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PMID: 7816338 Published · ppublish English Journal Article

Different modifications of the dopamine metabolism in the core and shell parts of the nucleus accumbens following CCK-A receptor stimulation in the shell region.

Neuroscience letters ·Vol. 178 ·No. 1 ·1994-08-29 ·Pages 5-10

Ladurelle N, Durieux C, Roques BP, Daugé V

Abstract

After the injection of CCK8 into the posterior N. Acc. of rats DA, DOPAC HVA contents were determined from punches of the anterior and posterior N. Acc. and VTA. CCK8 (20 pmol/side) modified these levels only in the posterior N. Acc. and these responses were inhibited by the CCK-A antagonist devazepide. Five min after treatment, DA, DOPAC and HVA were increased in the N. Acc.shell and 10 min later they were decreased in the N. Acc.core. These data suggest that in these regions CCK8 could both abolish the influence of DA from the core on the transmission of motor information and favor that of DA from the shell on emotional-like responses.

MeSH Terms
3,4-Dihydroxyphenylacetic Acid/metabolism Animals Benzodiazepinones/pharmacology Cholecystokinin/antagonists & inhibitors Devazepide Dopamine/metabolism Dose-Response Relationship, Drug Homovanillic Acid/metabolism Kinetics Male Microinjections Nucleus Accumbens/drug effects,metabolism Organ Specificity Rats Rats, Wistar Receptors, Cholecystokinin/antagonists & inhibitors,physiology Sincalide/administration & dosage,pharmacology Time Factors
Chemicals
Benzodiazepinones Receptors, Cholecystokinin 3,4-Dihydroxyphenylacetic Acid Cholecystokinin Devazepide Sincalide Dopamine Homovanillic Acid
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Ladurelle N
Département de Pharmacochimie Moléculaire et Structurale U 266 INSERM, URA D 1500 CNRS, Université René Descartes, Faculté des Sciences Pharmaceutiques et Biologiques, Paris, France.
Durieux C
Roques B P
Daugé V
Article Info
Journal
Neuroscience letters
Abbr.
Neurosci Lett
ISSN
0304-3940
Published
1994-08-29
Pages
5-10
Language
English
Region
Ireland
NLM ID
7600130
Subset
IM
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