Evidence map›Paper›PMID 37083584›Full record

ArticleeLife2023

Elucidating a locus coeruleus-dentate gyrus dopamine pathway for operant reinforcement.

Elijah A Petter, Isabella P Fallon, Ryan N Hughes, Glenn D R Watson, Warren H Meck, Francesco Paolo Ulloa Severino, Henry H Yin

Open access · goldAbstract read
In one paragraph

Article in eLife, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

9 citing papers in PubMed, 15 citations in OpenAlex.

  1. A Drd1-cre mouse line with nucleus accumbens gene dysregulation exhibits blunted fentanyl seeking.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2025
    Article
  2. Article
  3. A locus coeruleus to dorsal hippocampus pathway mediates cue-induced reinstatement of opioid self-administration in male and female rats.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2024
    Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Dopamine D2 receptors in hilar mossy cells regulate excitatory transmission and hippocampal function.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  9. Review
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 1 institution in 1 country.

Elijah A PetterDepartment of Psychology and Neuroscience, Duke University, Durham, United States.
Isabella P FallonDepartment of Psychology and Neuroscience, Duke University, Durham, United States.ORCID 0000-0002-1456-4152
Ryan N HughesDepartment of Psychology and Neuroscience, Duke University, Durham, United States.ORCID 0000-0002-4999-0215
Glenn D R WatsonDepartment of Psychology and Neuroscience, Duke University, Durham, United States.
Warren H MeckDepartment of Psychology and Neuroscience, Duke University, Durham, United States.
Francesco Paolo Ulloa SeverinoDepartment of Psychology and Neuroscience, Duke University, Durham, United States.ORCID 0000-0003-3725-9713
Henry H YinDepartment of Psychology and Neuroscience, Duke University, Durham, United States.ORCID 0000-0003-1546-6850
Duke University · US

Funding

The Role of Opponent Basal Ganglia Outputs in BehaviorR01NS094754 · NINDS · DUKE UNIVERSITY · PI Henry Yin · 2017 to 2026
$3.7M
Dissecting basal ganglia circuit mechanisms underlying instrumental learningR01DA040701 · NIDA · DUKE UNIVERSITY · PI Henry Yin · 2016 to 2026
$3.6M
NIDA NIH HHS R01 DA040701NINDS NIH HHS R01 NS094754
6 · The paper itself

Abstract

Animals can learn to repeat behaviors to earn desired rewards, a process commonly known as reinforcement learning. While previous work has implicated the ascending dopaminergic projections to the basal ganglia in reinforcement learning, little is known about the role of the hippocampus. Here, we report that a specific population of hippocampal neurons and their dopaminergic innervation contribute to operant self-stimulation. These neurons are located in the dentate gyrus, receive dopaminergic projections from the locus coeruleus, and express D1 dopamine receptors. Activation of D1 + dentate neurons is sufficient for self-stimulation: mice will press a lever to earn optogenetic activation of these neurons. A similar effect is also observed with selective activation of the locus coeruleus projections to the dentate gyrus, and blocked by D1 receptor antagonism. Calcium imaging of D1 + dentate neurons revealed significant activity at the time of action selection, but not during passive reward delivery. These results reveal the role of dopaminergic innervation of the dentate gyrus in supporting operant reinforcement.

Indexed as

DopamineLocus CoeruleusAnimalsDentate GyrusHippocampusMiceReceptors, Dopamine D1Reinforcement, PsychologyDopamineReceptors, Dopamine D1dentate gyrusdopaminehippocampuslocus coeruleusmouseneuroscienceoperantreinforcement

Identifiers

PMID37083584
PMCPMC10162798
OpenAlexW4366602886

What OpenQuestion holds

Textmetadata
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.