Evidence map›Paper›PMID 25716851›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2015

Dopamine directly modulates GABAA receptors.

Paul Hoerbelt, Tara A Lindsley, Mark W Fleck

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

22 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Phenols and GABAFrontiers in pharmacology · 2024
    Review
  6. Article
  7. A Novel and Functionally Diverse Class of Acetylcholine-Gated Ion Channels.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
    Article
  8. High Fat Diet Increases [Neurochemical research · 2022
    Article
  9. Article
  10. Intricacies of GABAInternational journal of molecular sciences · 2021
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Ethanol Dependence Abolishes Monoamine and GIRK (Kir3) Channel Inhibition of Orbitofrontal Cortex Excitability.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2017
    Article
  16. The Neuropeptide Orexin-A Inhibits the GABAJournal of molecular neuroscience : MN · 2017
    Article
  17. Article
  18. Article
  19. Review
  20. Article
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 1 institution in 1 country.

Paul HoerbeltCenter for Neuropharmacology and Neuroscience, Albany Medical College, Albany, New York 12208 HoerbeP@mail.amc.edu.ORCID http://orcid.org/0000-0002-8707-5376
Tara A LindsleyCenter for Neuropharmacology and Neuroscience, Albany Medical College, Albany, New York 12208.
Mark W FleckCenter for Neuropharmacology and Neuroscience, Albany Medical College, Albany, New York 12208.
Albany Medical Center Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dopamine is a critical neuromodulator that activates GPCRs in mammals or ligand-gated ion channels in invertebrates. The present study demonstrates that dopamine (0.1-10 mm) exerts novel, opposing effects on different populations of mammalian (rat) GABAA receptors. Using whole-cell patch-clamp electrophysiology, we observed direct dopamine-mediated inhibition of tonic-level (1 μm) GABA-evoked currents in untransfected striatal neurons that could be recapitulated in HEK293 cells containing α1β3 or α1β2γ2 subunits. Surprisingly, direct activation by dopamine was seen in the absence of GABA with α1β2γ2, α5β3γ2, or α1β3γ2 transfections. This activity was also present in α1β3γ2 receptors containing a mutant β3 subunit (H267A [(Z)β3]) insensitive to trace levels of inhibitory Zn(2+). Dopamine activation required β and γ subunits but not α subunits ((Z)β3γ2 EC50 value, 660 μm). Dopamine activity was fully blocked by picrotoxin but not GABAA competitive antagonists, and was strongly correlated with spontaneous receptor activity. We also report opposing effects of bicuculline and gabazine, such that bicuculline surprisingly activated non-α-containing (β3γ2) GABAA receptors, whereas gabazine suppressed spontaneous activity in these receptors. Our results suggest that dopamine may directly inhibit GABAA receptors that are both immediately adjacent to dopamine release sites in the striatum and activated by tonic GABA. Furthermore, synaptic/phasic release of dopamine may directly enhance signaling at some spontaneously active noncanonical GABAA receptors that lack α subunits.

Indexed as

Amino Acid SequenceAnimalsBicucullineCells, CulturedCorpus StriatumDopamineFemaleGABA-A Receptor AgonistsGABA-A Receptor AntagonistsHEK293 CellsHumansMaleMolecular Sequence DataMutationNeuronsPicrotoxinBicucullineDopamineGABA-A Receptor AgonistsGABA-A Receptor AntagonistsgabazinePicrotoxinProtein SubunitsPyridazinesReceptors, GABA-AZincdopamineelectrophysiologyGABAGABAALGICspontaneous activity

Identifiers

PMID25716851
PMCPMC6605556
OpenAlexW2168467160

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.