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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/75748
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dc.contributor.authorFalcão, Heloina de Sousa-
dc.contributor.authorMaia, Gabriela Lemos de Azevedo-
dc.contributor.authorBonamin, Flávia-
dc.contributor.authorKushima, Hélio-
dc.contributor.authorMoraes, Thiago Mello-
dc.contributor.authorHiruma Lima, Clélia Akiko-
dc.contributor.authorTakayama, Christiane-
dc.contributor.authorFerreira, Anderson Luiz-
dc.contributor.authorSouza Brito, Alba Regina Monteiro-
dc.contributor.authorAgra, Maria de Fátima-
dc.contributor.authorBarbosa Filho, José Maria-
dc.contributor.authorBatista, Leônia Maria-
dc.date.accessioned2014-05-27T11:29:48Z-
dc.date.accessioned2016-10-25T18:50:16Z-
dc.date.available2014-05-27T11:29:48Z-
dc.date.available2016-10-25T18:50:16Z-
dc.date.issued2013-07-01-
dc.identifierhttp://dx.doi.org/10.1007/s11418-012-0705-4-
dc.identifier.citationJournal of Natural Medicines, v. 67, n. 3, p. 480-491, 2013.-
dc.identifier.issn1340-3443-
dc.identifier.issn1861-0293-
dc.identifier.urihttp://hdl.handle.net/11449/75748-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/75748-
dc.description.abstractFlavonoid-rich Praxelis clematidea (Griseb.) R.M.King & H.Robinson (Asteraceae) is a native plant of South America. This study evaluates the gastroprotective activity and possible mechanisms for both the chloroform (CHCl3P) and ethyl acetate phases (AcOEtP) obtained from aerial parts of the plant. The activity was investigated using acute models of gastric ulcer. Gastric secretion biochemical parameters were determined after pylorus ligature. The participation of cytoprotective factors such as mucus, nitric oxide (NO), sulfhydryl (SH) groups, prostaglandin E2 (PGE 2), reduced glutathione (GSH), superoxide dismutase (SOD), glutathione peroxidase (GPx), glutathione reductase (GR), reduction of lipid peroxidation (malondialdehyde level), and polymorphonuclear infiltration (myeloperoxidase activity), was also investigated. CHCl3P (125, 250, and 500 mg/kg) and AcOEtP (62.5, 125, and 250 mg/kg) showed significant gastroprotective activity, reducing the ulcerative index by 75, 83, 88 % and 66, 66, 81 % for ethanol; 67, 67, 56 % and 56, 53, 58 % for a non-steroidal anti-inflammatory drug (NSAID); and 74, 58, 59 % and 64, 65, 61 % for stress-induced gastric ulcer, respectively. CHCl3P (125 mg/kg) and AcOEtP (62.5 mg/kg) significantly reduced the ulcerative area by 78 and 83 %, respectively, for the ischemia-reperfusion model. They also did not alter the biochemical parameters of gastric secretion, the GSH level or the activities of SOD, GPx or GR. They increased the quantity of gastric mucus, not dependent on NO, yet dependent on SH groups, and maintained PGE2 levels. The P. clematidea phases demonstrated gastroprotective activity related to cytoprotective factors. © 2012 The Japanese Society of Pharmacognosy and Springer.en
dc.format.extent480-491-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectAsteraceae-
dc.subjectCytoprotection-
dc.subjectGastric ulcer-
dc.subjectGastroprotective activity-
dc.subjectPraxelis clematidea-
dc.subject7,4' dimethylapigenin-
dc.subjectacetic acid ethyl ester-
dc.subjectapigenin-
dc.subjectchloroform-
dc.subjectcimetidine-
dc.subjectcirsimaritin-
dc.subjectgastrointestinal mucosa protective agent-
dc.subjectgenkwanin-
dc.subjectglutathione-
dc.subjectglutathione peroxidase-
dc.subjectglutathione reductase-
dc.subjectlansoprazole-
dc.subjectmalonaldehyde-
dc.subjectmyeloperoxidase-
dc.subjectnitric oxide-
dc.subjectplant extract-
dc.subjectplant medicinal product-
dc.subjectPraxelis clematidea extract-
dc.subjectprostaglandin E2-
dc.subjectsuperoxide dismutase-
dc.subjecttetramethylscutellarein-
dc.subjectthiol group-
dc.subjecttrimethylapigenin-
dc.subjectunclassified drug-
dc.subjectanimal experiment-
dc.subjectanimal model-
dc.subjectanimal tissue-
dc.subjectantioxidant activity-
dc.subjectcell infiltration-
dc.subjectcontrolled study-
dc.subjectdrug identification-
dc.subjectdrug isolation-
dc.subjectdrug mechanism-
dc.subjectdrug structure-
dc.subjectenzyme activity-
dc.subjectlipid peroxidation-
dc.subjectmale-
dc.subjectmouse-
dc.subjectnonhuman-
dc.subjectpolymorphonuclear cell-
dc.subjectsingle drug dose-
dc.subjectstomach mucus-
dc.subjectstomach protection-
dc.subjectstomach secretion-
dc.subjectstomach ulcer-
dc.titleGastroprotective mechanisms of the chloroform and ethyl acetate phases of Praxelis clematidea (Griseb.) R.M.King & H.Robinson (Asteraceae)en
dc.typeoutro-
dc.contributor.institutionUniversidade Federal da Paraíba (UFPB)-
dc.contributor.institutionUniversidade Estadual de Campinas (UNICAMP)-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationLaboratório de Tecnologia Farmacêutica (LTF) Departamento de Ciências Farmacêuticas Universidade Federal da Paraiba (UFPB), Cx. Postal 5009, João Pessoa PB, CEP 58051-970-
dc.description.affiliationDepartamento de Fisiologia e Biofísica Laboratório de Produtos Naturais Universidade Estadual de Campinas (UNICAMP), Cx. Postal 6109, Campinas SP, CEP 13083-970-
dc.description.affiliationDepartamento de Fisiologia Instituto de Biociências Universidade Estadual Paulista (UNESP), Cx. Postal 510, Botucatu SP, CEP 18618-000-
dc.description.affiliationUnespDepartamento de Fisiologia Instituto de Biociências Universidade Estadual Paulista (UNESP), Cx. Postal 510, Botucatu SP, CEP 18618-000-
dc.identifier.doi10.1007/s11418-012-0705-4-
dc.identifier.wosWOS:000320112500007-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofJournal of Natural Medicines-
dc.identifier.scopus2-s2.0-84879241660-
dc.identifier.orcid0000-0002-8645-3777pt
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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