Publicação:
Absence of chemopreventive influence of propolis on the rat liver altered foci development

dc.contributor.authorSaid, Roueda Abou
dc.contributor.authorGrassi, Tony Fernando [UNESP]
dc.contributor.authorScolastici, Clarissa [UNESP]
dc.contributor.authorAlves de Lima, Rodrigo Otavio [UNESP]
dc.contributor.authorDarros, Bruno R. [UNESP]
dc.contributor.authorBarbisan, Luis Fernando [UNESP]
dc.contributor.authorCamargo, João Lauro Viana de [UNESP]
dc.contributor.institutionUniv Estadual Santa Cruz
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T13:37:31Z
dc.date.available2014-05-20T13:37:31Z
dc.date.issued2010-07-01
dc.description.abstractPropolis (bee glue) is a complex mixture of natural substances that exhibits a broad spectrum of biological activities. As the possibility exists that it may exert a chemopreventive role against cancer development, the present study aimed to evaluate the chemopreventive influence of a Brazilian aqueous propolis extract (APE) in a rat two-stage (initiation-promotion) medium-term bioassay for chemical liver carcinogenesis. Male Wistar rats were sequentially initiated with diethylnitrosamine (DEN, 200 mg/kg b.w.) and, 2 weeks later, exposed to a diet containing hexachlorobenzene (HCB, 100 ppm) and to APE 0.1% through drinking water for 6 weeks. Appropriate control groups were also established. The animals were sacrificed at the weeks 8th and 30th when liver samples were processed to evaluate the development of altered hepatocyte foci (AHF) identified under hematoxylin and eosin (H&E) staining and by the immunohistochemical expression of the enzyme glutathione S-transferase placental form (GST-P). The results indicate that APE 0.1% did not protect against the development of any of the differentially identified putative preneoplastic foci in DEN-initiated animals, exposed or not to the promoting agent HCB. Also, APE 0.1% by itself did not significantly induce any AHF, what is in line with its already known absence of genotoxic potential. Our results indicate that an aqueous extract of Brazilian propolis did not exert chemoprevention on the hepatocarcinogenesis process chemically induced in the rat. (C) 2009 Elsevier GmbH. All rights reserved.en
dc.description.affiliationUniv Estadual Santa Cruz, Dept Environm & Agrarian Sci, Ilheus, Bahia, Brazil
dc.description.affiliationSão Paulo State Univ, TOXICAM Nucleus Evaluat Environm Impact Human Hlt, Dept Pathol, Sch Med, BR-18618000 Botucatu, SP, Brazil
dc.description.affiliationSão Paulo State Univ, Dept Morphol, Inst Biosci, BR-18618000 Botucatu, SP, Brazil
dc.description.affiliationUnespSão Paulo State Univ, TOXICAM Nucleus Evaluat Environm Impact Human Hlt, Dept Pathol, Sch Med, BR-18618000 Botucatu, SP, Brazil
dc.description.affiliationUnespSão Paulo State Univ, Dept Morphol, Inst Biosci, BR-18618000 Botucatu, SP, Brazil
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipIdFAPESP: 00/08000-0
dc.format.extent405-412
dc.identifierhttp://dx.doi.org/10.1016/j.etp.2009.05.012
dc.identifier.citationExperimental and Toxicologic Pathology. Jena: Elsevier Gmbh, Urban & Fischer Verlag, v. 62, n. 4, p. 405-412, 2010.
dc.identifier.doi10.1016/j.etp.2009.05.012
dc.identifier.issn0940-2993
dc.identifier.lattes3278528112652257
dc.identifier.urihttp://hdl.handle.net/11449/12996
dc.identifier.wosWOS:000280425200009
dc.language.isoeng
dc.publisherElsevier Gmbh, Urban & Fischer Verlag
dc.relation.ispartofExperimental and Toxicologic Pathology
dc.relation.ispartofjcr2.023
dc.relation.ispartofsjr0,551
dc.rights.accessRightsAcesso restrito
dc.sourceWeb of Science
dc.subjectPropolisen
dc.subjectDiethylnitrosamineen
dc.subjectHexachlorobenzeneen
dc.subjectGST-P-positive focien
dc.subjectHepatocarcinogenesisen
dc.subjectWistar ratsen
dc.titleAbsence of chemopreventive influence of propolis on the rat liver altered foci developmenten
dc.typeArtigo
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderElsevier Gmbh, Urban & Fischer Verlag
dspace.entity.typePublication
unesp.author.lattes3278528112652257[6]
unesp.author.orcid0000-0003-2257-7751[21]
unesp.author.orcid0000-0001-7040-9846[486]
unesp.author.orcid0000-0001-8809-8927[1038]
unesp.author.orcid0000-0002-5492-6920[1469]
unesp.author.orcid0000-0001-5847-0062[191]
unesp.author.orcid0000-0002-3865-4996[1362]
unesp.author.orcid0000-0002-0568-665X[119]
unesp.author.orcid0000-0001-7291-1979[817]
unesp.author.orcid0000-0002-6356-2655[1921]
unesp.author.orcid0000-0002-1653-1303[1181]
unesp.author.orcid0000-0003-4281
unesp.campusUniversidade Estadual Paulista (Unesp), Instituto de Biociências, Botucatupt
unesp.campusUniversidade Estadual Paulista (Unesp), Faculdade de Medicina, Botucatupt
unesp.departmentPatologia - FMBpt
unesp.departmentMorfologia - IBBpt

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