Inhibition of sleep and benzodiazepine receptor binding by a beta-carboline derivative

Pharmacol Biochem Behav. 1989 Sep;34(1):37-42. doi: 10.1016/0091-3057(89)90349-3.

Abstract

The effects of systemic injections of beta-carboline-3-carboxylate-t-butyl ester (beta-CCtB) were investigated with regard to normally occurring sleep and several measures of benzodiazepine receptor occupancy in rats. A dose of 30 mg/kg of beta-CCtB was found to have a long time-course of action as measured by an in vivo assay for benzodiazepine binding, with an 84% depletion of [3H]diazepam binding at one hour after the intraperitoneal injection. This dose of beta-CCtB was shown to delay sleep onset, decrease non-REM and total sleep in the first two hours after the injection, and to delay the appearance of REM sleep after the sleep onset. The dose- and time-dependence of the effects on sleep approximated the dose- and time-dependence of inhibitory effects of an IP injection of beta-CCtB on in vitro measures of benzodiazepine receptor affinity and number.

MeSH terms

  • Animals
  • Brain / drug effects
  • Brain / metabolism
  • Carbolines / metabolism
  • Carbolines / pharmacology*
  • Diazepam / metabolism
  • Dose-Response Relationship, Drug
  • GABA-A Receptor Antagonists
  • Male
  • Rats
  • Rats, Inbred Strains
  • Receptors, GABA-A / metabolism*
  • Sleep / drug effects*
  • Time Factors

Substances

  • Carbolines
  • GABA-A Receptor Antagonists
  • Receptors, GABA-A
  • tert-butyl beta-carboline-3-carboxylate
  • Diazepam