An in vitro study on the hippocampal electrophysiological properties of enkephalinase inhibitors in rats

Pharmacol Biochem Behav. 1991 May;39(1):119-21. doi: 10.1016/0091-3057(91)90407-s.

Abstract

The effects of two enkephalinase inhibitors were studied on the CA1 and dentate hippocampal extracellular field potentials (FPs). The enkephalinase inhibitors thiorphan and SCH 32615, at a concentration of 1-500 microM, failed to significantly affect CA1 and dentate FPs. Thiorphan and SCH 32615, at a concentration of 150 microM, were able to potentiate the enkephalin-induced epileptiform bursting, inducing an increase in the bursting duration and in the number of spikes per burst due to 3.5 microM DAEAM or 0.20 microM DAGO. The results suggest: 1) the potentiation of an electrophysiological opiate receptor-mediated response by enkephalinase inhibitors; 2) the inability to show a direct effect on the basal CA1FP as a result of the inhibition of the endogenous enkephalinase.

MeSH terms

  • Animals
  • Dipeptides / pharmacology
  • Electric Stimulation
  • Electrophysiology
  • Enkephalin, Ala(2)-MePhe(4)-Gly(5)-
  • Enkephalin, Methionine / analogs & derivatives
  • Enkephalin, Methionine / pharmacology
  • Enkephalins / pharmacology
  • Evoked Potentials / drug effects
  • Hippocampus / physiology*
  • In Vitro Techniques
  • Male
  • Neprilysin / antagonists & inhibitors*
  • Perfusion
  • Rats
  • Rats, Inbred Strains
  • Thiorphan / pharmacology

Substances

  • Dipeptides
  • Enkephalins
  • Enkephalin, Ala(2)-MePhe(4)-Gly(5)-
  • Enkephalin, Methionine
  • enkephalinamide-Met, Ala(2)-
  • SCH 32615
  • Thiorphan
  • Neprilysin