Evidence map›Paper›PMID 40161352›Full record

ArticleAddiction neuroscience2025

Evaluating the impact of concurrent sucrose availability on operant ethanol self-administration in male and female Long Evans rats.

Olivia A Ortelli, Jeffrey L Weiner

Abstract read
In one paragraph

Article in Addiction neuroscience, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

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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.

Olivia A OrtelliWake Forest University School of Medicine, Department of Translational Neuroscience, United States.ORCID 0000-0003-0330-3894
Jeffrey L WeinerWake Forest University School of Medicine, Department of Translational Neuroscience, United States.ORCID 0000-0002-8099-760X

Funding

Wake Forest Translational Alcohol Research Center (WF-TARC)P50AA026117 · NIAAA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Paul W. Czoty · 2018 to 2026
$16.2M
Synaptic Correlates of Vulnerability and Resilience to Alcohol Use DisordersR37AA017531 · NIAAA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI WEINER, JEFFREY L. · 2014 to 2023
$3.5M
Neural Substrates of Comorbid Alcohol Use Disorder and Post-Traumatic Stress DisorderR01AA026551 · NIAAA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI WEINER, JEFFREY L. · 2017 to 2021
$1.9M
Neuroscience Training at Wake ForestT32NS115704 · NINDS · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI CZOTY, PAUL W. · 2021 to 2025
$1.4M
Assessing the contributions of the ventral subiculum to the nucleus accumbens shell projection in a novel ethanol self-administration choice paradigmF31AA032154 · NIAAA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Olivia Colarusso · 2024 to 2026
$149k
NIAAA NIH HHS F31 AA032154NIAAA NIH HHS P50 AA026117NIAAA NIH HHS R01 AA026551NIAAA NIH HHS R37 AA017531NINDS NIH HHS T32 NS115704
6 · The paper itself

Abstract

Investigating how environmental factors, such as the availability of non-ethanol alternative reinforcers, influences ethanol self-administration is critical for understanding the pathology of alcohol use disorder (AUD). Here we established the first operant choice paradigm that leverages the strengths of the sipper tube self-administration model to investigate how concurrent access to sucrose altered ethanol self-administration in male and female Long Evans rats. Choice behavior was examined using two distinct paradigms, including a novel adaptation of the response requirement paradigm. Under both a fixed-ratio or response requirement paradigm, we observed that concurrent availability of an alternative reinforcer significantly reduced appetitive and consummatory ethanol drinking-related behaviors. Furthermore, we assessed the sensitivity of the response requirement choice paradigm by administering the pharmacological stressor yohimbine and by altering the taste of the ethanol solution. Yohimbine administration non-selectively increased ethanol and sucrose intake, but not seeking, while taste adulteration decreased ethanol seeking and intake. These experiments demonstrate the utility of two concurrent choice paradigms that can more accurately capture AUD-like phenotypes, such as ethanol-directed choice in the face of alternative reinforcers. Future studies should investigate how models of vulnerability and dependence alter ethanol choice behavior under these paradigms.

Indexed as

ChoiceEthanolSelf-administrationSex differencesSucrose

Identifiers

PMID40161352
PMCPMC11951412

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.