Evidence map›Paper›PMID 25712173›Full record

ArticlePharmacology, biochemistry, and behavior2015

Alcohol preferring (P) rats as a model for examining sex differences in alcohol use disorder and its treatment.

Catherine F Moore, Wendy J Lynch

Open access · greenAbstract read
In one paragraph

Article in Pharmacology, biochemistry, and behavior, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 10% 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

38 citing papers in PubMed, 1 synthesis or guideline pooled it, 62 citations in OpenAlex.

  1. Yohimbine as a pharmacological probe for alcohol research: a systematic review of rodent and human studies.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2022
    Pooled it
  2. Article
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  18. FACTORS CONTRIBUTING TO THE ESCALATION OF ALCOHOL CONSUMPTION.Neuroscience and biobehavioral reviews · 2022
    Review
  19. The GABAPsychopharmacology · 2021
    Article
  20. 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.

Catherine F MooreDepartment of Psychiatry and Neurobehavioral Sciences, University of Virginia, Charlottesville, VA 22902, United States.
Wendy J LynchDepartment of Psychiatry and Neurobehavioral Sciences, University of Virginia, Charlottesville, VA 22902, United States. Electronic address: wlynch@virginia.edu.
University of Virginia · US

Funding

Dopaminergic and Glutamatergic Mechanisms of Cocaine Addiction: Sex DifferencesR01DA024716 · NIDA · UNIVERSITY OF VIRGINIA · PI Wendy Jean Lynch · 2008 to 2026
$6.1M
Exercise as a Sex-Specific Intervention Strategy for Cocaine AddictionR01DA039093 · NIDA · UNIVERSITY OF VIRGINIA · PI LYNCH, WENDY JEAN · 2015 to 2019
$1.7M
Rat Models of Alcohol Dependence for Evaluating Combined Medication EffectsR01AA016554 · NIAAA · UNIVERSITY OF VIRGINIA · PI LYNCH, WENDY JEAN · 2008 to 2012
$1.6M
NIAAA NIH HHS R01 AA016554NIDA NIH HHS R01 DA024716NIDA NIH HHS R01 DA039093
6 · The paper itself

Abstract

rationaleDespite epidemiological and clinical data indicating marked gender differences in alcohol use disorders (AUDs), few preclinical studies have examined sex differences in animal models of AUDs.

objectiveThe purpose of this study was to first characterize sex differences in ethanol consumption and reinforcement in an alcohol preferring (P) rat model of alcoholism, then use this model to screen pharmacological treatments for sex-specific effects.

methodsEthanol consumption was first assessed in male and female P rats under a three-bottle free-choice procedure. Next, ethanol's reinforcing effects were assessed under a fixed-ratio 1 (FR1) schedule followed by a progressive-ratio (PR) schedule. Finally, the effects of two pharmacological treatments for AUDs, naltrexone (1mg/kg) and topiramate (10 or 20mg/kg), alone and in combination, were tested for sex-specific differences in their efficacy at reducing ethanol's reinforcing effects.

resultsAlthough females initially had higher consumption of and preference for ethanol, male rats increased their consumption and preference over time and rapidly became equal to females. Following prolonged 24-hour/day access, males and females self-administered similar levels of ethanol under FR1 and PR schedules. In response to pharmacological treatment, we observed some sex differences and similarities, most notably, a more robust effect of the combination of naltrexone and topiramate in males as compared to females.

conclusionsThis model of selectively bred P rats may be useful for understanding sex differences in AUDs and related behavior and their underlying neurobiological mechanisms and treatment.

Indexed as

Alcohol preferring (P) ratsCombination treatmentEthanolNaltrexoneSex differencesTopiramate

Identifiers

PMID25712173
PMCPMC4545742
OpenAlexW2089282986

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.