Evidence map›Paper›PMID 17625498›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2008

Alcohol inhibits NR2B-containing NMDA receptors in the ventral bed nucleus of the stria terminalis.

Thomas L Kash, Robert T Matthews, Danny G Winder

Open access · bronzeAbstract read
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
1.5field-weighted citation impact, top 21% 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

52 citing papers in PubMed, 71 citations in OpenAlex.

  1. Influence of combined treatment with naltrexone and memantine on alcohol drinking behaviors: a phase II randomized crossover trial.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2020
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  11. Ethanol-induced conditioned place preference and aversion differentially alter plasticity in the bed nucleus of stria terminalis.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2019
    Article
  12. Review
  13. Article
  14. Review
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  16. Ketamine administration during a critical period after forced ethanol abstinence inhibits the development of time-dependent affective disturbances.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2018
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  17. Article
  18. Review
  19. Review
  20. Titrating Tipsy Targets: The Neurobiology of Low-Dose Alcohol.Trends in pharmacological sciences · 2017
    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 2 institutions in 2 countries.

Thomas L KashDepartment of Molecular Physiology and Biophysics, Vanderbilt University School of Medicine, Nashville, TN 37232-0615, USA.
Robert T Matthews
Danny G Winder
Vanderbilt University · USKennedy Center · DK

Funding

Alcohol action on extended amygdala glutamate synapsesR01AA019455 · NIAAA · VANDERBILT UNIVERSITY · PI WINDER, DANNY G. · 2010 to 2014
$1.8M
Regulation of Synaptic Transmission in BNST by AlcoholU01AA015635 · NIAAA · VANDERBILT UNIVERSITY · PI WINDER, DANNY G. · 2005 to 2009
$1.7M
Neuropeptide Modulation of Inhibition in the BNSTF32AA016025 · NIAAA · VANDERBILT UNIVERSITY · PI KASH, THOMAS L. · 2006 to 2008
$110k
NIAAA NIH HHS F32 AA016025NIAAA NIH HHS R01 AA019455NIAAA NIH HHS U01 AA015635
6 · The paper itself

Abstract

Components of the mesolimbic dopamine system, in particular dopaminergic cells in the ventral tegmental area (VTA), have been implicated in the acute reinforcing actions of ethanol. The ventral bed nucleus of the stria terminalis (vBNST) potently regulates dopaminergic cell firing in the VTA, and has been implicated in the behavioral actions of ethanol. The N-methyl-D-asparate receptor (NMDAR) is a major molecular target of ethanol, however, current evidence suggests that ethanol regulation of NMDAR function is widely variable and likely depends on a number of factors. Thus, it is critical to investigate ethanol regulation of NMDAR function at synapses relevant to ethanol-regulated behaviors, such as in the vBNST. Here we show, using multiple techniques, that ethanol inhibits NMDAR function in vBNST neurons in a postsynaptic fashion. Further, we demonstrate the functional presence of both NR2A and NR2B-containing NMDARs in the vBNST. While genetic removal of NR2A did not alter the magnitude of ethanol inhibition, pharmacological blockade of NR2B rendered synaptically activated NMDARs insensitive to ethanol inhibition. Finally, we demonstrate that ethanol inhibits NMDARs in cells in the vBNST that project to the VTA, providing a direct means by which ethanol in the vBNST can modulate the dopaminergic system.

Indexed as

AnimalsBehavior, AnimalCentral Nervous System DepressantsDose-Response Relationship, DrugDrug InteractionsElectric StimulationEthanolExcitatory Amino Acid AntagonistsExcitatory Postsynaptic PotentialsGABA AntagonistsIn Vitro TechniquesMaleMiceMice, Inbred C57BLMice, KnockoutModels, BiologicalCentral Nervous System DepressantsEthanolExcitatory Amino Acid AntagonistsGABA AntagonistsN-MethylaspartateNR2B NMDA receptorPicrotoxinReceptors, N-Methyl-D-Aspartate

Identifiers

PMID17625498
PMCPMC2864636
OpenAlexW2047982498

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.