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dc.contributor.authorSilva, Luiz Francisco Rocha e-
dc.contributor.authorPinto, Ana Cristina da Silva-
dc.contributor.authorPohlit, Adrian Martin-
dc.contributor.authorQuignard, Etienne Louis Jacques-
dc.contributor.authorVieira, Pedro Paulo Ribeiro-
dc.contributor.authorTadei, Wanderli Pedro-
dc.contributor.authorChaves, Francisco Célio Maia-
dc.contributor.authorSamonek, Jean Francisco-
dc.contributor.authorLima, Carlos Alberto Jatoba-
dc.contributor.authorCosta, Mônica Regina Farias-
dc.contributor.authorAlecrim, Maria das Graças Costa-
dc.contributor.authorAndrade Neto, Valter Ferreira de-
dc.date.accessioned2020-06-15T21:52:15Z-
dc.date.available2020-06-15T21:52:15Z-
dc.date.issued2011-
dc.identifier.urihttps://repositorio.inpa.gov.br/handle/1/18169-
dc.description.abstract4-Nerolidylcatechol (4-NC) isolated from Piper peltatum L. (Piperaceae) was evaluated for in vitro antiplasmodial activity against Plasmodium falciparum (cultures of both standard CQR (K1) and CQS (3D7) strains and two Amazonian field isolates) and for in vivo antimalarial activity using the Plasmodium berghei-murine model. 4-NC exhibits significant in vitro and moderate in vivo antiplasmodial activity. 4-NC administered orally and subcutaneously at doses of 200, 400 and 600 mg/kg/day suppressed the growth of P. berghei by up to 63% after four daily treatments (days 1-4). Also, 4-NC exhibited important in vitro antiplasmodial activity against both standard and field P. falciparum strains in which 50% inhibition of parasite growth (IC 50) was produced at concentrations of 0.05-2.11 μg/mL and depended upon the parasite strain. Interestingly, healthy (non-infected) mice that received 4-NC orally presented (denatured) blood plasma which exhibited significant in vitro activity against P. falciparum. This is evidence that mouse metabolism allows 4-NC or active metabolites to enter the blood. Further chemical and pharmacological studies are necessary to confirm the potential of 4-NC as a new antimalarial prototype. Copyright © 2011 John Wiley & Sons, Ltd.en
dc.language.isoenpt_BR
dc.relation.ispartofVolume 25, Número 8, Pags. 1181-1188pt_BR
dc.rightsRestrito*
dc.subject4 Nerolidylcatecholen
dc.subjectAntimalarial Agenten
dc.subjectCatechol Derivativeen
dc.subjectChloroquineen
dc.subjectUnclassified Drugen
dc.subjectAnimals Cellen
dc.subjectAnimals Experimenten
dc.subjectAnimals Modelen
dc.subjectAntimalarial Activityen
dc.subjectBlood Samplingen
dc.subjectConcentration (parameters)en
dc.subjectControlled Studyen
dc.subjectDrug Determinationen
dc.subjectDrug Dose Comparisonen
dc.subjectDrug Inhibitionen
dc.subjectDrug Metabolismen
dc.subjectDrug Structureen
dc.subjectFemaleen
dc.subjectGrowth Inhibitionen
dc.subjectHumanen
dc.subjectHuman Cellen
dc.subjectIn Vitro Studyen
dc.subjectIn Vivo Studyen
dc.subjectMalariaen
dc.subjectMicrobial Growthen
dc.subjectMouseen
dc.subjectNonhumanen
dc.subjectPiper Peltatumen
dc.subjectPiperaceaeen
dc.subjectPlasmodium Bergheien
dc.subjectPlasmodium Falciparumen
dc.subjectTreatment Responseen
dc.subjectAnimalen
dc.subjectAntimalarialsen
dc.subjectCatecholsen
dc.subjectDisease Models, Animalsen
dc.subjectFemaleen
dc.subjectMalariaen
dc.subjectMalaria, Falciparumen
dc.subjectMiceen
dc.subjectPiperen
dc.subjectPlasmodium Bergheien
dc.subjectPlasmodium Falciparumen
dc.subjectMurinaeen
dc.subjectMusen
dc.subjectPiper Peltatumen
dc.subjectPiperaceaeen
dc.subjectPlasmodium Bergheien
dc.subjectPlasmodium Falciparumen
dc.titleIn vivo and in vitro antimalarial activity of 4-nerolidylcatecholen
dc.typeArtigopt_BR
dc.identifier.doi10.1002/ptr.3424-
dc.publisher.journalPhytotherapy Researchpt_BR
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