Abstract
Dopamine recognized and competed for a single population of [3H]-domperidone-binding sites in rat striatum and olfactory tubercle when tested in the presence of sodium ions and guanine nucleotide [Gpp(NH)p]. In the absence of Na+ and Gpp(NH)p, however, dopamine recognized two components of [3H]-domperidone binding. Thus, [3H]-domperidone labelled only a single population of dopamine receptors (type D2) which fully converted from high to low affinity for dopamine. These results agree with those found previously using [3H]-spiperone and [3H]-YM-09151-2.
MeSH Terms
Animals
Antipsychotic Agents/pharmacology
Benzamides/pharmacology
Binding, Competitive/drug effects
Brain/metabolism
Corpus Striatum/metabolism
Domperidone/pharmacology
Dopamine/metabolism
In Vitro Techniques
Kinetics
Male
Olfactory Bulb/metabolism
Rats
Rats, Inbred Strains
Receptors, Dopamine/drug effects,metabolism
Spiperone/pharmacology
Chemicals
Antipsychotic Agents
Benzamides
Receptors, Dopamine
Spiperone
Domperidone
nemonapride
Dopamine
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Grigoriadis D
Seeman P
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