首页> 外文期刊>Iranian Journal of Pharmaceutical Research >Cytotoxic and Apoptogenic Sesquiterpenoids from the Petroleum Ether Extract of Artemisia aucheri Aerial Parts
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Cytotoxic and Apoptogenic Sesquiterpenoids from the Petroleum Ether Extract of Artemisia aucheri Aerial Parts

机译:蒿蒿地上部分石油醚提取物的细胞毒性和凋亡倍半萜类化合物

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Different types of Artemisia aucheri extracts were reported to have various biological activities including a cytotoxic effect on some cancer cell lines. We investigated the antiproliferative activity of isolated sesquiterpenoids from petroleum ether extract of Artemisia aucheri (A. aucheri)aerial parts on SK-N-MC, MCF-7, and A2780 cell lines. Phytochemicals from the petroleum ether cold macerated extract were isolated using normal phase vacuum liquid chromatography and high pressure liquid chromatography (VLC and HPLC) and the structures of the components were determined by spectroscopic means. Cell viability was determined by 3-(4,5- dimethylthiazol-2yl)-2,5-diphenyltetrazolium bromide assay. Activation of caspases-3 and -9 was evaluated using a spectrophotometer. Mitochondrial membrane potential (MMP) was measured using rhodamine 123 fluorescent dye. Two tetrahydrofuran- type sesquiterpenoids, hydroperoxide of davanone (1) and hydroxydavanone (2) were isolated and characterized. Between these compounds, compound 1 exhibited the most potent activity against the MCF-7, SK-N-MC and A2780 cell lines with IC50 value of 8.45 ?± 0.81 ?μg/mL, 9.60 ?± 1.32 ?μg/mL and 10.9 ?± 2.03 ?μg/mL in A2780, MCF-7 and SK-N-MC cells, respectively. Compound 1 inhibited cell growth of human cancer cells by induction of apoptosis. To the best of our knowledge, this is the first comprehensive study on cytotoxic and apoptotic mechanism of two davanone derivatives isolated from A. aucheri in human cancer cells. Overall, our data suggest that hydroperoxide of davanone (1) should be further studied in-vivo as a potential antitumor agent.
机译:据报道,不同类型的青蒿提取物具有多种生物学活性,包括对某些癌细胞系的细胞毒性作用。我们调查了从蒿蒿(A. aucheri)空中部分的石油醚提取物中分离的倍半萜类化合物对SK-N-MC,MCF-7和A2780细胞系的抗增殖活性。使用正相真空液相色谱和高压液相色谱(VLC和HPLC)分离石油醚冷浸提取物中的植物化学物质,并通过光谱学方法确定其结构。通过3-(4,5-二甲基噻唑-2基)-2,5-二苯基溴化四氮唑测定法测定细胞活力。使用分光光度计评估caspases-3和-9的活化。使用若丹明123荧光染料测量线粒体膜电位(MMP)。分离并鉴定了两种四氢呋喃型倍半萜类化合物,达万酮的氢过氧化物(1)和羟基达万酮(2)。在这些化合物之间,化合物1对MCF-7,SK-N-MC和A2780细胞系表现出最强的活性,IC50值分别为8.45±0.81μg/ mL,9.60±1.32μg/ mL和10.9α。在A2780,MCF-7和SK-N-MC细胞中分别为±2.03μμg/ mL。化合物1通过诱导凋亡来抑制人癌细胞的细胞生长。据我们所知,这是首次分离出从Aucheri中分离到的两种达瓦酮衍生物在人癌细胞中的细胞毒性和凋亡机制。总体而言,我们的数据表明,达瓦酮(1)的氢过氧化物应作为潜在的抗肿瘤药物进行体内研究。

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