Please use this identifier to cite or link to this item: http://hdl.handle.net/1822/28678

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dc.contributor.authorBorges, Sónia Maria de Sousa-
dc.contributor.authorCoimbra, Bárbara Guimarães Salazar-
dc.contributor.authorCunha, Carina Isabel Soares da-
dc.contributor.authorSilva, Ana Paula Ventura-
dc.contributor.authorPinto, Luísa-
dc.contributor.authorCarvalho, Miguel-
dc.contributor.authorPêgo, José M.-
dc.contributor.authorRodrigues, Ana João-
dc.contributor.authorSousa, Nuno-
dc.date.accessioned2014-04-04T15:33:02Z-
dc.date.available2014-04-04T15:33:02Z-
dc.date.issued2013-12-
dc.identifier.issn1664-2392por
dc.identifier.urihttp://hdl.handle.net/1822/28678-
dc.description.abstractStress perception, response, adaptation, and coping strategies are individually distinct, and the sequel of stress and/or glucocorticoids (GCs) is also distinct between subjects. In the last years, it has become clear that early life stress is a powerful modulator of neuroendocrine stress-responsive circuits, programing intrinsic susceptibility to stress, and potentiating the appearance of stress-related disorders such as depression, anxiety, and addiction. Herein we were interested in understanding how early life experiences reset the normal processing of negative stimuli, leading to emotional dysfunction. Animals prenatally exposed to GCs (in utero glucocorticoid exposure, iuGC) present hyperanxiety, increased fear behavior, and hyper-reactivity to negative stimuli. In parallel, we found a remarkable increase in the number of aversive 22?kHz ultrasonic vocalizations in response to an aversive cue. Considering the suggested role of the mesopontine tegmentum cholinergic pathway, arising from the laterodorsal tegmental nucleus (LDT) and pedunculopontine tegmental nucleus (PPT), in the initiation of 22?kHz vocalizations and hypothetically in the control of emotional arousal and tone, we decided to evaluate the condition of this circuit in iuGC animals. Notably, in a basal situation, iuGC animals present increased choline acetyltransferase (ChAT) expression in the LDT and PPT, but not in other cholinergic nuclei, namely in the nucleus basalis of Meynert. In addition, and in accordance with the amplified response to an adverse stimulus of iuGC animals, we found marked changes in the cholinergic activation pattern of LDT and PPT regions. Altogether, our results suggest a specific cholinergic pathway programing by prenatal GC, and hint that this may be of relevance in setting individual stress vulnerability threshold.por
dc.language.isoengpor
dc.publisherFrontierspor
dc.rightsopenAccesspor
dc.subjectGlucocorticoidspor
dc.subjectStresspor
dc.subjectAcetylcholinepor
dc.subjectAnxietypor
dc.subjectFearpor
dc.subjectPedunculopontine tegmental nucleuspor
dc.subjectLaterodorsal tegmental nucleuspor
dc.subjectUltrasonic vocalizationspor
dc.titleGlucocorticoid programing of the mesopontine cholinergic systempor
dc.typearticle-
dc.peerreviewedyespor
dc.relation.publisherversionhttp://www.frontiersin.org/por
sdum.publicationstatuspublishedpor
degois.publication.firstPage1por
degois.publication.lastPage11por
degois.publication.issue190por
degois.publication.titleFrontiers in endocrinologypor
degois.publication.volume4por
dc.date.updated2014-03-06T14:19:56Z-
dc.identifier.doi10.3389/fendo.2013.00190por
sdum.journalFrontiers in endocrinologypor
Appears in Collections:ICVS - Artigos em Revistas Internacionais com Referee

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