Evidence map›Paper›PMID 29559384›Full record

ArticleNeuroscience2018

Region-specific Expression of NMDA Receptor GluN2C Subunit in Parvalbumin-Positive Neurons and Astrocytes: Analysis of GluN2C Expression using a Novel Reporter Model.

Aparna Ravikrishnan, Pauravi J Gandhi, Gajanan P Shelkar, Jinxu Liu, Ratnamala Pavuluri, Shashank M Dravid

Abstract read
In one paragraph

Article in Neuroscience, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing 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

39 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Discovery of GluN2A subtype-selectiveActa pharmaceutica Sinica. B · 2024
    Review
  7. Article
  8. Therapeutic potential of N-methyl-D-aspartate receptor modulators in psychiatry.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2024
    Review
  9. Ketamine and the neurobiology of depression: Toward next-generation rapid-acting antidepressant treatments.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Cell-Cell Communication AlterationsFrontiers in aging neuroscience · 2022
    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

6 authors.

Aparna RavikrishnanDepartment of Pharmacology, Creighton University, Omaha, NE 68178, USA.
Pauravi J GandhiDepartment of Pharmacology, Creighton University, Omaha, NE 68178, USA.
Gajanan P ShelkarDepartment of Pharmacology, Creighton University, Omaha, NE 68178, USA.
Jinxu LiuDepartment of Pharmacology, Creighton University, Omaha, NE 68178, USA.
Ratnamala PavuluriDepartment of Pharmacology, Creighton University, Omaha, NE 68178, USA.
Shashank M DravidDepartment of Pharmacology, Creighton University, Omaha, NE 68178, USA. Electronic address: ShashankDravid@creighton.edu.

Funding

Replacing an Animal Resource Facility Cage Washer.G20RR024001 · NCRR · CREIGHTON UNIVERSITY · PI DRESCHER, KRISTEN · 2007 to 2007
$638k
NMDA receptor subtypes in basal gangliaR21NS104705 · NINDS · CREIGHTON UNIVERSITY · PI DRAVID, SHASHANK MANOHAR · 2018 to 2019
$412k
NCRR NIH HHS G20 RR024001NINDS NIH HHS R21 NS104705Wellcome Trust
6 · The paper itself

Abstract

Hypofunction of NMDA receptors in parvalbumin (PV)-positive interneurons has been proposed as a potential mechanism for cortical abnormalities and symptoms in schizophrenia. GluN2C-containing receptors have been linked to this hypothesis due to the higher affinity of psychotomimetic doses of ketamine for GluN1/2C receptors. However, the precise cell-type expression of GluN2C subunit remains unknown. We describe the expression of the GluN2C subunit using a novel EGFP reporter model. We observed EGFP(GluN2C) localization in PV-positive neurons in the nucleus reticularis of the thalamus, globus pallidus externa and interna, ventral pallidum and substantia nigra. In contrast, EGFP(GluN2C)-expressing cells did not co-localize with PV-positive neurons in the cortex, striatum, hippocampus or amygdala. Instead, EGFP(GluN2C) expression in these regions co-localized with an astrocytic marker. We confirmed functional expression of GluN2C-containing receptors in the PV-neurons in substantia nigra and cortical astrocytes using electrophysiology. GluN2C was found to be enriched in several first-order and higher order thalamic nuclei. Interestingly, we found that a previous GluN2C β-gal reporter model excluded expression from PV-neurons and certain thalamic nuclei but exhibited expression in the retrosplenial cortex. GluN2C's unique distribution in neuronal and non-neuronal cells in a brain region-specific manner raises interesting questions regarding the role of GluN2C-containing receptors in the central nervous system.

Indexed as

AnimalsAstrocytesBrainGene Knock-In TechniquesGreen Fluorescent ProteinsMiceMice, Inbred C57BLMice, TransgenicModels, AnimalNeuronsParvalbuminsReceptors, N-Methyl-D-Aspartateenhanced green fluorescent proteinGreen Fluorescent ProteinsNR2C NMDA receptorParvalbuminsReceptors, N-Methyl-D-AspartateastrocytesGluN2CGRIN2CNMDA receptorNR2Cparvalbumin

Identifiers

PMID29559384
PMCPMC6086378

What OpenQuestion holds

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Read underepoch 390

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.