Grigore Alice, Neagu Georgeta, Dobre Nicoleta, Albulescu Adrian, Ionita Lucian, Ionita Carmen, Albulescu Radu
Department of Pharmaceutical Biotechnologies, National Institute of Chemical-Pharmaceutical Research and Development (ICCF) , Bucharest , Romania.
Department of Pharmacology, National Institute of Chemical-Pharmaceutical Research and Development (ICCF) , Bucharest , Romania.
Turk J Biol. 2018 Aug 9;42(4):334-344. doi: 10.3906/biy-1803-72. eCollection 2018.
Eupatorium cannabinum L. (Asteraceae) has been used for a long time for medicinal purposes due to its various pharmacological effects and richness in active compounds such as phenolics, sesquiterpenes, pyrrolizidine alkaloids, and polysaccharides. Despite the high content of compounds that have important roles in medicinal plants, there are still limited literature data regarding this valuable species. The plant was fractioned using chloroform (EC) and distilled water (EA) and HPLC analysis revealed the presence of eupatorin, eupatilin, and quercetin in EC and caefic acid and rutin in EA. The antiproliferative potential on BT-20, HepG2, Caco-2, and Jurkat cancer cell lines was assessed by MTS test. Jurkat cells were more sensitive to both extracts (IC50 of 7.35 ± 0.35 for EC and 13.77 ± 2.16 µg/mL for EA), while the other lines were susceptible only to EC (IC50 88.27 ± 1.34 on Caco-2 cells and over 100 µg/mL on BT20 and HepG2 cells) after 24 h of exposure. In an LPS-induced damage mouse model of endotoxemia, we showed that preventive administration increases the survival times of mice and leads to inhibition of proinflammatory cytokines. Both polar and nonpolar compounds are involved in exerting these effects, but further analytical studies are needed to identify the key responsible compounds and their biochemical pathways.
大麻叶泽兰(菊科)因其多种药理作用以及富含酚类、倍半萜、吡咯里西啶生物碱和多糖等活性化合物,长期以来一直被用于药用。尽管该植物中含有对药用植物具有重要作用的高含量化合物,但关于这种珍贵物种的文献数据仍然有限。使用氯仿(EC)和蒸馏水(EA)对该植物进行分离,高效液相色谱分析显示EC中存在泽兰素、泽兰苦素和槲皮素,EA中存在咖啡酸和芦丁。通过MTS试验评估了其对BT - 20、HepG2、Caco - 2和Jurkat癌细胞系的抗增殖潜力。Jurkat细胞对两种提取物都更敏感(EC的IC50为7.35±0.35,EA的IC50为13.77±2.16 µg/mL),而在暴露24小时后,其他细胞系仅对EC敏感(Caco - 2细胞的IC50为88.27±1.34,BT20和HepG2细胞的IC50超过100 µg/mL)。在脂多糖诱导的内毒素血症小鼠损伤模型中,我们发现预防性给药可延长小鼠存活时间并抑制促炎细胞因子。极性和非极性化合物都参与发挥这些作用,但需要进一步的分析研究来确定关键的责任化合物及其生化途径。