Evidence map›Paper›PMID 25515706›Full record

ArticleAlcohol (Fayetteville, N.Y.)2015

Genotypic and sex differences in anxiety-like behavior and alcohol-induced anxiolysis in High Drinking in the Dark selected mice.

Amanda M Barkley-Levenson, John C Crabbe

Open access · greenAbstract read
In one paragraph

Article in Alcohol (Fayetteville, N.Y.), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
0.8field-weighted citation impact, top 34% 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

17 citing papers in PubMed, 23 citations in OpenAlex.

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  12. Evidence for a Long-Lasting Compulsive Alcohol Seeking Phenotype in Rats.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2018
    Article
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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

2 authors at 2 institutions in 1 country.

Amanda M Barkley-LevensonDepartment of Behavioral Neuroscience, Oregon Health & Science University, Portland, OR 97239, USA; Portland Alcohol Research Center, VA Medical Center, Portland, OR 97239, USA. Electronic address: barkleya@ohsu.edu.
John C CrabbeDepartment of Behavioral Neuroscience, Oregon Health & Science University, Portland, OR 97239, USA; Portland Alcohol Research Center, VA Medical Center, Portland, OR 97239, USA.
Oregon Health & Science University · USPortland VA Medical Center · US

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
Selective Breeding for Drinking in the Circadian DarkU01AA013519 · NIAAA · OREGON HEALTH & SCIENCE UNIVERSITY · PI Angela Renee Ozburn · 2001 to 2026
$10.9M
THERMAL AND METABOLIC DYSFUNCTION DURING WITHDRAWALP50AA010760 · NIAAA · OREGON HEALTH AND SCIENCE UNIVERSITY · PI CRABBE, JOHN C. · 1996 to 2005
$10.7M
MODULATION OF ALCOHOL REINFORCEMENTR01AA007702 · NIAAA · OREGON HEALTH & SCIENCE UNIVERSITY · PI RYABININ, ANDREY E · 1988 to 2019
$4.0M
MODULATION OF ALCOHOL REINFORCEMENTR37AA007702 · NIAAA · OREGON HEALTH & SCIENCE UNIVERSITY · PI CUNNINGHAM, CHRISTOPHER L · 1998 to 2007
$2.3M
Mouse Genetic Models for Alcohol ResearchR24AA020245 · NIAAA · OREGON HEALTH & SCIENCE UNIVERSITY · PI PHILLIPS, TAMARA J. · 2011 to 2020
$2.3M
The role of neuropeptide Y in binge-like drinking in miceF31AA022009 · NIAAA · OREGON HEALTH & SCIENCE UNIVERSITY · PI BARKLEY-LEVENSON, AMANDA MALINA · 2012 to 2015
$109k
ALCOHOL-RELATED BIRTH DEFECTS: SCI. CURRIC. FOR HS &MSN01AA002009 · NIAAA · UNIVERSITY OF NORTH CAROLINA CHAPEL HILL · PI SULIK, KATHLEEN · 2000 to 2000
$67k
Genetic Models of AlcoholismI01BX000313 · VA · PORTLAND VA MEDICAL CENTER · PI CRABBE, JOHN C. · 2009 to 2019
–
BLRD VA I01 BX000313NIAAA NIH HHS AA007468NIAAA NIH HHS AA02009NIAAA NIH HHS AA020245NIAAA NIH HHS AA07702NIAAA NIH HHS AA10760NIAAA NIH HHS AA13519NIAAA NIH HHS F31 AA022009NIAAA NIH HHS P50 AA010760NIAAA NIH HHS P60 AA010760NIAAA NIH HHS R01 AA007702NIAAA NIH HHS R24 AA020245NIAAA NIH HHS R37 AA007702NIAAA NIH HHS T32 AA007468NIAAA NIH HHS U01 AA013519
6 · The paper itself

Abstract

Alcohol use disorders and anxiety disorders are highly comorbid in humans. In rodent lines selected for alcohol drinking, differences in anxiety-like behavior are also seen. The High Drinking in the Dark (HDID) lines of mice are selectively bred for drinking to intoxication during limited access to alcohol, and these mice represent a genetic model of risk for binge-like drinking. The present studies investigated whether these selected lines differ from control (HS) mice in basal anxiety behavior or in anxiolytic response to alcohol. We also assessed the genetic correlation between alcohol drinking in the dark (DID) and basal anxiety-like behavior using existing inbred strain data. Mice of both sexes and HDID replicates (HDID-1 and HDID-2) were tested on an elevated zero maze immediately following a DID test. In general, HDID mice showed more time spent in the open arms after drinking alcohol than HS mice, and open-arm time was significantly correlated with blood alcohol concentration. HDID-1 male mice also showed less anxiety-like behavior at baseline (water-drinking controls). In a separate experiment, HDID-1 and HS mice were tested for anxiolytic dose-response to acute alcohol injections. Both genotypes showed increasing time spent in the open arms with increasing alcohol doses, and HDID-1 and female mice had greater open-arm time across all doses. HDID-1 control males showed lower anxiety-like behavior than the HS control males. Inbred strain data analysis also showed no significant genetic relationship between alcohol DID and anxiety. These findings suggest that HDID selection has not produced systematic changes in anxiety-like behavior or sensitivity to alcohol-induced anxiolysis, though there is a tendency in the male mice of the first replicate toward reduced basal anxiety-like behavior. Therefore, anxiety state and sensitivity to alcohol's anxiolytic effects do not appear to contribute significantly to the high drinking behavior of the HDID mice.

Indexed as

GenotypeSex CharacteristicsAlcohol DrinkingAnimalsAnxietyBinge DrinkingFemaleMaleMiceMice, TransgenicSpecies SpecificityAlcoholAnxietyBehavioral geneticsBinge drinkingInbred strainsSelected lines

Identifiers

PMID25515706
PMCPMC4342118
OpenAlexW1975584111

What OpenQuestion holds

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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.