Amygdaloid involvement in the defensive behavior of mice exposed to the open elevated plus-maze

Detalhes bibliográficos
Autor(a) principal: Sorregotti, Tatiani [UNESP]
Data de Publicação: 2018
Outros Autores: Cipriano, Ana Cláudia [UNESP], Cruz, Fábio Cardoso, Mascarenhas, Diego Cardozo [UNESP], Rodgers, Robert John, 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.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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spelling 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
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