从 Aesculus glabra Willd 树皮中分离出的生物活性化合物

IF 1.3 4区 生物学 Q4 CHEMISTRY, MEDICINAL
Miriam Velazquez Cruz , Eric Salinas-Arellano , Ines Castro Dionicio, Jonathan G. Jeyaraj, Nathan P. Mirtallo Ezzone, Esperanza J. Carcache de Blanco
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引用次数: 0

摘要

Aesculus属有多个物种,其中最著名的是Aesculus hippocastanum,据报道具有细胞毒性和静脉张力作用。鉴于目前抗血管生成疗法的局限性,A. hippocastanum 的血管生成效果令人感兴趣。Aesculus glabra(Willdenow)被称为俄亥俄红豆杉,是一种原产于北美洲的树种,据报道美洲原住民将其作为药用植物。以前的植物化学研究主要集中在苁蓉树种子和叶子的成分上,其中大部分研究报告了其细胞毒性活性。在本研究中,我们利用斑马鱼(Danio rerio)模型初步评估了从草履虫树皮中分离出的化合物的抗血管生成活性和毒性。我们用斑马鱼测试了原花青素 A2 和表儿茶素这两种纯分离物,结果表明它们具有抗血管生成的作用,这表明它们的潜在机制与血管发育有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Bioactive compounds isolated from the bark of Aesculus glabra Willd

Bioactive compounds isolated from the bark of Aesculus glabra Willd

The Aesculus genus has several species, most notably Aesculus hippocastanum, with reported cytotoxic and venotonic effects. The angiogenic effect from A. hippocastanum is of interest given the current limitations of anti-angiogenic therapeutics. Aesculus glabra (Willdenow), known as the Ohio Buckeye Tree is a species native to North America with reported medicinal use by the Native Americans. Previous phytochemical studies have focused on the seed and leaf contents of the glabra species, with most of them reporting cytotoxic activity. In this study, we assessed preliminary anti-angiogenic activity and toxicity of isolated compounds from the bark of A. glabra utilizing a zebrafish (Danio rerio) model. Procyanidin A2 and epicatechin, two pure isolates, were tested using zebrafish and gave an anti-angiogenic response, suggesting an underlying mechanism involved in vascular development.

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来源期刊
Phytochemistry Letters
Phytochemistry Letters 生物-生化与分子生物学
CiteScore
3.00
自引率
11.80%
发文量
190
审稿时长
34 days
期刊介绍: Phytochemistry Letters invites rapid communications on all aspects of natural product research including: • Structural elucidation of natural products • Analytical evaluation of herbal medicines • Clinical efficacy, safety and pharmacovigilance of herbal medicines • Natural product biosynthesis • Natural product synthesis and chemical modification • Natural product metabolism • Chemical ecology • Biotechnology • Bioassay-guided isolation • Pharmacognosy • Pharmacology of natural products • Metabolomics • Ethnobotany and traditional usage • Genetics of natural products Manuscripts that detail the isolation of just one new compound are not substantial enough to be sent out of review and are out of scope. Furthermore, where pharmacology has been performed on one new compound to increase the amount of novel data, the pharmacology must be substantial and/or related to the medicinal use of the producing organism.
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