Pharmacological comparison of the sigma recognition site labelled by [3H]haloperidol in human and rat cerebellum

J M Barnes, N M Barnes, P C Barber, S Champaneria, B Costall, C D Hornsby, J W Ironside, R J Naylor

Research output: Contribution to journalArticlepeer-review

Abstract

The radioligand binding characteristics of [3H]haloperidol (in the presence of spiperone, 25 nmolL-1) were investigated in rat and human cerebellar membranes. In both rat and human cerebellar membrane preparations saturation studies with [3H]haloperidol (non-specific binding defined by pentazocine, 10 mumolsL-1) demonstrated high affinity saturable specific binding to a homogenous population of binding sites (rat, Bmax 6693 +/- 1242 fmol mg-1 protein, pKD 8.33 +/- 0.08; human, Bmax 2550 +/- 437 fmol mg-1 protein, pKD 8.59 +/- 0.11; mean +/- SEM, n = 3-6). Competition studies employing a wide range of structurally diverse competing compounds displayed that the [3H]haloperidol binding site was pharmacologically similar in both preparations and comparable to sigma recognition sites previously identified in various tissues originating from different species. In addition, with reference to the potential subtypes of sigma recognition sites, the labelling of these sites by low nanomolar concentrations of [3H]haloperidol provides evidence that they belong to the sigma-1 recognition site subtype. The present findings suggest that the pharmacology of the rat and human cerebellar sigma recognition site are directly comparable and provides further supporting evidence towards the use of [3H]haloperidol radioligand binding studies in the rat to detect sigma receptor ligands with potential therapeutic activity.

Original languageEnglish
Pages (from-to)197-202
Number of pages6
JournalNaunyn-Schmiedeberg's Archives of Pharmacology
Volume345
Issue number2
Publication statusPublished - Feb 1992

Keywords

  • Animals
  • Binding Sites
  • Binding, Competitive
  • Cerebellum
  • Female
  • Haloperidol
  • Humans
  • Male
  • Radioligand Assay
  • Rats
  • Receptors, Opioid
  • Receptors, sigma

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