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dc.contributor.authorPereira, Tiago B.-
dc.contributor.authorSilva, Luiz Francisco Rocha e-
dc.contributor.authorAmorim, Rodrigo C.N.-
dc.contributor.authorMelo, Márcia R.S.-
dc.contributor.authorZacardi de Souza, Rita C.-
dc.contributor.authorEberlin, M. N.-
dc.contributor.authorLima, Emerson Silva-
dc.contributor.authorVasconcellos, Marne Carvalho de-
dc.contributor.authorPohlit, Adrian Martin-
dc.date.accessioned2020-05-21T20:06:20Z-
dc.date.available2020-05-21T20:06:20Z-
dc.date.issued2014-
dc.identifier.urihttps://repositorio.inpa.gov.br/handle/1/15981-
dc.description.abstractBackground: Carapa guianensis is a cultivable tree used by traditional health practitioners in the Amazon region to treat several diseases and particularly symptoms related to malaria. Abundant residual pressed seed material (RPSM) results as a by-product of carapa or andiroba oil production. The objective of this study was to evaluate the in vitro and in vivo anti-malarial activity and cytotoxicity of limonoids isolated from C. guaianensis RPSM.Methods. 6-acetoxyepoxyazadiradione (1), andirobin (2), 6-acetoxygedunin (3) and 7-deacetoxy-7-oxogedunin (4) (all isolated from RPSM using extraction and chromatography techniques) and 6-hydroxy-deacetylgedunin (5) (prepared from 3) were evaluated using the micro test on the multi-drug-resistant Plasmodium falciparum K1 strain. The efficacy of limonoids 3 and 4 was then evaluated orally and subcutaneously in BALB/c mice infected with chloroquine-sensitive Plasmodium berghei NK65 strain in the 4-day suppressive test.Results: In vitro, limonoids 1-5 exhibited median inhibition concentrations (IC50) of 20.7-5.0 μM, respectively. In general, these limonoids were not toxic to normal cells (MRC-5 human fibroblasts). In vivo, 3 was more active than 4. At oral doses of 50 and 100 mg/kg/day, 3 suppressed parasitaemia versus untreated controls by 40 and 66%, respectively, evidencing a clear dose-response.Conclusion: 6-acetoxygedunin is an abundant natural product present in C. guianensis residual seed materials that exhibits significant in vivo anti-malarial properties. © 2014 Pereira et al.; licensee BioMed Central Ltd.x.en
dc.language.isoenpt_BR
dc.relation.ispartofVolume 13, Número 1pt_BR
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Brazil*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/br/*
dc.subject6alpha Acetoxyepoxyazadiradioneen
dc.subject6alpha Acetoxygeduninen
dc.subject6alpha Hydroxydeacetylgeduninen
dc.subject7 Deacetoxy 7 Oxogeduninen
dc.subjectAndirobinen
dc.subjectAntimalarial Agenten
dc.subjectLimonoiden
dc.subjectPlant Extracten
dc.subjectUnclassified Drugen
dc.subjectAntimalarial Agenten
dc.subjectLimonoiden
dc.subjectPlant Extracten
dc.subjectAnimals Experimenten
dc.subjectAnimals Modelen
dc.subjectAntimalarial Activityen
dc.subjectCarapa Guianensisen
dc.subjectControlled Studyen
dc.subjectDose Responseen
dc.subjectDrug Cytotoxicityen
dc.subjectDrug Efficacyen
dc.subjectDrug Screeningen
dc.subjectFibroblasten
dc.subjectHumanen
dc.subjectHuman Cellen
dc.subjectIc 50en
dc.subjectIn Vitro Studyen
dc.subjectIn Vivo Studyen
dc.subjectMedicinal Planten
dc.subjectMeliaceaeen
dc.subjectMinimum Inhibitory Concentrationen
dc.subjectMouseen
dc.subjectNonhumanen
dc.subjectSeed Planten
dc.subjectPlasmodium Berghei Infectionen
dc.subjectPlasmodium Falciparumen
dc.subjectAnimalsen
dc.subjectBagg Albino Mouseen
dc.subjectCell Lineen
dc.subjectChemistryen
dc.subjectDrug Effectsen
dc.subjectFemaleen
dc.subjectMalariaen
dc.subjectMeliaceaeen
dc.subjectPlasmodium Bergheien
dc.subjectAnimalen
dc.subjectAntimalarialsen
dc.subjectCell Lineen
dc.subjectFemaleen
dc.subjectHumansen
dc.subjectInhibitory Concentration 50en
dc.subjectLimoninsen
dc.subjectMalariaen
dc.subjectMeliaceaeen
dc.subjectMiceen
dc.subjectMice, Inbred Balb Cen
dc.subjectPlant Extractsen
dc.subjectPlasmodium Bergheien
dc.subjectPlasmodium Falciparumen
dc.subjectSeedsen
dc.titleIn vitro and in vivo anti-malarial activity of limonoids isolated from the residual seed biomass from Carapa guianensis (andiroba) oil productionen
dc.typeArtigopt_BR
dc.identifier.doi10.1186/1475-2875-13-317-
dc.publisher.journalMalaria Journalpt_BR
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