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PMID: 7931313 Published · ppublish English Comparative Study Journal Article

Are striatal dopamine D4 receptors increased in schizophrenia?

Journal of neurochemistry ·Vol. 63 ·No. 4 ·1994-10-00 ·Pages 1576-7

Reynolds GP, Mason SL

Abstract

The density of dopamine D2-like receptors was determined using [3H]emonapride binding in putamen tissue taken postmortem from schizophrenic subjects and matched controls. A 72% increase in number of these receptors was identified in the schizophrenics, although three patients not receiving antipsychotic drug treatment before death exhibited receptor densities in the control range. Displacement of 1 nM [3H]emonapride binding by raclopride was used to define the contribution of the D4 subtype of dopamine receptors to total [3H]emonapride binding. No evidence was obtained for the presence of D4 receptors in putamen tissue from either control or schizophrenic subjects, indicating that the increase in D2-like receptor density in schizophrenia is due not to an increase in number of D4 sites in the disease, but to an up-regulation of D2 or D3 receptors probably induced by chronic treatment with antipsychotic drugs.

MeSH Terms
Aged Animals Antipsychotic Agents/pharmacology Benzamides/metabolism Binding, Competitive Corpus Striatum/metabolism,pathology Dopamine D2 Receptor Antagonists Humans Kinetics Pyrrolidines/metabolism Raclopride Receptors, Dopamine/analysis,metabolism Receptors, Dopamine D4 Reference Values Salicylamides/pharmacology Schizophrenia/metabolism,pathology
Chemicals
Antipsychotic Agents Benzamides DRD4 protein, human Dopamine D2 Receptor Antagonists Pyrrolidines Receptors, Dopamine Salicylamides Receptors, Dopamine D4 Raclopride nemonapride
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Reynolds G P
Department of Biomedical Science, University of Sheffield, England, U.K.
Mason S L
Article Info
Journal
Journal of neurochemistry
Abbr.
J Neurochem
ISSN
0022-3042
Published
1994-10-00
Pages
1576-7
Language
English
Region
England
NLM ID
2985190R
Subset
IM
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