Evidence map›Paper›PMID 34029701›Full record

ArticleAlcohol (Fayetteville, N.Y.)2021

Binge ethanol consumption-associated behavioral impairments in male mice using a gelatin-based drinking-in-the dark model.

Meera Rath, Jasmin Tawfic, Aziza Abrorkhujaeva, Sam Sowell, Sara Wu, Shainnel O Eans, Joanna Peris, Jay P McLaughlin, Stanley M Stevens, Bin Liu

Open access · greenAbstract read
In one paragraph

Article in Alcohol (Fayetteville, N.Y.), 2021. 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
0.4field-weighted citation impact, top 47% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

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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

10 authors at 2 institutions in 1 country.

Meera RathDepartment of Pharmacodynamics, University of Florida, Gainesville, FL, 32610, United States.
Jasmin TawficDepartment of Pharmacodynamics, University of Florida, Gainesville, FL, 32610, United States.
Aziza AbrorkhujaevaDepartment of Pharmacodynamics, University of Florida, Gainesville, FL, 32610, United States.
Sam SowellDepartment of Pharmacodynamics, University of Florida, Gainesville, FL, 32610, United States.
Sara WuDepartment of Pharmacodynamics, University of Florida, Gainesville, FL, 32610, United States.
Shainnel O EansDepartment of Pharmacodynamics, University of Florida, Gainesville, FL, 32610, United States.
Joanna PerisDepartment of Pharmacodynamics, University of Florida, Gainesville, FL, 32610, United States.
Jay P McLaughlinDepartment of Pharmacodynamics, University of Florida, Gainesville, FL, 32610, United States.
Stanley M StevensDepartment of Cell Biology, Microbiology, and Molecular Biology, University of South Florida, Tampa, FL, 33620, United States.
Bin LiuDepartment of Pharmacodynamics, University of Florida, Gainesville, FL, 32610, United States. Electronic address: liu@cop.ufl.edu.
University of Florida · USUniversity of South Florida · US

Funding

The role of histone demethylase KDM5B in ethanol-induced microglial activation: link to tau pathologyR01AA026082 · NIAAA · UNIVERSITY OF SOUTH FLORIDA · PI STEVENS, STANLEY M · 2017 to 2021
$2.2M
Novel Proteomic Approaches for the Study of Alcohol NeuropathologyR03AA022790 · NIAAA · UNIVERSITY OF FLORIDA · PI LIU, BIN, STEVENS, STANLEY M · 2015 to 2016
$162k
NIAAA NIH HHS R01 AA026082NIAAA NIH HHS R03 AA022790
6 · The paper itself

Abstract

backgroundAcute intoxication caused by binge ethanol drinking is linked to widespread impairments in brain functions. Various alcohol administration paradigms have been used in animals to model the heterogeneous clinical manifestation of intoxication in people. It is challenging to model a procedure that produces "visible intoxication" in rodents; however, manipulation of variables such as route of alcohol administration, time of availability, frequency, and duration and amount of ethanol exposure has achieved some success. In the current study, we employed a modified drinking-in-the-dark model to assess the validity of this model in producing "post-ethanol consumption intoxication" impairments following prolonged repeated daily voluntary "binge" ethanol consumption.

methodsAdult male C57BL/6J mice were allowed a daily 3-h access to non-alcoholic plain or ethanol-containing gel during the dark cycle for a total of 83 days. After the initial 2-month daily DID, ethanol intake patterns were intensely characterized during the next 3 weeks. Immediately following the last DID session (day 83), plain and ethanol gel-consuming mice were then subjected to behavioral tests of locomotor ability and/or anxiety (cylinder, wire grip, open field) followed by blood ethanol concentration measurement.

resultMice exhibited a relatively consistent ethanol consumption pattern during and across daily access periods. Ethanol intake of individual mice positively correlated with blood ethanol concentration that averaged 61.64 ± 2.84 mg/dL (n = 12). Compared to the plain gel-consuming control mice, ethanol gel mice exhibited significant locomotor impairment as well as anxiety-like behavior, with the magnitude of impairments of key indices well correlated with blood ethanol levels.

conclusionThe gelatin vehicle-based voluntary ethanol drinking-in-the-dark model reliably produced post consumption acute movement impairments as well as anxiety-like behaviors even after 2 months of daily binge ethanol consumption in male mice. Taken together, this mouse binge ethanol model should facilitate the investigation of mechanisms of binge drinking in subjects chronically abusing ethanol and the search for effective novel treatment strategies.

Indexed as

Binge DrinkingAlcohol DrinkingAnimalsEthanolGelatinMaleMiceMice, Inbred C57BLEthanolGelatinanxietybinge drinkingethanolintoxicationlocomotion

Identifiers

PMID34029701
PMCPMC10629591
OpenAlexW3164444028

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.