Corticosterone does not change open elevated plus maze-induced antinociception in mice
Autor(a) principal: | |
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Data de Publicação: | 2011 |
Outros Autores: | , , |
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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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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1808128365838729216 |