Evidence map›Paper›PMID 34197448›Full record

ArticlePLoS biology2021

D1- and D2-like receptors differentially mediate the effects of dopaminergic transmission on cost-benefit evaluation and motivation in monkeys.

Yukiko Hori, Yuji Nagai, Koki Mimura, Tetsuya Suhara, Makoto Higuchi, Sebastien Bouret, Takafumi Minamimoto

Open access · goldAbstract read
In one paragraph

Article in PLoS biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.7field-weighted citation impact, top 17% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Functional Heterogeneity within the Primate Ventral Striatum for Motivational Regulation.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
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  7. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 2 countries.

Yukiko HoriDepartment of Functional Brain Imaging, National Institutes for Quantum and Radiological Science and Technology, Chiba, Japan.ORCID 0000-0003-1023-9587
Yuji NagaiDepartment of Functional Brain Imaging, National Institutes for Quantum and Radiological Science and Technology, Chiba, Japan.ORCID 0000-0001-7005-0749
Koki MimuraDepartment of Functional Brain Imaging, National Institutes for Quantum and Radiological Science and Technology, Chiba, Japan.ORCID 0000-0001-7069-6558
Tetsuya SuharaDepartment of Functional Brain Imaging, National Institutes for Quantum and Radiological Science and Technology, Chiba, Japan.
Makoto HiguchiDepartment of Functional Brain Imaging, National Institutes for Quantum and Radiological Science and Technology, Chiba, Japan.
Sebastien BouretTeam Motivation Brain & Behavior, Institut du Cerveau et de la Moelle épinière (ICM), Centre National de la Recherche Scientifique (CNRS), Hôpital Pitié Salpêtrière, Paris, France.ORCID 0000-0003-2279-6161
Takafumi MinamimotoDepartment of Functional Brain Imaging, National Institutes for Quantum and Radiological Science and Technology, Chiba, Japan.ORCID 0000-0003-4305-0174
The Open University of Japan · JPCentre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It has been widely accepted that dopamine (DA) plays a major role in motivation, yet the specific contribution of DA signaling at D1-like receptor (D1R) and D2-like receptor (D2R) to cost-benefit trade-off remains unclear. Here, by combining pharmacological manipulation of DA receptors (DARs) and positron emission tomography (PET) imaging, we assessed the relationship between the degree of D1R/D2R blockade and changes in benefit- and cost-based motivation for goal-directed behavior of macaque monkeys. We found that the degree of blockade of either D1R or D2R was associated with a reduction of the positive impact of reward amount and increasing delay discounting. Workload discounting was selectively increased by D2R antagonism. In addition, blocking both D1R and D2R had a synergistic effect on delay discounting but an antagonist effect on workload discounting. These results provide fundamental insight into the distinct mechanisms of DA action in the regulation of the benefit- and cost-based motivation, which have important implications for motivational alterations in both neurological and psychiatric disorders.

Indexed as

Cost-Benefit AnalysisMotivationAnimalsDelay DiscountingDopamineDopamine AntagonistsMacaca fuscataMacaca mulattaMalePositron-Emission TomographyReceptors, Dopamine D1Receptors, Dopamine D2WorkloadDopamineDopamine AntagonistsReceptors, Dopamine D1Receptors, Dopamine D2

Identifiers

PMID34197448
PMCPMC8248602
OpenAlexW3177365212

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.