Evidence map›Paper›PMID 42327123›Full record

ArticlebioRxiv : the preprint server for biology2026

Attenuated conditioned taste aversion for sucrose in female mice with a history of chronic low-dose ethanol exposure.

Christina M Curran-Alfaro, Christine M Side, Ankith Alluri, Wesley Corey, Conor Sheehan, Jacqueline M Barker

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Christina M Curran-AlfaroDepartment of Pharmacology and Physiology, Drexel University College of Medicine Philadelphia, PA, 19102.
Christine M SideDepartment of Pharmacology and Physiology, Drexel University College of Medicine Philadelphia, PA, 19102.
Ankith AlluriDepartment of Pharmacology and Physiology, Drexel University College of Medicine Philadelphia, PA, 19102.
Wesley CoreyDepartment of Pharmacology and Physiology, Drexel University College of Medicine Philadelphia, PA, 19102.
Conor SheehanDepartment of Pharmacology and Physiology, Drexel University College of Medicine Philadelphia, PA, 19102.
Jacqueline M BarkerDepartment of Pharmacology and Physiology, Drexel University College of Medicine Philadelphia, PA, 19102.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It is becoming increasingly clear that chronic exposure to lower levels of ethanol impact learning and behavior. To determine the impact of chronic low-dose ethanol exposure on sensitivity to changes in stimulus value, a conditioned taste aversion procedure was used. Adult male and female mice underwent a sucrose two bottle-choice drinking paradigm. Each day, mice received an injection of either low-dose ethanol (0.5g/kg) or saline two hours after sucrose access for 20 days. This was followed by a lithium chloride (LiCl)-induced conditioned taste aversion (CTA) paradigm in which 0.15M LiCl or vehicle injection was administered immediately after sucrose consumption for three days. On the fourth day, changes in sucrose consumption were analyzed. Chronic exposure to low-dose ethanol did not affect sucrose consumption in either female of male mice during two-bottle choice. In female mice, a history of chronic low-dose ethanol exposure blocked the development of LiCl-induced CTA. A history of chronic low-dose ethanol did not impact LiCl-induced CTA in male mice as both ethanol-naïve and -exposed male mice who underwent LiCl pairing reduced sucrose consumption. This suggests that low-dose ethanol alters aversion-related learning in female mice which may have implication for development of aberrant behavior and risk for alcohol use disorder (AUD).

Identifiers

PMID42327123
PMCPMC13277867

What OpenQuestion holds

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Registered trials

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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.