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<dc:title xml:lang="fr">Circuits neuronaux sous-tendant la régulation émotionnelle par le système ocytocinergique</dc:title>
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<dc:subject xml:lang="fr">Ocytocine</dc:subject>
<dc:subject xml:lang="fr">Neuropeptide S</dc:subject>
<dc:subject xml:lang="fr">Dopamine</dc:subject>
<dc:subject xml:lang="fr">Hypothalamus</dc:subject>
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<dc:subject xml:lang="fr">Électrophysiologie</dc:subject>
<dc:subject xml:lang="fr">Conditionnement de peur</dc:subject>
<dc:subject xml:lang="en">Oxytocin</dc:subject>
<dc:subject xml:lang="en">Neuropeptide S</dc:subject>
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<dc:subject xml:lang="en">Hypothalamus</dc:subject>
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<tef:elementdEntree autoriteExterne="148171907" autoriteSource="Sudoc">Récepteurs couplés aux protéines G</tef:elementdEntree>
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<tef:elementdEntree autoriteExterne="027733130" autoriteSource="Sudoc">Hormones hypothalamiques</tef:elementdEntree>
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<tef:elementdEntree autoriteExterne="028272412" autoriteSource="Sudoc">Neuropeptides</tef:elementdEntree>
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<dcterms:abstract xml:lang="fr">L’ocytocine (OT) est un neuropeptide synthétisé au sein de l’hypothalamus. On sait aujourd’hui que l’OT est fortement impliquée dans la modulation de nombreux comportements et émotions. Pourtant, il reste encore difficile d’expliquer comment s’organise le système ocytocinergique, par exemple en sous-ensembles spécifiques. De même, les circuits neuronaux impliqués dans leur recrutement restent obscures, tout comme leur potentielle plasticité. C’est pourquoi, au cours de ma thèse, je me suis attachée à mieux comprendre ces différents points. Les résultats obtenus ont montré que i) un sous-ensemble spécifique de neurones OT est recruté par la peur ; ii) le système OT fait preuve d’une grande plasticité après une exposition à un contexte effrayant ; iii) le neuropeptide S est capable de recruter une sous-population de neurones OT afin d’exercer une action anxiolytique ; iv) les neurotransmetteurs monoaminergiques sont eux-mêmes capables de recruter différents sous-ensembles de neurones OT. En conclusion, mon travail a mis en évidence la plasticité de ce système peptidergique et différentes manières de recruter de manière spécifiques certains sous-ensembles existants de neurones OT.</dcterms:abstract>
<dcterms:abstract xml:lang="en">Oxytocin (OT) is a peptide synthesized within the hypothalamus. We now know that OT is strongly involved in the modulation of many behaviors and emotions. However, it is still difficult to explain how the oxytocinergic system is organized, for example in specific sub-populations. Similarly, the neuronal circuits involved in their recruitment remain obscure, like their potential plasticity. That is why, during my thesis, I tried to better understand these different points. The results obtained showed that i) a specific sub-population of OT neurons is recruited by fear; ii) the OT system exhibits great plasticity after exposure to a scary context; iii) the neuropeptide S is able to recruit an OT neuron sub-population in order to exert an anxiolytic effect; iv) monoaminergic neurotransmitters are themselves able to recruit different sub-populations of OT neurons. In conclusion, my work has highlighted the plasticity of this peptidergic system and different ways to recruit in a specific manner some existing sub-populations of OT neurons.</dcterms:abstract>
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