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Inhibition of chlorpromazine-induced catalepsy by the 5-HT-1A ligands pindolol and Buspirone in mice
Braz. j. med. biol. res ; 23(9): 869-71, 1990. ilus
Artículo en Inglés | LILACS | ID: lil-92445
RESUMO
Neuroleptcs such as chlorpromazine and haloperidol are capable of inducing catalepsy in rodents. Non-selective 5-hydroxytryptamine (5-HT) antagonists such as methysergide reduce the cataleptic effect of haloperidol. The present study was designed to evaluate the particpation of 5-HT-1A receptors in chlorpromazine-induced catalepsy in mice. Pundolol and buspirone, two putative 5-HT-1A receptor ligands, were used. Pretreatment with these drugs reduced the cataleptic effect of chlorpromazine. Clomipramine, a 5-HT neuronal uptake blocker, reversed the inhibitory effect of buspirone. Pretreatment with clomipramine alone caused a potentiation of neuroleptic-induced catalepsy. These results suggest that central 5-HT-1A receptors play an important role in neuroleptic-induced catalepsy in mice
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Índice: LILACS (Américas) Asunto principal: Pindolol / Buspirona / Catalepsia / Clorpromazina / Clomipramina / Haloperidol Límite: Animales Idioma: Inglés Revista: Braz. j. med. biol. res Asunto de la revista: Biologia / Medicina Año: 1990 Tipo del documento: Artículo / Congreso y conferencia

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Índice: LILACS (Américas) Asunto principal: Pindolol / Buspirona / Catalepsia / Clorpromazina / Clomipramina / Haloperidol Límite: Animales Idioma: Inglés Revista: Braz. j. med. biol. res Asunto de la revista: Biologia / Medicina Año: 1990 Tipo del documento: Artículo / Congreso y conferencia