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Role of glutamate NMDA receptors and nitric oxide located within the periaqueductal gray on defensive behaviors in mice confronted by predator

dc.contributor.authorCarvalho-Netto, Eduardo F. [UNESP]
dc.contributor.authorGomes, Karina S. [UNESP]
dc.contributor.authorAmaral, Vanessa C. S. [UNESP]
dc.contributor.authorNunes-de-Souza, Ricardo L. [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionUniversidade Federal de São Carlos (UFSCar)
dc.date.accessioned2014-05-20T13:24:58Z
dc.date.available2014-05-20T13:24:58Z
dc.date.issued2009-07-01
dc.description.abstractThe midbrain periaqueductal gray (PAG) is part of the brain system involved in active defense reactions to threatening stimuli. Glutamate N-methyl-d-aspartate (NMDA) receptor activation within the dorsal column of the PAG (dPAG) leads to autonomic and behavioral responses characterized as the fear reaction. Nitric oxide (NO) has been proposed to be a mediator of the aversive action of glutamate, since the activation of NMDA receptors in the brain increases NO synthesis.We investigated the effects of intra-dPAG infusions of NMDA on defensive behaviors in mice pretreated with a neuronal nitric oxide synthase (nNOS) inhibitor [N omega-propyl-l-arginine (NPLA)], in the same midbrain site, during a confrontation with a predator in the rat exposure test (RET).Male Swiss mice received intra-dPAG injections of NPLA (0.1 or 0.4 nmol/0.1 mu l), and 10 min later, they were infused with NMDA (0.04 nmol/0.1 mu l) into the dPAG. After 10 min, each mouse was placed in the RET.NMDA treatment enhanced avoidance behavior from the predator and markedly increased freezing behavior. These proaversive effects of NMDA were prevented by prior injection of NPLA. Furthermore, defensive behaviors (e.g., avoidance, risk assessment, freezing) were consistently reduced by the highest dose of NPLA alone, suggesting an intrinsic effect of nitric oxide on defensive behavior in mice exposed to the RET.These findings suggest a potential role of glutamate NMDA receptors and NO in the dPAG in the regulation of defensive behaviors in mice during a confrontation with a predator in the RET.en
dc.description.affiliationUNESP, FCF, Farmacol Lab, BR-14801902 Araraquara, SP, Brazil
dc.description.affiliationUniv São Paulo, Psychobiol Grad Program, BR-14040901 Ribeirao Preto, SP, Brazil
dc.description.affiliationSão Paulo State Univ, Pharmacol Lab, BR-14801902 Araraquara, SP, Brazil
dc.description.affiliationUniversidade Federal de São Carlos (UFSCar), Physiol Sci Grad Program, BR-13565905 São Carlos, SP, Brazil
dc.description.affiliationUnespUNESP, FCF, Farmacol Lab, BR-14801902 Araraquara, SP, Brazil
dc.description.affiliationUnespSão Paulo State Univ, Pharmacol Lab, BR-14801902 Araraquara, SP, Brazil
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipPrograma de Apoio ao Desenvolvimento Científico da Faculdade de Ciências Farmacêuticas da UNESP (PADC)
dc.format.extent617-625
dc.identifierhttp://dx.doi.org/10.1007/s00213-009-1492-9
dc.identifier.citationPsychopharmacology. New York: Springer, v. 204, n. 4, p. 617-625, 2009.
dc.identifier.doi10.1007/s00213-009-1492-9
dc.identifier.issn0033-3158
dc.identifier.urihttp://hdl.handle.net/11449/7888
dc.identifier.wosWOS:000266486700006
dc.language.isoeng
dc.publisherSpringer
dc.relation.ispartofPsychopharmacology
dc.relation.ispartofjcr3.222
dc.relation.ispartofsjr1,494
dc.rights.accessRightsAcesso restritopt
dc.sourceWeb of Science
dc.subjectGlutamateen
dc.subjectNitric oxideen
dc.subjectPeriaqueductal grayen
dc.subjectDefenseen
dc.subjectAnxietyen
dc.subjectAnimal model and miceen
dc.titleRole of glutamate NMDA receptors and nitric oxide located within the periaqueductal gray on defensive behaviors in mice confronted by predatoren
dc.typeArtigopt
dcterms.licensehttp://www.springer.com/open+access/authors+rights?SGWID=0-176704-12-683201-0
dcterms.rightsHolderSpringer
dspace.entity.typePublication
relation.isOrgUnitOfPublication95697b0b-8977-4af6-88d5-c29c80b5ee92
relation.isOrgUnitOfPublication.latestForDiscovery95697b0b-8977-4af6-88d5-c29c80b5ee92
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências Farmacêuticas, Araraquarapt

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