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| Research article summary (published 23 Mar 2008): |
The role of dopamine in alcohol self-administration in humans: individual differences.
Full Abstract
OBJECTIVE:
To clarify dopamine's role in alcohol self-administration in a heterogeneous sample of drinkers using acute phenylalanine/tyrosine depletion (APTD).
METHODS:
Sixteen men with variable drinking histories were characterized on their ethanol-induced cardiac response, a marker previously proposed to index dopamine system reactivity and vulnerability to alcohol abuse. During separate sessions participants were administered (i) a nutritionally balanced (BAL) amino acid (AA) mixture, (ii) a mixture lacking the dopamine precursors, phenylalanine and tyrosine, and (iii) APTD followed by the dopamine precursor, L-DOPA. Five hours after AA administration, participants could earn units of alcohol using a progressive ratio breakpoint task.
RESULTS:
Alcohol self-administration was reduced in the APTD and APTD+L-DOPA conditions relative to the BAL condition. In both cases the changes were predicted by ethanol-induced cardiac change.
CONCLUSIONS:
The motivation to drink is likely regulated by more than one neurobiological mechanism. Individual differences in cardiac responsivity to ethanol might provide a peripheral marker of responsiveness to pharmacological manipulations of dopamine.
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Author information
Author/s: Barrett, Sean P (SP); Pihl, Robert O (RO); Benkelfat, Chawki (C); Brunelle, Caroline (C); Young, Simon N (SN); Leyton, Marco (M);
Affiliation: Psychology Department, McGill University, 1033 Pine Avenue West, Montreal, Quebec, Canada.
Journal and publication information
Publication Type: Clinical Trial; Journal Article; Randomized Controlled Trial; Research Support, Non-U.S. Gov't
Journal: European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology (Eur Neuropsychopharmacol), published in Netherlands. (Language: eng)
Reference: 2008-Jun; vol 18 (issue 6) : pp 439-47
Dates: Created 2008/05/02; Completed 2008/08/13;
PMID: 18367384, status: MEDLINE (last retrieval date: 11/6/2008)
Sourced from the National Library of Medicine. Abstract text and other information may be subject to copyright.
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