Panic-like escape response elicited in mice by exposure to CO2, but not hypoxia

Detalhes bibliográficos
Autor(a) principal: Spiacci, Ailton
Data de Publicação: 2018
Outros Autores: Vilela-Costa, Heloisa H., Sant'Ana, Ana Beatriz, Fernandes, Gabriel Gripp, Frias, Alana Tercino, da Silva, Glauber S. Ferreira [UNESP], Antunes-Rodrigues, José, Zangrossi, Hélio
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1016/j.pnpbp.2017.10.018
http://hdl.handle.net/11449/175462
Resumo: Exposure to elevated concentrations of CO2 or hypoxia has been widely used in psychiatric research as a panic provoking stimulus. However, the use of these respiratory challenges to model panic-like responses in experimental animals has been less straightforward. Little data is available, from behavioral and endocrine perspectives, to support the conclusion that a marked aversive situation, such as that experienced during panic attacks, was evoked in these animals. We here compared the behavioral responses of male CB57BL/6 mice during exposure to 20% CO2 or 7% O2 and its consequence on plasma levels of corticosterone. We also evaluated whether clinically-effective panicolytic drugs affect the behavioral responses expressed during CO2 exposure. The results showed that whereas hypoxia caused a marked reduction in locomotion, inhalation of CO2-enriched air evoked an active escape response, characterized by bouts of upward leaps directed to the border of the experimental cage, interpreted as escape attempts. Corticosterone levels were increased 30 min after either of the respiratory challenges used, but it was higher in the hypoxia group. Chronic (21 days), but not acute, treatment with fluoxetine or imipramine (5, 10 or 15 mg/kg) or a single injection of alprazolam (0.025, 0.05 or 0.1 mg/kg), but not of the anxiolytic diazepam (0.025, 0.05 or 0.1 and 1 mg/kg) reduced the number of escape attempts, indicating a panicolytic-like effect. Altogether, the results suggest that whereas hypoxia increased anxiety, exposure to 20% CO2 evoked a panic-like state. The latter condition/test protocol seems to be a simple and validated model for studying in mice pathophysiological mechanisms and the screening of novel drugs for panic disorder.
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spelling Panic-like escape response elicited in mice by exposure to CO2, but not hypoxiaCO2-exposureCorticosteroneEscapeHypoxiaPanicExposure to elevated concentrations of CO2 or hypoxia has been widely used in psychiatric research as a panic provoking stimulus. However, the use of these respiratory challenges to model panic-like responses in experimental animals has been less straightforward. Little data is available, from behavioral and endocrine perspectives, to support the conclusion that a marked aversive situation, such as that experienced during panic attacks, was evoked in these animals. We here compared the behavioral responses of male CB57BL/6 mice during exposure to 20% CO2 or 7% O2 and its consequence on plasma levels of corticosterone. We also evaluated whether clinically-effective panicolytic drugs affect the behavioral responses expressed during CO2 exposure. The results showed that whereas hypoxia caused a marked reduction in locomotion, inhalation of CO2-enriched air evoked an active escape response, characterized by bouts of upward leaps directed to the border of the experimental cage, interpreted as escape attempts. Corticosterone levels were increased 30 min after either of the respiratory challenges used, but it was higher in the hypoxia group. Chronic (21 days), but not acute, treatment with fluoxetine or imipramine (5, 10 or 15 mg/kg) or a single injection of alprazolam (0.025, 0.05 or 0.1 mg/kg), but not of the anxiolytic diazepam (0.025, 0.05 or 0.1 and 1 mg/kg) reduced the number of escape attempts, indicating a panicolytic-like effect. Altogether, the results suggest that whereas hypoxia increased anxiety, exposure to 20% CO2 evoked a panic-like state. The latter condition/test protocol seems to be a simple and validated model for studying in mice pathophysiological mechanisms and the screening of novel drugs for panic disorder.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Department of Pharmacology School of Medicine of Ribeirão Preto University of São Paulo, Av. Bandeirantes, 3900Department of Animal Morphology and Physiology São Paulo State University UNESP FCAVDepartment of Physiology School of Medicine of Ribeirao Preto University of São PauloDepartment of Animal Morphology and Physiology São Paulo State University UNESP FCAVFAPESP: 12/17626-7CAPES: 1281474CNPq: 466796/2014-5Universidade de São Paulo (USP)Universidade Estadual Paulista (Unesp)Spiacci, AiltonVilela-Costa, Heloisa H.Sant'Ana, Ana BeatrizFernandes, Gabriel GrippFrias, Alana Tercinoda Silva, Glauber S. Ferreira [UNESP]Antunes-Rodrigues, JoséZangrossi, Hélio2018-12-11T17:15:56Z2018-12-11T17:15:56Z2018-02-02info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article178-186application/pdfhttp://dx.doi.org/10.1016/j.pnpbp.2017.10.018Progress in Neuro-Psychopharmacology and Biological Psychiatry, v. 81, p. 178-186.1878-42160278-5846http://hdl.handle.net/11449/17546210.1016/j.pnpbp.2017.10.0182-s2.0-850334094732-s2.0-85033409473.pdfScopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengProgress in Neuro-Psychopharmacology and Biological Psychiatry1,714info:eu-repo/semantics/openAccess2024-01-17T06:28:59Zoai:repositorio.unesp.br:11449/175462Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-01-17T06:28:59Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Panic-like escape response elicited in mice by exposure to CO2, but not hypoxia
title Panic-like escape response elicited in mice by exposure to CO2, but not hypoxia
spellingShingle Panic-like escape response elicited in mice by exposure to CO2, but not hypoxia
Spiacci, Ailton
CO2-exposure
Corticosterone
Escape
Hypoxia
Panic
title_short Panic-like escape response elicited in mice by exposure to CO2, but not hypoxia
title_full Panic-like escape response elicited in mice by exposure to CO2, but not hypoxia
title_fullStr Panic-like escape response elicited in mice by exposure to CO2, but not hypoxia
title_full_unstemmed Panic-like escape response elicited in mice by exposure to CO2, but not hypoxia
title_sort Panic-like escape response elicited in mice by exposure to CO2, but not hypoxia
author Spiacci, Ailton
author_facet Spiacci, Ailton
Vilela-Costa, Heloisa H.
Sant'Ana, Ana Beatriz
Fernandes, Gabriel Gripp
Frias, Alana Tercino
da Silva, Glauber S. Ferreira [UNESP]
Antunes-Rodrigues, José
Zangrossi, Hélio
author_role author
author2 Vilela-Costa, Heloisa H.
Sant'Ana, Ana Beatriz
Fernandes, Gabriel Gripp
Frias, Alana Tercino
da Silva, Glauber S. Ferreira [UNESP]
Antunes-Rodrigues, José
Zangrossi, Hélio
author2_role author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade de São Paulo (USP)
Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Spiacci, Ailton
Vilela-Costa, Heloisa H.
Sant'Ana, Ana Beatriz
Fernandes, Gabriel Gripp
Frias, Alana Tercino
da Silva, Glauber S. Ferreira [UNESP]
Antunes-Rodrigues, José
Zangrossi, Hélio
dc.subject.por.fl_str_mv CO2-exposure
Corticosterone
Escape
Hypoxia
Panic
topic CO2-exposure
Corticosterone
Escape
Hypoxia
Panic
description Exposure to elevated concentrations of CO2 or hypoxia has been widely used in psychiatric research as a panic provoking stimulus. However, the use of these respiratory challenges to model panic-like responses in experimental animals has been less straightforward. Little data is available, from behavioral and endocrine perspectives, to support the conclusion that a marked aversive situation, such as that experienced during panic attacks, was evoked in these animals. We here compared the behavioral responses of male CB57BL/6 mice during exposure to 20% CO2 or 7% O2 and its consequence on plasma levels of corticosterone. We also evaluated whether clinically-effective panicolytic drugs affect the behavioral responses expressed during CO2 exposure. The results showed that whereas hypoxia caused a marked reduction in locomotion, inhalation of CO2-enriched air evoked an active escape response, characterized by bouts of upward leaps directed to the border of the experimental cage, interpreted as escape attempts. Corticosterone levels were increased 30 min after either of the respiratory challenges used, but it was higher in the hypoxia group. Chronic (21 days), but not acute, treatment with fluoxetine or imipramine (5, 10 or 15 mg/kg) or a single injection of alprazolam (0.025, 0.05 or 0.1 mg/kg), but not of the anxiolytic diazepam (0.025, 0.05 or 0.1 and 1 mg/kg) reduced the number of escape attempts, indicating a panicolytic-like effect. Altogether, the results suggest that whereas hypoxia increased anxiety, exposure to 20% CO2 evoked a panic-like state. The latter condition/test protocol seems to be a simple and validated model for studying in mice pathophysiological mechanisms and the screening of novel drugs for panic disorder.
publishDate 2018
dc.date.none.fl_str_mv 2018-12-11T17:15:56Z
2018-12-11T17:15:56Z
2018-02-02
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.pnpbp.2017.10.018
Progress in Neuro-Psychopharmacology and Biological Psychiatry, v. 81, p. 178-186.
1878-4216
0278-5846
http://hdl.handle.net/11449/175462
10.1016/j.pnpbp.2017.10.018
2-s2.0-85033409473
2-s2.0-85033409473.pdf
url http://dx.doi.org/10.1016/j.pnpbp.2017.10.018
http://hdl.handle.net/11449/175462
identifier_str_mv Progress in Neuro-Psychopharmacology and Biological Psychiatry, v. 81, p. 178-186.
1878-4216
0278-5846
10.1016/j.pnpbp.2017.10.018
2-s2.0-85033409473
2-s2.0-85033409473.pdf
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Progress in Neuro-Psychopharmacology and Biological Psychiatry
1,714
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 178-186
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
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