Publicação:
Gastroprotective mechanisms of the chloroform and ethyl acetate phases of Praxelis clematidea (Griseb.) R.M.King & H.Robinson (Asteraceae)

dc.contributor.authorFalcão, Heloina de Sousa
dc.contributor.authorMaia, Gabriela Lemos de Azevedo
dc.contributor.authorBonamin, Flávia [UNESP]
dc.contributor.authorKushima, Hélio [UNESP]
dc.contributor.authorMoraes, Thiago Mello [UNESP]
dc.contributor.authorHiruma Lima, Clélia Akiko [UNESP]
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.contributor.institutionUniversidade Federal da Paraíba (UFPB)
dc.contributor.institutionUniversidade Estadual de Campinas (UNICAMP)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-27T11:29:48Z
dc.date.available2014-05-27T11:29:48Z
dc.date.issued2013-07-01
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.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.format.extent480-491
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.doi10.1007/s11418-012-0705-4
dc.identifier.issn1340-3443
dc.identifier.issn1861-0293
dc.identifier.lattes3814504901386844
dc.identifier.orcid0000-0002-8645-3777
dc.identifier.scopus2-s2.0-84879241660
dc.identifier.urihttp://hdl.handle.net/11449/75748
dc.identifier.wosWOS:000320112500007
dc.language.isoeng
dc.relation.ispartofJournal of Natural Medicines
dc.relation.ispartofjcr1.920
dc.relation.ispartofsjr0,643
dc.rights.accessRightsAcesso restrito
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.typeArtigo
dcterms.licensehttp://www.springer.com/open+access/authors+rights
dspace.entity.typePublication
unesp.author.lattes3814504901386844[6]
unesp.author.orcid0000-0002-8645-3777[6]
unesp.campusUniversidade Estadual Paulista (Unesp), Instituto de Biociências, Botucatupt
unesp.departmentFisiologia - IBBpt

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