Evidence map›Paper›PMID 41887015›Full record

ArticleDrug and alcohol dependence2026

Effects of nonpharmacological manipulations and repeated xanomeline treatment on methamphetamine-vs-food choice in Sprague Dawley and Long Evans rats.

Amber N Baldwin, Matthew L Banks

Abstract read
In one paragraph

Article in Drug and alcohol dependence, 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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1 · What the graph read from it

What it found

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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

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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

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5 · Who and what money

Authors and funding

2 authors.

Amber N BaldwinDepartment of Pharmacology and Toxicology, Virginia Commonwealth University School of Medicine, Richmond, VA 23298, USA.
Matthew L BanksDepartment of Pharmacology and Toxicology, Virginia Commonwealth University School of Medicine, Richmond, VA 23298, USA. Electronic address: mbanks7@vcu.edu.

Funding

Pharmacology of Stimulant ChoiceR01DA055825 · NIDA · VIRGINIA COMMONWEALTH UNIVERSITY · PI Matthew L Banks, Jose Miguel Eltit · 2023 to 2026
$1.4M
NIDA NIH HHS R01 DA055825
6 · The paper itself

Abstract

backgroundThe absence of Food and Drug Administration (FDA)-approved pharmacotherapies for methamphetamine use disorder (MUD) highlights the need for preclinical research to understand both the basic biological mechanisms of methamphetamine reinforcement and evaluate novel MUD pharmacotherapies. Recent studies demonstrated that repeated treatment with the muscarinic receptor agonist xanomeline attenuated cocaine self-administration. Whether these xanomeline treatment effects extend to methamphetamine self-administration remains unknown.

methodsThe first aim established sensitivity of methamphetamine-vs-food choice in male and female Sprague Dawley (SD) and Long Evans (LE) rats to reinforcer magnitude and response requirement manipulations. A within-session methamphetamine choice dose-effect function (0.032-0.32mg/kg/infusion) was determined daily, and food reinforcer magnitude was manipulated weekly by changing the concentration (0, 10, 32, and 100%) of vanilla-flavored Ensure. Additionally, methamphetamine response requirement (i.e., fixed ratio (FR) 1, 5, 25, 125) was manipulated each week while holding the food FR constant. The second aim determined the effectiveness of repeated 5-day xanomeline (3.2-10mg/kg, SC) to attenuate methamphetamine choice.

resultsBoth increasing Ensure concentrations and methamphetamine FR values resulted in rightward shifts in the methamphetamine choice dose-effect function in both SD and LE rats. Repeated 5-day xanomeline treatment significantly decreased methamphetamine choice across all doses tested in LE, but not SD, rats. Time course of xanomeline treatment effectiveness revealed effects were greatest during the first 30min of choice session.

conclusionsThese results demonstrate that methamphetamine-vs-food choice was sensitive to parametric manipulations in rats and that xanomeline may warrant further consideration as a MUD pharmacotherapy.

Indexed as

Central Nervous System StimulantsChoice BehaviorFood PreferencesMethamphetamineMuscarinic AgonistsPyridinesAnimalsConditioning, OperantDose-Response Relationship, DrugFemaleMaleRatsRats, Long-EvansRats, Sprague-DawleyReinforcement, PsychologySelf AdministrationCentral Nervous System StimulantsMethamphetamineMuscarinic AgonistsPyridinesChoiceLong EvansMethamphetamineRatsReinforcer magnitude: Sprague DawleyXanomeline

Identifiers

PMID41887015
PMCPMC13138848

What Socratic 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 Socratic graph.