齐墩果酸(8)、齐墩果酸(9)、3β-O-乙酰齐墩果酸(10)、2α,23-二羟基小酸(11)。所有这些化合物都在人脐静脉内皮细胞(HUVEC)增殖和管形成测定中,以及齐墩果酸(用作对照)和化合物 2、3、4 和 8 的浓度范围内,评估了它们的抗血管生成活性。结果表明,中华猕猴桃的抗肿瘤作用部分是通过三萜类化合物抑制肿瘤血管生成,化合物 2、3、4 和 8 作为新型潜在的抗血管生成剂,值得进一步转化研究。

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