Evidence map›Paper›PMID 22855801›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2012

D1 receptor modulation of action potential firing in a subpopulation of layer 5 pyramidal neurons in the prefrontal cortex.

Hannah J Seong, Adam G Carter

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

73 citing papers in PubMed, 104 citations in OpenAlex.

  1. Article
  2. Activation by Alcohol of Prefrontal Layer 5 Pyramidal Neurons Depends on Ascending Dopaminergic Input.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
    Article
  3. Intrinsic Dendritic Integration Features of Prefrontal Layer 5 Pyramidal Cell Subclasses.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Arrestin-3 Agonism at Dopamine DBiological psychiatry · 2023
    Article
  10. Review
  11. Article
  12. Distinct Roles for Prefrontal Dopamine D1 and D2 Neurons in Social Hierarchy.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Article
  13. Review
  14. Article
  15. Increased Synaptic Strength and mGluAlcoholism, clinical and experimental research · 2021
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Upregulated 5-HTMolecular brain · 2020
    Article

13 more citing papers are in PubMed but not listed here.

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

2 authors at 1 institution in 1 country.

Hannah J SeongCenter for Neural Science, New York University, New York, New York 10003, USA.
Adam G Carter
New York University · US

Funding

Synaptic and Dendritic Physiology in the Prefrontal CortexR01MH085974 · NIMH · NEW YORK UNIVERSITY · PI CARTER, ADAM G · 2010 to 2024
$6.4M
Training Systems and Integrative NeuroscienceT32MH019524 · NIMH · NEW YORK UNIVERSITY · PI KIORPES, LYNNE · 1992 to 2025
$5.2M
NIMH NIH HHS 5T32 MH019524NIMH NIH HHS R01 MH085974NIMH NIH HHS T32 MH019524
6 · The paper itself

Abstract

Dopamine modulation in the prefrontal cortex is important for cognitive processing and disrupted in diverse neuropsychiatric diseases. Activation of D1 receptors is thought to enable working memory by enhancing the firing properties of pyramidal neurons. However, these receptors are only sparsely expressed in the prefrontal cortex, and how they impact individual neurons remains unknown. Here we study D1 receptor modulation of layer 5 pyramidal neurons in acute slices of the mouse prefrontal cortex. Using whole-cell recordings and two-photon microscopy, we show that neurons expressing D1 receptors have unique morphological and physiological properties. We then demonstrate that activation of these receptors selectively enhances the firing of these neurons by signaling via the protein kinase A pathway. This finding of robust D1 receptor modulation in only a subpopulation of neurons has important implications for cognitive function and disease.

Indexed as

Action PotentialsAnimalsAnimals, NewbornBiophysicsDopamine AntagonistsElectric StimulationEnzyme InhibitorsExcitatory Amino Acid AntagonistsFemaleGABA AntagonistsIn Vitro TechniquesMaleMiceMice, TransgenicMicroscopy, ConfocalPatch-Clamp Techniques2,3-dioxo-6-nitro-7-sulfamoylbenzo(f)quinoxaline3-(2-carboxypiperazin-4-yl)propyl-1-phosphonic acidDopamine AntagonistsEnzyme InhibitorsExcitatory Amino Acid AntagonistsGABA AntagonistsgabazinePiperazinesPlant LectinsPyridazinesQuinoxalinesReceptors, Dopamine D1tomato lectin

Identifiers

PMID22855801
PMCPMC3429120
OpenAlexW2109660229

What OpenQuestion holds

Textmetadata
LicenceTDM
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.