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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/41902
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dc.contributor.authorMendes-Gomes, Joyce-
dc.contributor.authorSantana Amaral, Vanessa Cristiane-
dc.contributor.authorNunes-de-Souza, Ricardo Luiz-
dc.date.accessioned2014-05-20T15:33:12Z-
dc.date.accessioned2016-10-25T18:09:42Z-
dc.date.available2014-05-20T15:33:12Z-
dc.date.available2016-10-25T18:09:42Z-
dc.date.issued2011-06-01-
dc.identifierhttp://dx.doi.org/10.1016/j.bbr.2011.01.012-
dc.identifier.citationBehavioural Brain Research. Amsterdam: Elsevier B.V., v. 219, n. 2, p. 248-253, 2011.-
dc.identifier.issn0166-4328-
dc.identifier.urihttp://hdl.handle.net/11449/41902-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/41902-
dc.description.abstractThe exposure of rodents to an open elevated plus-maze (oEPM: four open arms raised from the floor) elicits naloxone-insensitive antinociception. Midazolam infusion into the dorsal portion of the periaque-ductal gray (dPAG), a structure of the descending inhibitory system of pain, failed to alter oEPM-induced antinociception. Chemical lesion of dorsomedial and dorsolateral PAG attenuated defensive behavior in the standard EPM (sEPM), an animal model of anxiety, but failed to change oEPM-induced antinociception. The present study investigated the effects of bilateral lesion, with the injection of NMDA (N-methyl-D-aspartic acid), of the ventrolateral column of PAG (vIPAG) (i) on nociceptive response induced by 2.5% formalin injected into the right hind paw (nociception test) in mice exposed to the enclosed EPM (eEPM: four enclosed arms - a non-aversive situation) or to the oEPM and (ii) on anxiety indices in mice exposed to the sEPM without prior formalin injection. Results showed that oEPM-induced antinociception was not altered by lesion of vIPAG. Nevertheless, the lesion reduced the nociceptive response in mice exposed to the eEPM and increased general locomotor activity during the eEPM and oEPM exposure. Furthermore, vIPAG lesion did not alter anxiety-like indices in mice exposed to the sEPM. The results suggest that vIPAG does not play a role in oEPM-induced antinociception or in defensive reactions assessed in the sEPM. Moreover, vIPAG inactivation induces pain inhibition in mice not exposed to an aversive situation and seems to increase general activity. (C) 2011 Elsevier B.V. All rights reserved.en
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.extent248-253-
dc.language.isoeng-
dc.publisherElsevier B.V.-
dc.sourceWeb of Science-
dc.subjectAnxietyen
dc.subjectFearen
dc.subjectDifferent types of EPMen
dc.subjectAntinociceptionen
dc.subjectFormalin testen
dc.subjectNMDA lesionen
dc.subjectVentrolateral periaqueductal grayen
dc.subjectMiceen
dc.titleVentrolateral periaqueductal gray lesion attenuates nociception but does not change anxiety-like indices or fear-induced antinociception in miceen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.description.affiliationUNESP, Lab Neuropsicofarmacol, Fac Ciencias Farmaceut, BR-14801902 Araraquara, SP, Brazil-
dc.description.affiliationUSP, FFCLRP, Programa Posgrad Psicobiol, BR-14040901 Ribeirao Preto, SP, Brazil-
dc.description.affiliationUNESP, UFSCAR, Programa Interinst Posgrad Ciencias Fisiol, BR-13565905 São Carlos, SP, Brazil-
dc.description.affiliationUnespUNESP, Lab Neuropsicofarmacol, Fac Ciencias Farmaceut, BR-14801902 Araraquara, SP, Brazil-
dc.description.affiliationUnespUNESP, UFSCAR, Programa Interinst Posgrad Ciencias Fisiol, BR-13565905 São Carlos, SP, Brazil-
dc.description.sponsorshipIdFAPESP: 05/01988-3-
dc.description.sponsorshipIdCNPq: 142266/2008-6-
dc.description.sponsorshipIdCNPq: 309407/2006-0-
dc.identifier.doi10.1016/j.bbr.2011.01.012-
dc.identifier.wosWOS:000289703700011-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofBehavioural Brain Research-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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