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Proconvulsant effects in baboons of beta-carboline, a putative endogenous ligand for benzodiazepine receptors.

Abstract
beta-Carboline-3-carboxylic acid ethyl ester (beta-CCE) was tested on two models of epilepsy in the baboon: kainic acid-induced limbic status epilepticus and photosensitive epilepsy. Beta-CCE, at very low doses ranging from 8 to 100 microgram/kg (i.v.), induced a reactivation of the limbic focus and photomyoclonic and generalized seizures in photosensitive and non-photosensitive baboons. The proconvulsant effect of beta-CCE may be associated with its binding to a particular subclass of benzodiazepine receptors.
AuthorsC Cepeda, T Tanaka, R Besselièvre, P Potier, R Naquet, J Rossier
JournalNeuroscience letters (Neurosci Lett) Vol. 24 Issue 1 Pg. 53-7 (Jun 12 1981) ISSN: 0304-3940 [Print] Ireland
PMID6267525 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Carbolines
  • Indoles
  • Ligands
  • Receptors, Drug
  • Receptors, GABA-A
  • Benzodiazepines
  • beta-carboline-3-carboxylic acid ethyl ester
  • Kainic Acid
Topics
  • Amygdala (drug effects, physiopathology)
  • Animals
  • Benzodiazepines (metabolism)
  • Carbolines (pharmacology)
  • Indoles (pharmacology)
  • Kainic Acid
  • Ligands
  • Light
  • Papio
  • Receptors, Drug (drug effects, metabolism)
  • Receptors, GABA-A
  • Seizures (chemically induced, physiopathology)

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