Evidence map›Paper›PMID 26631477›Full record

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

NMDA Receptors Containing the GluN2D Subunit Control Neuronal Function in the Subthalamic Nucleus.

Sharon A Swanger, Katie M Vance, Jean-François Pare, Florence Sotty, Karina Fog, Yoland Smith, Stephen F Traynelis

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 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
5.5field-weighted citation impact, top 4% 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

47 citing papers in PubMed, 78 citations in OpenAlex.

  1. Review
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  12. Therapeutic potential of N-methyl-D-aspartate receptor modulators in psychiatry.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2024
    Review
  13. Selective Cell-Surface Expression of Triheteromeric NMDA Receptors.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  14. Potential Roles for the GluN2D NMDA Receptor Subunit in Schizophrenia.International journal of molecular sciences · 2023
    Review
  15. Article
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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 3 institutions in 3 countries.

Sharon A SwangerDepartment of Pharmacology and.ORCID http://orcid.org/0000-0003-0615-6244
Katie M VanceDepartment of Pharmacology and.
Jean-François PareYerkes National Primate Research Center and Morris K. Udall Center of Excellence for Parkinson's Disease Research, Emory University, Atlanta, Georgia 30329, and.
Florence SottyH. Lundbeck A/S, Division of Neurodegeneration and Biologics, Ottiliavej 9, DK-2500 Valby, Denmark.
Karina FogH. Lundbeck A/S, Division of Neurodegeneration and Biologics, Ottiliavej 9, DK-2500 Valby, Denmark.
Yoland SmithDepartment of Neurology, Emory University School of Medicine, Atlanta, Georgia 30322, Yerkes National Primate Research Center and Morris K. Udall Center of Excellence for Parkinson's Disease Research, Emory University, Atlanta, Georgia 30329, and.
Stephen F TraynelisDepartment of Pharmacology and strayne@emory.edu.ORCID http://orcid.org/0000-0002-3750-9615
Emory University · USInstitute of Pharmacology · CZLundbeck (Denmark) · DK

Funding

Yerkes National Primate Research Center Role of type-I IFN in regulating COVID-19 induced inflammation and pathogenesisP51OD011132 · OD · EMORY UNIVERSITY · PI Joon Sup Lee · 2012 to 2026
$167.0M
TRAINING IN TRANSLATIONAL RESEARCH IN NEUROLOGYT32NS007480 · NINDS · EMORY UNIVERSITY · PI LEVEY, ALLAN I · 2000 to 2020
$4.5M
Control of Glutamate Receptor FunctionR01NS036654 · NINDS · EMORY UNIVERSITY · PI TRAYNELIS, STEPHEN F · 1998 to 2018
$3.7M
Training Program in Neurobiology of Drug AbuseT32DA015040 · NIDA · EMORY UNIVERSITY · PI KUHAR, MICHAEL J · 2003 to 2012
$3.6M
Mechanism of Action of Novel Subunit-Selective NMDA Receptor ModulatorsR01NS065371 · NINDS · EMORY UNIVERSITY · PI TRAYNELIS, STEPHEN F · 2009 to 2018
$3.4M
Control of glutamate receptor functionR37NS036654 · NINDS · EMORY UNIVERSITY · PI TRAYNELIS, STEPHEN F · 2007 to 2013
$2.4M
Subunit-specific NMDA receptor function in the subthalamic nucleusF32NS086368 · NINDS · EMORY UNIVERSITY · PI SWANGER, SHARON ANN · 2013 to 2015
$126k
NIDA NIH HHS T32 DA015040NIDA NIH HHS T32-DA015040NINDS NIH HHS F32 NS086368NINDS NIH HHS F32-NS086368NINDS NIH HHS NS036654NINDS NIH HHS NS065371NINDS NIH HHS R01 NS036654NINDS NIH HHS R01 NS065371NINDS NIH HHS R37 NS036654NINDS NIH HHS T32 NS007480NINDS NIH HHS T32-NS007480
6 · The paper itself

Abstract

The GluN2D subunit of the NMDA receptor is prominently expressed in the basal ganglia and associated brainstem nuclei, including the subthalamic nucleus (STN), globus pallidus, striatum, and substantia nigra. However, little is known about how GluN2D-containing NMDA receptors contribute to synaptic activity in these regions. Using Western blotting of STN tissue punches, we demonstrated that GluN2D is expressed in the rat STN throughout development [age postnatal day 7 (P7)-P60] and in the adult (age P120). Immunoelectron microscopy of the adult rat brain showed that GluN2D is predominantly expressed in dendrites, unmyelinated axons, and axon terminals within the STN. Using subunit-selective allosteric modulators of NMDA receptors (TCN-201, ifenprodil, CIQ, and DQP-1105), we provide evidence that receptors containing the GluN2B and GluN2D subunits mediate responses to exogenously applied NMDA and glycine, as well as synaptic NMDA receptor activation in the STN of rat brain slices. EPSCs in the STN were mediated primarily by AMPA and NMDA receptors and GluN2D-containing NMDA receptors controlled the slow deactivation time course of EPSCs in the STN. In vivo recordings from the STN of anesthetized adult rats demonstrated that the spike firing rate was increased by the GluN2C/D potentiator CIQ and decreased by the GluN2C/D antagonist DQP-1105, suggesting that NMDA receptor activity can influence STN output. These data indicate that the GluN2B and GluN2D NMDA receptor subunits contribute to synaptic activity in the STN and may represent potential therapeutic targets for modulating subthalamic neuron activity in neurological disorders such as Parkinson's disease.

Indexed as

Action PotentialsAnimalsAnimals, NewbornDendritesExcitatory Amino Acid AgentsExcitatory Amino Acid AntagonistsExcitatory Postsynaptic PotentialsFemaleGene Expression Regulation, DevelopmentalHEK293 CellsHumansMaleMiceMice, Inbred C57BLMice, TransgenicNeuronsExcitatory Amino Acid AgentsExcitatory Amino Acid AntagonistsFG 9041NR2D NMDA receptorQuinoxalinesReceptors, N-Methyl-D-Aspartateexcitatory synapseGluN2BGluN2Dglutamate receptorNMDAsubthalamic nucleus

Identifiers

PMID26631477
PMCPMC4666920
OpenAlexW2182506513

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.