Publicação:
Epicatechin Used in the Treatment of Intestinal Inflammatory Disease: An Analysis by Experimental Models

dc.contributor.authorde Paula Vasconcelos, Paulo Cesar [UNESP]
dc.contributor.authorSeito, Leonardo Noboru [UNESP]
dc.contributor.authorDi Stasi, Luiz Claudio [UNESP]
dc.contributor.authorHiruma-Lima, Clélia Akiko [UNESP]
dc.contributor.authorPellizzon, Claudia Helena [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T13:49:17Z
dc.date.available2014-05-20T13:49:17Z
dc.date.issued2012-01-01
dc.description.abstractBackground. This study was pathway of (-)-epicatechin (EC) in the prevention and treatment of intestine inflammation in acute and chronic rat models. Methods. Intestine inflammation was induced in rats using TNBS. The morphological, inflammatory, immunohistochemical, and immunoblotting characteristics of colon samples were examined. The effects of EC were evaluated in an acute model at doses of 5, 10, 25, and 50 mg/kg by gavage for 5 days. The chronic colitis model was induced 1st day, and treated for 21 days. For the colitis relapse model, the induction was repeated on 14th. Results. EC10 and EC50 effectively reduced the lesion size, as assessed macroscopically; and confirmed by microscopy for EC10. The glutathione levels were higher in EC10 group but decreased COX-2 expression and increased cell proliferation (PC) were observed, indicating an anti-inflammatory activity and a proliferation-stimulating effect. In the chronic colitis model, EC10 showed lower macroscopic and microscopic lesion scores and increase in glutathione levels. As in the acute model, a decrease in COX-2 expression and an increase in PC in EC10, the chronic model this increase maybe by the pathway EGF expression. Conclusion. These results confirm the activity of EC as an antioxidant that reduces of the lesion and that has the potential to stimulate tissue healing, indicating useful for preventing and treating intestine inflammation.en
dc.description.affiliationUNESP Univ Estadual Paulista, Biosci Inst, Morphol Dept, BR-18618970 Botucatu, SP, Brazil
dc.description.affiliationUNESP Univ Estadual Paulista, Biosci Inst, Pharmacol Dept, BR-18618970 Botucatu, SP, Brazil
dc.description.affiliationUNESP Univ Estadual Paulista, Biosci Inst, Physiol Dept, BR-18618970 Botucatu, SP, Brazil
dc.description.affiliationUnespUNESP Univ Estadual Paulista, Biosci Inst, Morphol Dept, BR-18618970 Botucatu, SP, Brazil
dc.description.affiliationUnespUNESP Univ Estadual Paulista, Biosci Inst, Pharmacol Dept, BR-18618970 Botucatu, SP, Brazil
dc.description.affiliationUnespUNESP Univ Estadual Paulista, Biosci Inst, Physiol Dept, BR-18618970 Botucatu, SP, Brazil
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipIdFAPESP: 02/05503-6
dc.description.sponsorshipIdFAPESP: 06/55542-9
dc.description.sponsorshipIdFAPESP: 07/53201-2
dc.description.sponsorshipIdFAPESP: 09-52237-9
dc.description.sponsorshipIdFAPESP: 10/08536-9
dc.format.extent12
dc.identifierhttp://dx.doi.org/10.1155/2012/508902
dc.identifier.citationEvidence-based Complementary and Alternative Medicine. New York: Hindawi Publishing Corporation, p. 12, 2012.
dc.identifier.doi10.1155/2012/508902
dc.identifier.fileWOS000313444900001.pdf
dc.identifier.issn1741-427X
dc.identifier.lattes1697547325096457
dc.identifier.lattes0019393779801069
dc.identifier.lattes3814504901386844
dc.identifier.orcid0000-0002-8645-3777
dc.identifier.orcid0000-0002-4494-4180
dc.identifier.urihttp://hdl.handle.net/11449/17550
dc.identifier.wosWOS:000313444900001
dc.language.isoeng
dc.publisherHindawi Publishing Corporation
dc.relation.ispartofEvidence-based Complementary and Alternative Medicine
dc.relation.ispartofjcr2.064
dc.rights.accessRightsAcesso aberto
dc.sourceWeb of Science
dc.titleEpicatechin Used in the Treatment of Intestinal Inflammatory Disease: An Analysis by Experimental Modelsen
dc.typeArtigo
dcterms.licensehttp://www.hindawi.com/journals/apm/apc/
dcterms.rightsHolderHindawi Publishing Corporation
dspace.entity.typePublication
unesp.author.lattes1697547325096457
unesp.author.lattes0019393779801069[5]
unesp.author.lattes3814504901386844[4]
unesp.author.orcid0000-0002-8645-3777[4]
unesp.author.orcid0000-0002-4494-4180[5]
unesp.campusUniversidade Estadual Paulista (Unesp), Instituto de Biociências, Botucatupt
unesp.departmentFarmacologia - IBBpt
unesp.departmentFisiologia - IBBpt
unesp.departmentMorfologia - IBBpt

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