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Cytotoxicity of alkaloids isolated from Argemone mexicana on SW480 human colon cancer cell line

机译:墨西哥Argemone分离的生物碱对SW480人结肠癌细胞系的细胞毒性

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Context: Argemone mexicana Linn. (Papaveraceae) has been used as traditional medicine in India and Taiwan for the treatment of skin diseases, inflammations, bilious, fever, etc. Some alkaloids of A. mexicana have been screened for their cytotoxicity on different cancer cell lines.Objective: The study investigates potential cytotoxic effects of alkaloids isolated from aerial part of A. mexicana on SW480 human colon cancer cell line.Materials and methods: Six alkaloids, 13-oxoprotopine, protomexicine, 8-methoxydihydrosanguinarine, dehydrocorydalmine, jatrorrhizine, and 8-oxyberberine were isolated from the methanol extract of A. mexicana. Cytotoxicity of these alkaloids was studied on SW480 human colon cancer cell line at 1, 25, 50, 75, 100, 125, 150, and 200 mu g/mL for 24 and 48h. Cells were seeded in a 96-well micro-plate at a concentration of 2x10(4) cells per well and MTS assay was performed to assess cytotoxicity in terms of cell viability.Results: At 200 mu g/mL, protomexicine and 13-oxoprotopine showed mild cytotoxicity (approximate to 24-28%) whereas dehydrocorydalmine exhibited moderate cytotoxicity (approximate to 48%). 8-Oxyberberine was mildly cytotoxic (approximate to 27%) at 24h but was more potent (approximate to 76%) at 48h. Jatrorrhizine and 8-methoxydihydrosanguinarine were most potent (approximate to 95-100%) in inhibiting the human colon cancer cell proliferation showing complete reduction in cell viability.Discussion and conclusion: This is the first study on the effect of these alkaloids on SW480 human colon cancer cell line. This study indicates that some alkaloids of A. mexicana strongly inhibit the cell proliferation in human colon cancer cells, and it might be a basis for future development of a potent chemotherapeutic drug.
机译:背景:Argemone mexicana Linn。罂粟科(Papaveraceae)已在印度和台湾用作治疗皮肤疾病,炎症,胆汁,发烧等的传统药物。已经筛选了墨西哥曲霉某些生物碱对不同癌细胞系的细胞毒性。目的:该研究研究了从墨西哥农杆菌的空中部分分离出的生物碱对SW480人结肠癌细胞系的潜在细胞毒性作用。材料与方法:分离了六种生物碱,13-氧代普鲁托品,原生化霉素,8-甲氧基二氢血红姜碱,脱氢花丹参碱,麻疯子碱和8-氧黄连碱墨西哥曲霉的甲醇提取物。在SW480人结肠癌细胞系上以1、25、50、75、100、125、150和200μg / mL的浓度对这些生物碱的细胞毒性进行了24小时和48小时的研究。将细胞以每孔2x10(4)个细胞的浓度接种到96孔微孔板中,并进行MTS分析以评估细胞活力,以评估细胞毒性。结果:200μg / mL时,原生抗氧化剂和13-氧代甲氧平表现出轻度的细胞毒性(约24-28%),而脱氢钴精胺表现出中度的细胞毒性(约48%)。 8-Oxberberine在24h时具有轻度的细胞毒性(约27%),但在48h时具有更强的细胞毒性(约76%)。麻风树碱和8-甲氧基二氢血红蛋白碱在抑制人结肠癌细胞增殖方面最有效(约95-100%),显示出细胞活力的完全降低。讨论和结论:这是这些生物碱对SW480人结肠的影响的首次研究。癌细胞系。这项研究表明,墨西哥曲霉的某些生物碱能强烈抑制人结肠癌细胞的细胞增殖,这可能是未来开发强效化疗药物的基础。

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