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Campo DCValorIdioma
dc.contributor.authorDa Costa, Miriani-
dc.contributor.authorXimenes, Valdecir Farias-
dc.contributor.authorDa Fonseca, Luiz Marcos-
dc.date.accessioned2014-05-27T11:21:07Z-
dc.date.accessioned2016-10-25T18:19:47Z-
dc.date.available2014-05-27T11:21:07Z-
dc.date.available2016-10-25T18:19:47Z-
dc.date.issued2004-08-01-
dc.identifierhttp://dx.doi.org/10.1248/bpb.27.1183-
dc.identifier.citationBiological and Pharmaceutical Bulletin, v. 27, n. 8, p. 1183-1187, 2004.-
dc.identifier.issn0918-6158-
dc.identifier.issn1347-5215-
dc.identifier.urihttp://hdl.handle.net/11449/67820-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/67820-
dc.description.abstractType-1 diabetic patients experience hyperketonemia caused by an increase in fatty acid metabolism. Thus, the aim of this study was to measure the effect of ketone bodies as suppressors of oxidizing species produced by stimulated neutrophils. Both acetoacetate and 3-hydroxybutyrate have suppressive effect on the respiratory burst measured by luminol-enhanced chemiluminescence. Through measurements of hypochlorous acid production, using neutrophils or the myeloperoxidase/H2O2/Cl- system, it was found that acetoacetate but not 3-hydroxybutyrate is able to inhibit the generation of this antimicrobial oxidant. The superoxide anion scavenging properties were confirmed by ferricytochrome C reduction and lucigenin-enhanced chemiluminescence assays. However, ketone bodies did not alter the rate of oxygen uptake by stimulated neutrophils, measured with an oxygen electrode. A strong inhibition of the expression of the cytokine IL-8 by cultured neutrophils was also observed; this is discussed with reference to the antioxidant-like property of acetoacetate. © 2004 Pharmaceutical Society of Japan.en
dc.format.extent1183-1187-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectCytokine-
dc.subjectHypochlorous acid-
dc.subjectKetone body-
dc.subjectMyeloperoxidase-
dc.subjectNeutrophil-
dc.subjectRespiratory burst-
dc.subject3 hydroxybutyric acid-
dc.subjectacetoacetic acid-
dc.subjectcytochrome c-
dc.subjecthypochlorous acid-
dc.subjectinterleukin 18-
dc.subjectketone body-
dc.subjectlucigenin-
dc.subjectmyeloperoxidase-
dc.subjectoxygen-
dc.subjectsuperoxide-
dc.subjectacetoacetic acid derivative-
dc.subjectinterleukin 8-
dc.subjectcell culture-
dc.subjectcell function-
dc.subjectcell stimulation-
dc.subjectchemoluminescence-
dc.subjectcontrolled study-
dc.subjecthuman-
dc.subjecthuman cell-
dc.subjectneutrophil-
dc.subjectoxygen electrode-
dc.subjectrespiratory burst-
dc.subjectbiosynthesis-
dc.subjectdrug antagonism-
dc.subjectin vitro study-
dc.subjectluminescence-
dc.subjectmetabolism-
dc.subjectphysiology-
dc.subjectAcetoacetates-
dc.subjectHumans-
dc.subjectHypochlorous Acid-
dc.subjectInterleukin-8-
dc.subjectKetone Bodies-
dc.subjectLuminescence-
dc.subjectNeutrophils-
dc.titleHypochlorous acid inhibition by acetoacetate: Implications on neutrophil functionsen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationDepartment of Clinical Analysis (LAC) State University of São Paulo (UNESP) School of Pharmaceutical Science, Araraquara, SP, CEP 14801-902-
dc.description.affiliationUnespDepartment of Clinical Analysis (LAC) State University of São Paulo (UNESP) School of Pharmaceutical Science, Araraquara, SP, CEP 14801-902-
dc.identifier.doi10.1248/bpb.27.1183-
dc.identifier.wosWOS:000223206400007-
dc.rights.accessRightsAcesso aberto-
dc.identifier.fileWOS000223206400007.pdf-
dc.relation.ispartofBiological and Pharmaceutical Bulletin-
dc.identifier.scopus2-s2.0-16644386300-
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