Evidence map›Paper›PMID 25833024›Full record

ArticleAlcoholism, clinical and experimental research2015

Relative fluid novelty differentially alters the time course of limited-access ethanol and water intake in selectively bred high-alcohol-preferring mice.

David N Linsenbardt, Stephen L Boehm

Open access · greenAbstract read
In one paragraph

Article in Alcoholism, clinical and experimental research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.1field-weighted citation impact, top 52% 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

11 citing papers in PubMed, 14 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

2 authors at 1 institution in 1 country.

David N LinsenbardtAddiction Neuroscience, Department of Psychology and Indiana Alcohol Research Center, Indiana University-Purdue University Indianapolis, Indianapolis, Indiana.
Stephen L Boehm
Indiana University – Purdue University Indianapolis · US

Funding

Translational Research and Science Education (OUT)P60AA007611 · NIAAA · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI Marian Lee Logrip · 2003 to 2026
$45.5M
TRAINING GRANT ON GENETICS ASPECTS OF ALCOHOLISMT32AA007462 · NIAAA · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI CRISTINE L CZACHOWSKI · 1985 to 2026
$10.7M
GABAergic Mechanisms in the Modulation of Binge-Like Ethanol Intake in MiceR01AA016789 · NIAAA · STATE UNIVERSITY OF NY,BINGHAMTON · PI BOEHM, STEPHEN LEE · 2009 to 2013
$1.8M
Role of GABA-A alpha1 in Locomotor Sensitization to EthanolK01AA015434 · NIAAA · STATE UNIVERSITY OF NY,BINGHAMTON · PI BOEHM, STEPHEN LEE · 2005 to 2009
$762k
Electrophysiological ensembles organization during alcohol cue-induced intake andF32AA022268 · NIAAA · INDIANA UNIVERSITY INDIANAPOLIS · PI LINSENBARDT, DAVID NATHANIEL · 2013 to 2015
$155k
NIAAA NIH HHS AA015434NIAAA NIH HHS AA016789NIAAA NIH HHS AA022268NIAAA NIH HHS AA07462NIAAA NIH HHS F32 AA022268NIAAA NIH HHS K01 AA015434NIAAA NIH HHS P60 AA007611NIAAA NIH HHS R01 AA016789NIAAA NIH HHS T32 AA007462
6 · The paper itself

Abstract

backgroundThe influence of previous alcohol (ethanol [EtOH])-drinking experience on increasing the rate and amount of future EtOH consumption might be a genetically regulated phenomenon critical to the development and maintenance of repeated excessive EtOH abuse. We have recently found evidence supporting this view, wherein inbred C57BL/6J (B6) mice develop progressive increases in the rate of binge EtOH consumption over repeated drinking-in-the-dark (DID) EtOH access sessions (i.e., "front loading"). The primary goal of this study was to evaluate identical parameters in high-alcohol-preferring (HAP) mice to determine whether similar temporal alterations in limited-access EtOH drinking develop in a population selected for high EtOH preference/intake under continuous (24-hour) access conditions.

methodsUsing specialized volumetric drinking devices, HAP mice received 14 daily 2-hour DID EtOH or water access sessions. A subset of these mice was then given 1 day access to the opposite assigned fluid on day 15. Home cage locomotor activity was recorded concomitantly on each day of these studies. The possibility of behavioral/metabolic tolerance was evaluated on day 16 using experimenter-administered EtOH.

resultsThe amount of EtOH consumed within the first 15 minutes of access increased markedly over days. However, in contrast to previous observations in B6 mice, EtOH front loading was also observed on day 15 in mice that only had previous DID experience with water. Furthermore, a decrease in the amount of water consumed within the first 15 minutes of access compared to animals given repeated water access was observed on day 15 in mice with 14 previous days of EtOH access.

conclusionsThese data further illustrate the complexity and importance of the temporal aspects of limited-access EtOH consumption and suggest that previous procedural/fluid experience in HAP mice selectively alters the time course of EtOH and water consumption.

Indexed as

Alcohol DrinkingAnimalsDrinkingDrug ToleranceEthanolFemaleMaleMiceMice, Inbred StrainsMotor ActivityTime FactorsEthanolAlcohol/Ethanol Front LoadingDrinking-in-the-DarkGenetic Regulation of Binge Alcohol/Ethanol ConsumptionHigh-Alcohol-/Ethanol-Preferring MiceNovelty of Alcohol/Ethanol AccessRate of Alcohol/Ethanol Intake

Identifiers

PMID25833024
PMCPMC4384188
OpenAlexW2140151540

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.