Modulation by GABAB receptors of spontaneous synchronous activities induced by 4-aminopyridine in the rat hippocampus

Neurosci Lett. 1992 Dec 14;148(1-2):159-63. doi: 10.1016/0304-3940(92)90829-v.

Abstract

Field potential recordings were made in the CA3 and/or CA1 subfields of rat hippocampal slices maintained in vitro during perfusion with medium containing the convulsant drug 4-aminopyridine (4AP, 50 microM). In this experimental condition, spontaneous interictal epileptiform discharges caused by the activation of excitatory amino acid receptors and synchronous, GABA-mediated potentials occurred regularly in both areas. Interictal discharges and GABA-mediated potentials were reduced and eventually abolished in both subfields by bath application of baclofen (0.5-100 microM), which is a selective agonist for the GABAB receptor. However, interictal epileptiform events disappeared in the presence of baclofen concentrations (i.e., 4.75 +/- 0.7 microM; IC50 = 3.4 microM; n = 9) that were lower than those required for abolishing the GABA-mediated potential (i.e., 96.1 +/- 19.4 microM; IC50 = 9.8 microM; n = 12). The effects of baclofen were antagonized by the GABAB receptor antagonists saclofen (1 mM; n = 3 slices) or CGP 35348 (0.2-1 mM; IC50 = 240 microM; n = 12 slices). Our findings indicate that activation of GABAB receptors by baclofen inhibits both types of 4AP-induced activities in the rat hippocampus although epileptiform discharges appear to be more sensitive than GABA-mediated potentials to this pharmacological procedure. Although our data do not indicate whether the action of baclofen is pre- or postsynaptic, they demonstrate that this mechanism is sensitive to available GABAB receptor antagonists.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 4-Aminopyridine / pharmacology*
  • Animals
  • Baclofen / pharmacology*
  • Dose-Response Relationship, Drug
  • Epilepsy / physiopathology
  • Evoked Potentials / drug effects
  • GABA-A Receptor Antagonists
  • Hippocampus / drug effects
  • Hippocampus / physiology*
  • In Vitro Techniques
  • Organophosphorus Compounds / pharmacology*
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, GABA-A / physiology*
  • gamma-Aminobutyric Acid / physiology*

Substances

  • GABA-A Receptor Antagonists
  • Organophosphorus Compounds
  • Receptors, GABA-A
  • gamma-Aminobutyric Acid
  • CGP 35348
  • 4-Aminopyridine
  • Baclofen