...
首页> 外文期刊>Journal of Ethnopharmacology: An Interdisciplinary Journal Devoted to Bioscientific Research on Indigenous Drugs >Cytotoxic, apoptotic and anti-alpha-glucosidase activities of 3,4-di-O-caffeoyl quinic acid, an antioxidant isolated from the polyphenolic-rich extract of Elephantopus mollis Kunth.
【24h】

Cytotoxic, apoptotic and anti-alpha-glucosidase activities of 3,4-di-O-caffeoyl quinic acid, an antioxidant isolated from the polyphenolic-rich extract of Elephantopus mollis Kunth.

机译:3,4-二-O-咖啡酰奎尼酸的细胞毒性,凋亡和抗α-葡糖苷酶活性,这是一种从富含多酚的象草提取物中分离出来的抗氧化剂。

获取原文
获取原文并翻译 | 示例
           

摘要

ETHNOPHARMACOLOGICAL RELEVANCE: The decoction of the whole plant of Elephantopus mollis Kunth. is traditionally consumed to treat various free radical-mediated diseases including cancer and diabetes. AIM OF THE STUDY: This study was initiated to determine whether the most effective antioxidant compound isolated from the whole plant of Elephantopus mollis can also contribute to its claimed traditional values as anticancer and antidiabetes agents. MATERIALS AND METHODS: An active antiradical phenolic compound (3,4-di-O-caffeoyl quinic acid) was isolated from the methanol extract (with the highest in polyphenolic content) and their antioxidant activities were compared using four different assays, that are DPPH, FRAP, metal chelating, and beta-carotene bleaching tests. The compound was also evaluated for its cytotoxic activity, apoptotic induction and anti-glucosidase efficacies using methylene blue, DeadEnd assay and alpha-glucosidase assays, respectively. RESULTS: The compound acted as a greater primary antioxidant than its methanol extract, by having higher ferric reducing activity (EC 2.18+/-0.05 mug/ml), beta-carotene bleaching activity (EC 23.85+/-0.65 mug/ml) and DPPH scavenging activity (EC 68.91+/-5.44mug/ml), whereas the methanol extract exhibited higher secondary antioxidant activity as a metal chelator with lower EC value (49.39+/-3.68 mug/ml) than the compound. Cytotoxicity screening of this compound exhibited a remarkable dose-dependent inhibitory effect on NCI-H23 (human lung adenocarcinoma) cell lines (EC 3.26+/-0.35 mug/ml) and was found to be apoptotic in nature based on a clear indication of DNA fragmentation. This compound also displayed a concentration-dependent alpha-glucosidase inhibition with EC 241.80+/-14.29 mug/ml. CONCLUSIONS: The findings indicate the major role of 3,4-di-O-caffeoyl quinic acid to antioxidant capacities of Elephantopus mollis extracts. The compound also exerted apoptosis-mediated cytotoxicity and alpha-glucosidase inhibitory effects and is thus a promising non toxic agent in treating cancer and type 2 diabetes mellitus.
机译:族裔药理关系:象草全植物的汤剂。传统上被用于治疗各种自由基介导的疾病,包括癌症和糖尿病。研究的目的:这项研究是为了确定从整个象脚草植物中分离出的最有效的抗氧化剂化合物是否也可以作为抗癌药和抗糖尿病药发挥其传统价值。材料与方法:从甲醇提取物中(多酚含量最高)分离出一种活性的抗自由基酚类化合物(3,4-二-O-咖啡酰奎尼酸),并通过四种不同的测定方法(DPPH)对它们的抗氧化活性进行了比较。 ,FRAP,金属螯合和β-胡萝卜素漂白测试。还分别使用亚甲基蓝,DeadEnd试验和α-葡萄糖苷酶试验评估了该化合物的细胞毒性活性,凋亡诱导作用和抗葡萄糖苷酶作用。结果:该化合物具有更高的三价铁还原活性(EC 2.18 +/- 0.05杯/毫升),β-胡萝卜素漂白活性(EC 23.85 +/- 0.65杯/毫升)和比其甲醇提取物更高的主要抗氧化剂。 DPPH清除活性(EC 68.91 +/- 5.44ug / ml),而甲醇提取物作为金属螯合剂表现出较高的次级抗氧化剂活性,其EC值(49.39 +/- 3.68 mug / ml)比该化合物低。对该化合物的细胞毒性筛选对NCI-H23(人肺腺癌)细胞系(EC 3.26 +/- 0.35 mug / ml)表现出显着的剂量依赖性抑制作用,并且根据DNA的明确指示,发现其在自然界具有凋亡性碎片化。该化合物还表现出浓度依赖性的α-葡糖苷酶抑制,EC 241.80 +/- 14.29马克杯/毫升。结论:研究结果表明3,4-二-O-咖啡酰奎尼酸对象牙草提取物的抗氧化能力具有重要作用。该化合物还发挥细胞凋亡介导的细胞毒性和α-葡萄糖苷酶抑制作用,因此是治疗癌症和2型糖尿病的有前途的无毒剂。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号