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Antiepileptic action of the beta-carboline ZK 91296 in a genetic petit mal model in rats.

Abstract
The anticonvulsant action of the benzodiazepine (BZ) receptor partial agonist, ethyl 5-benzyloxy-4-methoxymethyl-beta-carboline-3-carboxylate (ZK 91296) was studied in rats of Wistar origin exhibiting spontaneous bilateral cortical synchronous spike and wave discharges with a symptomatology paralleling that of human petit mal seizures. ZK 91296 1-16 mg/kg i.p.) attenuated the absence seizures without inducing signs of sedation or disorganized EEG patterns at any dose. Diazepam (1-8 mg/kg i.p.) suppressed seizures but also induced sedation and modified EEG background activity in a dose-related manner.
AuthorsL H Jensen, C Marescaux, M Vergnes, G Micheletti, E N Petersen
JournalEuropean journal of pharmacology (Eur J Pharmacol) Vol. 102 Issue 3-4 Pg. 521-4 (Jul 20 1984) ISSN: 0014-2999 [Print] Netherlands
PMID6436039 (Publication Type: Journal Article)
Chemical References
  • Anticonvulsants
  • Carbolines
  • Indoles
  • ZK 91296
  • Diazepam
Topics
  • Animals
  • Anticonvulsants
  • Behavior, Animal (drug effects)
  • Carbolines (pharmacology)
  • Diazepam (pharmacology)
  • Dose-Response Relationship, Drug
  • Electroencephalography
  • Epilepsy, Absence (drug therapy)
  • Indoles (pharmacology)
  • Male
  • Rats
  • Rats, Inbred Strains

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