Brazilian cerrado Qualea grandiflora Mart. leaves exhibit antiplasmodial and trypanocidal activities In vitro

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Abstract
Pharmacognosy Magazine ,2017,13,52,668-672.
Published:November 2017
Type:Original Article
Authors:
Author(s) affiliations:

Thuany de Moura Cordeiro1, Fabian Borghetti2, Sarah C Caldas Oliveira3, Izabela Marques Dourado Bastos4, Jaime Martins de Santana4, Philippe Grellier5, Sébastien Charneau1
1Department of Cell Biology, Laboratory of Biochemistry and Protein Chemistry, Institute of Biology, University of Brasilia, Darcy Ribeiro Campus, 70910-900, Brasilia, DF, Brazil
2Department of Botany, Laboratory of Thermobiology, Institute of Biology, University of Brasilia, Darcy Ribeiro Campus, 70910-900, Brasilia, DF, Brazil
3Department of Botany, Laboratory of Allelopathy, Institute of Biology, University of Brasilia, Darcy Ribeiro Campus, 70910-900, Brasilia, DF, Brazil
4Department of Cell Biology, Laboratory of Host-Pathogen Interaction, Institute of Biology, University of Brasilia, Darcy Ribeiro Campus, 70910-900, Brasilia, DF, Brazil
5UMR 7245 CNRS, Communication Molecules and Adaptation of Microorganisms, CP 52, 61 rue Buffon, 75231 PARIS CEDEX 05, France

Abstract:

Background: The rapid spread of drug-resistant strains of protozoan parasites required the urgent need for new effective drugs. Natural products offer a variety of chemical structures, which make them a valuable source of lead compounds for the development of such new drugs. Cerrado is the second largest biome in Brazil and has the richest flora of all the world savannahs. We selected Qualea grandiflora, a plant species known for its proprieties in folk medicine and its antibacterial activity. Objective: However, its antiprotozoal activity was not yet explored. Materials and Methods: We investigated the activities of fractions from the ethyl acetate extract of Q. grandiflora leaves against human life forms of Plasmodium falciparumTrypanosoma cruzi, and Trypanosoma brucei gambiense, and for its cytotoxicity upon the rat L6-myoblast cell line. Ten fractions were produced by ethyl acetate:hexane chromatography. Results and Conclusion: The fractions showed no cytotoxicity against L-6 cells (IC50 > 100 μg/mL) and no hemolysis propriety. Three fractions had a moderate activity against P. falciparum, anyone was active against T. cruzi but four fractions demonstrated a high activity against bloodstream forms of T. brucei gambiense (8.0< IC50 <15 μg/mL). Identification and characterization of the active compounds are currently under investigation.

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