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The role of monoamines for the central effects of Baclofen on behavior of rats.

Abstract
Male albino rats given a bilateral injection of Baclofen (Lioresal) (12 micrograms/rat) in the cerebral ventricles showed a behavioral syndrome of activation + ataxia, paddling, tail-pinch hyperresponse and anesthesia. The phase of activation + ataxia was reduced by pretreatment of rats with H 44/68, FLA 63, reserpine, pimozide, phenoxybenzamine, oxypertine or chlorpromazine. The phase of paddling was reduced by pretreatment with FLA 63, reserpine, phenoxybenzamine, oxypertine, chlorpromazine, pimozide + phenoxybenzamine or apomorphine, while administration of clonidine instead of Baclofen caused paddling in non-pretreated rats. The phase of tail-pinch hyperresponse was reduced by reserpine, oxypertine, chlorpromazine or pimozide + phenoxybenzamine, while none of the pretreatments affected Baclofen-induced anesthesia. Drugs which affect mainly tryptaminergic or GABA-ergic functions failed to affect Baclofen-induced behaviors consistently. The findings suggest that dopaminergic and noradrenergic functions play a role in the central effects of Baclofen on behavior of rats.
AuthorsD F Smith, P Vestergaard
JournalJournal of neural transmission (J Neural Transm) Vol. 46 Issue 3 Pg. 215-23 ( 1979) Austria
PMID528996 (Publication Type: Journal Article)
Chemical References
  • Catecholamines
  • Baclofen
  • Clonidine
  • Dopamine
  • Norepinephrine
Topics
  • Anesthesia
  • Animals
  • Ataxia (chemically induced)
  • Baclofen (administration & dosage, pharmacology)
  • Catecholamines (physiology)
  • Clonidine (pharmacology)
  • Dopamine (physiology)
  • Injections, Intraventricular
  • Male
  • Motor Activity (drug effects)
  • Norepinephrine (physiology)
  • Rats

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