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In vitro activity of extracts and isolated polyphenols from West African medicinal plants against Plasmodium falciparum

机译:西非药用植物提取物和分离的多酚对恶性疟原虫的体外活性

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The aim of the study was to screen 11 selected traditional medicinal plants from West Africa for their in vitro antiplasmodial activity in order to determine the activity of single and of combination of plant extracts and to examine the activity of isolated pure compounds. Ethanolic and aqueous extracts of the 11 selected plants and pure compounds from Phyllanthus muellerianus and Anogeissus leiocarpus were tested in vitro against Plasmodium falciparum 3D7. Proliferation inhibitory effects were monitored after 48 h. Among the plants and pure compounds investigated in this study, geraniin from P. muellerianus, ellagic, gentisic, and gallic acids from A. leiocarpus, and extracts from A. leiocarpus, P. muellerianus and combination of A. leiocarpus with P. muellerianus affected the proliferation of P. falciparum most potently. Significant inhibitory activity was observed in combination of A. leiocarpus with P. muellerianus (IC 50=10.8 μg/ml), in combination of A. leiocarpus with Khaya senegalensis (IC 50=12.5 μg/ml), ellagic acid (IC 50=2.88 μM), and geraniin (IC 50=11.74 μM). In general growth inhibition was concentration-dependent revealing IC 50 values ranging between 10.8 and -40.1 μg/ml and 2.88 and 11.74 μM for plant extracts and pure substances respectively. Comparison with literature sources of in vivo and in vitro toxicity data revealed that thresholds are up to two times higher than the determined IC 50 values. Thus, the present study suggests that geraniin from P. muellerianus; ellagic acid, gallic acid, and gentisic acid from A. leiocarpus; and combination of extracts from A. leiocarpus with either P. muellerianus or K. senegalensis could be a potential option for malaria treatment.
机译:该研究的目的是筛选11种选自西非的传统药用植物的体外抗疟原虫活性,以确定植物提取物的单一和组合活性,并研究分离出的纯化合物的活性。在体外针对恶性疟原虫3D7对11种选定植物的乙醇提取物和水提取物以及来自Phyllanthus muellerianus和Anogeissus leiocarpus的纯化合物进行了测试。 48小时后监测增殖抑制作用。在这项研究中研究的植物和纯净化合物中,来自穆勒疟原虫的香叶素,来自leiocarpus的鞣花酸,龙胆酸和没食子酸,以及来自leiocarpus,P。muellerianus的提取物以及A. leiocarpus与muellerianus的组合。恶性疟原虫的增殖最有效。观察结果表明,在阿波罗酸杆菌和穆勒疟原虫的组合中(IC 50 = 10.8μg/ ml),在阿波罗酸杆菌和塞内加尔海藻的结合中(IC 50 = 12.5μg/ ml),鞣花酸(IC 50 = 2.88μM)和香叶素(IC 50 = 11.74μM)。通常,生长抑制是浓度依赖性的,揭示植物提取物和纯物质的IC 50值分别在10.8至-40.1μg/ ml和2.88至11.74μM之间。与体内和体外毒性数据的文献来源进行比较后发现,阈值比确定的IC 50值高两倍。因此,本研究表明,来自鼠疫假单胞菌的香叶素;得自Leocarpus的鞣花酸,没食子酸和龙胆酸;以及将Leocarpus提取物与P. muellerianus或K.senegalensis组合使用可能是治疗疟疾的潜在选择。

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