Evidence map›Paper›PMID 38747563›Full record

ArticleeLife2024

Functional diversity of dopamine axons in prefrontal cortex during classical conditioning.

Kenta Abe, Yuki Kambe, Kei Majima, Zijing Hu, Makoto Ohtake, Ali Momennezhad, Hideki Izumi, Takuma Tanaka, Ashley Matunis, Emma Stacy and 3 more

Abstract read
In one paragraph

Article in eLife, 2024. 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
–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

11 citing papers in PubMed.

  1. Article
  2. Article
  3. Dopamine Responses in Medial Frontal Cortex Are More Consistent with a Generalized Arousal Signal Than Signed Reward Prediction Errors.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Synergistic deficits in parvalbumin interneurons and dopamine signaling drive ACC dysfunction in chronic pain.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  9. Article
  10. Review
  11. bioRxiv : the preprint server for biology · 2024
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors.

Kenta Abe *Department of Neuroscience, Medical University of South Carolina, Charleston, United States.
Yuki Kambe *Department of Pharmacology, Kagoshima University, Kagoshima, Japan.
Kei Majima *Institute for Quantum Life Science, National Institutes for Quantum Science and Technology, Chiba, Japan.ORCID https://orcid.org/0000-0002-2405-4113
Zijing Hu *Department of Physiology, Monash University, Clayton, Australia.
Makoto Ohtake *Department of Neuroscience, Medical University of South Carolina, Charleston, United States.
Ali MomennezhadDepartment of Pharmacology, Kagoshima University, Kagoshima, Japan.ORCID https://orcid.org/0000-0002-8046-4387
Hideki IzumiFaculty of Data Science, Shiga University, Shiga, Japan.
Takuma TanakaFaculty of Data Science, Shiga University, Shiga, Japan.
Ashley MatunisDepartment of Neuroscience, Medical University of South Carolina, Charleston, United States.
Emma StacyDepartment of Neuroscience, Medical University of South Carolina, Charleston, United States.
Takahide ItokazuDepartment of Neuro-Medical Science, Osaka University, Osaka, Japan.
Takashi R SatoDepartment of Neuroscience, Medical University of South Carolina, Charleston, United States.ORCID https://orcid.org/0000-0002-7623-9021
Tatsuo SatoDepartment of Pharmacology, Kagoshima University, Kagoshima, Japan.ORCID https://orcid.org/0000-0002-1279-5125

Funding

The Role of Early Life Stress in Feeding BehaviorsP20GM148302 · NIGMS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI Jose H Ledo · 2023 to 2026
$11.5M
COCA: Project 4. Neurocircuit Strategy to Decrease Cocaine Cue ReactivityP50DA046373 · NIDA · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI HANLON, COLLEEN A · 2019 to 2023
$9.9M
Cortical Circuits Underlying Functional Recovery Following StrokeR01NS131549 · NINDS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI Takashi Sato · 2023 to 2026
$1.5M
The Role of Motor Cortex Output Circuits in Stroke RecoveryR21NS125571 · NINDS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI SATO, TAKASHI · 2021 to 2021
$415k
Effects of cell-type specific brain stimulation in Alzheimer's model miceR03AG070517 · NIA · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI SATO, TAKASHI · 2021 to 2022
$301k
BBRF Young Investigator Grant 29268Japan Science and Technology Agency 10.52926/jpmjpr1883Japan Science and Technology Agency 10.52926/jpmjpr2128Japan Science and Technology Agency JPMJFR2245Japan Society for the Promotion of Science 20K16465Japan Society for the Promotion of Science 20K23378Japan Society for the Promotion of Science 23K06151Japan Society for the Promotion of Science JP21K07459National Health and Medical Research Council APP1184899NIA NIH HHS R03 AG070517NIDA NIH HHS COCA Pilot grant P50 DA046373NIDA NIH HHS P50 DA046373NIGMS NIH HHS P20 GM148302NINDS NIH HHS R01 NS131549NINDS NIH HHS R21 NS125571
6 · The paper itself

Abstract

Midbrain dopamine neurons impact neural processing in the prefrontal cortex (PFC) through mesocortical projections. However, the signals conveyed by dopamine projections to the PFC remain unclear, particularly at the single-axon level. Here, we investigated dopaminergic axonal activity in the medial PFC (mPFC) during reward and aversive processing. By optimizing microprism-mediated two-photon calcium imaging of dopamine axon terminals, we found diverse activity in dopamine axons responsive to both reward and aversive stimuli. Some axons exhibited a preference for reward, while others favored aversive stimuli, and there was a strong bias for the latter at the population level. Long-term longitudinal imaging revealed that the preference was maintained in reward- and aversive-preferring axons throughout classical conditioning in which rewarding and aversive stimuli were paired with preceding auditory cues. However, as mice learned to discriminate reward or aversive cues, a cue activity preference gradually developed only in aversive-preferring axons. We inferred the trial-by-trial cue discrimination based on machine learning using anticipatory licking or facial expressions, and found that successful discrimination was accompanied by sharper selectivity for the aversive cue in aversive-preferring axons. Our findings indicate that a group of mesocortical dopamine axons encodes aversive-related signals, which are modulated by both classical conditioning across days and trial-by-trial discrimination within a day.

Indexed as

AxonsConditioning, ClassicalDopaminergic NeuronsPrefrontal CortexAnimalsCuesDopamineMaleMiceMice, Inbred C57BLRewardDopamineaversiveclassical conditioningdopaminemesocorticalmouseneurosciencerewardtwo-photon imaging

Identifiers

PMID38747563
PMCPMC11095940

What OpenQuestion holds

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Registered trials

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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.