Ndjonka D, Abladam E D, Djafsia B, Ajonina-Ekoti I, Achukwi M D, Liebau E
Faculty of Science, University of Ngaoundere,PO Box 454,Ngaoundere,Cameroon.
Institute for Zoophysiology,Schlossplatz 8,48143Muenster,Germany.
J Helminthol. 2014 Dec;88(4):481-8. doi: 10.1017/S0022149X1300045X. Epub 2013 Jun 17.
The effect of three phenols (ellagic, gentisic and gallic acids) from the axlewood tree Anogeissus leiocarpus on Onchocerca ochengi and drug-resistant strains of Caenorhabditis elegans, a model organism for research on nematode parasites, is investigated. Worms were incubated in different concentrations of phenols and their survival was monitored after 48 h. Among the three acids, ellagic acid strongly affected the survival of O. ochengi microfilariae, O. ochengi adults, a wild-type C. elegans and anthelmintic-resistant strains of C. elegans, namely albendazole (CB3474), levamisole (CB211, ZZ16) and ivermectin (VC722, DA1316), with LC50 values ranging from 0.03 mm to 0.96 mm. These results indicate that the binding of ellagic acid in the worm differs from that of resistant strains of C. elegans. The efficacy of both gallic and gentisic acids was not significantly changed in resistant strains of C. elegans treated with levamisole (ZZ16, LC50= 9.98 mm, with gallic acid), albendazole (CB3474, LC50= 7.81 mm, with gentisic acid) and ivermectin (DA1316, LC50= 10.62 mm, with gentisic acid). The efficacy of these three pure compounds is in accordance with the use of A. leiocarpus from its locality of origin. The in vivo toxicity data reveal that the thresholds are up to 200 times higher than the determined LC50 values. Thus, ellagic acid could be a potential option for the treatment of nematode infections, even in cases of drug resistance towards established anthelmintic drugs.
研究了来自轴木(Anogeissus leiocarpus)的三种酚类物质(鞣花酸、龙胆酸和没食子酸)对线虫寄生虫研究的模式生物——奥氏盘尾丝虫(Onchocerca ochengi)以及秀丽隐杆线虫(Caenorhabditis elegans)耐药菌株的影响。将蠕虫置于不同浓度的酚类物质中孵育,并在48小时后监测其存活率。在这三种酸中,鞣花酸强烈影响奥氏盘尾丝虫微丝蚴、奥氏盘尾丝虫成虫、野生型秀丽隐杆线虫以及秀丽隐杆线虫的抗驱虫药菌株,即阿苯达唑(CB3474)、左旋咪唑(CB211、ZZ16)和伊维菌素(VC722、DA1316)的存活,其半数致死浓度(LC50)值在0.03毫米至0.96毫米之间。这些结果表明,鞣花酸在蠕虫中的结合方式与秀丽隐杆线虫耐药菌株不同。在用左旋咪唑(ZZ16,LC50 = 9.98毫米,与没食子酸联用)、阿苯达唑(CB3474,LC50 = 7.81毫米,与龙胆酸联用)和伊维菌素(DA1316,LC50 = 10.62毫米,与龙胆酸联用)处理的秀丽隐杆线虫耐药菌株中,没食子酸和龙胆酸的效力没有显著变化。这三种纯化合物的效力与轴木在其原产地的使用情况相符。体内毒性数据显示,阈值比测定的LC50值高出200倍。因此,即使在对现有驱虫药产生耐药性的情况下,鞣花酸也可能是治疗线虫感染的潜在选择。