Participação de receptores noradrenérgicos na substância cinzenta periaquedutal dorsal na modulação de comportamentos defensivos relacionados à ansiedade
Ano de defesa: | 2016 |
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Autor(a) principal: | |
Orientador(a): | |
Banca de defesa: | |
Tipo de documento: | Dissertação |
Tipo de acesso: | Acesso aberto |
Idioma: | por |
Instituição de defesa: |
Universidade Federal do Espírito Santo
BR Mestrado em Ciências Farmacêuticas Centro de Ciências da Saúde UFES Programa de Pós-Graduação em Ciências Farmacêuticas |
Programa de Pós-Graduação: |
Não Informado pela instituição
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Departamento: |
Não Informado pela instituição
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País: |
Não Informado pela instituição
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Palavras-chave em Português: | |
Link de acesso: | http://repositorio.ufes.br/handle/10/8358 |
Resumo: | The role of the dorsal periaqueductal gray matter (DPAG) in fear and anxiety has been studied over the last decades. The evidence regarding the involvement of the noradrenergic system in anxiety is conflicting, depending on brain structure studied. Thus, in the present study we tested the hypothesis that noradrenaline injected directly into the DPAG of rats has anxiolytic-like effect in the light-dark transition test. The lightdark transition test is an ethological model of anxiety, quick and easy to perform, that does not require animal training. For this, Wistar rats were given intra-DPAG administration of noradrenaline (30, 60 or 90 nmol) or saline and tested in light-dark test. In addition, we investigated the effect of pre-treatment with intra-DPAG nonselective antagonists of alpha and beta-adrenergic receptors, phentolamine and propranolol, respectively, in the effect of noradrenaline injection in the same structure. After the tests, the animals were placed for five minutes in the open field, for measurement of locomotor activity. Our results show that noradrenaline (30 and 60 nmols) administered directly into the SCPD increased time spent in the light compartment and the number of transitions of the animals submitted to the light-dark transition test, suggesting an anxiolytic-like effect. In addition, intra-SCPD injection of norepinephrine did not change locomotor activity of animals in the open field test. The results also show that pre-treatment with intra-SCPD propranolol or phentolamine attenuated anxiolytic-like effect of norepinephrine when analyzing the time spent in the light compartment of the model. Thus, this work suggests an involvement of noradrenergic neurotransmission in the SCPD, via alpha and beta-adrenergics receptors in defensive reactions associated with generalized anxiety disorder in animals in the light-dark transition model. |