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Antiproliferative Antimicrobial and Apoptosis Inducing Effects of Compounds Isolated from Inula viscosa

机译:粘稠旋覆花中化合物的抗增殖抗菌和凋亡诱导作用

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摘要

The antiproliferative and antimicrobial effects of thirteen compounds isolated from Inula viscosa (L.) were tested in this study. The antiproliferative activity was tested against three cell lines using the MTT assay. The microdilution method was used to study the antimicrobial activity against two Gram positive bacteria, two Gram negative bacteria and one fungus. The apoptotic activity was determined using a TUNEL colorimetric assay. Scanning electron microscopy was used to study the morphological changes in treated cancer cells and bacteria. Antiproliferative activity was observed in four flavonoids (nepetin, 3,3′-di-O-methylquercetin, hispidulin, and 3-O-methylquercetin). 3,3′-di-O-Methylquercetin and 3-O-methylquercetin showed selective antiproliferative activity against MCF-7 cells, with IC50 values of 10.11 and 11.23 µg/mL, respectively. Both compounds exert their antiproliferative effect by inducing apoptosis as indicted by the presence of DNA fragmentation, nuclear condensation, and formation of apoptotic bodies in treated cancer cells. The antimicrobial effect of Inula viscosa were also noticed in 3,3′-di-O-methylquercetin and 3-O-methyquercetin that inhibited Bacillus cereus at MIC of 62.5 and 125 µg/mL, respectively. Salmonella typhimurium was inhibited by both compounds at MIC of 125 µg/mL. 3,3′-di-O-Methylquercetin induced damage in bacterial cell walls and cytoplasmic membranes. Methylated quercetins isolated from Inula viscosa have improved anticancer and antimicrobial properties compared with other flavonoids and are promising as potential anticancer and antimicrobial agents.
机译:在这项研究中测试了从Inula viscosa(L.)分离出的13种化合物的抗增殖和抗菌作用。使用MTT测定法测试了针对三种细胞系的抗增殖活性。微稀释法用于研究对两种革兰氏阳性菌,两种革兰氏阴性菌和一种真菌的抗菌活性。使用TUNEL比色测定法确定凋亡活性。扫描电子显微镜用于研究处理过的癌细胞和细菌的形态变化。在四个类黄酮(荆芥,3,3'-二-O-甲基槲皮素,组蛋白和3-O-甲基槲皮素)中观察到了抗增殖活性。 3,3'-di-O-甲基槲皮素和3-O-甲基槲皮素对MCF-7细胞具有选择性的抗增殖活性,IC50值分别为10.11和11.23 µg / mL。两种化合物均通过诱导凋亡而发挥抗增殖作用,这是由治疗的癌细胞中DNA片段化,核浓缩和凋亡小体形成所指示的。在3,3'-二-O-甲基槲皮素和3-O-甲基槲皮素中也观察到了Inula viscosa的抗菌作用,它们分别以62.5和125μg/ mL的MIC抑制蜡状芽孢杆菌。两种化合物均以125 µg / mL的MIC抑制鼠伤寒沙门氏菌。 3,3'-二-O-甲基槲皮素诱导细菌细胞壁和细胞质膜的损伤。与其他类黄酮相比,从Inula viscosa分离的甲基化槲皮素具有改进的抗癌和抗菌特性,并有望作为潜在的抗癌和抗菌剂。

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