Evidence map›Paper›PMID 24485881›Full record

ArticleDrug and alcohol dependence2014

Behavioral disinhibition in mice bred for high drinking in the dark (HDID) and HS controls increases following ethanol.

Megan E Tipps, Travis M Moschak, Suzanne H Mitchell

Abstract read
In one paragraph

Article in Drug and alcohol dependence, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Article
  2. Animal Models of the Behavioral Symptoms of Substance Use Disorders.Cold Spring Harbor perspectives in medicine · 2021
    Review
  3. Article
  4. Article
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.

Megan E TippsDepartment of Behavioral Neuroscience, Oregon Health & Science University, United States.
Travis M MoschakDepartment of Behavioral Neuroscience, Oregon Health & Science University, United States.
Suzanne H MitchellDepartment of Behavioral Neuroscience, Oregon Health & Science University, United States; Department of Psychiatry, Oregon Health & Science University, United States; Portland Alcohol Research Center, Oregon Health & Science University, United States. Electronic address: mitchesu@ohsu.edu.

Funding

Translational measures of risk for excessive alcohol consumptionP60AA010760 · NIAAA · OREGON HEALTH & SCIENCE UNIVERSITY · PI Suzanne S. Fei · 2006 to 2026
$34.5M
BIOLOGICAL BASES OF ALCOHOLISMT32AA007468 · NIAAA · OREGON HEALTH & SCIENCE UNIVERSITY · PI Andrey E Ryabinin · 1987 to 2026
$11.3M
BIOLOGICAL BASES OF DRUG-SEEKING BEHAVIORT32DA007262 · NIDA · OREGON HEALTH & SCIENCE UNIVERSITY · PI WILLIAMS, JOHN T · 1991 to 2022
$9.4M
Determining the neurological and behavioral substrates of ethanol and discountingF31AA020741 · NIAAA · OREGON HEALTH & SCIENCE UNIVERSITY · PI MOSCHAK, TRAVIS M · 2011 to 2013
$119k
The role of GIRK3 in ethanol withdrawal-induced changes in learning and memoryF32AA022011 · NIAAA · OREGON HEALTH & SCIENCE UNIVERSITY · PI TIPPS, MEGAN E. · 2012 to 2014
$87k
NIAAA NIH HHS F31 AA020741NIAAA NIH HHS F32 AA022011NIAAA NIH HHS F32AA022011NIAAA NIH HHS P60 AA010760NIAAA NIH HHS P60 AA10760NIAAA NIH HHS T32 AA007468NIDA NIH HHS T32 DA007262
6 · The paper itself

Abstract

backgroundAlcohol consumption and behavioral inhibition share some common underlying genetic mechanisms. The current study examined whether lines of mice selected for high blood ethanol concentrations, attained by heavy drinking in the dark period (DID) of the light-dark cycle that models binge drinking, also exhibit higher levels of drug-naïve inhibition. It also examined whether the administration of ethanol would result in higher levels of disinhibition in these selected lines compared to the founder stock (HS).

methodsA Go/No-Go task was used to assess baseline inhibition and the effects of acute ethanol on disinhibition (response to a No-Go cue) in the HS line and in mice selected for high levels of DID (HDID-1 and HDID-2).

resultsLines did not differ in inhibition at baseline and all lines showed increased disinhibition following moderate doses of ethanol. Ethanol decreased responding to Go cues for HDID-2 and HS lines at high doses but not HDID-1 mice.

conclusionsThese data corroborate previous work showing ethanol-induced increases in behavioral disinhibition. The selection paradigm did not result in differential sensitivity to the disinhibiting effects of ethanol, but did result in differential sensitivity to the suppressant effects of ethanol on operant behavior between the two HDID lines.

Indexed as

Inhibition, PsychologicalAlcohol DrinkingAnimalsBehavior, AnimalBinge DrinkingCentral Nervous System DepressantsConditioning, OperantDarknessData Interpretation, StatisticalDisease Models, AnimalEthanolFemaleMaleMiceSpecies SpecificityCentral Nervous System DepressantsEthanolAlcoholDrinking in the darkGo/No-GoImpulsivityInhibitionSelected lines

Identifiers

PMID24485881
PMCPMC3956112

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Registered trials

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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.