Evidence map›Paper›PMID 27012890›Full record

ArticleNeuropharmacology2017

GluN1 deletions in D1- and A2A-expressing cell types reveal distinct modes of behavioral regulation.

Max E Joffe, Sophie R Vitter, Brad A Grueter

Abstract read
In one paragraph

Article in Neuropharmacology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.7field-weighted citation impact, top 18% 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

14 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. mGluNeuron · 2020
    Article
  10. Review
  11. Genetic loss of GluN2B in D1-expressing cell types enhances long-term cocaine reward and potentiation of thalamo-accumbens synapses.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2018
    Article
  12. Toll-like receptor 4 deficiency alters nucleus accumbens synaptic physiology and drug reward behavior.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  13. Review
  14. Review
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.

Max E JoffeDept. of Pharmacology, Vanderbilt University School of Medicine, Nashville, TN, 37232, USA.
Sophie R VitterVanderbilt University, Nashville, TN, 37232, USA.
Brad A GrueterDept. of Anesthesiology, Vanderbilt University School of Medicine, Nashville, TN, 37232, USA; Dept. of Molecular Physiology and Biophysics, Vanderbilt University School of Medicine, Nashville, TN, 37232, USA; Dept. of Psychiatry, Vanderbilt University School of Medicine, Nashville, TN, 37232, USA. Electronic address: brad.grueter@vanderbilt.edu.
Vanderbilt University · US

Funding

Research Project: Sensory and Multisensory Contributions to AutismU54HD083211 · NICHD · VANDERBILT UNIVERSITY MEDICAL CENTER · PI MIRNICS, KAROLY · 2015 to 2019
$7.1M
Synaptic Mechanisms of Addiction-Related Behaviors in the Nucleus AccumbensR00DA031699 · NIDA · VANDERBILT UNIVERSITY MEDICAL CENTER · PI GRUETER, BRAD ALAN · 2013 to 2015
$743k
NICHD NIH HHS U54 HD083211NIDA NIH HHS R00 DA031699
6 · The paper itself

Abstract

N-methyl-d-aspartate receptors (NMDARs) are profound regulators of glutamate neurotransmission and behavior. To coordinate components of the limbic system, the dorsal and ventral striatum integrate cognitive and emotional information towards the execution of complex behaviors. Striatal outflow is conveyed by medium spiny neurons (MSNs), which can be dichotomized by expression of dopamine receptor subtype 1 (D1) or adenosine receptor subtype 2A (A2A). To examine how striatal NMDAR function modulates reward-related behaviors, we generated D1- and A2A-specific genetic deletions of the obligatory GluN1 subunit. Interestingly, we observed no differences in any GluN1

Indexed as

AnimalsAnxietyBehavior, AnimalCocaineDrug-Seeking BehaviorExploratory BehaviorExtinction, PsychologicalFemaleMaleMiceMice, KnockoutNerve Tissue ProteinsNeuronsNucleus AccumbensReceptor, Adenosine A2AReceptors, Dopamine D1CocaineGprin1 protein, mouseNerve Tissue ProteinsReceptor, Adenosine A2AReceptors, Dopamine D1Receptors, N-Methyl-D-AspartateCocaineDespairNMDARNucleus accumbensReinstatementStriatum

Identifiers

PMID27012890
PMCPMC5031515
OpenAlexW2305610512

What OpenQuestion holds

Textmetadata
LicenceTDM
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.