Evidence map›Paper›PMID 26048424›Full record

ArticleBehavioural brain research2015

Binge alcohol drinking elicits persistent negative affect in mice.

Kaziya M Lee, Michal Coehlo, Hadley A McGregor, Ryan S Waltermire, Karen K Szumlinski

Abstract read
In one paragraph

Article in Behavioural brain research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 74 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
74citing papers in PubMed, 1 pooled it
–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

74 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Selective dysregulation of serotonin dynamics in the anterior cingulate cortex and central amygdala following binge alcohol consumption.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
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  9. Mouse parasubthalamicbioRxiv : the preprint server for biology · 2024
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14 more citing papers are in PubMed but not listed here.

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

5 authors.

Kaziya M LeeDepartment of Psychological and Brain Sciences, Neuroscience Research Institute, University of California, Santa Barbara, CA, USA.
Michal CoehloDepartment of Psychological and Brain Sciences, Neuroscience Research Institute, University of California, Santa Barbara, CA, USA.
Hadley A McGregorDepartment of Psychological and Brain Sciences, Neuroscience Research Institute, University of California, Santa Barbara, CA, USA.
Ryan S WaltermireDepartment of Psychological and Brain Sciences, Neuroscience Research Institute, University of California, Santa Barbara, CA, USA.
Karen K SzumlinskiDepartment of Psychological and Brain Sciences, Neuroscience Research Institute, University of California, Santa Barbara, CA, USA. Electronic address: karen.szumlinski@psych.ucsb.edu.

Funding

Molecular regulation of CeA glutamate and binge drinkingR01AA016650 · NIAAA · UNIVERSITY OF CALIFORNIA SANTA BARBARA · PI SZUMLINSKI, KAREN KATHLEEN · 2010 to 2014
$1.7M
mGluR-Homer interactions in excessive drinkingU01AA016650 · NIAAA · UNIVERSITY OF CALIFORNIA SANTA BARBARA · PI SZUMLINSKI, KAREN KATHLEEN · 2006 to 2008
$475k
NIAAA NIH HHS AA016650NIAAA NIH HHS R01 AA016650NIAAA NIH HHS U01 AA016650
6 · The paper itself

Abstract

Cessation from chronic alcohol abuse often produces a dysphoric state that can persist into protracted withdrawal. This dysphoric state is theorized to function as a negative reinforcer that maintains excessive alcohol consumption and/or precipitates relapse in those struggling to abstain from alcohol. However, we know relatively little regarding the impact of cessation from binge drinking on behavioral measures of negative affect and related neurobiology. Male C57BL/6J mice were given access to unsweetened 20% alcohol for 6 weeks under modified Drinking-in-the-dark procedures, followed by behavioral testing beginning either 1 or 21 days into withdrawal. Mice were administered a behavioral test battery consisting of: the elevated plus maze, light/dark box, novel object test, marble burying test, Porsolt forced swim test and sucrose preference test to assess anxiogenic and depressive signs. Egr1 immunostaining was used to quantify cellular activity within the central nucleus of the amygdala (CEA), basolateral amygdala (BLA), bed nucleus of the stria terminalis (BNST), and the nucleus accumbens (Acb) shell (AcbSh) and core (AcbC). Compared to water controls, alcohol-drinking mice exhibited higher indices of emotionality in the majority of behavioral assays. The hyper-emotionality exhibited by binge drinking mice was apparent at both withdrawal time-points and correlated with higher Egr1+ cell counts in the CEA and BNST, compared to controls. These data show that affective symptoms emerge very early after cessation of binge drinking and persist into protracted withdrawal. A history of binge drinking is capable of producing enduring neuroadaptations within brain circuits mediating emotional arousal.

Indexed as

AnxietyDepressionAmygdalaAnhedoniaAnimalsBinge DrinkingCentral Nervous System DepressantsDietary SucroseDisease Models, AnimalEthanolMaleMice, Inbred C57BLMotor ActivityNucleus AccumbensRandom AllocationSeptal NucleiCentral Nervous System DepressantsDietary SucroseEthanolAmygdalaAnxietyBinge drinkingBNSTNucleus accumbens

Identifiers

PMID26048424
PMCPMC4513951

What OpenQuestion holds

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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.