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Dopamine receptor-specific contributions to the computation of value

Burke, Christopher J; Soutschek, Alexander; Weber, Susanna; Raja Beharelle, Anjali; Fehr, Ernst; Haker, Helene; Tobler, Philippe N (2018). Dopamine receptor-specific contributions to the computation of value. Neuropsychopharmacology, 43(6):1415-1424.

Abstract

Dopamine is thought to play a crucial role in value-based decision making. However, the specific contributions of different dopamine receptor subtypes to the computation of subjective value remain unknown. Here we demonstrate how the balance between D1 and D2 dopamine receptor subtypes shapes subjective value computation during risky decision-making. We administered the D2 receptor antagonist amisulpride or placebo before participants made choices between risky options. Compared to placebo, D2 receptor blockade resulted in more frequent choice of higher risk and higher expected value options. Using a novel model fitting procedure, we concurrently estimated the three parameters that define individual risk attitude according to an influential theoretical account of risky decision making. This analysis revealed that the observed reduction in risk aversion under amisulpride was driven by increased sensitivity to reward magnitude and decreased distortion of outcome probability, resulting in more linear value coding. Our data suggest that different components that govern individual risk attitude are under dopaminergic control, such that D2 receptor blockade facilitates risk taking and expected value processing.

Additional indexing

Item Type:Journal Article, refereed, original work
Communities & Collections:03 Faculty of Economics > Department of Economics
04 Faculty of Medicine > Institute of Biomedical Engineering
Dewey Decimal Classification:330 Economics
Scopus Subject Areas:Life Sciences > Pharmacology
Health Sciences > Psychiatry and Mental Health
Scope:Discipline-based scholarship (basic research)
Language:English
Date:2018
Deposited On:23 Jan 2018 19:58
Last Modified:19 May 2025 03:45
Publisher:Nature Publishing Group
ISSN:0893-133X
OA Status:Hybrid
Free access at:PubMed ID. An embargo period may apply.
Publisher DOI:https://doi.org/10.1038/npp.2017.302
PubMed ID:29251282
Other Identification Number:merlin-id:15867
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