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Facilitation of contextual fear extinction by orexin-1 receptor antagonism is associated with the activation of specific amygdala cell subpopulations

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dc.contributor.author Flores de los Heros, África, 1985-
dc.contributor.author Herry, Cyril
dc.contributor.author Maldonado, Rafael, 1961-
dc.contributor.author Berrendero Díaz, Fernando, 1971-
dc.date.accessioned 2018-03-06T16:07:38Z
dc.date.available 2018-03-06T16:07:38Z
dc.date.issued 2017
dc.identifier.citation Flores A, Herry C, Maldonado R, Berrendero F. Facilitation of Contextual Fear Extinction by Orexin-1 Receptor Antagonism IsAssociated with the Activation of Specific Amygdala Cell Subpopulations. Int J Neuropsychopharmacol. 2017 Aug 1;20(8):654-9. DOI: 10.1093/ijnp/pyx029
dc.identifier.issn 1461-1457
dc.identifier.uri http://hdl.handle.net/10230/34051
dc.description.abstract BACKGROUND: Orexins are hypothalamic neuropeptides recently involved in the regulation of emotional memory. The basolateral amygdala, an area orchestrating fear memory processes, appears to be modulated by orexin transmission during fear extinction. However, the neuronal types within the basolateral amygdala involved in this modulation remain to be elucidated. METHODS: We used retrograde tracing combined with immunofluorescence techniques in mice to identify basolateral amygdala projection neurons and cell subpopulations in this brain region influenced by orexin transmission during contextual fear extinction consolidation. RESULTS: Treatment with the orexin-1 receptor antagonist SB334867 increased the activity of basolateral amygdala neurons projecting to infralimbic medial prefrontal cortex during fear extinction. GABAergic interneurons expressing calbindin, but not parvalbumin, were also activated by orexin-1 receptor antagonism in the basolateral amygdala. CONCLUSIONS: These data identify neuronal circuits and cell populations of the amygdala associated with the facilitation of fear extinction consolidation induced by the orexin-1 receptor antagonist SB334867.
dc.description.sponsorship This work was supported by “Plan Nacional sobre Drogas” (no. 2014I019 to F.B.), the “Ministerio de Economía y Competitividad-MINECO” (no. SAF2014-59648-P to R.M.), the “Instituto de Salud Carlos III” (no. PI13/00042 to F.B. and RETICS-RTA, no. RD12/0028/0023 to R.M.), the “Generalitat de Catalunya-AGAUR” (no. 2014-SGR-1547 and ICREA-Acadèmia (2015) to R.M.). AF was recipient of an EMBO Short-Term Fellowship (281-2015).
dc.format.mimetype application/pdf
dc.language.iso eng
dc.publisher Oxford University Press
dc.relation.ispartof International Journal of Neuropsychopharmacology. 2017 Aug 1;20(8):654-9
dc.rights © The Author 2017. Published by Oxford University Press on behalf of CINP. This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
dc.rights.uri http://creativecommons.org/licenses/by-nc/4.0/
dc.title Facilitation of contextual fear extinction by orexin-1 receptor antagonism is associated with the activation of specific amygdala cell subpopulations
dc.type info:eu-repo/semantics/article
dc.identifier.doi http://dx.doi.org/10.1093/ijnp/pyx029
dc.subject.keyword Fear extinction
dc.subject.keyword Orexin
dc.subject.keyword Amygdala
dc.subject.keyword Retrograde labeling
dc.subject.keyword Calbindin
dc.relation.projectID info:eu-repo/grantAgreement/ES/1PE/SAF2014-59648-P
dc.rights.accessRights info:eu-repo/semantics/openAccess
dc.type.version info:eu-repo/semantics/publishedVersion

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