Anthelmintic activity in vivo of epiisopiloturine against juvenile and adult worms of Schistosoma mansoni

PLoS Negl Trop Dis. 2015 Mar 27;9(3):e0003656. doi: 10.1371/journal.pntd.0003656. eCollection 2015 Mar.

Abstract

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 4-Butyrolactone / analogs & derivatives*
  • 4-Butyrolactone / pharmacology
  • Animals
  • Dose-Response Relationship, Drug
  • Feces / parasitology
  • Granuloma / pathology
  • Imidazoles / pharmacology*
  • Liver / drug effects
  • Liver / parasitology
  • Mice
  • Microscopy, Electron, Scanning
  • Schistosoma mansoni / drug effects*
  • Schistosoma mansoni / ultrastructure
  • Schistosomiasis mansoni / drug therapy*
  • Schistosomicides / pharmacology*

Substances

  • Imidazoles
  • Schistosomicides
  • epiisopiloturine
  • 4-Butyrolactone

Grants and funding

This study was supported by the Coordenação de Aperfeiçoamento de Pessoal de Nível Supeior, Brazilian Ministry of Education (CAPES, Grant 705/2009, Nanobiomed Network), the authors ACM, YM, JRSAL, MAG, and LMCV. This work has also been supported by the Fundação para a Ciência e a Tecnologia (FCT) (grants number PEst-C/EQB/LA0006/2011 and PTDC/CTM-NAN/109877/2009) (The author PE) and through a joint Conselho Nacional de Desenvolvimento Cientifico e Tecnologico, Brazilian Ministry of Science and Technology (CNPq/FCT Bilateral Grant 490585/2010-8) (The authors JRSA, PE and LMCV). The author JM is grateful to the Faculdade de Ciências de Guarulhos FACIG/UNIESP and Conselho Nacional de Desenvolvimento Cientifico e Tecnologico, Brazilian Ministry of Science and Technology (MCTI/CNPq/MS-SCTIE) (Grant number 40/2012, 404134/2012-2 - Projeto sobre Doenças Negligenciadas). The author ACM is grateful to Fundação e Amparo a Pesquisa do Estado de São Paulo (FAPESP) (Grant number 2014/02282-6). TZV is grateful to Ministry of Education, Science, and Technological Development of Serbia (Grant number 172008). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.