Evidence map›Paper›PMID 35633038›Full record

ArticleAlcoholism, clinical and experimental research2022

The development, but not expression, of alcohol front-loading in C57BL/6J mice maintained on LabDiet 5001 is abolished by maintenance on Teklad 2920x rodent diet.

Nicole M Maphis, Radcliff T Huffman, David N Linsenbardt

Open access · greenAbstract read
In one paragraph

Article in Alcoholism, clinical and experimental research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 15% 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, 1 synthesis or guideline pooled it, 22 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

3 authors at 1 institution in 1 country.

Nicole M MaphisDepartment of Neurosciences, University of New Mexico, Albuquerque, New Mexico, USA.ORCID 0000-0003-3833-1027
Radcliff T HuffmanDepartment of Neurosciences, University of New Mexico, Albuquerque, New Mexico, USA.ORCID 0000-0002-0216-3829
David N LinsenbardtDepartment of Neurosciences, University of New Mexico, Albuquerque, New Mexico, USA.ORCID 0000-0003-2447-0683
University of New Mexico · US

Funding

WOMEN'S CANCERS RESEARCH PROGRAMP30CA118100 · NCI · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI Yolanda Sanchez · 2005 to 2026
$57.1M
Understanding neurophysiological deficits in response inhibition in children with FASDP50AA022534 · NIAAA · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI Carlos Fernando Valenzuela · 2014 to 2026
$21.5M
FAIR Data Competency and Machine Learning Readiness for Biomedical ScientistsK12GM088021 · NIGMS · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI REBECCA S. HARTLEY, Diane Lidke · 2009 to 2026
$16.4M
Repeated Binge Drinking and the Genetic Regulation of Corticostriatal SynchronyR00AA025120 · NIAAA · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI LINSENBARDT, DAVID NATHANIEL · 2020 to 2022
$993k
Repeated Binge Drinking and the Genetic Regulation of Corticostriatal SynchronyK99AA025120 · NIAAA · INDIANA UNIVERSITY INDIANAPOLIS · PI LINSENBARDT, DAVID NATHANIEL · 2017 to 2018
$316k
NCI NIH HHS P30 CA118100NIAAA NIH HHS K99 AA025120NIAAA NIH HHS P50 AA022534NIAAA NIH HHS R00 AA025120NIGMS NIH HHS K12 GM088021
6 · The paper itself

Abstract

backgroundExcessive alcohol (ethanol) consumption, such as binge drinking, is extremely commonplace and represents a major health concern. Through modeling excessive drinking in rodents, we are beginning to uncover the neurobiological and neurobehavioral causes and consequences of this pattern of ethanol intake. One important factor for modeling binge drinking in mice is that they reliably drink to blood ethanol concentrations (BECs) of 80 mg/dl or higher. Drinking-in-the-dark (DID) is a commonly used mouse model of binge drinking, and we have shown that this method reliably results in robust ethanol front-loading and binge-level BECs in C57BL/6J (B6) mice and other ethanol-preferring mouse strains/lines. However, establishing the DID model in a new vivarium space forced us to consider the use of rodent diet formulations that we had not previously used.

methodsThe current set of experiments were designed to investigate the role of two standard rodent diet formulations on binge drinking and the development of ethanol front-loading using DID.

resultsWe found that BECs in animals maintained on LabDiet 5001 (LD01) were double those found in mice maintained on Teklad 2920x (TL20). Interestingly, this effect was paralleled by differences in the degree of front-loading, such that LD01-fed mice consumed approximately twice as much ethanol in the first 15 min of the 2-h DID sessions as the TL20-fed mice. Surprisingly, however, mice that developed front-loading during maintenance on the LD01 diet continued to display front-loading behavior after being switched to the TL20 diet.

conclusionsThese data emphasize the importance of choosing and reporting diet formulations when conducting voluntary drinking studies and support the need for further investigation into the mechanisms behind diet-induced differences in binge drinking, particularly front-loading.

Indexed as

Binge DrinkingAlcohol DrinkingAnimalsBlood Alcohol ContentDietEthanolMiceMice, Inbred C57BLRodentiaBlood Alcohol ContentEthanolalcohol front-loadingbinge drinking mouse modeldrinking in the darkEtOHrodent diet

Identifiers

PMID35633038
PMCPMC9357207
OpenAlexW4281633342

What OpenQuestion 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 OpenQuestion graph.