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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/130436
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dc.contributor.authorMonteiro, Diana Amaral-
dc.contributor.authorCarlos, Iracilda Zeppone-
dc.contributor.authorPinto, Fábio Gonçalves-
dc.date.accessioned2014-05-27T11:23:41Z-
dc.date.accessioned2016-10-25T21:21:09Z-
dc.date.available2014-05-27T11:23:41Z-
dc.date.available2016-10-25T21:21:09Z-
dc.date.issued2008-10-01-
dc.identifierhttp://www.scielo.br/scielo.php?script=sci_arttext&pid=S1516-93322008000400007&lng=pt&nrm=iso&tlng=pt-
dc.identifier.citationRevista Brasileira de Ciências Farmaceuticas. São Paulo: Univ São Paulo, Conjunto Quimicas, v. 44, n. 4, p. 613-620, 2008.-
dc.identifier.issn1516-9332-
dc.identifier.urihttp://hdl.handle.net/11449/130436-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/130436-
dc.description.abstractBenzodiazepines are one of the most frequently prescribed drugs due to their anxiolytic properties. The aim of this study was to evaluate the effects of diazepam on lipopolysaccharide-induced peritoneal acute inflammatory responses. Swiss mice were treated with diazepam in a single dose of 1 or 10 mg/kg- subcutaneously 1 h before an intraperitoneal injection of lipopolysaccharide or sterile saline solution. The mice were killed 16 h after and the cells were washed from the peritoneal cavity to determine the total number of cells and the mononuclear and polimorfonuclear subpopulations, as well as the TNF-alpha activity and percentage of spread macrophages. Our results showed that the diazepam treatment (1 and 10 mg/kg) induced a significant reduction in the LPS-induced macrophage stimulation and TNF-α activity. Diazepam (10 mg/kg) also reduced the inflammatory cellular migration when compared to the control. It can be concluded that the diazepam treatment in a single dose is able to influence the inflammatory cellular influx, macrophage stimulation and TNF-α activity in the acute inflammatory response in mice, having possible implications on the anti-infectious response efficiency.en
dc.format.extent613-620-
dc.language.isopor-
dc.publisherUniversidade de São Paulo (USP), Conjunto Quimicas-
dc.sourceScopus-
dc.subjectAcute inflammatory response-
dc.subjectCellular migration/inhibition-
dc.subjectDiazepam-
dc.subjectLipopolysaccharide-
dc.subjectMacrophages/stimulation-
dc.subjectTnf-α-
dc.subjectDiazepam-
dc.subjectTumor necrosis factor alpha-
dc.subjectAnimal cell-
dc.subjectAnimal experiment-
dc.subjectAntiinflammatory activity-
dc.subjectAscites fluid cytology-
dc.subjectCell count-
dc.subjectChemotaxis-
dc.subjectControlled study-
dc.subjectDrug dose comparison-
dc.subjectDrug effect-
dc.subjectDrug mechanism-
dc.subjectFemale-
dc.subjectInflammation-
dc.subjectInflammatory cell-
dc.subjectMacrophage-
dc.subjectMacrophage migration-
dc.subjectMononuclear cell-
dc.subjectMouse-
dc.subjectNonhuman-
dc.subjectPolymorphonuclear cell-
dc.subjectSingle drug dose-
dc.subjectSwiss webster mouse-
dc.titleDiazepam, em dose única, inibe a migração celular, a estimulação macrofágica e a atividade de TNF-α na reação inflamatória aguda induzida por LPS em camundongospt
dc.title.alternativeDiazepam, in a single dose, inhibits cellular chemotaxis, macrophage stimulation, and TNF-α activity in LPS-induced acute inflammatory responses in miceen
dc.typeoutro-
dc.contributor.institutionUniversidade Federal de São Carlos (UFSCar)-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationDepartamento de Morfologia e Patologia Universidade Federal de São Carlos-
dc.description.affiliationDepartamento de Análises Clínicas Faculdade de Ciências Farmacêuticas Universidade Estadual Paulista Júlio de Mesquita Filho-
dc.description.affiliationDepartamento de Morfologia e Patologia Centro de Ciências Biológicas e da Saúde Universidade Federal de São Carlos, Rodovia Washington Luiz, km 235, 13565-905 - São Carlos - SP-
dc.description.affiliationUnespDepartamento de Análises Clínicas Faculdade de Ciências Farmacêuticas Universidade Estadual Paulista Júlio de Mesquita Filho-
dc.identifier.doihttp://dx.doi.org/10.1590/S1516-93322008000400007-
dc.identifier.scieloS1516-93322008000400007-
dc.identifier.wosWOS:000263804500007-
dc.rights.accessRightsAcesso aberto-
dc.identifier.file2-s2.0-59649119535.pdf-
dc.relation.ispartofRevista Brasileira de Ciências Farmacêuticas-
dc.identifier.scopus2-s2.0-59649119535-
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