Evidence map›Paper›PMID 25797622›Full record

ArticleBiochemical and biophysical research communications2015

Deficient copper concentrations in dried-defatted hepatic tissue from ob/ob mice: A potential model for study of defective copper regulation in metabolic liver disease.

Stephanie J Church, Paul Begley, Nina Kureishy, Selina McHarg, Paul N Bishop, David A Bechtold, Richard D Unwin, Garth J S Cooper

Open access · hybridAbstract read
In one paragraph

Article in Biochemical and biophysical research communications, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.2field-weighted citation impact, top 9% 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

14 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
  2. Article
  3. Full-length ATP7B reconstituted through proteinMolecular therapy. Methods & clinical development · 2022
    Article
  4. Article
  5. Copper Ionophores as Novel Antiobesity Therapeutics.Molecules (Basel, Switzerland) · 2020
    Article
  6. Review
  7. Chloride regulates dynamic NLRP3-dependent ASC oligomerization and inflammasome priming.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  8. Plasma metals as potential biomarkers in dementia: a case-control study in patients with sporadic Alzheimer's disease.Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine · 2018
    Article
  9. Micronutrients in Nonalcoholic Fatty Liver Disease Pathogenesis.Cellular and molecular gastroenterology and hepatology · 2018
    Review
  10. Low Hepatic Tissue Copper in Pediatric Nonalcoholic Fatty Liver Disease.Journal of pediatric gastroenterology and nutrition · 2017
    Article
  11. Thiol oxidase ability of copper ion is specifically retained upon chelation by aldose reductase.Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry · 2017
    Article
  12. Review
  13. In vivo bioluminescence imaging reveals copper deficiency in a murine model of nonalcoholic fatty liver disease.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  14. 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

8 authors at 3 institutions in 2 countries.

Stephanie J ChurchCentre for Advanced Discovery and Experimental Therapeutics, Central Manchester University Hospitals NHS Foundation Trust (CMFT), Manchester M13 9WL, United Kingdom; Centre for Endocrinology & Diabetes, Institute of Human Development, Manchester Academic Health Science Centre, University of Manchester, Manchester, United Kingdom.
Paul BegleyCentre for Advanced Discovery and Experimental Therapeutics, Central Manchester University Hospitals NHS Foundation Trust (CMFT), Manchester M13 9WL, United Kingdom; Centre for Endocrinology & Diabetes, Institute of Human Development, Manchester Academic Health Science Centre, University of Manchester, Manchester, United Kingdom.
Nina KureishyCentre for Advanced Discovery and Experimental Therapeutics, Central Manchester University Hospitals NHS Foundation Trust (CMFT), Manchester M13 9WL, United Kingdom; Centre for Endocrinology & Diabetes, Institute of Human Development, Manchester Academic Health Science Centre, University of Manchester, Manchester, United Kingdom.
Selina McHargCentre for Advanced Discovery and Experimental Therapeutics, Central Manchester University Hospitals NHS Foundation Trust (CMFT), Manchester M13 9WL, United Kingdom; Centre for Endocrinology & Diabetes, Institute of Human Development, Manchester Academic Health Science Centre, University of Manchester, Manchester, United Kingdom.
Paul N BishopCentre for Advanced Discovery and Experimental Therapeutics, Central Manchester University Hospitals NHS Foundation Trust (CMFT), Manchester M13 9WL, United Kingdom; Centre for Endocrinology & Diabetes, Institute of Human Development, Manchester Academic Health Science Centre, University of Manchester, Manchester, United Kingdom.
David A BechtoldFaculty of Life Sciences, University of Manchester, Manchester M13 9PT, United Kingdom.
Richard D UnwinCentre for Advanced Discovery and Experimental Therapeutics, Central Manchester University Hospitals NHS Foundation Trust (CMFT), Manchester M13 9WL, United Kingdom; Centre for Endocrinology & Diabetes, Institute of Human Development, Manchester Academic Health Science Centre, University of Manchester, Manchester, United Kingdom. Electronic address: r.unwin@manchester.ac.uk.
Garth J S CooperCentre for Advanced Discovery and Experimental Therapeutics, Central Manchester University Hospitals NHS Foundation Trust (CMFT), Manchester M13 9WL, United Kingdom; Centre for Endocrinology & Diabetes, Institute of Human Development, Manchester Academic Health Science Centre, University of Manchester, Manchester, United Kingdom; School of Biological Sciences, Faculty of Science, and Department of Medicine, Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand; Department of Pharmacology, Medical Sciences Division, University of Oxford, Oxford OX1 3QT, United Kingdom. Electronic address: g.cooper@auckland.ac.nz.
Manchester Academic Health Science Centre · GBUniversity of Auckland · NZUniversity of Manchester · GB

Funding

Biotechnology and Biological Sciences Research Council BB/I018654/1Medical Research Council MR/L010445/1
6 · The paper itself

Abstract

Ob/ob mice provide an animal model for non-alcoholic fatty liver disease/non-alcoholic steatohepatitis (NAFLD/NASH) in patients with obesity and type-2 diabetes. Low liver copper has been linked to hepatic lipid build-up (steatosis) in animals with systemic copper deficiency caused by low-copper diets. However, hepatic copper status in patients with NAFLD or NASH is uncertain, and a validated animal model useful for the study of hepatic copper regulation in common forms of metabolic liver disease is lacking. Here, we report parallel measurements of essential metal levels in whole-liver tissue and defatted-dried liver tissue from ob/ob and non-obese control mice. Measurements in whole-liver tissue from ob/ob mice at an age when they have developed NAFLD/NASH, provide compelling evidence for factitious lowering of copper and all other essential metals by steatosis, and so cannot be used to study hepatic metal regulation in this model. By marked contrast, metal measurements in defatted-dried liver samples reveal that most essential metals were actually normal and indicate specific lowering of copper in ob/ob mice, consistent with hepatic copper deficiency. Thus ob/ob mice can provide a model useful for the study of copper regulation in NAFLD and NASH, provided levels are measured in defatted-dried liver tissue.

Indexed as

AnimalsCopperFatsLiverLiver DiseasesMaleMass SpectrometryMiceMice, Inbred C57BLCopperFatsCopperDiabetesLiverNon-alcoholic fatty liver diseaseNon-alcoholic steatohepatitisObesity

Identifiers

PMID25797622
PMCPMC4427106
OpenAlexW2030922339

What OpenQuestion holds

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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.