Brasil | Dissertação
dc.contributorNogueira, Cristina Wayne
dc.contributorhttp://lattes.cnpq.br/2877042401245169
dc.contributorLuchese, Cristiane
dc.contributorhttp://lattes.cnpq.br/3420684025232526
dc.contributorMagni, Danieli Valnes
dc.contributorhttp://lattes.cnpq.br/5452391689473129
dc.creatorPesarico, Ana Paula
dc.date.accessioned2015-10-29
dc.date.available2015-10-29
dc.date.created2015-10-29
dc.date.issued2014-03-11
dc.identifierPESARICO, Ana Paula. Involvement of serotonergic and dopaminergic systems in the antidepressant-like action of 7-fluoro-1,3 diphenylisoquinoline in mice. 2014. 62 f. Dissertação (Mestrado em Ciências Biológicas) - Universidade Federal de Santa Maria, Santa Maria, 2014.
dc.identifierhttp://repositorio.ufsm.br/handle/1/11237
dc.description.abstractDepression is a psychiatric disorder associated with a negative impact on quality of life. Monoaminergic system has been involved in this disease and in the action of antidepressants. This study aimed to investigate the potential antidepressant-like of 7-fluoro-1,3-diphenylisoquinoline-1-amine (FDPI) and the possible involvement of monoaminergic system. Results showed that FDPI (1, 10 and 20 mg/kg, intragastric (i.g.)) reduced the immobility time, increased swimming time, but did not alter climbing time of mice in the modified forced swimming test (FST). These effects were similar to those of paroxetine (8 mg/kg, intraperitoneally (i.p.)), a selective serotonin reuptake inhibitor, which was used as positive control. Pretreatments with p-chlorophenylalanine (pCPA, an inhibitor of serotonin (5-HT) synthesis, 100 mg/kg, i.p., once a day for 4 consecutive days), N-[1]-N-(2-pyridinyl) cyclohexanecarboxamide (WAY 100635, a 5-HT1A receptor antagonist, 0.1 mg/kg, subcutaneous injection (s.c.)) and ondansetron (a 5-HT3 receptor antagonist, 1 mg/kg, i.p.) reversed the antidepressant-like effect of FDPI at the dose 1 mg/kg in FST, this did not occurs with ritanserin (a 5-HT2A/2C receptor antagonist, 1 mg/kg, i.p.). Antagonist related with dopaminergic system, as haloperidol (a D2 receptor antagonist, 0.2 mg/kg, i.p.) and SCH23390 (a D1 receptor antagonist, 0.05 mg/kg, s.c.) were able to reverse the antidepressant-like effect of FDPI at the dose 1 mg/kg in FST, this did not occurs with sulpiride (a D2 and D3 receptors antagonist, 50 mg/kg, i.p.). FDPI, at doses of 10 and 20 mg/kg, inhibited monoamine oxidase-B activity in prefrontal cortex of mice. These results suggest that FDPI produced an antidepressant-like action in the FST in mice, possibly by an involvement of the monoaminergic system. Additional studies are necessary in order to propose FDPI as a drug for depression treatment.
dc.publisherUniversidade Federal de Santa Maria
dc.publisherBR
dc.publisherBioquímica
dc.publisherUFSM
dc.publisherPrograma de Pós-Graduação em Ciências Biológicas: Bioquímica Toxicológica
dc.rightsAcesso Aberto
dc.subjectTeste do nado forçado modificado
dc.subjectIsoquinolina
dc.subjectSerotoninérgico
dc.subjectDopaminérgico
dc.subjectAntidepressivo
dc.subjectMonoamino oxidase
dc.subjectModified forced swim test
dc.subjectIsoquinoline
dc.subjectSerotonergic
dc.subjectDopaminergic
dc.subjectAntidepressant-like
dc.subjectMonoamine oxidase
dc.titleEnvolvimento dos sistemas serotoninérgico e dopaminérgico na ação do tipo antidepressiva do 7-flúor-1,3 difenilisoquinolina-1-amino em camundongos
dc.typeDissertação


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