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Antileishmanial and antitrypanosomal activity of the cutaneous secretion of Siphonops annulatus
Pinto, Erika Gracielle; Antoniazzi, Marta Maria; Jared, Carlos; Tempone, Andre Gustavo.
Afiliação
  • Pinto, Erika Gracielle; Instituto Adolfo Lutz. Departamento de Parasitologia e Micologia. São Paulo. BR
  • Antoniazzi, Marta Maria; Butantan Institute. Laboratory of Cell Biology. São Paulo. BR
  • Jared, Carlos; Butantan Institute. Laboratory of Cell Biology. São Paulo. BR
  • Tempone, Andre Gustavo; Instituto Adolfo Lutz. Departamento de Parasitologia e Micologia. São Paulo. BR
J. venom. anim. toxins incl. trop. dis ; J. venom. anim. toxins incl. trop. dis;20: 1-9, 04/02/2014. graf, ilus, tab
Article em En | LILACS, VETINDEX | ID: biblio-1484599
Biblioteca responsável: BR68.1
Localização: BR68.1
ABSTRACT
Background Among the tropical parasitic diseases, those caused by protozoans are considered a challenge to public health, being represented by leishmaniasis and Chagas disease. In view of the low effectiveness and toxicity of the current therapy, animal venoms such as amphibian secretions have been used as a promising source of new drug prototypes. The present work aimed to achieve bioguided fractionation of metabolites present in a cutaneous secretion of the caecilian Siphonops annulatus (Amphibia Gymnophiona Siphonopidae) with antileishmanial and antitrypanosomal activity.Methods Through liquid-liquid partition and chromatographic techniques, the secretion was fractionated using bioguided assays. The 50% inhibitory concentration (IC50) of the main fraction (SaFr1) was studied against Leishmania (L.) infantumpromastigotes and intracellular amastigotes, trypomastigotes ofTrypanosoma cruzi and mammalian cells; viability was detected by the colorimetric MTT assay. By using a spectrofluorimetric assay with the probe SYTOX® Green and transmission electron microscopy (TEM), we also investigated the potential damage caused by SaFr1 in the plasma membrane and mitochondria of Leishmania.Results The bioguided assay enabled isolation of a highly purified fraction (SaFr1) with an IC50 of 0.065 g/mL against promastigotes and 2.75 g/mL against trypomastigotes. Due to its high toxicity to peritoneal macrophages, SaFr1 showed no selectivity towards the intracellular forms ofLeishmania. Ultrastructural studies withLeishmania demonstrated severe mitochondrial damage and the formation of large cytoplasmic vacuoles, leading to the parasites death within a few hours...
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Texto completo: 1 Coleções: 01-internacional Base de dados: LILACS / VETINDEX Assunto principal: Trypanosoma cruzi / Preparações Farmacêuticas / Venenos de Anfíbios / Leishmania / Antiprotozoários Limite: Animals Idioma: En Revista: J. venom. anim. toxins incl. trop. dis Assunto da revista: TOXICOLOGIA Ano de publicação: 2014 Tipo de documento: Article / Project document País de afiliação: Brasil

Texto completo: 1 Coleções: 01-internacional Base de dados: LILACS / VETINDEX Assunto principal: Trypanosoma cruzi / Preparações Farmacêuticas / Venenos de Anfíbios / Leishmania / Antiprotozoários Limite: Animals Idioma: En Revista: J. venom. anim. toxins incl. trop. dis Assunto da revista: TOXICOLOGIA Ano de publicação: 2014 Tipo de documento: Article / Project document País de afiliação: Brasil