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Provedor de dados:  BJMBR
País:  Brazil
Título:  Gender-related differences in the effects of nitric oxide donors on neuroleptic-induced catalepsy in mice
Autores:  Pires,J.G.P.
Costa,P.G.
Saraiva,F.P.
Bonikovski,V.
Futuro Neto,H.A.
Data:  2003-02-01
Ano:  2003
Palavras-chave:  Neuroleptic-induced catalepsy
Nitric oxide donors
Gender differences
Linsidomine
SNAP
Isosorbide dinitrate
Resumo:  It has been suggested that nigrostriatal dopaminergic transmission is modulated by nitric oxide (NO). Since there is evidence that gonadal hormones can affect extrapyramidal motor behavior in mammals, we investigated the effects of isosorbide dinitrate (ISD), linsidomine (SIN-1) and S-nitroso-N-acetylpenicillamine (SNAP), three pharmacologically different NO donors, on neuroleptic-induced catalepsy in 60- to 80-day-old male and female albino mice. Catalepsy was induced with haloperidol (1 mg/kg, ip) and measured at 30-min intervals by means of a bar test. Drugs (or appropriate vehicle) were injected ip 30 min before haloperidol, with each animal being used only once. ISD (5, 20 and 50 mg/kg) caused a dose-dependent inhibition of catalepsy in male mice (maximal effect 120 min after haloperidol: 64% inhibition). In the females only at the highest dose of ISD was an attenuation of catalepsy observed, which was mild and short lasting. SIN-1 (10 and 50 mg/kg) did not significantly affect catalepsy in female mice, while a significant attenuation was observed in males at the dose of 50 mg/kg (maximal inhibition: 60%). SNAP (20 mg/kg) significantly attenuated catalepsy in males 120 min after haloperidol (44% inhibition), but had no significant effect on females. These results basically agree with literature data showing that NO facilitates central dopaminergic transmission, although the mechanisms are not fully understood. They also reveal the existence of gender-related differences in this nitrergic modulation in mice, with females being less affected than males.
Tipo:  Info:eu-repo/semantics/article
Idioma:  Inglês
Identificador:  http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2003000200012
Editor:  Associação Brasileira de Divulgação Científica
Relação:  10.1590/S0100-879X2003000200012
Formato:  text/html
Fonte:  Brazilian Journal of Medical and Biological Research v.36 n.2 2003
Direitos:  info:eu-repo/semantics/openAccess
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