甲壳Lindernia (L.)的抗癌活性研究f . Muell。var。甲壳纲动物

S. Barusrux, N. Weerapreeyakul, Preeyaporn Plaimee Phiboonchaiyanan, Munthipha Khamphio, W. Tanthanuch, Kanjana Thummanu
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引用次数: 2

摘要

甲壳linderia (L.)f . Muell。变种甲壳类动物或“Ya Kap Hoi: YKH”被误解为“Ya Yad Nam Kang”和癌症治疗。本研究旨在通过对提取物化学成分的分析,探讨其抗癌活性,并在体外筛选提取物的生物活性,如癌细胞毒性活性、免疫细胞增殖活性、还原力活性、烷基化活性等。高效液相色谱分析表明,水提液和醇提液均未见白丹苷峰。YKH乙醇提取物比YKH水提取物产生更多的化学成分。YKH水提物对所有癌细胞均无活性。有趣的是,YKH乙醇提取物对HCT116结肠癌、HepG2肝癌和Jurkat白血病细胞系的癌细胞死亡呈浓度依赖关系。在HCT116、HepG2和Jurkat细胞系中,暴露24 h后细胞死亡率达到50%的YKH乙醇提取物的IC50浓度分别为195.4±12、171.7±8.7和48.8±5.7µg/mL。YKH的水提液和醇提液均表现出较高的抗氧化活性,但不具有烷基化活性。在高浓度(250µg/mL)时,YKH乙醇提取物比YKH水提物更能抑制免疫细胞的增殖活性。我们研究的一个意想不到但关键的结果是发现选择极性较小的植物提取溶剂具有抗癌活性。用乙醇提取了黄芪的潜在抗癌成分,这些成分在黄芪的水溶液中找不到。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Investigation of Anticancer Activity of Lindernia crustacea (L.) F. Muell. var. Crustacean
Lindernia crustacea (L.) F. Muell. var. crustacean or “Ya Kap Hoi: YKH” was misunderstood as “Ya Yad Nam Kang” and cancer curative. This study aimed to investigate anticancer activity by the analysis of chemical constituent in extracts and in vitro screening of biological activities of the extract in several aspects such as cancer cell lines cytotoxic activity, immune cell proliferating activity, reducing power activity, alkylation activity. The HPLC analysis showed the absence of plumbagin peak observed in the HPLC chromatograms of both YKH aqueous and YKH ethanolic extracts. The YKH ethanolic extract yielded more chemical constituents than that of the YKH aqueous extract. The YKH aqueous extract was inactive against all cancer cells tested. Interestingly, YKH ethanolic extract caused cancer cell death in HCT116 colon cancer, HepG2 liver cancer, and Jurkat leukemic cancer cell lines in the concentration dependent manner. The following IC50 concentrations of the YKH ethanolic extract that possessed 50 % cell death after 24 h exposure in HCT116, HepG2, and Jurkat cell line were 195.4 ± 12, 171.7 ± 8.7, and 48.8 ± 5.7 µg/mL, respectively. Both aqueous and ethanolic extracts of YKH showed high antioxidant activity based on reducing power activity but did not have alkylation activity. At high concentration (250 µg/mL), YKH ethanolic extract can inhibit immune cells proliferation activity more than the YKH aqueous extract. An unexpected but critical outcome of our studies was the finding that anticancer activity is promised by selecting the plant extraction solvent with less polarity. Potential anticancer constituents were extracted from YKH using ethanol and these constituents cannot be found in aqueous solution of YKH.
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