Evidence map›Paper›PMID 25454537›Full record

ArticleAlcohol (Fayetteville, N.Y.)2014

The effect of prior alcohol consumption on the ataxic response to alcohol in high-alcohol preferring mice.

Brandon M Fritz, Stephen L Boehm

Open access · bronzeAbstract read
In one paragraph

Article in Alcohol (Fayetteville, N.Y.), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact, top 91% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Article
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.

Brandon M FritzIndiana Alcohol Research Center, Department of Psychology, Indiana University - Purdue University Indianapolis, Indiana, USA. Electronic address: bmfritz@iupui.edu.
Stephen L BoehmIndiana Alcohol Research Center, Department of Psychology, Indiana University - Purdue University Indianapolis, Indiana, USA.
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
NIAAA NIH HHS AA016789NIAAA NIH HHS AA07462NIAAA NIH HHS P60 AA007611NIAAA NIH HHS R01 AA016789NIAAA NIH HHS T32 AA007462
6 · The paper itself

Abstract

We have previously shown that ethanol-naïve high-alcohol preferring (HAP) mice, genetically predisposed to consume large quantities of alcohol, exhibited heightened sensitivity and more rapid acute functional tolerance (AFT) to alcohol-induced ataxia compared to low-alcohol preferring mice. The goal of the present study was to evaluate the effect of prior alcohol self-administration on these responses in HAP mice. Naïve male and female adult HAP mice from the second replicate of selection (HAP2) underwent 18 days of 24-h, 2-bottle choice drinking for 10% ethanol vs. water, or water only. After 18 days of fluid access, mice were tested for ataxic sensitivity and rapid AFT following a 1.75 g/kg injection of ethanol on a static dowel apparatus in Experiment 1. In Experiment 2, a separate group of mice was tested for more protracted AFT development using a dual-injection approach where a second, larger (2.0 g/kg) injection of ethanol was given following the initial recovery of performance on the task. HAP2 mice that had prior access to alcohol exhibited a blunted ataxic response to the acute alcohol challenge, but this pre-exposure did not alter rapid within-session AFT capacity in Experiment 1 or more protracted AFT capacity in Experiment 2. These findings suggest that the typically observed increase in alcohol consumption in these mice may be influenced by ataxic functional tolerance development, but is not mediated by a greater capacity for ethanol exposure to positively influence within-session ataxic tolerance.

Indexed as

Alcohol DrinkingAnimalsAtaxiaEthanolFemaleMaleMiceSelf AdministrationEthanolAlcoholAlcohol consumptionAtaxiaMouseSelected linesTolerance

Identifiers

PMID25454537
PMCPMC4254582
OpenAlexW2038914433

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.