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PMID: 1974064 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Chronic cocaine treatment impairs the regulation of synaptosomal 3H-DA release by D2 autoreceptors.

Pharmacology, biochemistry, and behavior ·Vol. 36 ·No. 3 ·1990-07-00 ·Pages 457-61

Yi SJ, Johnson KM

Abstract

The effect of repeated administration of cocaine on presynaptic D2 autoreceptor sensitivity in synaptosomes was studied. In rats treated chronically with saline, the dopamine D2 agonist 2-(N-propyl-N-2-thienylethylamino)-5-hydroxytetralin (N-0437) caused a significant inhibition of the Ca2(+)-evoked 3H-DA release from synaptosomes prepared from the nucleus accumbens and from the striatum; this effect was blocked by the D2 antagonist sulpiride. However, chronic cocaine pretreatment abolished the effect of N-0437 in both areas, suggesting a subsensitivity of release-modulating terminal DA autoreceptors. Subsensitive DA autoreceptors would enhance stimulated DA release from mesolimbic and nigrostriatal terminals and may play a role in the behavioral sensitization observed in this paradigm.

MeSH Terms
Animals Behavior, Animal/drug effects Calcium/pharmacology Cocaine/pharmacology Corpus Striatum/drug effects,metabolism Dopamine/metabolism Dopamine Agents/pharmacology Female Nucleus Accumbens/drug effects,metabolism Rats Rats, Inbred Strains Receptors, Dopamine/drug effects,metabolism Receptors, Dopamine D2 Sulpiride/pharmacology Synaptosomes/drug effects,metabolism Tetrahydronaphthalenes/pharmacology Thiophenes/pharmacology
Chemicals
Dopamine Agents Receptors, Dopamine Receptors, Dopamine D2 Tetrahydronaphthalenes Thiophenes Sulpiride rotigotine Cocaine Calcium Dopamine
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Yi S J
Department of Pharmacology and Toxicology, University of Texas Medical Branch, Galveston 77550.
Johnson K M
Article Info
Journal
Pharmacology, biochemistry, and behavior
Abbr.
Pharmacol Biochem Behav
ISSN
0091-3057
Published
1990-07-00
Pages
457-61
Language
English
Region
United States
NLM ID
0367050
Subset
IM
Grants
NIDA NIH HHS · DA-05159 · United States
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