The potent 5-HT3 receptor antagonist (R)-zacopride labels an additional high affinity site in the central nervous system

Eur J Pharmacol. 1992 Jan 28;211(1):133-6. doi: 10.1016/0014-2999(92)90276-a.

Abstract

The binding characteristics of [3H](R)- and [3H](S)-zacopride were investigated in membranes from the rat entorhinal cortex and NG 108-15 clonal cells. In contrast to [3H](S)-zacopride which bound solely to 5-HT3 receptors, [3H](R)-zacopride recognized another class of binding sites, called the (R)-sites, in both membrane preparations. In addition to (R)-zacopride (Ki = 3-11 nM), only (R)-iodo-zacopride, (R)-dechloro-zacopride, prazosin and mianserin exhibited high to moderate affinity for the (R)-sites, whose possible functions remain to be established.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Benzamides / pharmacology*
  • Binding Sites
  • Brain / metabolism*
  • Bridged Bicyclo Compounds / pharmacology*
  • Bridged Bicyclo Compounds, Heterocyclic*
  • Cell Membrane / metabolism
  • Clone Cells
  • In Vitro Techniques
  • Rats
  • Serotonin Antagonists*
  • Tritium

Substances

  • Benzamides
  • Bridged Bicyclo Compounds
  • Bridged Bicyclo Compounds, Heterocyclic
  • Serotonin Antagonists
  • Tritium
  • zacopride