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dc.contributor.authorGomez-Nieto, Ricardo-
dc.contributor.authorHorta-Junior, Jose de Anchieta C.-
dc.contributor.authorCastellano, Orlando-
dc.contributor.authorMillian-Morell, Lymarie-
dc.contributor.authorRubio, Maria E.-
dc.contributor.authorLopez, Dolores E.-
dc.date.accessioned2015-03-18T15:56:20Z-
dc.date.accessioned2016-10-25T20:35:32Z-
dc.date.available2015-03-18T15:56:20Z-
dc.date.available2016-10-25T20:35:32Z-
dc.date.issued2014-07-25-
dc.identifierhttp://dx.doi.org/10.3389/fnins.2014.00216-
dc.identifier.citationFrontiers In Neuroscience. Lausanne: Frontiers Research Foundation, v. 8, 18 p., 2014.-
dc.identifier.issn1662-453X-
dc.identifier.urihttp://hdl.handle.net/11449/117509-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/117509-
dc.description.abstractThe acoustic startle reflex (ASR) is a survival mechanism of alarm, which rapidly alerts the organism to a sudden loud auditory stimulus. In rats, the primary ASR circuit encompasses three serially connected structures: cochlear root neurons (CRNs), neurons in the caudal pontine reticular nucleus (PnC), and motoneurons in the medulla and spinal cord. It is well-established that both CRNs and PnC neurons receive short-latency auditory inputs to mediate the ASR. Here, we investigated the anatomical origin and functional role of these inputs using a multidisciplinary approach that combines morphological, electrophysiological and behavioral techniques. Anterograde tracer injections into the cochlea suggest that CRNs somata and dendrites receive inputs depending, respectively, on their basal or apical cochlear origin. Confocal colocalization experiments demonstrated that these cochlear inputs are immunopositive for the vesicular glutamate transporter 1 (VGLUT1). Using extracellular recordings in vivo followed by subsequent tracer injections, we investigated the response of PnC neurons after contra-, ipsi-, and bilateral acoustic stimulation and identified the source of their auditory afferents. Our results showed that the binaural firing rate of PnC neurons was higher than the monaural, exhibiting higher spike discharges with contralateral than ipsilateral acoustic stimulations. Our histological analysis confirmed the CRNs as the principal source of short-latency acoustic inputs, and indicated that other areas of the cochlear nucleus complex are not likely to innervate PnC. Behaviorally, we observed a strong reduction of ASR amplitude in monaural earplugged rats that corresponds with the binaural summation process shown in our electrophysiological findings. Our study contributes to understand better the role of neuronal mechanisms in auditory alerting behaviors and provides strong evidence that the CRNs-PnC pathway mediates fast neurotransmission and binaural summation of the ASR.en
dc.description.sponsorshipSpanish Ministry of Science and Innovation (MICINN)-
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)-
dc.format.extent18-
dc.language.isoeng-
dc.publisherFrontiers Research Foundation-
dc.sourceWeb of Science-
dc.subjectalertness systemen
dc.subjectbinaural summationen
dc.subjectcochlear root neuronsen
dc.subjectextracellular recordingsen
dc.subjectneuronal tracersen
dc.subjectpontine reticular formationen
dc.subjectraten
dc.subjectvglut1-auditory nerveen
dc.titleOrigin and function of short-latency inputs to the neural substrates underlying the acoustic startle reflexen
dc.typeoutro-
dc.contributor.institutionUniv Salamanca-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniv Pittsburgh-
dc.description.affiliationUniv Salamanca, Neurosci Inst Castilla & Leon, Salamanca 37007, Spain-
dc.description.affiliationUniv Salamanca, Dept Cell Biol & Pathol, Salamanca 37007, Spain-
dc.description.affiliationUniv Salamanca, Inst Biomed Res Salamanca IBSAL, Salamanca 37007, Spain-
dc.description.affiliationSao Paulo State Univ Botucatu, Biosci Inst, Dept Anat, Sao Paulo, Brazil-
dc.description.affiliationUniv Pittsburgh, Dept Otolaryngol, Pittsburgh, PA 15260 USA-
dc.description.affiliationUnespSao Paulo State Univ Botucatu, Biosci Inst, Dept Anat, Sao Paulo, Brazil-
dc.description.sponsorshipIdSpanish Ministry of Science and Innovation (MICINN)BFU2010-17754-
dc.description.sponsorshipIdFAPESP: 08/02771-6-
dc.description.sponsorshipId1R01DC013048-01-
dc.identifier.doi10.3389/fnins.2014.00216-
dc.identifier.wosWOS:000346501100001-
dc.rights.accessRightsAcesso aberto-
dc.identifier.fileWOS000346501100001.pdf-
dc.relation.ispartofFrontiers In Neuroscience-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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