Evidence map›Paper›PMID 42341209›Full record

ArticleAlcohol and alcoholism (Oxford, Oxfordshire)2026

Reduced ethanol consumption by mice treated orally with arachidonic acid alone or in combination with the benign yeast Saccharomyces cerevisiae.

Andrew W Day, Katrina Blandino, Emma Hayes, Jamie Maguire, Carol A Kumamoto

Abstract read
In one paragraph

Article in Alcohol and alcoholism (Oxford, Oxfordshire), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Andrew W DayGraduate School of Biomedical Sciences, Tufts University, 150 Harrison Ave., Boston, MA 02111, United States.
Katrina BlandinoGraduate School of Biomedical Sciences, Tufts University, 150 Harrison Ave., Boston, MA 02111, United States.
Emma HayesDepartment of Molecular Biology and Microbiology, Tufts University, 150 Harrison Ave., Boston, MA 02111, United States.
Jamie MaguireDepartment of Neuroscience, Tufts University, 150 Harrison Ave., Boston, MA 02111, United States.
Carol A KumamotoDepartment of Molecular Biology and Microbiology, Tufts University, 150 Harrison Ave., Boston, MA 02111, United States.

Funding

MOLECULAR ANALYSIS OF MICROBIAL PATHOGENST32AI007422 · NIAID · TUFTS UNIVERSITY BOSTON · PI Ralph R. Isberg · 1992 to 2026
$5.7M
C ALBICANS IN THE GI TRACT ENVIRONMENTR01AI118898 · NIAID · TUFTS UNIVERSITY BOSTON · PI KUMAMOTO, CAROL A. · 2016 to 2020
$2.5M
Interneurons tune the neural circuits mediating the anxiolytic effects of alcoholR01AA026256 · NIAAA · TUFTS UNIVERSITY BOSTON · PI MAGUIRE, JAMIE LYNN · 2018 to 2022
$1.9M
Pathogenicity of ethanol tolerant strains of Candida albicans in the oral cavityR21DE034446 · NIDCR · TUFTS UNIVERSITY BOSTON · PI DONGARI-BAGTZOGLOU, ANNA I, KUMAMOTO, CAROL A. · 2025 to 2025
$464k
NIAAA NIH HHS R01 AA026256NIAID NIH HHS R01 AI118898NIAID NIH HHS T32 AI007422NIDCR NIH HHS R21 DE034446NIH HHS R01AA026256NIH HHS R01AI118898NIH HHS R21DE034446NIH HHS T32AI007422Tufts Initiative on Substance Use and Addiction
6 · The paper itself

Abstract

aimsThe goal of this study was to determine the effect of administering arachidonic acid (ARA) with or without the yeast Saccharomyces cerevisiae, on voluntary ethanol consumption by mice.

methodsEthanol consumption was measured using a continuous access two-bottle choice experiment with water and 15% ethanol (vol/vol). Ethanol naïve C57BL/6J mice were orally inoculated with ARA (or acidic PBS as the control), S. cerevisiae, or both each evening for three evenings. Ethanol consumption and preference were measured on the following days. In additional experiments, male and female mice underwent chronic intermittent exposure to ethanol vapor. After a 2-week exposure protocol, these mice were given access to 15% ethanol (vol/vol) via a two-bottle choice and inoculated nightly with ARA and S. cerevisiae (or acidic PBS and mock as the control). RESULTS AND

conclusionsAdministration of ARA initially reduced ethanol preference and consumption by ethanol naïve female mice but the effects waned. In contrast, administration of ARA together with a fungus had a sustained effect that reduced preference and consumption. The effects of ARA and fungi were statistically significantly different from ARA alone on Day 3 of ethanol access. Chronically exposed mice that showed low initial consumption of ethanol in the two-bottle choice maintained low consumption when administered ARA and S. cerevisiae. These findings support the future development of a therapeutic regimen utilizing ARA and yeast, or targeting eicosanoids, that could be developed as a supplement to current approaches to reduce ethanol consumption.

Indexed as

Alcohol DrinkingArachidonic AcidEthanolSaccharomyces cerevisiaeAdministration, OralAnimalsFemaleMaleMiceMice, Inbred C57BLArachidonic AcidEthanolarachidonic acidethanolmousepreferenceSaccharomyces cerevisiae

Identifiers

PMID42341209
PMCPMC13293251

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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.