Evidence map›Paper›PMID 38178638›Full record

ArticleMetallomics : integrated biometal science2024

Evidence for decreased copper associated with demyelination in the corpus callosum of cuprizone-treated mice.

James B W Hilton, Kai Kysenius, Jeffrey R Liddell, Stephen W Mercer, Dominic J Hare, Gojko Buncic, Bence Paul, YouJia Wang, Simon S Murray, Trevor J Kilpatrick and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Metallomics : integrated biometal science, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
4.3field-weighted citation impact, top 5% of its field
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

10 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Copper homeostasis and cuproptosis in Alzheimer's disease (Review).International journal of molecular medicine · 2025
    Review
  7. Review
  8. Article
  9. Article
  10. Integrated elemental analysis supports targeting copper perturbations as a therapeutic strategy in multiple sclerosis.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2024
    Article
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

13 authors at 5 institutions in 2 countries.

James B W HiltonDepartment of Anatomy & Physiology, The University of Melbourne, Victoria 3010, Australia.
Kai KyseniusDepartment of Anatomy & Physiology, The University of Melbourne, Victoria 3010, Australia.
Jeffrey R LiddellDepartment of Anatomy & Physiology, The University of Melbourne, Victoria 3010, Australia.
Stephen W MercerDepartment of Anatomy & Physiology, The University of Melbourne, Victoria 3010, Australia.
Dominic J HareAtomic Medicine Initiative, University of Technology Sydney, Sydney, New South Wales 2007, Australia.
Gojko BuncicSchool of Chemistry and Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, Victoria 3010, Australia.
Bence PaulSchool of Earth Sciences, The University of Melbourne, Victoria 3010, Australia.
YouJia WangDepartment of Anatomy & Physiology, The University of Melbourne, Victoria 3010, Australia.
Simon S MurrayDepartment of Anatomy & Physiology, The University of Melbourne, Victoria 3010, Australia.
Trevor J KilpatrickDepartment of Anatomy & Physiology, The University of Melbourne, Victoria 3010, Australia.
Anthony R WhiteQueensland Institute of Medical Research Berghofer, Herston, Queensland 4006, Australia.
Paul S DonnellySchool of Chemistry and Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, Victoria 3010, Australia.
Peter J CrouchDepartment of Anatomy & Physiology, The University of Melbourne, Victoria 3010, Australia.
The University of Melbourne · AUBiotechnology Institute · USFlorey Institute of Neuroscience and Mental Health · AUQIMR Berghofer Medical Research Institute · AUUniversity of Technology Sydney · AU

Funding

Agilent TechnologiesAustralian Research CouncilMichael Hirshorn Medical Research Commercialisation FundNHMRC 1084927
6 · The paper itself

Abstract

Demyelination within the central nervous system (CNS) is a significant feature of debilitating neurological diseases such as multiple sclerosis and administering the copper-selective chelatorcuprizone to mice is widely used to model demyelination in vivo. Conspicuous demyelination within the corpus callosum is generally attributed to cuprizone's ability to restrict copper availability in this vulnerable brain region. However, the small number of studies that have assessed copper in brain tissue from cuprizone-treated mice have produced seemingly conflicting outcomes, leaving the role of CNS copper availability in demyelination unresolved. Herein we describe our assessment of copper concentrations in brain samples from mice treated with cuprizone for 40 d. Importantly, we applied an inductively coupled plasma mass spectrometry methodology that enabled assessment of copper partitioned into soluble and insoluble fractions within distinct brain regions, including the corpus callosum. Our results show that cuprizone-induced demyelination in the corpus callosum was associated with decreased soluble copper in this brain region. Insoluble copper in the corpus callosum was unaffected, as were pools of soluble and insoluble copper in other brain regions. Treatment with the blood-brain barrier permeant copper compound CuII(atsm) increased brain copper levels and this was most pronounced in the soluble fraction of the corpus callosum. This effect was associated with significant mitigation of cuprizone-induced demyelination. These results provide support for the involvement of decreased CNS copper availability in demyelination in the cuprizone model. Relevance to human demyelinating disease is discussed.

Indexed as

CuprizoneDemyelinating DiseasesAnimalsCopperCorpus CallosumDisease Models, AnimalHumansMiceMice, Inbred C57BLMyelin SheathOligodendrogliaCopperCuprizonecoppercorpus callosumCu(atsm)cuprizonedemyelinationmultiple sclerosismyelinprotectiontherapy

Identifiers

PMID38178638
PMCPMC10797489
OpenAlexW4390600907

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.