Corticosterone does not change open elevated plus maze-induced antinociception in mice

Detalhes bibliográficos
Autor(a) principal: Mendes-Gomes, Joyce [UNESP]
Data de Publicação: 2011
Outros Autores: Miguel, Tarciso Tadeu [UNESP], Santana Amaral, Vanessa Cristiane [UNESP], Nunes-de-Souza, Ricardo Luiz [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1016/j.yhbeh.2011.07.004
http://hdl.handle.net/11449/42601
Resumo: It has been demonstrated that the exposure of rodents to the standard elevated plus-maze (sEPM: 2 open and 2 enclosed arms) elicits defensive behavioral reactions and antinociception and also activates the hypothalamo-pituitary-adrenal (HPA) axis. We have recently reported that EPM-induced antinociception is particularly observed when rats and mice are exposed to a totally open EPM (oEPM: 4 open arms). Given that the oEPM seems to be a more aversive situation than the sEPM, we hypothesized that oEPM exposure would induce higher plasma levels of corticosterone than sEPM exposure in mice. In this study, we investigated the influence of exposure to eEPM (enclosed EPM: 4 enclosed arms), sEPM or oEPM on plasma corticosterone levels in mice, with or without prior nociceptive stimulation (2.5% formalin injection into the right hind paw). We also tested whether the nociceptive response in the formalin test and oEPM-induced antinociception are altered by adrenalectomy. Results showed that oEPM-exposed mice spent less time licking the injected paw than sEPM- and eEPM-exposed animals. All three types of EPM exposure increased plasma corticosterone when compared to the basal group, but sEPM- and oEPM-exposed mice showed higher corticosterone levels than eEPM-exposed mice. Prior nociceptive stimulation (formalin injection) did not enhance the plasma corticosterone response induced by the three types of EPM exposure. Indeed, formalin injection appeared to provoke a ceiling effect on plasma corticosterone concentration. Furthermore, neither the nociceptive response in the formalin test nor oEPM-induced antinociception was changed by adrenalectomy. Present results suggest that oEPM antinociception does not depend on corticosterone release in mice. (C) 2011 Elsevier B.V. All rights reserved.
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spelling Corticosterone does not change open elevated plus maze-induced antinociception in miceAnxietyFearDifferent types of EPMAntinociceptionFormalin testCorticosteroneAdrenalectomyMiceIt has been demonstrated that the exposure of rodents to the standard elevated plus-maze (sEPM: 2 open and 2 enclosed arms) elicits defensive behavioral reactions and antinociception and also activates the hypothalamo-pituitary-adrenal (HPA) axis. We have recently reported that EPM-induced antinociception is particularly observed when rats and mice are exposed to a totally open EPM (oEPM: 4 open arms). Given that the oEPM seems to be a more aversive situation than the sEPM, we hypothesized that oEPM exposure would induce higher plasma levels of corticosterone than sEPM exposure in mice. In this study, we investigated the influence of exposure to eEPM (enclosed EPM: 4 enclosed arms), sEPM or oEPM on plasma corticosterone levels in mice, with or without prior nociceptive stimulation (2.5% formalin injection into the right hind paw). We also tested whether the nociceptive response in the formalin test and oEPM-induced antinociception are altered by adrenalectomy. Results showed that oEPM-exposed mice spent less time licking the injected paw than sEPM- and eEPM-exposed animals. All three types of EPM exposure increased plasma corticosterone when compared to the basal group, but sEPM- and oEPM-exposed mice showed higher corticosterone levels than eEPM-exposed mice. Prior nociceptive stimulation (formalin injection) did not enhance the plasma corticosterone response induced by the three types of EPM exposure. Indeed, formalin injection appeared to provoke a ceiling effect on plasma corticosterone concentration. Furthermore, neither the nociceptive response in the formalin test nor oEPM-induced antinociception was changed by adrenalectomy. Present results suggest that oEPM antinociception does not depend on corticosterone release in mice. (C) 2011 Elsevier B.V. All rights reserved.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Programa de Apoio ao Desenvolvimento Científico da Faculdade de Ciências Farmacêuticas da UNESP (PADC)FFCLRP USP Av, Programa Posgrad Psicobiol, BR-14040901 Ribeirao Preto, SP, BrazilFac Ciencias Farmaceut UNESP Rod, Lab Neuropsicofarmacol, BR-14801902 Araraquara, SP, BrazilUFSCAR UNESP Rod, Programa Interinst Posgrad Ciencias Fisiol, BR-13565 São Carlos, SP, BrazilUnidade Univ Ciencias Exatas & Tecnol, BR-75132903 Anapolis, GO, BrazilFac Ciencias Farmaceut UNESP Rod, Lab Neuropsicofarmacol, BR-14801902 Araraquara, SP, BrazilUFSCAR UNESP Rod, Programa Interinst Posgrad Ciencias Fisiol, BR-13565 São Carlos, SP, BrazilFAPESP: 05/01988-3FAPESP: 05/05171-1CNPq: 142266/2008-6CNPq: 303580/2009-7Academic Press Inc. Elsevier B.V.Universidade de São Paulo (USP)Universidade Estadual Paulista (Unesp)Unidade Univ Ciencias Exatas & TecnolMendes-Gomes, Joyce [UNESP]Miguel, Tarciso Tadeu [UNESP]Santana Amaral, Vanessa Cristiane [UNESP]Nunes-de-Souza, Ricardo Luiz [UNESP]2014-05-20T15:34:36Z2014-05-20T15:34:36Z2011-09-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article408-413application/pdfhttp://dx.doi.org/10.1016/j.yhbeh.2011.07.004Hormones and Behavior. San Diego: Academic Press Inc. Elsevier B.V., v. 60, n. 4, p. 408-413, 2011.0018-506Xhttp://hdl.handle.net/11449/4260110.1016/j.yhbeh.2011.07.004WOS:000294834100012WOS000294834100012.pdfWeb of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengHormones and Behavior4.418info:eu-repo/semantics/openAccess2024-06-24T14:51:25Zoai:repositorio.unesp.br:11449/42601Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T14:29:05.514817Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Corticosterone does not change open elevated plus maze-induced antinociception in mice
title Corticosterone does not change open elevated plus maze-induced antinociception in mice
spellingShingle Corticosterone does not change open elevated plus maze-induced antinociception in mice
Mendes-Gomes, Joyce [UNESP]
Anxiety
Fear
Different types of EPM
Antinociception
Formalin test
Corticosterone
Adrenalectomy
Mice
title_short Corticosterone does not change open elevated plus maze-induced antinociception in mice
title_full Corticosterone does not change open elevated plus maze-induced antinociception in mice
title_fullStr Corticosterone does not change open elevated plus maze-induced antinociception in mice
title_full_unstemmed Corticosterone does not change open elevated plus maze-induced antinociception in mice
title_sort Corticosterone does not change open elevated plus maze-induced antinociception in mice
author Mendes-Gomes, Joyce [UNESP]
author_facet Mendes-Gomes, Joyce [UNESP]
Miguel, Tarciso Tadeu [UNESP]
Santana Amaral, Vanessa Cristiane [UNESP]
Nunes-de-Souza, Ricardo Luiz [UNESP]
author_role author
author2 Miguel, Tarciso Tadeu [UNESP]
Santana Amaral, Vanessa Cristiane [UNESP]
Nunes-de-Souza, Ricardo Luiz [UNESP]
author2_role author
author
author
dc.contributor.none.fl_str_mv Universidade de São Paulo (USP)
Universidade Estadual Paulista (Unesp)
Unidade Univ Ciencias Exatas & Tecnol
dc.contributor.author.fl_str_mv Mendes-Gomes, Joyce [UNESP]
Miguel, Tarciso Tadeu [UNESP]
Santana Amaral, Vanessa Cristiane [UNESP]
Nunes-de-Souza, Ricardo Luiz [UNESP]
dc.subject.por.fl_str_mv Anxiety
Fear
Different types of EPM
Antinociception
Formalin test
Corticosterone
Adrenalectomy
Mice
topic Anxiety
Fear
Different types of EPM
Antinociception
Formalin test
Corticosterone
Adrenalectomy
Mice
description It has been demonstrated that the exposure of rodents to the standard elevated plus-maze (sEPM: 2 open and 2 enclosed arms) elicits defensive behavioral reactions and antinociception and also activates the hypothalamo-pituitary-adrenal (HPA) axis. We have recently reported that EPM-induced antinociception is particularly observed when rats and mice are exposed to a totally open EPM (oEPM: 4 open arms). Given that the oEPM seems to be a more aversive situation than the sEPM, we hypothesized that oEPM exposure would induce higher plasma levels of corticosterone than sEPM exposure in mice. In this study, we investigated the influence of exposure to eEPM (enclosed EPM: 4 enclosed arms), sEPM or oEPM on plasma corticosterone levels in mice, with or without prior nociceptive stimulation (2.5% formalin injection into the right hind paw). We also tested whether the nociceptive response in the formalin test and oEPM-induced antinociception are altered by adrenalectomy. Results showed that oEPM-exposed mice spent less time licking the injected paw than sEPM- and eEPM-exposed animals. All three types of EPM exposure increased plasma corticosterone when compared to the basal group, but sEPM- and oEPM-exposed mice showed higher corticosterone levels than eEPM-exposed mice. Prior nociceptive stimulation (formalin injection) did not enhance the plasma corticosterone response induced by the three types of EPM exposure. Indeed, formalin injection appeared to provoke a ceiling effect on plasma corticosterone concentration. Furthermore, neither the nociceptive response in the formalin test nor oEPM-induced antinociception was changed by adrenalectomy. Present results suggest that oEPM antinociception does not depend on corticosterone release in mice. (C) 2011 Elsevier B.V. All rights reserved.
publishDate 2011
dc.date.none.fl_str_mv 2011-09-01
2014-05-20T15:34:36Z
2014-05-20T15:34:36Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1016/j.yhbeh.2011.07.004
Hormones and Behavior. San Diego: Academic Press Inc. Elsevier B.V., v. 60, n. 4, p. 408-413, 2011.
0018-506X
http://hdl.handle.net/11449/42601
10.1016/j.yhbeh.2011.07.004
WOS:000294834100012
WOS000294834100012.pdf
url http://dx.doi.org/10.1016/j.yhbeh.2011.07.004
http://hdl.handle.net/11449/42601
identifier_str_mv Hormones and Behavior. San Diego: Academic Press Inc. Elsevier B.V., v. 60, n. 4, p. 408-413, 2011.
0018-506X
10.1016/j.yhbeh.2011.07.004
WOS:000294834100012
WOS000294834100012.pdf
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Hormones and Behavior
4.418
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 408-413
application/pdf
dc.publisher.none.fl_str_mv Academic Press Inc. Elsevier B.V.
publisher.none.fl_str_mv Academic Press Inc. Elsevier B.V.
dc.source.none.fl_str_mv Web of Science
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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