Evidence map›Paper›PMID 34815314›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2022

D1/D5 Dopamine Receptors and mGluR5 Jointly Enable Non-Hebbian Long-Term Potentiation at Sensory Synapses onto Lamina I Spinoparabrachial Neurons.

Jie Li, Theodore J Price, Mark L Baccei

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.6field-weighted citation impact, top 38% 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

10 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Cell Type-Dependent Short-Term Plasticity and Dopaminergic Modulation of Sensory Synapses onto Mouse Superficial Dorsal Horn Neurons.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  5. Article
  6. Sex differences in the transition to chronic pain.The Journal of clinical investigation · 2025
    Review
  7. Review
  8. Article
  9. Article
  10. An Overview of the Mechanisms Involved in Neuralgia.Journal of inflammation research · 2023
    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

3 authors at 2 institutions in 1 country.

Jie LiPain Research Center, Department of Anesthesiology, University of Cincinnati College of Medicine, Cincinnati, Ohio 45267.
Theodore J PriceCenter for Advanced Pain Studies, Department of Neuroscience, University of Texas at Dallas, Richardson, Texas 75080.ORCID 0000-0002-6971-6221
Mark L BacceiPain Research Center, Department of Anesthesiology, University of Cincinnati College of Medicine, Cincinnati, Ohio 45267 mark.baccei@uc.edu.ORCID 0000-0003-3337-7480
University of Cincinnati Medical Center · USThe University of Texas at Dallas · US

Funding

Translation Control of Pain PlasticityR01NS065926 · NINDS · UNIVERSITY OF TEXAS DALLAS · PI PRICE, THEODORE J. · 2010 to 2023
$5.7M
Synaptic Function within Mature Central Pain Networks after Neonatal InjuryR01NS080889 · NINDS · UNIVERSITY OF CINCINNATI · PI Mark L Baccei · 2013 to 2026
$4.5M
NINDS NIH HHS R01 NS065926NINDS NIH HHS R01 NS080889
6 · The paper itself

Abstract

Highly correlated firing of primary afferent inputs and lamina I projection neurons evokes synaptic long-term potentiation (LTP), a mechanism by which ascending nociceptive transmission can be amplified at the level of the spinal dorsal horn. However, the degree to which neuromodulatory signaling shapes the temporal window governing spike-timing-dependent plasticity (STDP) at sensory synapses onto projection neurons remains unclear. The present study demonstrates that activation of spinal D1/D5 dopamine receptors (D1/D5Rs) creates a highly permissive environment for the production of LTP in male and female adult mouse spinoparabrachial neurons by promoting non-Hebbian plasticity. Bath application of the mixed D1/D5R agonist SKF82958 unmasked LTP at STDP pairing intervals that normally fail to alter synaptic efficacy. Furthermore, during D1/D5R signaling, action potential discharge in projection neurons became dispensable for LTP generation, and primary afferent stimulation alone was sufficient to induce strengthening of sensory synapses. This non-Hebbian LTP was blocked by the D1/D5R antagonist SCH 39166 or genetic deletion of D5R, and required activation of mGluR5 and intracellular Ca

Indexed as

Action PotentialsAnimalsBenzazepinesCalciumDopamine AgonistsFemaleLong-Term PotentiationMaleMiceMice, KnockoutNeuronsReceptor, Metabotropic Glutamate 5Receptors, Dopamine D1Receptors, Dopamine D5Spinal Cord Dorsal HornSynapsesBenzazepinesCalciumDopamine AgonistsReceptor, Metabotropic Glutamate 5Receptors, Dopamine D1Receptors, Dopamine D5SK&F 82958dorsal hornlong-term potentiationprojection neuronspike-timing-dependent plasticityspinal cordsynaptic plasticity

Identifiers

PMID34815314
PMCPMC8802920
OpenAlexW3217614600

What OpenQuestion holds

Textmetadata
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.