Amygdaloid involvement in the defensive behavior of mice exposed to the open elevated plus-maze
Autor(a) principal: | |
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Data de Publicação: | 2018 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1016/j.bbr.2017.10.022 http://hdl.handle.net/11449/179332 |
Resumo: | Previous studies have shown that the exposure to an open elevated plus maze (oEPM, an EPM with all four open arms) elicits fear/anxiety-related responses in laboratory rodents. However, very little is known about the underlying neural substrates of these defensive behaviors. Accordingly, the present study investigated the effects of chemical inactivation of the amygdala [through local injection of cobalt chloride (CoCl2: a nonspecific synaptic blocker)] on the behavior of oEPM-exposed mice. In a second experiment, the pattern of activation of the basolateral (BLA) and central (CeA) nuclei of the amygdala was assessed through quantification of Fos protein expression in mice subjected to one of several behavioral manipulations. To avoid the confound of acute handling stress, 4 independent groups of mice were habituated daily for 10 days to an enclosed EPM (eEPM) and, on day 11 prior to immunohistochemistry, were either taken directly from their home cage (control) or individually exposed for 10 min to a new clean holding cage (novelty), an eEPM, or the oEPM. An additional group of mice (maze-naïve) was not subjected to either the habituation or exposure phase but were simply chosen at random from their home cages to undergo an identical immunohistochemistry procedure. Results showed that amygdala inactivation produced an anxiolytic-like profile comprising reductions in time spent in the proximal portions of the open arms and total stretched attend postures (SAP) as well as increases in time spent in the distal portions of the open arms and total head-dipping. Moreover, Fos-positive labeled cells were bilaterally increased in the amygdaloid complex, particularly in the BLA, of oEPM-exposed animals compared to all other groups. These results suggest that the amygdala (in particular, its BLA nucleus) plays a key role in the modulation of defensive behaviors in oEPM-exposed mice. |
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Amygdaloid involvement in the defensive behavior of mice exposed to the open elevated plus-mazeAmygdalaCobalt chlorideDefensive behaviorImmunohistochemistryMiceOpen elevated plus mazePrevious studies have shown that the exposure to an open elevated plus maze (oEPM, an EPM with all four open arms) elicits fear/anxiety-related responses in laboratory rodents. However, very little is known about the underlying neural substrates of these defensive behaviors. Accordingly, the present study investigated the effects of chemical inactivation of the amygdala [through local injection of cobalt chloride (CoCl2: a nonspecific synaptic blocker)] on the behavior of oEPM-exposed mice. In a second experiment, the pattern of activation of the basolateral (BLA) and central (CeA) nuclei of the amygdala was assessed through quantification of Fos protein expression in mice subjected to one of several behavioral manipulations. To avoid the confound of acute handling stress, 4 independent groups of mice were habituated daily for 10 days to an enclosed EPM (eEPM) and, on day 11 prior to immunohistochemistry, were either taken directly from their home cage (control) or individually exposed for 10 min to a new clean holding cage (novelty), an eEPM, or the oEPM. An additional group of mice (maze-naïve) was not subjected to either the habituation or exposure phase but were simply chosen at random from their home cages to undergo an identical immunohistochemistry procedure. Results showed that amygdala inactivation produced an anxiolytic-like profile comprising reductions in time spent in the proximal portions of the open arms and total stretched attend postures (SAP) as well as increases in time spent in the distal portions of the open arms and total head-dipping. Moreover, Fos-positive labeled cells were bilaterally increased in the amygdaloid complex, particularly in the BLA, of oEPM-exposed animals compared to all other groups. These results suggest that the amygdala (in particular, its BLA nucleus) plays a key role in the modulation of defensive behaviors in oEPM-exposed mice.Joint Graduate Program in Physiological Sciences UFSCar/UNESPPharmacology Laboratory of Neuropsychopharmacology School of Pharmaceutical Sciences Univ. Estadual Paulista UNESPDepartment of Pharmacology Federal University of São PauloSchool of Psychology University of LeedsJoint Graduate Program in Physiological Sciences UFSCar/UNESPPharmacology Laboratory of Neuropsychopharmacology School of Pharmaceutical Sciences Univ. Estadual Paulista UNESPUniversidade Estadual Paulista (Unesp)Universidade de São Paulo (USP)University of LeedsSorregotti, Tatiani [UNESP]Cipriano, Ana Cláudia [UNESP]Cruz, Fábio CardosoMascarenhas, Diego Cardozo [UNESP]Rodgers, Robert JohnNunes-de-Souza, Ricardo Luiz [UNESP]2018-12-11T17:34:44Z2018-12-11T17:34:44Z2018-02-15info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article159-165application/pdfhttp://dx.doi.org/10.1016/j.bbr.2017.10.022Behavioural Brain Research, v. 338, p. 159-165.1872-75490166-4328http://hdl.handle.net/11449/17933210.1016/j.bbr.2017.10.0222-s2.0-850329016352-s2.0-85032901635.pdfScopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengBehavioural Brain Research1,413info:eu-repo/semantics/openAccess2024-06-24T14:51:52Zoai:repositorio.unesp.br:11449/179332Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-06-24T14:51:52Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Amygdaloid involvement in the defensive behavior of mice exposed to the open elevated plus-maze |
title |
Amygdaloid involvement in the defensive behavior of mice exposed to the open elevated plus-maze |
spellingShingle |
Amygdaloid involvement in the defensive behavior of mice exposed to the open elevated plus-maze Sorregotti, Tatiani [UNESP] Amygdala Cobalt chloride Defensive behavior Immunohistochemistry Mice Open elevated plus maze |
title_short |
Amygdaloid involvement in the defensive behavior of mice exposed to the open elevated plus-maze |
title_full |
Amygdaloid involvement in the defensive behavior of mice exposed to the open elevated plus-maze |
title_fullStr |
Amygdaloid involvement in the defensive behavior of mice exposed to the open elevated plus-maze |
title_full_unstemmed |
Amygdaloid involvement in the defensive behavior of mice exposed to the open elevated plus-maze |
title_sort |
Amygdaloid involvement in the defensive behavior of mice exposed to the open elevated plus-maze |
author |
Sorregotti, Tatiani [UNESP] |
author_facet |
Sorregotti, Tatiani [UNESP] Cipriano, Ana Cláudia [UNESP] Cruz, Fábio Cardoso Mascarenhas, Diego Cardozo [UNESP] Rodgers, Robert John Nunes-de-Souza, Ricardo Luiz [UNESP] |
author_role |
author |
author2 |
Cipriano, Ana Cláudia [UNESP] Cruz, Fábio Cardoso Mascarenhas, Diego Cardozo [UNESP] Rodgers, Robert John Nunes-de-Souza, Ricardo Luiz [UNESP] |
author2_role |
author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (Unesp) Universidade de São Paulo (USP) University of Leeds |
dc.contributor.author.fl_str_mv |
Sorregotti, Tatiani [UNESP] Cipriano, Ana Cláudia [UNESP] Cruz, Fábio Cardoso Mascarenhas, Diego Cardozo [UNESP] Rodgers, Robert John Nunes-de-Souza, Ricardo Luiz [UNESP] |
dc.subject.por.fl_str_mv |
Amygdala Cobalt chloride Defensive behavior Immunohistochemistry Mice Open elevated plus maze |
topic |
Amygdala Cobalt chloride Defensive behavior Immunohistochemistry Mice Open elevated plus maze |
description |
Previous studies have shown that the exposure to an open elevated plus maze (oEPM, an EPM with all four open arms) elicits fear/anxiety-related responses in laboratory rodents. However, very little is known about the underlying neural substrates of these defensive behaviors. Accordingly, the present study investigated the effects of chemical inactivation of the amygdala [through local injection of cobalt chloride (CoCl2: a nonspecific synaptic blocker)] on the behavior of oEPM-exposed mice. In a second experiment, the pattern of activation of the basolateral (BLA) and central (CeA) nuclei of the amygdala was assessed through quantification of Fos protein expression in mice subjected to one of several behavioral manipulations. To avoid the confound of acute handling stress, 4 independent groups of mice were habituated daily for 10 days to an enclosed EPM (eEPM) and, on day 11 prior to immunohistochemistry, were either taken directly from their home cage (control) or individually exposed for 10 min to a new clean holding cage (novelty), an eEPM, or the oEPM. An additional group of mice (maze-naïve) was not subjected to either the habituation or exposure phase but were simply chosen at random from their home cages to undergo an identical immunohistochemistry procedure. Results showed that amygdala inactivation produced an anxiolytic-like profile comprising reductions in time spent in the proximal portions of the open arms and total stretched attend postures (SAP) as well as increases in time spent in the distal portions of the open arms and total head-dipping. Moreover, Fos-positive labeled cells were bilaterally increased in the amygdaloid complex, particularly in the BLA, of oEPM-exposed animals compared to all other groups. These results suggest that the amygdala (in particular, its BLA nucleus) plays a key role in the modulation of defensive behaviors in oEPM-exposed mice. |
publishDate |
2018 |
dc.date.none.fl_str_mv |
2018-12-11T17:34:44Z 2018-12-11T17:34:44Z 2018-02-15 |
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.bbr.2017.10.022 Behavioural Brain Research, v. 338, p. 159-165. 1872-7549 0166-4328 http://hdl.handle.net/11449/179332 10.1016/j.bbr.2017.10.022 2-s2.0-85032901635 2-s2.0-85032901635.pdf |
url |
http://dx.doi.org/10.1016/j.bbr.2017.10.022 http://hdl.handle.net/11449/179332 |
identifier_str_mv |
Behavioural Brain Research, v. 338, p. 159-165. 1872-7549 0166-4328 10.1016/j.bbr.2017.10.022 2-s2.0-85032901635 2-s2.0-85032901635.pdf |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Behavioural Brain Research 1,413 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
159-165 application/pdf |
dc.source.none.fl_str_mv |
Scopus 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 |
repositoriounesp@unesp.br |
_version_ |
1834484453355814912 |