Evidence map›Paper›PMID 31821815›Full record

ArticlePhysiology & behavior2020

Phasic dopamine responses to a food-predictive cue are suppressed by the glucagon-like peptide-1 receptor agonist Exendin-4.

Vaibhav R Konanur, Ted M Hsu, Scott E Kanoski, Matthew R Hayes, Mitchell F Roitman

Abstract read
In one paragraph

Article in Physiology & behavior, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed, 1 pooled it
–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

42 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Nucleus of the solitary tract regulation of cue-induced appetitive behaviors via midbrain dopamine neurons.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
    Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
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  9. Article
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  11. Article
  12. Article
  13. The Enteric Neuronal Circuitry: A Key Ignored Player in Nutrient Sensing Along the Gut-Brain Axis.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Review
  14. Article
  15. Article
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  17. Article
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  19. Current neuropharmacology · 2025
    Article
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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

5 authors.

Vaibhav R KonanurGraduate Program in Neuroscience, University of Illinois at Chicago, Chicago, IL, United States.
Ted M HsuDepartment of Psychology, University of Illinois at Chicago, 1007W. Harrison St., Chicago, IL 60607-7137, United States.
Scott E KanoskiDepartment of Biological Sciences, Human and Evolutionary Biology Section, University of Southern California, Los Angeles, CA, United States.
Matthew R HayesDepartment of Psychiatry, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States.
Mitchell F RoitmanDepartment of Psychology, University of Illinois at Chicago, 1007W. Harrison St., Chicago, IL 60607-7137, United States. Electronic address: mroitman@uic.edu.

Funding

Modulation of NAc-DA Signaling by Learning Motivational State and PeptidesR01DA025634 · NIDA · UNIVERSITY OF ILLINOIS AT CHICAGO · PI ROITMAN, MITCHELL F · 2009 to 2024
$5.1M
Amylin Modulates Food RewardR01DK105155 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI HAYES, MATTHEW R · 2016 to 2025
$4.1M
The effects of context and physiological state on mesolimbic encoding of rewardF32DA047052 · NIDA · UNIVERSITY OF ILLINOIS AT CHICAGO · PI HSU, TED · 2019 to 2021
$209k
NIDA NIH HHS F32 DA047052NIDA NIH HHS R01 DA025634NIDDK NIH HHS R01 DK105155
6 · The paper itself

Abstract

Phasic dopamine activity is evoked by reliable predictors of food reward and plays a role in cue-triggered, goal-directed behavior. While this important signal is modulated by physiological state (e.g. hunger, satiety), the mechanisms by which physiological state is integrated by dopamine neurons is only beginning to be elucidated. Activation of central receptors for glucagon-like peptide-1 (GLP-1R) via long-acting agonists (e.g., Exendin-4) suppresses food intake and food-directed motivated behavior, in part, through action in regions with dopamine cell bodies, terminals, and/or neural populations that directly target the mesolimbic dopamine system. However, the effects of GLP-1R activation on cue-evoked, phasic dopamine signaling remain unknown. Here, in vivo fiber photometry was used to capture real-time signaling dynamics selectively from dopamine neurons in the ventral tegmental area of male and female transgenic (tyrosine hydroxylase-Cre; TH:Cre+) rats trained to associate an audio cue with the brief availability of a sucrose solution. Cue presentation evoked a brief spike in dopamine activity. Administration of Exendin-4 (Ex4; 0, 0.05, 0.1 μg) to the lateral ventricle both dose-dependently suppressed sucrose-directed behaviors and the magnitude of cue-evoked dopamine activity. Moreover, the amplitude of cue evoked dopamine activity was significantly correlated with subsequent sucrose-directed behaviors. While female rats exhibited overall reduced dopamine responses to the sucrose-paired cue relative to males, there was no significant interaction with Ex4. Together, these findings support a role for central GLP-1Rs in modulating a form of dopamine signaling that influences approach behavior and provide a potential mechanism whereby GLP-1 suppresses food-directed behaviors.

Indexed as

CuesFoodGlucagon-Like Peptide-1 Receptor AgonistsAcoustic StimulationAnimalsDopamineDopaminergic NeuronsDose-Response Relationship, DrugEatingExenatideFeeding BehaviorFemaleGlucagon-Like Peptide-1 ReceptorInjections, IntraventricularMaleMotivationDopamineExenatideGlp1r protein, ratGlucagon-Like Peptide-1 ReceptorGlucagon-Like Peptide-1 Receptor AgonistsSucroseDopamineFiber photometryMotivationRewardSatietyVentral tegmental area

Identifiers

PMID31821815
PMCPMC8112128

What OpenQuestion holds

Textmetadata
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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.