Ethanol Extracts from Selected Tanzanian Medicinal Plants Selectively Inhibit Plasmodium falciparum Growth In Vitro

R. Christopher, Amina Msonga, H. Hoppe, F. Boyom
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Abstract

This study aimed to assess the in vitro antiplasmodial and cytotoxic activities of ethanol extracts from the root barks, leaves and stem barks of seven medicinal plant species growing in Tanzania. The antiplasmodial activities of extracts against chloroquine-sensitive (3D7) and multidrug-resistant (Dd2) strains of Plasmodium falciparum were determined using a SYBR green I-based fluorescence assay, while the cytotoxicity of active extracts was determined against the human HepG2 cell line using a resazurin-based assay. Out of twenty-one extracts screened, two of them, namely, DFRE from Dracaena fragrans root bark (IC50Pf3D7 = 2.4 mg/mL) and EHSE from Erythrina haerdii stem bark (IC50Pf3D7 = 8.6 mg/mL and IC50PfDd2 = 7.6 mg/mL), exhibited good potencies against P. falciparum parasites. The two extracts emerged as the most promising and selective inhibitors (inhibited the growth of P. falciparum strains and were not toxic to the human HepG2 cell line) of chloroquine-sensitive (3D7) and multidrug-resistant (Dd2) strains of P. falciparum. Eight other extracts showed moderate potencies with IC50 values ranging from 11–25 mg/mL against both plasmodial strains, while the remaining 11 extracts were mildly active with IC50 values ranging from 25.1 to 96.7 mg/mL. The results of the cytotoxicity test indicated that the median cytotoxic concentrations (CC50) of the tested extracts were all ≥ 224.8 mg/mL, leading to selectivity indices (SI) > 10-fold for most of the extracts. The findings described in this article support the traditional use of the investigated medicinal plants to treat malaria. Keywords: Antiplasmodial; Cytotoxicity; Ethanol extracts; Plasmodium falciparum  
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坦桑尼亚药用植物乙醇提取物对恶性疟原虫体外生长的选择性抑制
本研究旨在评估坦桑尼亚七种药用植物根皮、叶皮和茎皮乙醇提取物的体外抗疟原虫和细胞毒活性。采用SYBR绿i荧光法测定提取物对氯喹敏感(3D7)和多重耐药(Dd2)恶性疟原虫的抗疟原虫活性,采用瑞沙脲法测定活性提取物对人HepG2细胞株的细胞毒性。筛选出的21个提取物中,龙血树根皮DFRE (IC50Pf3D7 = 2.4 mg/mL)和赤螺旋藻茎皮EHSE (IC50Pf3D7 = 8.6 mg/mL和IC50PfDd2 = 7.6 mg/mL)对恶性疟原虫具有较好的抑制作用。这两种提取物是对氯喹敏感(3D7)和多重耐药(Dd2)恶性疟原虫最有希望和选择性的抑制剂(抑制恶性疟原虫菌株的生长,对人HepG2细胞系无毒性)。8个提取物对两种疟原虫的IC50值在11 ~ 25 mg/mL之间,其余11个提取物对两种疟原虫的IC50值在25.1 ~ 96.7 mg/mL之间,表现为中度活性。细胞毒性试验结果表明,所测提取物的中位细胞毒浓度(CC50)均≥224.8 mg/mL,大部分提取物的选择性指数(SI) > 10倍。本文中描述的发现支持了所研究的药用植物治疗疟疾的传统用途。关键词:Antiplasmodial;细胞毒性;乙醇提取物;恶性疟原虫
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