Ndjonka Dieudonné, Djafsia Boursou, Liebau Eva
Department of Biological Sciences, Faculty of Science, University of Ngaoundere, P.O. Box 454, Ngaoundere, Cameroon.
Saint Jerome School of Health Sciences, Saint Jerome Catholic University of Douala, Douala, Cameroon.
Parasitol Res. 2018 Sep;117(9):2697-2713. doi: 10.1007/s00436-018-6003-7. Epub 2018 Jul 15.
Onchocerciasis is a filarial vector borne disease which affects several million people mostly in Africa. The therapeutic approach of its control was based on a succession of drugs which always showed limits. The last one: ivermectin is not the least. It was shown to be only microfilaricidal and induced resistance to the human parasite Onchocerca volvulus. The approach using medicinal plants used in traditional medicine is a possible alternative method to cure onchocerciasis. Onchocerca ochengi and Onchocerca gutturosa are the parasite models used to assess anthelmintic activity of potentially anthelmintic plants. Numerous studies assessed the in vitro and/or in vivo anthelmintic activity of medicinal plants. Online electronic databases were consulted to gather publications on in vitro and in vivo studies of anti-Onchocerca activity of plants from 1990 to 2017. Globally, 13 plant families were investigated for anti-Onchocerca activity in 13 studies. The most active species were Anacardium occidentale, Euphorbia hirta and Acacia nilotica each with an LC value of 2.76, 6.25 and 1.2 μg/mL, respectively. Polycarpol, voacamine, voacangine, ellagic acid, gallic acid, gentisic acid, 3-O-acetyl aleuritolic acid and (-)-epigallocatechin 3-O-gallate were the isolated plant compounds with anti-Onchocerca activity. Most of the assessed extract/compounds showed a good safety after in vivo acute toxicity assays and/or in vitro cytotoxicity test. The exception was the ethanol extract of Trichilia emetica, which killed completely and drastically mice at a dose of 3000 mg/kg. Several plant groups of compounds were shown active against Onchocerca sp. such as tannins, alkaloids, triterpenoids and essential oils. Nevertheless, none of the active compounds was subjected to clinical trial, to assessment of its diffusibility through nodular wall or its capability to induce genetic resistance of Onchocerca sp.
盘尾丝虫病是一种由丝虫媒介传播的疾病,主要影响非洲的数百万人。其控制的治疗方法基于一系列始终存在局限性的药物。最后一种药物:伊维菌素也不例外。它仅显示出杀微丝蚴作用,并诱导了对人体寄生虫旋盘尾丝虫的抗性。使用传统医学中使用的药用植物的方法是治疗盘尾丝虫病的一种可能替代方法。奥氏盘尾丝虫和喉盘尾丝虫是用于评估潜在驱虫植物驱虫活性的寄生虫模型。许多研究评估了药用植物的体外和/或体内驱虫活性。查阅了在线电子数据库,以收集1990年至2017年关于植物抗盘尾丝虫活性的体外和体内研究的出版物。在全球范围内,13项研究对13个植物科进行了抗盘尾丝虫活性研究。活性最强的物种是西方腰果、麻疯树和阿拉伯金合欢,其LC值分别为2.76、6.25和1.2μg/mL。聚卡波醇、沃卡明、沃坎京、鞣花酸、没食子酸、龙胆酸、3 - O - 乙酰齐墩果酸和(-)-表没食子儿茶素3 - O - 没食子酸酯是具有抗盘尾丝虫活性的分离植物化合物。大多数评估的提取物/化合物在体内急性毒性试验和/或体外细胞毒性试验后显示出良好的安全性。例外的是吐根美登木的乙醇提取物,在剂量为3000mg/kg时会完全且剧烈地杀死小鼠。几组植物化合物对盘尾丝虫属显示出活性,如单宁、生物碱、三萜类化合物和精油。然而,没有一种活性化合物进行过临床试验,也没有评估其通过结节壁的扩散性或诱导盘尾丝虫属遗传抗性的能力。