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从 Digitalis trojana 中提取的具有抗增殖活性的甾体糖苷。

Steroidal glycosides with antiproliferative activities from Digitalis trojana.

机构信息

Department of Pharmacognosy, Faculty of Pharmacy, University of Yeditepe, 34755, Kayisdagi, Istanbul, Turkey.

出版信息

Phytother Res. 2014 Apr;28(4):534-8. doi: 10.1002/ptr.5012. Epub 2013 May 31.

DOI:10.1002/ptr.5012
PMID:23722601
Abstract

The phytochemical investigation of Digitalis trojana led to the isolation of two cardiac glycosides (1, 2), one pregnane glycoside (3), three furostanol type saponins (4-6), along with three cleroindicins (7-9), four phenylethanoid glycosides (10-13), two flavonoids (14, 15) and two phenolic acid derivatives (16, 17). The structure elucidation of the isolates was carried out by NMR experiments as well as ESI-MS. The cytotoxic activity of compounds 1-13 against a small panel of cancer cell lines, namely MCF-7, T98G, HT-29, PC-3, A375 and SH-SY5Y, was investigated. Compounds 1-6 showed antiproliferative activity against human breast MCF-7 and colon HT-29 cancer cell lines with IC50 values ranging from 8.3 to 50 μM. In order to understand the mechanism involved in the cell death, the active compounds were tested as pro-apoptotic agents using propidium iodide staining by flow cytometry method. No significant increase was observed in the apoptosis of the MCF-7 and HT-29 cancer cells. Moreover, the effects of the active compounds on cell proliferation were assessed on the same cancer cell lines by cell cycle analysis of DNA content using flow cytometry. No significative changes were observed in the cell cycle of MCF-7, while significant changes in G2 /M cell cycle phase of HT-29 cells were observed after treatment with digitalin (1), cariensoside (3) and 22-O-methylparvispinoside B (6) at 10 μM.

摘要

从紫花毛地黄中分离得到了两个强心苷(1、2)、一个孕烷糖苷(3)、三个呋甾烷醇型皂苷(4-6),以及三个 clerodindins(7-9)、四个苯乙醇苷(10-13)、两个黄酮类化合物(14、15)和两个酚酸衍生物(16、17)。通过 NMR 实验和 ESI-MS 对分离物的结构进行了阐明。对化合物 1-13 对一组小的癌细胞系(即 MCF-7、T98G、HT-29、PC-3、A375 和 SH-SY5Y)的细胞毒性进行了研究。化合物 1-6 对人乳腺癌 MCF-7 和结肠 HT-29 癌细胞系具有增殖抑制活性,IC50 值范围为 8.3 至 50μM。为了了解细胞死亡涉及的机制,通过流式细胞术用碘化丙啶染色法测试了活性化合物作为促凋亡剂。在 MCF-7 和 HT-29 癌细胞中,未观察到明显的凋亡增加。此外,通过流式细胞术检测 DNA 含量的细胞周期分析,在相同的癌细胞系上评估了活性化合物对细胞增殖的影响。在 MCF-7 中未观察到细胞周期有明显变化,而在 10μM 时,毛地黄苷(1)、cariensoside(3)和 22-O-甲基 parvispinoside B(6)处理后 HT-29 细胞的 G2/M 细胞周期阶段发生了显著变化。

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