Evidence map›Paper›PMID 17446041›Full record

ArticleJournal of chemical neuroanatomy2007

Differential localization of the GluR1 and GluR2 subunits of the AMPA-type glutamate receptor among striatal neuron types in rats.

Y P Deng, J P Xie, H B Wang, W L Lei, Q Chen, A Reiner

Open access · greenAbstract read
In one paragraph

Article in Journal of chemical neuroanatomy, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

28 citing papers in PubMed, 54 citations in OpenAlex.

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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

6 authors at 2 institutions in 2 countries.

Y P DengDepartment of Anatomy and Neurobiology, University of Tennessee Health Science Center, Memphis, TN 38163, USA.
J P Xie
H B Wang
W L Lei
Q Chen
A Reiner
University of Tennessee Health Science Center · USSun Yat-sen University · CN

Funding

PATHOGENETIC MECHANISMS OF HUNTINGTON'S DISEASER01NS028721 · NINDS · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI REINER, ANTON J. · 1990 to 2004
$1.7M
Organization of the Cortical Projection to the Basal GangliaR01NS057722 · NINDS · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI REINER, ANTON J. · 2008 to 2012
$1.6M
NEUROPEPTIDE SYSTEMS IN AVIAN AND RETILLIAN BRAINR01NS019620 · NINDS · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI REINER, ANTON J. · 1985 to 2003
$900k
Neuropathology and Pathogenesis of Huntington's DiseaseR56NS028721 · NINDS · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI REINER, ANTON J. · 2008 to 2008
$322k
NINDS NIH HHS NS-19620NINDS NIH HHS NS 28721NINDS NIH HHS R01 NS019620NINDS NIH HHS R01 NS028721NINDS NIH HHS R01 NS057722NINDS NIH HHS R56 NS028721
6 · The paper itself

Abstract

Differences among the various striatal projection neuron and interneuron types in cortical input, function, and vulnerability to degenerative insults may be related to differences among them in AMPA-type glutamate receptor abundance and subunit configuration. We therefore used immunolabeling to assess the frequency and abundance of GluR1 and GluR2, the most common AMPA subunits in striatum, in the main striatal neuron types. All neurons projecting to the external pallidum (GPe), internal pallidum (GPi) or substantia nigra, as identified by retrograde labeling, possessed perikaryal GluR2, while GluR1 was more common in striato-GPe than striato-GPi perikarya. The frequency and intensity of immunostaining indicated the rank order of their perikaryal GluR1:GluR2 ratio to be striato-GPe>striatonigral>striato-GPi. Ultrastructural studies suggested a differential localization of GluR1 and GluR2 to striatal projection neuron dendritic spines as well, with GluR1 seemingly more common in striato-GPe spines and GluR2 more common in striato-GPi and/or striatonigral spines. Comparisons among projection neurons and interneurons revealed GluR1 to be most common and abundant in parvalbuminergic interneurons, and GluR2 most common and abundant in projection neurons, with the rank order for the GluR1:GluR2 ratio being parvalbuminergic interneurons>calretinergic interneurons>cholinergic interneurons>projection neurons>somatostatinergic interneurons. Striosomal projection neurons had a higher GluR1:GluR2 ratio than did matrix projection neurons. The abundance of both GluR1 and GluR2 in striatal parvalbuminergic interneurons and projection neurons is consistent with their prominent cortical input and susceptibility to excitotoxic insult, while differences in GluR1:GluR2 ratio among projection neurons are likely to yield differences in Ca(2+) permeability, desensitization, and single channel current, which may contribute to differences among them in plasticity, synaptic integration, and excitotoxic vulnerability. The apparent association of the GluR1 subunit with synaptic plasticity, in particular, suggests striato-GPe neuron spines as a particular site of corticostriatal synaptic plasticity, presumably associated with motor learning.

Indexed as

AcetylcholineAnimalsCalcium-Binding ProteinsCalcium SignalingCorpus StriatumDendritic SpinesEntopeduncular NucleusFluorescent Antibody TechniqueGlobus PallidusGlutamic AcidInterneuronsMaleMicroscopy, Electron, TransmissionNeostriatumNeural PathwaysNeuronal PlasticityAcetylcholineCalcium-Binding Proteinsglutamate receptor ionotropic, AMPA 2Glutamic AcidReceptors, AMPASomatostatin

Identifiers

PMID17446041
PMCPMC1993922
OpenAlexW2081116653

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.