Evidence map›Paper›PMID 30392132›Full record

ReviewPsychopharmacology2018

Vasopressin and alcohol: a multifaceted relationship.

Kathryn M Harper, Darin J Knapp, Hugh E Criswell, George R Breese

Abstract readReview
In one paragraph

Review in Psychopharmacology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

18 citing papers in PubMed, 35 citations in OpenAlex.

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  7. How Does ADPKD Severity Differ Between Family Members?Kidney international reports · 2024
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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

4 authors at 1 institution in 1 country.

Kathryn M HarperBowles Center for Alcohol Studies, The University of North Carolina at Chapel Hill, CB #7178, Thurston Bowles Building, Chapel Hill, NC, 27599-7178, USA. kathryn_harper@med.unc.edu.ORCID http://orcid.org/0000-0002-6297-0032
Darin J KnappBowles Center for Alcohol Studies, The University of North Carolina at Chapel Hill, CB #7178, Thurston Bowles Building, Chapel Hill, NC, 27599-7178, USA.
Hugh E CriswellBowles Center for Alcohol Studies, The University of North Carolina at Chapel Hill, CB #7178, Thurston Bowles Building, Chapel Hill, NC, 27599-7178, USA.
George R BreeseBowles Center for Alcohol Studies, The University of North Carolina at Chapel Hill, CB #7178, Thurston Bowles Building, Chapel Hill, NC, 27599-7178, USA.
University of North Carolina at Chapel Hill · US

Funding

UNC ARC Information/Dissemination CoreP60AA011605 · NIAAA · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Thomas L. Kash · 2003 to 2026
$46.3M
Central amygdala input circuits control stress-induced anxiety after chronic ETOHR01AA022234 · NIAAA · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BREESE, GEORGE R, STUBER, GARRET D · 2013 to 2017
$1.7M
Chronic alcohol affects stress-induced cytokines and cytokine neural functionR01AA021275 · NIAAA · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BREESE, GEORGE R · 2014 to 2018
$1.4M
Foundation for the National Institutes of Health P60AA01165Foundation for the National Institutes of Health R01AA021275Foundation for the National Institutes of Health R01AA022234NIAAA NIH HHS P60 AA011605NIAAA NIH HHS R01 AA021275NIAAA NIH HHS R01 AA022234
6 · The paper itself

Abstract

backgroundArginine vasopressin (VP) has been implicated in a number of neuropsychiatric disorders with an emphasis on situations where stress increased the severity of the disorder. Based on this hypothesized role for VP in neuropsychiatric disorders, much research is currently being undertaken in humans and animals to test VP as a target for treatment of a number of these disorders including alcohol abuse.

objectivesTo provide a summary of the literature regarding the role of VP in alcohol- and stress-related behaviors including the use of drugs that target VP in clinical trials.

resultsChanges in various components of the VP system occur with alcohol and stress. Manipulating VP or its receptors can alter alcohol- and stress-related behaviors including tolerance to alcohol, alcohol drinking, and anxiety-like behavior. Finally, the hypothalamic-pituitary-adrenal axis response to alcohol is also altered by manipulating the VP system. However, clinical trials of VP antagonists have had mixed results.

conclusionsA review of VP's involvement in alcohol's actions demonstrates that there is much to be learned about brain regions involved in VP-mediated effects on behavior. Thus, future work should focus on elucidating relevant brain regions. By using previous knowledge of the actions of VP and determining the brain regions and/or systems involved in its different behavioral effects, it may be possible to identify a specific receptor subtype target, drug treatment combination, or specific clinical contexts that may point toward a more successful treatment.

Indexed as

Alcohol DrinkingAlcoholismAnimalsAntidiuretic Hormone Receptor AntagonistsAnxietyArginine VasopressinEthanolHumansHypothalamo-Hypophyseal SystemNeurophysinsPituitary-Adrenal SystemProtein PrecursorsStress, PsychologicalVasopressinsAntidiuretic Hormone Receptor AntagonistsArginine VasopressinAVP protein, humanEthanolNeurophysinsProtein PrecursorsVasopressinsAlcohol intakeAmygdalaAntagonistsAnxietyClinical trialsEthanolHypothalamusStressToleranceVasopressin

Identifiers

PMID30392132
PMCPMC6286152
OpenAlexW2899052433

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.