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dc.contributor.authorLopes, F.D.T.Q.S.-
dc.contributor.authorToledo, A.C.-
dc.contributor.authorOlivo, C.R.-
dc.contributor.authorPrado, C.M.-
dc.contributor.authorLeick, E.A.-
dc.contributor.authorMedeiros, M.C.-
dc.contributor.authorSantos, A.B.G.-
dc.contributor.authorGarippo, A.-
dc.contributor.authorMartins, M.A.-
dc.contributor.authorMauad, T.-
dc.date.accessioned2018-02-19T11:53:58Z-
dc.date.available2018-02-19T11:53:58Z-
dc.date.issued2013-
dc.identifier.citationHistology and Histopathology, vol. 28, nº 2, (2013)es
dc.identifier.issn1699-5848-
dc.identifier.issn0213-3911-
dc.identifier.urihttp://hdl.handle.net/10201/56238-
dc.description.abstractA single instillation of porcine pancreatic elastase (PPE) results in significant airspace enlargement on the 28th day after instillation, whereas cigarette smoke (CS) exposure requires 6 months to produce mild emphysema in rodents. Considering that there are differences in the pathogenesis of parenchymal destruction in these different experimental models, it is likely that there may be different patterns of extracellular matrix (ECM) remodeling. To evaluate ECM remodeling, C57BL/6 mice were submitted to either a nasal drop of PPE (PPE 28 Days) or exposed for 6 months to cigarette smoke (CS 6 months). Control groups received either an intranasal instillation of saline solution (Saline 28 Days) or remained without any smoke inhalation for six months (Control 6 months). We measured the mean linear intercept and the volume proportion of collagen type I, collagen type III, elastin and fibrillin. We used emission-scanning confocal microscopy to verify the fiber distribution. Both models induced increased mean linear intercept in relation to the respective controls, being larger in the elastase model in relation to the CS model. In the CS model, emphysema was associated with an increase in the volume proportion of fibrillin, whereas in the PPE model there was an increase in the parenchymal elastin content. In both models, there was an increase in collagen type III, which was higher in the CS-exposed mice. We concluded that ECM remodeling is different in the two most used experimental models of emphysema.es
dc.formatapplication/pdfes
dc.format.extent8es
dc.languageenges
dc.publisherF. Hernández y Juan F. Madrid. Universidad de Murcia: Departamento de Biología Celular e Histologíaes
dc.rightsinfo:eu-repo/semantics/openAccesses
dc.subjectEmphysemaes
dc.subjectExtracellular matrix remodelinges
dc.subjectCollagenes
dc.subject.otherCDU::6 - Ciencias aplicadas::61 - Medicinaes
dc.titleA comparative study of extracellular matrix remodeling in two murine models of emphysemaes
dc.typeinfo:eu-repo/semantics/articlees
Aparece en las colecciones:Vol.28, nº 2 (2013)

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