Evidence map›Paper›PMID 26549202›Full record

ArticleAddiction biology2017

Chronic intermittent alcohol disrupts the GluN2B-associated proteome and specifically regulates group I mGlu receptor-dependent long-term depression.

Tiffany A Wills, Anthony J Baucum, Katherine M Holleran, Yaoyi Chen, Johanna G Pasek, Eric Delpire, David L Tabb, Roger J Colbran, Danny G Winder

Abstract read
In one paragraph

Article in Addiction biology, 2017. 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
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

28 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Synaptic Effects Induced by Alcohol.Current topics in behavioral neurosciences · 2025
    Review
  3. Article
  4. Article
  5. Article
  6. Chronic MAP4343 reverses escalated alcohol drinking in a mouse model of alcohol use disorder.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2023
    Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Review
  12. Adolescent alcohol exposure produces sex differences in negative affect-like behavior and group I mGluR BNST plasticity.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2020
    Article
  13. Intermittent ethanol exposure during adolescence impairs cannabinoid type 1 receptor-dependent long-term depression and recognition memory in adult mice.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2020
    Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. Synaptic plasticity mechanisms common to learning and alcohol use disorder.Learning & memory (Cold Spring Harbor, N.Y.) · 2018
    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

9 authors at 5 institutions in 2 countries.

Tiffany A WillsDepartment of Molecular Physiology & Biophysics.
Anthony J BaucumDepartment of Biology, Indiana University Purdue University Indianapolis, Indianapolis, IN, USA.
Katherine M HolleranVanderbilt Brain Institute.
Yaoyi ChenDepartment of Biomedical Informatics, Vanderbilt University School of Medicine, Nashville, TN, USA.
Johanna G PasekDepartment of Molecular Physiology & Biophysics.
Eric DelpireDepartment of Molecular Physiology & Biophysics.
David L TabbDepartment of Biomedical Informatics, Vanderbilt University School of Medicine, Nashville, TN, USA.
Roger J ColbranDepartment of Molecular Physiology & Biophysics.
Danny G WinderDepartment of Molecular Physiology & Biophysics.
Allen Institute for Brain Science · USVanderbilt University · USIndiana University – Purdue University Indianapolis · USKennedy Center · DKLouisiana State University Health Sciences Center New Orleans · US

Funding

Research Project: Sensory and Multisensory Contributions to AutismU54HD083211 · NICHD · VANDERBILT UNIVERSITY MEDICAL CENTER · PI CUTTING, LAURIE E · 2015 to 2019
$7.1M
Mechanisms of CaM Kinase II Signal TransductionR01MH063232 · NIMH · VANDERBILT UNIVERSITY · PI COLBRAN, ROGER J · 2001 to 2015
$5.4M
Gene-Targeted Mouse CoreU01AA013514 · NIAAA · VANDERBILT UNIVERSITY MEDICAL CENTER · PI DELPIRE, ERIC J · 2002 to 2016
$4.3M
Vanberbilt Biomarker Developmental LaboratoryU01CA152647 · NCI · VANDERBILT UNIVERSITY · PI LIEBLER, DANIEL C, TABB, DAVID L · 2010 to 2014
$3.1M
Alcohol action on extended amygdala glutamate synapsesR01AA019455 · NIAAA · VANDERBILT UNIVERSITY · PI WINDER, DANNY G. · 2010 to 2014
$1.8M
Spinophilin Signaling in the StriatumK01NS073700 · NINDS · VANDERBILT UNIVERSITY · PI BAUCUM, ANTHONY J. · 2012 to 2016
$693k
Alcohol Regulation of Synaptic and Extrasynaptic GluN2B-NMDA Receptors in BNSTK99AA022651 · NIAAA · VANDERBILT UNIVERSITY · PI WILLS, TIFFANY A · 2014 to 2015
$235k
Modulation of CaMKII and endocannabinoid signaling by Calcium ChannelsF32MH100747 · NIMH · VANDERBILT UNIVERSITY · PI GANDY, JOHANNA C · 2013 to 2013
$52k
Modulation of Plasticity and Alcohol Preference by GRs within the BNST and CeAF31AA021623 · NIAAA · VANDERBILT UNIVERSITY · PI HOLLERAN, KATHERINE MERCEDES · 2014 to 2015
$50k
NCI NIH HHS U01 CA152647NIAAA NIH HHS F31 AA021623NIAAA NIH HHS K99 AA022651NIAAA NIH HHS R01 AA019455NIAAA NIH HHS U01 AA013514NICHD NIH HHS U54 HD083211NIMH NIH HHS F32 MH100747NIMH NIH HHS R01 MH063232NINDS NIH HHS K01 NS073700
6 · The paper itself

Abstract

N-Methyl-d-aspartate receptors (NMDARs) are major targets of both acute and chronic alcohol, as well as regulators of plasticity in a number of brain regions. Aberrant plasticity may contribute to the treatment resistance and high relapse rates observed in alcoholics. Recent work suggests that chronic alcohol treatment preferentially modulates both the expression and subcellular localization of NMDARs containing the GluN2B subunit. Signaling through synaptic and extrasynaptic GluN2B-NMDARs has already been implicated in the pathophysiology of various other neurological disorders. NMDARs interact with a large number of proteins at the glutamate synapse, and a better understanding of how alcohol modulates this proteome is needed. We employed a discovery-based proteomic approach in subcellular fractions of hippocampal tissue from chronic intermittent alcohol (CIE)-exposed C57Bl/6J mice to gain insight into alcohol-induced changes in GluN2B signaling complexes. Protein enrichment analyses revealed changes in the association of post-synaptic proteins, including scaffolding, glutamate receptor and PDZ-domain binding proteins with GluN2B. In particular, GluN2B interaction with metabotropic glutamate (mGlu)

Indexed as

AnimalsCentral Nervous System DepressantsCytoskeletal ProteinsEthanolHippocampusHomer Scaffolding ProteinsLong-Term Synaptic DepressionMaleMiceMice, Inbred C57BLMice, KnockoutNerve Tissue ProteinsProteomeReceptors, Metabotropic GlutamateReceptors, N-Methyl-D-AspartateSignal Transductionactivity regulated cytoskeletal-associated proteinCentral Nervous System DepressantsCytoskeletal ProteinsEthanolHomer Scaffolding ProteinsNerve Tissue ProteinsNR2B NMDA receptorProteomeReceptors, Metabotropic GlutamateReceptors, N-Methyl-D-AspartateAlcohol addictionNMDA receptorproteomicssynaptic plasticity

Identifiers

PMID26549202
PMCPMC4860359
OpenAlexW2117953650

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.