Evidence map›Paper›PMID 39900665›Full record

ArticleCommunications biology2025

Devaluing memories of reward: a case for dopamine.

Benjamin R Fry, Nicolette Russell, Victoria Fex, Bing Mo, Nathan Pence, Joseph A Beatty, Fredric P Manfredsson, Brandon A Toth, Christian R Burgess, Samuel Gershman and 1 more

Abstract read
In one paragraph

Article in Communications biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. The mesolimbic reward pathway is necessary for disruptions in cocaine-seeking behavior following mediated devaluation.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2025
    Article
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

11 authors.

Benjamin R Fry *Department of Psychology, Michigan State University, East Lansing, MI, USA.
Nicolette Russell *Department of Psychology, Michigan State University, East Lansing, MI, USA.
Victoria Fex *Lyman Briggs College, Michigan State University, East Lansing, MI, USA.
Bing MoDepartment of Psychology, Michigan State University, East Lansing, MI, USA.
Nathan PenceDepartment of Psychology, Michigan State University, East Lansing, MI, USA.
Joseph A BeattyDepartment of Physiology, Michigan State University, East Lansing, MI, USA.
Fredric P ManfredssonDepartment of Translational Neuroscience, Barrow Neurological Institute, Phoenix, AZ, USA.ORCID http://orcid.org/0000-0001-5802-5487
Brandon A TothMichigan Neuroscience Institute, University of Michigan, Ann Arbor, MI, USA.ORCID http://orcid.org/0000-0003-1046-6499
Christian R BurgessMichigan Neuroscience Institute, University of Michigan, Ann Arbor, MI, USA.
Samuel GershmanDepartment of Psychology, Harvard University, Cambridge, MA, USA.ORCID http://orcid.org/0000-0002-6546-3298
Alexander W JohnsonDepartment of Psychology, Michigan State University, East Lansing, MI, USA. awj@msu.edu.ORCID http://orcid.org/0000-0001-8166-7189

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Midbrain dopamine cells encode differences in predictive and expected value to support learning through reward prediction error. Recent findings have questioned whether reward prediction error can fully account for dopamine function and suggest a more complex role for dopamine in encoding detailed features of the reward environment. In this series of studies, we describe a novel role for dopamine in devaluing sensory features of reward. Mesencephalic dopamine cells activated during a mediated devaluation phase were later chemogenetically reactivated. This retrieval of the devalued reward memory elicited a reduction in the hedonic evaluation of sucrose reward. Through optogenetic and chemogenetic manipulations, we confirm dopamine cells are both sufficient and necessary for mediated devaluation, and retrieval of these memories reflected dopamine release in the nucleus accumbens. Consistent with our computational modeling data, our findings indicate a critical role for dopamine in encoding predictive representations of the sensory features of reinforcement. Overall, we elucidate a novel role for dopamine function in mediated devaluation and illuminate a more elaborate framework through which dopamine encodes reinforcement signals.

Indexed as

DopamineDopaminergic NeuronsMemoryRewardAnimalsNucleus AccumbensDopamine

Identifiers

PMID39900665
PMCPMC11790953

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.