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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/35331
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dc.contributor.authorda Silva, Alexandre O. Fernandes-
dc.contributor.authorGargaglioni, Luciane H.-
dc.contributor.authorBranco, Luiz G. S.-
dc.date.accessioned2014-05-20T15:24:47Z-
dc.date.accessioned2016-10-25T17:59:07Z-
dc.date.available2014-05-20T15:24:47Z-
dc.date.available2016-10-25T17:59:07Z-
dc.date.issued2007-05-01-
dc.identifierhttp://dx.doi.org/10.1139/Y07-038-
dc.identifier.citationCanadian Journal of Physiology and Pharmacology. Ottawa: Natl Research Council Canada-n R C Research Press, v. 85, n. 5, p. 497-501, 2007.-
dc.identifier.issn0008-4212-
dc.identifier.urihttp://hdl.handle.net/11449/35331-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/35331-
dc.description.abstractThis study was aimed at testing the hypothesis that serotoninergic receptors in the locus coeruleus (LC) play a role in bacterial lipopolysaccharide-induced fever. To this end, 5-HT1A (WAY-100635; 3 mu g/100 nL) and 5-HT2A (ketanserin; 2 mu g/100 nL) antagonists were microinjected into the LC and body temperature was monitored by biotelemetry. Intra-LC microinjections of ketanserin or WAY-100635 caused no change in body temperature of euthermic animals. 5-HT2A antagonism abolished the first phase of the lipopolysaccharide-induced fever. Taken together, these results indicate that serotonin acting on 5-HT2A receptors in the LC mediates the first phase of the febrile response, whereas 5-HT1A receptors are not involved in the lipopolysaccharide-induced fever.en
dc.format.extent497-501-
dc.language.isoeng-
dc.publisherNatl Research Council Canada-n R C Research Press-
dc.sourceWeb of Science-
dc.subjectserotoninpt
dc.subjectBody temperaturept
dc.subjectfebrile responsept
dc.subjectketanserinpt
dc.subjectWAY-100635pt
dc.subjectsystemic infectionpt
dc.title5-HT2A serotoninergic receptor in the locus coeruleus participates in the first phase of lipopolysaccharide-induced feveren
dc.typeoutro-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationUniv São Paulo, Dent Sch Ribeirao Preto, Dept Morphol Estomatol & Physiol, BR-14040904 Ribeirao Preto, SP, Brazil-
dc.description.affiliationUniv São Paulo, Med Sch Ribeirao Preto, Dept Physiol, Ribeirao Preto, SP, Brazil-
dc.description.affiliationSão Paulo State Univ, FCAV, Dept Anim Morphol & Physiol, Jaboticabal, SP, Brazil-
dc.description.affiliationUnespSão Paulo State Univ, FCAV, Dept Anim Morphol & Physiol, Jaboticabal, SP, Brazil-
dc.identifier.doi10.1139/Y07-038-
dc.identifier.wosWOS:000249010900002-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofCanadian Journal of Physiology and Pharmacology-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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