"Peripheral-type" binding sites for benzodiazepines in brain: relationship to the convulsant actions of Ro 5-4864

J Neurochem. 1985 May;44(5):1494-9. doi: 10.1111/j.1471-4159.1985.tb08787.x.

Abstract

Previous studies have shown that Ro 5-4864 is a potent convulsant and increases the firing rate of substantia nigra zona reticulata neurons. The pharmacologic profile of compounds that antagonize these actions suggested that the effects of Ro 5-4864 were not mediated by "brain-type" benzodiazepine receptors. We examined a number of compounds that are structurally related to Ro 5-4864 for their capacities to displace [3H]Ro 5-4864 from "peripheral-type" binding sites and their potencies as convulsants (or as antagonists of Ro 5-4864-induced convulsions). It was observed that compounds such as KW 3600 (the N-desmethyl analog of Ro 5-4864), which have very low affinities for "peripheral-type" sites, are convulsants with a potency nearly equal to that of Ro 5-4864. In contrast, compounds such as Ro 5-6900 and PK 11195, which bind with very high affinities to "peripheral-type" binding sites, are neither convulsants nor do they antagonize the convulsant actions of Ro 5-4864. Within a series of compounds that are structurally related to Ro 5-4864 there is a good correlation (r = 0.93; p less than 0.01) between their potencies as convulsants and their capacities to displace [35S]t-butylbicyclophosphorothionate from sites that may be associated with the chloride ionophore. Thus, it appears that occupation of "peripheral-type" binding sites by high-affinity ligands may not be directly involved in the convulsant actions of Ro 5-4864 and related compounds.

MeSH terms

  • Animals
  • Benzodiazepinones / metabolism
  • Benzodiazepinones / pharmacology*
  • Chlorides / metabolism
  • Convulsants / metabolism
  • Convulsants / pharmacology*
  • Ion Channels / drug effects
  • Male
  • Rats
  • Rats, Inbred Strains
  • Receptors, GABA-A / drug effects*
  • Receptors, GABA-A / metabolism
  • Structure-Activity Relationship

Substances

  • Benzodiazepinones
  • Chlorides
  • Convulsants
  • Ion Channels
  • Receptors, GABA-A
  • 4'-chlorodiazepam