dc.contributorTort, Adriano Bretanha Lopes
dc.contributor
dc.contributor
dc.contributorLaplagne, Diego Andres
dc.contributor
dc.contributorLeão, Emelie Katarina Svahn
dc.contributor
dc.contributorPereira, Rodrigo Neves Romcy
dc.contributor
dc.contributorMoraes, Márcio Flávio Dutra
dc.contributor
dc.contributorMinetti, Pablo Daniel Torterolo
dc.contributor
dc.creatorLockmann, André Luiz Vieira
dc.date.accessioned2019-02-14T22:01:33Z
dc.date.accessioned2022-10-06T12:25:32Z
dc.date.available2019-02-14T22:01:33Z
dc.date.available2022-10-06T12:25:32Z
dc.date.created2019-02-14T22:01:33Z
dc.date.issued2018-12-13
dc.identifierLOCKMANN, André Luiz Vieira. Oscilações neurais sincronizando circuitos olfatórios e hipocampais. 2018. 73f. Tese (Doutorado em Neurociências) - Universidade Federal do Rio Grande do Norte, Universidade Federal do Rio Grande do Norte, Natal, 2018.
dc.identifierhttps://repositorio.ufrn.br/jspui/handle/123456789/26650
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3951946
dc.description.abstractLocal field potentials (LFPs) in the rodent brain exhibit prominent oscillations, which have been suggested to coordinate information flow across neuronal circuits. This thesis investigated oscillations that simultaneously emerge in the rat olfactory and hippocampal systems and supposedly mediate their communication. The main results and insights are presented in four publications – two commentary (1 and 4) and two experimental (2 and 3) papers. Paper 1 discusses the controversial origin of low-frequency LFP oscillations (~ 1 Hz) that appear in the rodent hippocampus during sleep and anesthesia. Do these oscillations reflect internal processing with the neocortex or do they couple to external inputs from rhythmic nasal respiration? This question is experimentally addressed in paper 2. By simultaneously recording nasal respiration and LFPs from urethane-anesthetized rats, we show that the hippocampus exhibits two independent low-frequency oscillations: one that entrains to neocortical “up-and-down” state transitions and another that entrains to the olfactory bulb respiration-coupled rhythm (RR) – and to respiration itself. Paper 3 further shows that the olfactory bulb also drives beta oscillations (10-20 Hz) in the hippocampus. Together, papers 2 and 3 indicate that related network mechanisms generate hippocampal beta and RR: both rhythms are relayed to the hippocampus by entorhinal cortex inputs to the dentate gyrus and, additionally, the phase of RR modulates beta amplitude. Based on our own results and on publications from other groups, in paper 4 we defend that the recently described delta-band oscillations coupling prefrontal cortex and hippocampus correspond to RR. In all, this thesis supports that respiration-coupled and beta oscillations mediate olfacto-hippocampal communication.
dc.publisherBrasil
dc.publisherUFRN
dc.publisherPROGRAMA DE PÓS-GRADUAÇÃO EM NEUROCIÊNCIAS
dc.rightsAcesso Aberto
dc.subjectPotenciais de campo local
dc.subjectOscilações neurais acopladas à respiração
dc.subjectOscilações beta
dc.subjectBulbo olfatório
dc.subjectHipocampo
dc.titleOscilações neurais sincronizando circuitos olfatórios e hipocampais
dc.typedoctoralThesis


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