Résumé
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.
Langue d'origine | English |
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Pages (de-à) | 439-447 |
Nombre de pages | 9 |
Journal | European Neuropsychopharmacology |
Volume | 18 |
Numéro de publication | 6 |
DOI | |
Statut de publication | Published - juin 2008 |
Publié à l'externe | Oui |
Note bibliographique
Funding Information:This work was supported by an operating grant from the Canadian Institutes of Health Research (CIHR) to R.O.P and M.L. M.L. and C.B. are both recipients of salary awards from Fonds de la recherche en santé du Québec and funded research chairs from McGill University. S.P.B. is the recipient of a salary award from CIHR. We thank Franceen Lenoff for her excellent technical assistance.
ASJC Scopus Subject Areas
- Pharmacology
- Neurology
- Clinical Neurology
- Psychiatry and Mental health
- Biological Psychiatry
- Pharmacology (medical)
PubMed: MeSH publication types
- Clinical Trial
- Journal Article
- Randomized Controlled Trial
- Research Support, Non-U.S. Gov't