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Toxicological evaluation of an aqueous suspension from leaves and stems of Petiveria alliacea L. (Phytolaccaceae)

dc.contributor.authorGarcía-Pérez, Martha-Estrella
dc.contributor.authorAlfonso-Castillo, Alfredo
dc.contributor.authorLores, Onel Fong
dc.contributor.authorBatista-Duharte, Alexander [UNESP]
dc.contributor.authorLemus-Rodríguez, Zoe
dc.contributor.institutionLaboratorio Farmacéutico Oriente
dc.contributor.institutionInstituto Superior de Ciencias Médicas
dc.contributor.institutionUniversidad Michoacana de San Nicolás de Hidalgo
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2018-12-11T16:49:44Z
dc.date.available2018-12-11T16:49:44Z
dc.date.issued2018-01-30
dc.description.abstractEthnopharmacological relevance Petiveria alliacea L. (Phytolaccaceae) is used in folk medicine due to its antispasmodic, diuretic, hypoglycemic, abortive, anti-inflammatory and anticancerogenic properties. Although P. alliacea is considered toxic by people, its toxicity remains a concern since it is strongly dependent on the extraction method and the part of the plant used during tests. Even if some healers prefer to use the aerial parts in a liquefied form or by chewing them, instead of decoctions or infusions, no toxicological studies exist using whole dried stems and leaves. Materials and methods The toxicity of a suspension of the powder from the leaves and stems of P. alliacea was assessed in Sprague Dawley rats by oral administration using two tests: 1) the acute toxic class method, which allows classification of substances according to their intrinsic toxicity and 2) the repeated dose 28-day method, following the guidelines 423 and 407 respectively from the Organization for the Economic Cooperation and Development. Chemical characterization of this powder was performed by GC-MS, UV-fluorescence, proximate and elemental analysis. Results and conclusions P. alliacea powder from stems and leaves was classed in the hazard category 5 (LD50 > 2000 mg/kg) according to the acute toxicology study. There were no toxicity signs at 1000 mg/kg in the repeated dose study, although higher values of total leukocytes were found in the satellite and males of the experimental group, which were attributed to the immunomodulatory properties of this plant. According to GC-MS, the prevailing compounds identified were phytol, (R)-(-)-(Z)-14-methyl-8-hexadecen-1-ol, 1-(2-hydrohyethyl)-1,2,4-triazole and methyl β-dimethylaminoisobutyrate. In conclusion, the oral administration of the P. alliacea powder to Sprague Dawley rats did not result in deaths and was not associated with adverse effects reflected in the general condition, body weights or histopathological abnormalities.en
dc.description.affiliationLaboratorio Farmacéutico Oriente
dc.description.affiliationCentro de Toxicología y Biomedicina (TOXIMED) Instituto Superior de Ciencias Médicas
dc.description.affiliationFacultad de Químico-Farmacobiología Universidad Michoacana de San Nicolás de Hidalgo
dc.description.affiliationSão Paulo State University (UNESP) School of Pharmaceutical Sciences Department of Clinica Analysis
dc.description.affiliationUnespSão Paulo State University (UNESP) School of Pharmaceutical Sciences Department of Clinica Analysis
dc.format.extent29-37
dc.identifierhttp://dx.doi.org/10.1016/j.jep.2017.09.022
dc.identifier.citationJournal of Ethnopharmacology, v. 211, p. 29-37.
dc.identifier.doi10.1016/j.jep.2017.09.022
dc.identifier.file2-s2.0-85029871421.pdf
dc.identifier.issn1872-7573
dc.identifier.issn0378-8741
dc.identifier.scopus2-s2.0-85029871421
dc.identifier.urihttp://hdl.handle.net/11449/170200
dc.language.isoeng
dc.relation.ispartofJournal of Ethnopharmacology
dc.relation.ispartofsjr1,150
dc.rights.accessRightsAcesso abertopt
dc.sourceScopus
dc.subjectAcute toxic class method
dc.subjectLeaves
dc.subjectPetiveria alliacea
dc.subjectRepeated dose toxicity
dc.subjectStems
dc.titleToxicological evaluation of an aqueous suspension from leaves and stems of Petiveria alliacea L. (Phytolaccaceae)en
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublication95697b0b-8977-4af6-88d5-c29c80b5ee92
relation.isOrgUnitOfPublication.latestForDiscovery95697b0b-8977-4af6-88d5-c29c80b5ee92
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências Farmacêuticas, Araraquarapt

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