Your browser doesn't support javascript.
loading
Anthelmintic activity in vivo of epiisopiloturine against juvenile and adult worms of Schistosoma mansoni.
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; Lolic, Aleksandar; Verbic, Tatjana; Leite, José Roberto S A.
Afiliação
  • Guimarães MA; Biotechnology and Biodiversity Center Research, BIOTEC, Federal University of Piauí, Parnaíba, Piauí, Brazil.
  • de Oliveira RN; Department of Animal Biology, Institute of Biology, State University of Campinas, Campinas, São Paulo, Brazil.
  • Véras LM; Biotechnology and Biodiversity Center Research, BIOTEC, Federal University of Piauí, Parnaíba, Piauí, Brazil; Graduate Program in Biotechnology, RENORBIO, Focal Point Federal University of Piauí, Teresina, Piauí, Brazil.
  • Lima DF; Biotechnology and Biodiversity Center Research, BIOTEC, Federal University of Piauí, Parnaíba, Piauí, Brazil; Graduate Program in Biotechnology, RENORBIO, Focal Point Federal University of Piauí, Teresina, Piauí, Brazil; Collegiate Academic Medicine, Federal University of São Francisco Valley, Campu
  • Campelo YD; Biotechnology and Biodiversity Center Research, BIOTEC, Federal University of Piauí, Parnaíba, Piauí, Brazil; Graduate Program in Biotechnology, RENORBIO, Focal Point Federal University of Piauí, Teresina, Piauí, Brazil.
  • Campos SA; Biotechnology and Biodiversity Center Research, BIOTEC, Federal University of Piauí, Parnaíba, Piauí, Brazil.
  • Kuckelhaus SA; Faculty of Medicine, University of Brasilia, UNB Campus Dacy Ribeiro, Brasília, Distrito Federal, Brazil.
  • Pinto PL; Adolfo Lutz Institute, Central Laboratory, São Paulo, Brazil.
  • Eaton P; UCIBIO, REQUIMTE, Department of Chemistry and Biochemistry, Faculty of Science, University of Porto, Portugal.
  • Mafud AC; Group of Crystallography, Institute of Physics of São Carlos, University of São Paulo, São Carlos, São Paulo, Brazil.
  • Mascarenhas YP; Group of Crystallography, Institute of Physics of São Carlos, University of São Paulo, São Carlos, São Paulo, Brazil.
  • Allegretti SM; Department of Animal Biology, Institute of Biology, State University of Campinas, Campinas, São Paulo, Brazil.
  • de Moraes J; Research Center for Neglected Diseases (NPDN/FACIG), Guarulhos, São Paulo, Brazil.
  • Lolic A; Faculty of Chemistry, University of Belgrade, Belgrade, Serbia.
  • Verbic T; Faculty of Chemistry, University of Belgrade, Belgrade, Serbia.
  • Leite JR; Biotechnology and Biodiversity Center Research, BIOTEC, Federal University of Piauí, Parnaíba, Piauí, Brazil.
PLoS Negl Trop Dis ; 9(3): e0003656, 2015 Mar.
Article em En | MEDLINE | ID: mdl-25816129
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.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Schistosoma mansoni / Esquistossomicidas / Esquistossomose mansoni / 4-Butirolactona / Imidazóis Limite: Animals Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Schistosoma mansoni / Esquistossomicidas / Esquistossomose mansoni / 4-Butirolactona / Imidazóis Limite: Animals Idioma: En Ano de publicação: 2015 Tipo de documento: Article