Impulsivity moderates the effects of dopamine D2 and mixed D1-D2 antagonists in individuals with gambling disorder.


Journal

Journal of psychopharmacology (Oxford, England)
ISSN: 1461-7285
Titre abrégé: J Psychopharmacol
Pays: United States
ID NLM: 8907828

Informations de publication

Date de publication:
08 2019
Historique:
pubmed: 21 6 2019
medline: 28 7 2020
entrez: 21 6 2019
Statut: ppublish

Résumé

The functional role of dopamine D1 and D2 receptors in gambling disorder (GD) remains unclear. This study aimed to investigate the role of D1 activation and the moderating effects of impulsivity, a trait linked with weaker D2-mediated inhibition of dopamine release, in GD subjects. Thirty (nine female) non-comorbid GD subjects with low (LI), moderate (MI), or high impulsivity (HI) received the preferential D2 antagonist haloperidol (HAL; 3 mg) or the mixed D1-D2 antagonist fluphenazine (FLU; 3 mg), on separate sessions before a 15-minute slot machine game or amphetamine (AMPH; 20 mg), in a placebo-controlled, double-blind, counterbalanced design. On their own, HAL and FLU led to linear increases and decreases, respectively, in desire to gamble across increasing levels of impulsivity. The slot machine and AMPH each evoked an inverted-U pattern of desire to gamble across increasing impulsivity. HAL reversed this effect of the game, whereas FLU did not alter post-game desire. HAL and FLU decreased and increased psychostimulant-like effects of the game, respectively, in LI and MI subjects, but consistently reduced these effects in HI subjects. HAL also altered the salience of negative affective words on a reading task, such that greater salience of negative words coincided with lower post-game desire to gamble. D1 receptors appear to gauge the incentive value of gambling in GD subjects. D1 activation has negative reinforcing effects in HI gamblers and positive reinforcing effects in LI gamblers. Medications that activate D1 could curtail chasing in HI gamblers. D1 blockade could benefit HI gamblers whose main concern is craving.

Sections du résumé

BACKGROUND
The functional role of dopamine D1 and D2 receptors in gambling disorder (GD) remains unclear.
AIMS
This study aimed to investigate the role of D1 activation and the moderating effects of impulsivity, a trait linked with weaker D2-mediated inhibition of dopamine release, in GD subjects.
METHODS
Thirty (nine female) non-comorbid GD subjects with low (LI), moderate (MI), or high impulsivity (HI) received the preferential D2 antagonist haloperidol (HAL; 3 mg) or the mixed D1-D2 antagonist fluphenazine (FLU; 3 mg), on separate sessions before a 15-minute slot machine game or amphetamine (AMPH; 20 mg), in a placebo-controlled, double-blind, counterbalanced design.
RESULTS
On their own, HAL and FLU led to linear increases and decreases, respectively, in desire to gamble across increasing levels of impulsivity. The slot machine and AMPH each evoked an inverted-U pattern of desire to gamble across increasing impulsivity. HAL reversed this effect of the game, whereas FLU did not alter post-game desire. HAL and FLU decreased and increased psychostimulant-like effects of the game, respectively, in LI and MI subjects, but consistently reduced these effects in HI subjects. HAL also altered the salience of negative affective words on a reading task, such that greater salience of negative words coincided with lower post-game desire to gamble.
CONCLUSIONS
D1 receptors appear to gauge the incentive value of gambling in GD subjects. D1 activation has negative reinforcing effects in HI gamblers and positive reinforcing effects in LI gamblers. Medications that activate D1 could curtail chasing in HI gamblers. D1 blockade could benefit HI gamblers whose main concern is craving.

Identifiants

pubmed: 31219367
doi: 10.1177/0269881119855972
doi:

Substances chimiques

Central Nervous System Stimulants 0
Dopamine D2 Receptor Antagonists 0
Receptors, Dopamine D1 0
Receptors, Dopamine D2 0
Amphetamine CK833KGX7E
Haloperidol J6292F8L3D
Fluphenazine S79426A41Z

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1015-1029

Subventions

Organisme : CIHR
ID : 97817
Pays : Canada

Auteurs

Martin Zack (M)

1 Molecular Brain Sciences Research Department, Centre for Addiction and Mental Health (CAMH), Toronto, ON, Canada.
2 Department of Pharmacology and Toxicology, University of Toronto, Toronto, ON, Canada.

Daniela Lobo (D)

1 Molecular Brain Sciences Research Department, Centre for Addiction and Mental Health (CAMH), Toronto, ON, Canada.
3 Department of Psychiatry, University of Toronto, Toronto, ON, Canada.

Candice Biback (C)

2 Department of Pharmacology and Toxicology, University of Toronto, Toronto, ON, Canada.
4 Leslie Dan School of Pharmacy, University of Toronto, Toronto, ON, Canada.

Tim Fang (T)

2 Department of Pharmacology and Toxicology, University of Toronto, Toronto, ON, Canada.

Kelly Smart (K)

2 Department of Pharmacology and Toxicology, University of Toronto, Toronto, ON, Canada.

Daniel Tatone (D)

2 Department of Pharmacology and Toxicology, University of Toronto, Toronto, ON, Canada.

Aditi Kalia (A)

2 Department of Pharmacology and Toxicology, University of Toronto, Toronto, ON, Canada.

Daniel Digiacomo (D)

3 Department of Psychiatry, University of Toronto, Toronto, ON, Canada.

James L Kennedy (JL)

1 Molecular Brain Sciences Research Department, Centre for Addiction and Mental Health (CAMH), Toronto, ON, Canada.
3 Department of Psychiatry, University of Toronto, Toronto, ON, Canada.
5 Institute of Medical Science, University of Toronto, Toronto, ON, Canada.

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Classifications MeSH