Guimarães Maria A, de Oliveira Rosimeire N, Véras Leiz M C, Lima David F, Campelo Yuri D M, Campos Stefano Augusto, Kuckelhaus Selma A S, Pinto Pedro L S, Eaton Peter, Mafud Ana C, Mascarenhas Yvonne P, Allegretti Silmara M, de Moraes Josué, Lolić Aleksandar, Verbić Tatjana, Leite José Roberto S A
Biotechnology and Biodiversity Center Research, BIOTEC, Federal University of Piauí, Parnaíba, Piauí, Brazil.
Department of Animal Biology, Institute of Biology, State University of Campinas, Campinas, São Paulo, Brazil.
PLoS Negl Trop Dis. 2015 Mar 27;9(3):e0003656. doi: 10.1371/journal.pntd.0003656. eCollection 2015 Mar.
Schistosomiasis is a serious disease currently estimated to affect more that 207 million people worldwide. Due to the intensive use of praziquantel, there is increasing concern about the development of drug-resistant strains. Therefore, it is necessary to search for and investigate new potential schistosomicidal compounds. This work reports the in vivo effect of the alkaloid epiisopiloturine (EPI) against adults and juvenile worms of Schistosoma mansoni. EPI was first purified its thermal behavior and theoretical solubility parameters charaterised. In the experiment, mice were treated with EPI over the 21 days post-infection with the doses of 40 and 200 mg/kg, and 45 days post-infection with single doses of 40, 100 and 300 mg/kg. The treatment with EPI at 40 mg/kg was more effective in adult worms when compared with doses of 100 and 300 mg/kg. The treatment with 40 mg/kg in adult worms reduced parasite burden significantly, lead to reduction in hepatosplenomegaly, reduced the egg burden in faeces, and decreased granuloma diameter. Scanning electron microscopy revealed morphological changes to the parasite tegument after treatment, including the loss of important features. Additionally, the in vivo treatment against juvenile with 40 mg/kg showed a reduction of the total worm burden of 50.2%. Histopathological studies were performed on liver, spleen, lung, kidney and brain and EPI was shown to have a DL50 of 8000 mg/kg. Therefore EPI shows potential to be used in schistosomiasis treatment. This is the first time that schistosomicidal in vivo activity of EPI has been reported.
血吸虫病是一种严重疾病,目前估计全球有超过2.07亿人受其影响。由于吡喹酮的大量使用,人们越来越担心耐药菌株的出现。因此,有必要寻找和研究新的潜在杀血吸虫化合物。这项工作报道了生物碱表异舵尾尿碱(EPI)对曼氏血吸虫成虫和幼虫的体内作用。首先对EPI进行了纯化,并对其热行为和理论溶解度参数进行了表征。在实验中,感染后21天,小鼠分别以40和200mg/kg的剂量接受EPI治疗;感染后45天,小鼠分别接受40、100和300mg/kg的单剂量治疗。与100和300mg/kg的剂量相比,40mg/kg的EPI治疗对成虫更有效。40mg/kg的EPI治疗显著降低了成虫的寄生虫负荷,减轻了肝脾肿大,减少了粪便中的虫卵负荷,并减小了肉芽肿直径。扫描电子显微镜显示治疗后寄生虫体表出现形态变化,包括重要特征的丧失。此外,40mg/kg的EPI对幼虫的体内治疗使总虫负荷降低了50.2%。对肝脏、脾脏、肺、肾脏和大脑进行了组织病理学研究,结果显示EPI的半数致死剂量为8000mg/kg。因此,EPI显示出用于治疗血吸虫病的潜力。这是首次报道EPI的体内杀血吸虫活性。