Literature DB >> 17659386

Comparative studies of the anti-leishmanial activity of three Crotalus durissus ssp. venoms.

L F D Passero1, T Y Tomokane, C E P Corbett, M D Laurenti, M H Toyama.   

Abstract

In this study, we compared the anti-leishmanial activity of three crotalic venoms (Crotalus durissus terrificus-Cdt, Crotalus durissus cascavella-Cdca, and Crotalus durissus collilineatus-Cdcol). Different concentrations of each venom incubated with Leishmania (Leishmania) amazonensis promastigotes were used. Cdt venom exhibited a higher anti-leishmanial activity (Inhibitory concentration-IC50-value of 4.70+/-1.72 microg/ml) in comparison with that of Cdca venom (IC50 value of 9.41+/-1.21 microg/ml), while Cdcol venom increased parasite numbers in 50% at a concentration of 44.30+/-2.18 microg/ml. In addition, this venom showed a low anti-leishmanial activity in higher concentrations (IC50 value of 281.00+/-9.50 microg/ml). The main fractions of Cdca venom were isolated and assayed under similar conditions used for assessing crude venom. The most active fractions were gyroxin and crotamine that had IC50 values of 3.80+/-0.52 microg/ml and 19.95+/-4.21 microg/ml, respectively. Convulxin also inhibited parasite growth rate, although this effect was not dose-dependent. Crotoxin was the least effective fraction with an IC50 value of 99.80+/-2.21 microg/ml. None of the protein fractions presented cytotoxic effects against J774 cells in culture. In vivo assays using BALB/c mice revealed that crotoxin and crotamine were the main toxic fractions. In conclusion, C. durissus cascavella venom has three main fractions with anti-leishmanial activity. These results open new possibilities to find proteins that might be used as possible agents against cutaneous leishmaniasis.

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Year:  2007        PMID: 17659386     DOI: 10.1007/s00436-007-0653-1

Source DB:  PubMed          Journal:  Parasitol Res        ISSN: 0932-0113            Impact factor:   2.289


  21 in total

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4.  Biochemistry and pharmacology of the crotoxin complex. I. Subfractionation and recombination of the crotoxin complex.

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7.  Structure-function relationship of new crotamine isoform from the Crotalus durissus cascavella.

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Authors:  Marcos Hikari Toyama; Daniela Garcia de Oliveira; Luis O S Beriam; José Camillo Novello; Léa Rodrigues-Simioni; Sergio Marangoni
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  12 in total

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Authors:  Luiz Felipe D Passero; Alexis Bonfim-Melo; Carlos Eduardo P Corbett; Márcia D Laurenti; Marcos H Toyama; Daniela O de Toyama; Paulete Romoff; Oriana A Fávero; Simone S dos Grecco; Cynthia A Zalewsky; João Henrique G Lago
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2.  The effect of phospholipase A2 from Crotalus durissus collilineatus on Leishmania (Leishmania) amazonensis infection.

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Authors:  Lídia J Tasima; Caroline Serino-Silva; Daniela M Hatakeyama; Erika S Nishiduka; Alexandre K Tashima; Sávio S Sant'Anna; Kathleen F Grego; Karen de Morais-Zani; Anita M Tanaka-Azevedo
Journal:  J Venom Anim Toxins Incl Trop Dis       Date:  2020-04-06

7.  Evaluation of macroalgae sulfated polysaccharides on the Leishmania (L.) amazonensis promastigote.

Authors:  Camila Lehnhardt Pires; Selma Dzimidas Rodrigues; Daniel Bristot; Henrique Hessel Gaeta; Daniela de Oliveira Toyama; Wladimir Ronald Lobo Farias; Marcos Hikari Toyama
Journal:  Mar Drugs       Date:  2013-03-20       Impact factor: 5.118

8.  Identification of two novel cytolysins from the hydrozoan Olindias sambaquiensis (Cnidaria).

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9.  In vitro activity of phospholipase A2 and of peptides from Crotalus durissus terrificus venom against amastigote and promastigote forms of Leishmania (L.) infantum chagasi.

Authors:  Gustavo A C Barros; Andreia V Pereira; Luciana C Barros; Airton Lourenço; Sueli A Calvi; Lucilene D Santos; Benedito Barraviera; Rui Seabra Ferreira
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10.  The Metabolomic Profiles of Sera of Mice Infected with Plasmodium berghei and Treated by Effective Fraction of Naja naja oxiana Using 1H Nuclear Magnetic Resonance Spectroscopy.

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