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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/72789
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dc.contributor.authorLima, Zeila P.-
dc.contributor.authorBonamin, Flavia-
dc.contributor.authorCalvo, Tamara R.-
dc.contributor.authorVilegas, Wagner-
dc.contributor.authorSantos, Lourdes C.-
dc.contributor.authorRozza, Ariane L.-
dc.contributor.authorPellizzon, Claudia H.-
dc.contributor.authorRocha, Lucia R. M.-
dc.contributor.authorHiruma-Lima, Clélia A.-
dc.date.accessioned2014-05-27T11:26:07Z-
dc.date.accessioned2016-10-25T18:35:00Z-
dc.date.available2014-05-27T11:26:07Z-
dc.date.available2016-10-25T18:35:00Z-
dc.date.issued2011-11-09-
dc.identifierhttp://dx.doi.org/10.3390/ph4111423-
dc.identifier.citationPharmaceuticals, v. 4, n. 11, p. 1423-1433, 2011.-
dc.identifier.issn1424-8247-
dc.identifier.urihttp://hdl.handle.net/11449/72789-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/72789-
dc.description.abstractAlchornea triplinervia (Spreng.) Muell. Arg (Euphorbiaceae) is a medicinal plant commonly used by people living in the Cerrado region of Brazil to treat gastrointestinal ulcers. We previously described the gastroprotective action of methanolic extract (ME) of Alchornea triplinervia and the ethyl acetate fraction (EAF) in increasing of prostaglandin E 2 (PGE 2) gastric levels in the mucosa. In this work we evaluated the effect of EAF in promoting the healing process in rats with acetic acid-induced gastric ulcers. In addition, toxicity was investigated during treatment with EAF. After 14 days of treatment with EAF, the potent stimulator of gastric cell proliferation contributed to the acceleration of gastric ulcer healing. Upon immunohistochemical analysis, we observed a pronounced expression of COX-2, mainly in the submucosal layer. The 14-day EAF treatment also significantly increased the number of neutrophils in the gastric mucosa regeneration area. The EAF induced angiogenesis on gastric mucosa, observed as an increase of the number of blood vessels supplying the stomach in rats treated with EAF. Oral administration for 14 days of the ethyl acetate fraction from Alchornea triplinervia accelerated the healing of gastric ulcers in rats by promoting epithelial cell proliferation, increasing the number of neutrophils and stimulation of mucus production. This fraction, which contained mainly phenolic compounds, contributed to gastric mucosa healing. © 2011 by the authors; licensee MDPI, Basel, Switzerland.en
dc.format.extent1423-1433-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectAlchornea triplinervia-
dc.subjectAngiogenesis-
dc.subjectEuphorbiaceae-
dc.subjectHealing ulcer effect-
dc.subjectPhenolic compounds-
dc.subjectacetic acid ethyl ester-
dc.subjectAlchornea triplinervia extract-
dc.subjectantiulcer agent-
dc.subjectcimetidine-
dc.subjectcyclooxygenase 2-
dc.subjectplant extract-
dc.subjectunclassified drug-
dc.subjectangiogenesis-
dc.subjectanimal cell-
dc.subjectanimal experiment-
dc.subjectanimal model-
dc.subjectanimal tissue-
dc.subjectcell proliferation-
dc.subjectcontrolled study-
dc.subjectdose response-
dc.subjectdrug effect-
dc.subjectdrug mechanism-
dc.subjectdrug screening-
dc.subjectEuphorbia-
dc.subjectimmunohistochemistry-
dc.subjectmale-
dc.subjectmucus secretion-
dc.subjectneutrophil count-
dc.subjectnonhuman-
dc.subjectplant leaf-
dc.subjectprotein expression-
dc.subjectrat-
dc.subjectsingle drug dose-
dc.subjectstomach mucosa injury-
dc.subjectstomach protection-
dc.subjectstomach ulcer-
dc.subjecttissue regeneration-
dc.subjecttoxicity testing-
dc.subjectulcer healing-
dc.subjectulcerogenesis-
dc.titleEffects of the ethyl acetate fraction of Alchornea triplinervia on healing gastric ulcer in ratsen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationDepartment of Physiology Univ. Estadual Paulista-UNESP, Rubião Junior, cp 510, CEP 18618-000, Botucatu, São Paulo-
dc.description.affiliationInstitute of Chemistry Univ. Estadual Paulista-UNESP, cp 355, CEP 14801-970, Araraquara, São Paulo-
dc.description.affiliationDepartment of Morphology Univ. Estadual Paulista-UNESP, cp 610, CEP 18618-000, UNESP, Botucatu, São Paulo-
dc.description.affiliationUnespDepartment of Physiology Univ. Estadual Paulista-UNESP, Rubião Junior, cp 510, CEP 18618-000, Botucatu, São Paulo-
dc.description.affiliationUnespInstitute of Chemistry Univ. Estadual Paulista-UNESP, cp 355, CEP 14801-970, Araraquara, São Paulo-
dc.description.affiliationUnespDepartment of Morphology Univ. Estadual Paulista-UNESP, cp 610, CEP 18618-000, UNESP, Botucatu, São Paulo-
dc.identifier.doi10.3390/ph4111423-
dc.rights.accessRightsAcesso aberto-
dc.identifier.file2-s2.0-80455131271.pdf-
dc.relation.ispartofPharmaceuticals-
dc.identifier.scopus2-s2.0-80455131271-
dc.identifier.orcid0000-0002-8645-3777pt
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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