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Research article summary (published 11 May 2009):

Cue-induced dopamine release predicts cocaine preference: positron emission tomography studies in freely moving rodents.

Full Abstract

Positron emission tomography studies in drug-addicted patients have shown that exposure to drug-related cues increases striatal dopamine, which displaces binding of the D(2) ligand, [(11)C]-raclopride. However, it is not known if animals will also show cue-induced displacement of [(11)C]-raclopride binding. In this study, we use [(11)C]-raclopride imaging in awake rodents to capture cue-induced changes in dopamine release associated with the conditioned place preference model of drug craving. Ten animals were conditioned to receive cocaine in a contextually distinct environment from where they received saline. Following conditioning, each animal was tested for preference and then received two separate [(11)C]-raclopride scans. For each scan, animals were confined to the cocaine and/or the saline-paired environment for the first 25 min of uptake, after which they were anesthetized and scanned. [(11)C]-raclopride uptake in the saline-paired environment served as a within-animal control for uptake in the cocaine-paired environment. Cocaine produced a significant place preference (p = 0.004) and exposure to the cocaine-paired environment decreased [(11)C]-raclopride binding relative to the saline-paired environment in both the dorsal (20%; p < 0.002) and ventral striatum (22%; p < 0.05). The change in [(11)C]-raclopride binding correlated with preference in the ventral striatum (R(2) = -0.87; p = 0.003). In this region, animals who showed little or no preference exhibited little or no change in [(11)C]-raclopride binding in the cocaine-paired environment. This noninvasive procedure of monitoring neurochemical events in freely moving, behaving animals advances preclinical molecular imaging by interrogating the degree to which animal models reflect the human condition on multiple dimensions, both biological and behavioral.

 

Author information

Author/s: Schiffer, Wynne K (WK); Liebling, Courtney N B (CN); Reiszel, Corinne (C); Hooker, Jacob M (JM); Brodie, Jonathan D (JD); Dewey, Stephen L (SL);

Affiliation: Medical Department, Brookhaven National Laboratory, Upton, New York 11973, USA. wynne(-atsign-)bnl.gov

Grants: DA15041 (Agency:NIDA NIH HHS) ; DA22346 (Agency:NIDA NIH HHS)

Journal and publication information

Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, Non-P.H.S.

Journal: The Journal of neuroscience : the official journal of the Society for Neuroscience (J Neurosci), published in United States. (Language: eng)

Reference: 2009-May; vol 29 (issue 19) : pp 6176-85

Dates: Created 2009/05/14; Completed 2009/05/28;

PMID: 19439595, status: MEDLINE (last retrieval date: 5/28/2009, IMS Date: 28 May 2009 00:00:00)

Sourced from the National Library of Medicine. Abstract text and other information may be subject to copyright.

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MeSH headings (categories)

This article was linked to the MESH Headings shown below.

Associated Chemicals: Carbon Radioisotopes (0) ; Dopamine Antagonists (0) ; Receptors, Dopamine D2 (0) ; Cocaine (50-36-2) ; Raclopride (84225-95-6)

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