Evidence map›Paper›PMID 41692411›Full record

ArticleJournal of the American Association for Laboratory Animal Science : JAALAS2026

Cuprizone in Peanut Butter: An Alternative Method of Cuprizone Administration to Model Demyelination of the Central Nervous System.

Brooke Hawker, Ethan Chiddicks, Jack Flanagan, Bronwen Connor, Amy McCaughey-Chapman

Abstract read
In one paragraph

Article in Journal of the American Association for Laboratory Animal Science : JAALAS, 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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0cells of the map it votes in
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.

Brooke HawkerDepartment of Pharmacology and Clinical Pharmacology, Centre for Brain Research, School of Medical Science, Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand.
Ethan ChiddicksDepartment of Pharmacology and Clinical Pharmacology, Centre for Brain Research, School of Medical Science, Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand.
Jack FlanaganDepartment of Pharmacology and Clinical Pharmacology, Centre for Brain Research, School of Medical Science, Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand.
Bronwen ConnorDepartment of Pharmacology and Clinical Pharmacology, Centre for Brain Research, School of Medical Science, Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand.
Amy McCaughey-ChapmanDepartment of Pharmacology and Clinical Pharmacology, Centre for Brain Research, School of Medical Science, Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Modeling disease in rodents is essential for preclinical research, particularly in the development of drugs and therapies. Traditional disease modeling approaches often rely on invasive and stressful procedures such as repeated injections and/or surgical approaches. These methods raise welfare concerns and can introduce stress-related variables that compromise model reliability. Cuprizone (CPZ) is a copper-chelating compound widely used to induce CNS demyelination in mice over a 6-week period via incorporation into ground rodent chow. However, the presumed adverse taste of CPZ reduces food intake, resulting in weight loss, inconsistent consumption, and variable levels of demyelination, complicating disease comparison. To address this, we proposed that mixing CPZ into peanut butter (CPZ-PB) would promote voluntary intake, standardize daily dosing, and minimize weight loss, while maintaining effective demyelination. Thirty mice were divided into control, CPZ-PB, or CPZ-chow groups and received treatment daily for 6 weeks. Body weight and CPZ intake were recorded daily. The effect of demyelination through mechanical allodynia was assessed via the dynamic plantar aesthesiometer. Immunohistochemical analysis of myelin proteins and astrocyte activation was conducted on the brain and spinal cord after 6 weeks of treatment. Voluntary consumption of CPZ-PB successfully ameliorated weight loss concerns and achieved consistent daily CPZ dosing. Behavioral and immunohistochemical analyses confirmed effective demyelination comparable to traditional CPZ-chow methods. This study introduces an improved CPZ administration strategy that enhances animal welfare and provides a more reliable model for demyelination research.

Indexed as

CPZ, cuprizoneDPA, dynamic plantar aesthesiometerPB, peanut butter

Identifiers

PMID41692411
PMCPMC13086187

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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.