The University of Adelaide, School of Animal and Veterinary Science, Roseworthy, South Australia, 5352, Australia; Murdoch University, School of Veterinary and Life Science, Murdoch, Western Australia, 6150, Australia.
Murdoch University, School of Veterinary and Life Science, Murdoch, Western Australia, 6150, Australia.
Int J Parasitol Drugs Drug Resist. 2019 Aug;10:38-44. doi: 10.1016/j.ijpddr.2019.04.003. Epub 2019 Apr 8.
Giardia duodenalis is an ubiquitous parasitic pathogen that causes significant morbidity and mortality worldwide. Failures in drug therapy are commonly due to poor patient compliance as a result of the need for repeated administration, off target drug effects and increasing parasite drug resistance. In this study the in vitro efficacy and selectivity of the aminoguanidine compound robenidine and 2 structural analogues against Giardia were determined. After 5 h exposure to each compound the IC was as low as 0.2 μM with corresponding MLCs as low as 2.8 μM. This is in contrast to metronidazole which required 24 h to exhibit inhibitory activity. A modified adherence assay, developed for this study, demonstrated that three of the compounds inhibited in vitro adherence of the parasite. The lead compound exhibited rapid giardicidal activity (<5hr). In addition, microscopy studies demonstrated damage to the plasma membrane of trophozoites. In conclusion, a class of aminoguanidines, represented by robenidine, has shown antigiardial activity warranting further investigation.
十二指肠贾第鞭毛虫是一种普遍存在的寄生虫病原体,在全球范围内造成了很大的发病率和死亡率。药物治疗的失败通常是由于需要重复给药、药物靶向外的副作用以及寄生虫耐药性的增加,导致患者顺应性差。在这项研究中,测定了氨基胍化合物罗贝林和 2 种结构类似物对贾第鞭毛虫的体外疗效和选择性。暴露于每种化合物 5 小时后,IC 低至 0.2 μM,相应的 MLC 低至 2.8 μM。这与甲硝唑形成对比,甲硝唑需要 24 小时才能表现出抑制活性。为这项研究开发的改良黏附测定法表明,三种化合物抑制了寄生虫的体外黏附。先导化合物表现出快速杀贾第虫活性(<5 小时)。此外,显微镜研究表明滋养体的质膜受损。总之,以罗贝林为代表的一类氨基胍类化合物表现出抗贾第虫活性,值得进一步研究。