Evidence map›Paper›PMID 24440368›Full record

ArticleNeuropharmacology2014

Probing NMDA receptor GluN2A and GluN2B subunit expression and distribution in cortical neurons.

Rashna D Balsara, Ashley N Ferreira, Deborah L Donahue, Francis J Castellino, Patrick L Sheets

Abstract read
In one paragraph

Article in Neuropharmacology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 50% 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

2 citing papers in PubMed, 8 citations in OpenAlex.

  1. 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

5 authors at 2 institutions in 1 country.

Rashna D BalsaraW.M. Keck Center for Transgene Research, University of Notre Dame, Notre Dame, IN, USA.
Ashley N FerreiraDepartment of Biological Sciences, University of Notre Dame, Notre Dame, IN, USA.
Deborah L DonahueW.M. Keck Center for Transgene Research, University of Notre Dame, Notre Dame, IN, USA.
Francis J CastellinoW.M. Keck Center for Transgene Research, University of Notre Dame, Notre Dame, IN, USA; Department of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, IN, USA. Electronic address: fcastell@nd.edu.
Patrick L SheetsDepartment of Biological Sciences, University of Notre Dame, Notre Dame, IN, USA; Department of Pharmacology and Toxicology, Indiana University School of Medicine-South Bend, South Bend, IN, USA. Electronic address: plsheets@iupui.edu.
University of Notre Dame · USIndiana University South Bend · US

Funding

BLOOD COAGULATION PROTEIN-METAL ION-LIPID INTERACTIONSR01HL019982 · NHLBI · UNIVERSITY OF NOTRE DAME · PI CASTELLINO, FRANCIS J · 1985 to 2013
$4.9M
NHLBI NIH HHS HL019982NHLBI NIH HHS R01 HL019982
6 · The paper itself

Abstract

The spatial distribution of N-methyl-d-aspartate receptor (NMDAR) subunits in layer 5 (L5) neurons of the medial prefrontal cortex (mPFC) is important for integrating input-output signals involved in cognitive functions and motor behavior. In this study, focal laser scanning photostimulation of caged glutamate, slice electrophysiology, and small peptide pharmacology, were used to map the distribution of functional GluN2A and GluN2B subunits of the NMDAR from L5 neurons of wild-type (WT) and GluN2A(-/-) mice. Focal uncaging of glutamate evoked spatially-restricted glutamatergic responses on various dendritic locations of pyramidal neurons in the mPFC. Analyses of the spatial arrangements of the GluN2A and GluN2B subunits were performed by comparing inhibition of glutamatergic responses in the presence of the GluN2A-selective pharmacological antagonist, NVP-AAM077 (NVP), and the GluN2B-selective peptidic antagonist, conantokin-G (con-G). We found that apical and basal expression and distribution of GluN2A and GluN2B were similar in L5 mPFC neurons of WT mice. However, the inhibition of glutamatergic responses by NVP in brain slices of GluN2A(-/-) mice were dramatically decreased, while con-G inhibition remained similar to that observed in WT brain slices. The data obtained show that expression and spatial arrangement of GluN2B subunits is independent of GluN2A in L5 neurons of the mPFC. These findings have important ramifications for NMDAR organization and function in L5 pyramidal neurons of the mPFC, and show that specific populations of NMDARs can be antagonized, while sparing other subgroups of NMDARs, thus preserving selective NMDAR functions, an important therapeutic advantage.

Indexed as

AnimalsConotoxinsDendritesExcitatory Amino Acid AntagonistsGlutamic AcidIn Vitro TechniquesMembrane PotentialsMiceMice, KnockoutOptical ImagingPatch-Clamp TechniquesPrefrontal CortexPyramidal CellsQuinoxalinesReceptors, N-Methyl-D-Aspartate5-(alpha-methyl-4-bromobenzylamino)phosphonomethyl-1,4-dihydroquinoxaline-2,3-dioneconotoxin GVConotoxinsExcitatory Amino Acid AntagonistsGlutamic AcidNR2B NMDA receptorQuinoxalinesReceptors, N-Methyl-D-AspartateConantokinsLaser-scanning photostimulationMedial prefrontal cortexNMDARsPyramidal L5 neuronsSlice electrophysiology

Identifiers

PMID24440368
PMCPMC3951114
OpenAlexW1974410814

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.