Evidence map›Paper›PMID 31012186›Full record

ArticleAddiction biology2020

Ethanol induces maladaptive impulse control and decreased seeking behaviors in mice.

Phillip Starski, Sa-Ik Hong, Lee Peyton, Alfredo Oliveros, Katheryn Wininger, Colleen Hutchison, Seungwoo Kang, Victor Karpyak, Doo-Sup Choi

Open access · greenAbstract read
In one paragraph

Article in Addiction biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.2field-weighted citation impact, top 25% 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

12 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
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  8. Review
  9. NPsychopharmacology · 2022
    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

9 authors at 1 institution in 1 country.

Phillip StarskiNeuroscience Program, Mayo Clinic College of Medicine Rochester, Rochester, Minnesota.
Sa-Ik HongDepartment of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic College of Medicine Rochester, Rochester, Minnesota.
Lee PeytonDepartment of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic College of Medicine Rochester, Rochester, Minnesota.
Alfredo OliverosDepartment of Neurological Surgery, Mayo Clinic College of Medicine Rochester, Rochester, Minnesota.
Katheryn WiningerNeuroscience Program, Mayo Clinic College of Medicine Rochester, Rochester, Minnesota.
Colleen HutchisonNeuroscience Program, Mayo Clinic College of Medicine Rochester, Rochester, Minnesota.
Seungwoo KangDepartment of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic College of Medicine Rochester, Rochester, Minnesota.
Victor KarpyakDepartment of Psychiatry and Psychology, Mayo Clinic College of Medicine Rochester, Rochester, Minnesota.
Doo-Sup ChoiNeuroscience Program, Mayo Clinic College of Medicine Rochester, Rochester, Minnesota.ORCID 0000-0002-6796-9938
Mayo Clinic · US

Funding

Alcohol and Adenosine-Mediated Glutamate Signaling in Neuro-Glial InteractionR01AA018779 · NIAAA · MAYO CLINIC ROCHESTER · PI CHOI, DOO-SUP · 2009 to 2019
$3.8M
NIAAA NIH HHS R01 AA018779
6 · The paper itself

Abstract

Waiting impulsivity is a risk factor for many psychiatric disorders including alcohol use disorder (AUD). Highly impulsive individuals are vulnerable to alcohol abuse. However, it is not well understood whether chronic alcohol use increases the propensity for impulsive behavior. Here, we establish a novel experimental paradigm demonstrating that continuous binge-like ethanol exposure progressively leads to maladaptive impulsive behavior. To test waiting impulsivity, we employed the 5-choice serial reaction time task (5-CSRTT) in C57BL/6J male mice. We assessed premature responses in the fixed and variable intertrial interval (ITI) 5-CSRTT sessions. We further characterized our ethanol-induced impulsive mice using Open Field, y-maze, two-bottle choice, and an action-outcome task. Our results indicate that continuous binge-like ethanol exposure significantly increased premature responses when mice were tested in variable ITI sessions even during a prolonged abstinent period. Ethanol-induced impulsive mice exhibited anxiety-like behavior during chronic exposures. This behavior was also observed in a separate cohort that was subjected to 20 days of abstinence. Ethanol-treated mice were less motivated for a sucrose reward compared with air-exposed control mice, while also demonstrating reduced responding during action-outcome testing. Overall, ethanol-treated mice demonstrated increased impulsive behavior, but a reduced motivation for a sucrose reward. Although waiting impulsivity has been hypothesized to be a trait or risk factor for AUD, our findings indicate that maladaptive impulse control can also be potentiated or induced by continuous chronic ethanol exposure in mice.

Indexed as

AnimalsAnxietyBehavior, AnimalBinge DrinkingCentral Nervous System DepressantsChoice BehaviorEthanolImpulsive BehaviorMaleMiceMotivationOpen Field TestReaction TimeRewardCentral Nervous System DepressantsEthanolalcoholAUDimpulsivitymotivationoperant

Identifiers

PMID31012186
PMCPMC6810713
OpenAlexW2941821790

What Socratic 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 Socratic graph.