Evidence map›Paper›PMID 24947366›Full record

ArticleDiabetes2014

Heterozygous SOD2 deletion impairs glucose-stimulated insulin secretion, but not insulin action, in high-fat-fed mice.

Li Kang, Chunhua Dai, Mary E Lustig, Jeffrey S Bonner, Wesley H Mayes, Shilpa Mokshagundam, Freyja D James, Courtney S Thompson, Chien-Te Lin, Christopher G R Perry and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Diabetes, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.8field-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

25 citing papers in PubMed, 46 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
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  9. Article
  10. Article
  11. Can antioxidants be effective therapeutics for type 2 diabetes?Yeungnam University journal of medicine · 2021
    Article
  12. Article
  13. Article
  14. Review
  15. Diabetes, metabolic syndrome and obesity : targets and therapy · 2018
    Article
  16. Astragalus polysaccharides improve cardiomyopathy in STZ-induced diabetic mice and heterozygous (SOD2+/-) knockout mice.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2017
    Article
  17. Article
  18. Article
  19. Article
  20. SIRT3 regulates progression and development of diseases of aging.Trends in endocrinology and metabolism: TEM · 2015
    Review
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

14 authors at 3 institutions in 1 country.

Li KangDepartment of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN Mouse Metabolic Phenotyping Center, Vanderbilt University, Nashville, TN Division of Cardiovascular and Diabetes Medicine, Ninewells Hospital and Medical School, University of Dundee, Dundee, U.K. l.kang@dundee.ac.uk.
Chunhua DaiDivision of Diabetes, Endocrinology, and Metabolism, Department of Medicine, Vanderbilt University, Nashville, TN.
Mary E LustigDepartment of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN.
Jeffrey S BonnerDepartment of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN.
Wesley H MayesDepartment of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN.
Shilpa MokshagundamDepartment of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN.
Freyja D JamesDepartment of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN.
Courtney S ThompsonDivision of Diabetes, Endocrinology, and Metabolism, Department of Medicine, Vanderbilt University, Nashville, TN.
Chien-Te LinEast Carolina Diabetes and Obesity Institute and Departments of Physiology and Kinesiology, East Carolina University, Greenville, NC.
Christopher G R PerryEast Carolina Diabetes and Obesity Institute and Departments of Physiology and Kinesiology, East Carolina University, Greenville, NC.
Ethan J AndersonEast Carolina Diabetes and Obesity Institute and Departments of Physiology and Kinesiology, East Carolina University, Greenville, NC.
P Darrell NeuferEast Carolina Diabetes and Obesity Institute and Departments of Physiology and Kinesiology, East Carolina University, Greenville, NC.
David H WassermanDepartment of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN Mouse Metabolic Phenotyping Center, Vanderbilt University, Nashville, TN.
Alvin C PowersDepartment of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN Division of Diabetes, Endocrinology, and Metabolism, Department of Medicine, Vanderbilt University, Nashville, TN Veterans Affairs Tennessee Valley Healthcare System, Nashville, TN.
Vanderbilt University · USEast Carolina University · USVA Tennessee Valley Healthcare System · US

Funding

Coordinating Center for Beta Cell Biology ConsortiumU01DK072473 · NIDDK · VANDERBILT UNIVERSITY · PI MAGNUSON, MARK A · 2005 to 2014
$61.0M
Vanderbilt Diabetes Research CenterP30DK020593 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Marcela Brissova · 2012 to 2026
$29.3M
TRANSGENIC MOUSE/ ES CELL SHARES RESOURCESP60DK020593 · NIDDK · VANDERBILT UNIVERSITY · PI ELASY, TOM A · 1986 to 2011
$28.1M
Vanderbilt Mouse Metabolic Physiology CenterU24DK059637 · NIDDK · VANDERBILT UNIVERSITY · PI WASSERMAN, DAVID H · 2001 to 2015
$14.9M
Molecular Mechanisms of Human and Murine Beta Cell Proliferation and RegenerationU01DK089572 · NIDDK · VANDERBILT UNIVERSITY · PI GREINER, DALE LESLIE, HARLAN, DAVID MARSHALL · 2010 to 2014
$8.4M
Vanderbilt Mouse Metabolic Phenotyping CenterU2CDK059637 · NIDDK · VANDERBILT UNIVERSITY · PI WASSERMAN, DAVID H · 2016 to 2021
$6.3M
INTEGRATED CONTROL OF MUSCLE GLUCOSE UPTAKE IN VIVOR01DK054902 · NIDDK · VANDERBILT UNIVERSITY · PI WASSERMAN, DAVID H · 1999 to 2020
$5.9M
Exercise and Fuel MetabolismR37DK050277 · NIDDK · VANDERBILT UNIVERSITY · PI WASSERMAN, DAVID H · 2008 to 2017
$4.2M
Multi-Disciplinary Approaches to Driving Therapeutic Human Beta Cell ReplicationU01DK089538 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI STEWART, ANDREW F. · 2010 to 2014
$3.6M
GLP-1 to Enhance Islet TransplantationR33DK066636 · NIDDK · VANDERBILT UNIVERSITY · PI POWERS, ALVIN C · 2005 to 2007
$1.5M
VEGF and Islet VascularizationR01DK069603 · NIDDK · VANDERBILT UNIVERSITY · PI POWERS, ALVIN C · 2005 to 2010
$1.3M
Mitochondrial Bioenergetics and Etiology of Insulin ResistanceR01DK073488 · NIDDK · EAST CAROLINA UNIVERSITY · PI NEUFER, P DARRELL · 2007 to 2010
$1.2M
BLRD VA I01 BX000666NIDDK NIH HHS DK-054902NIDDK NIH HHS DK-059637NIDDK NIH HHS DK-072473NIDDK NIH HHS DK-089538NIDDK NIH HHS DK-089572NIDDK NIH HHS DK-20593NIDDK NIH HHS DK-66636NIDDK NIH HHS DK-69603NIDDK NIH HHS P30 DK020593NIDDK NIH HHS P60 DK020593NIDDK NIH HHS R01 DK054902NIDDK NIH HHS R01 DK069603NIDDK NIH HHS R01 DK073488NIDDK NIH HHS R21 DK066636NIDDK NIH HHS R33 DK066636NIDDK NIH HHS R37 DK050277NIDDK NIH HHS R56 DK054902NIDDK NIH HHS U01 DK072473NIDDK NIH HHS U01 DK089538NIDDK NIH HHS U01 DK089572NIDDK NIH HHS U24 DK059637
6 · The paper itself

Abstract

Elevated reactive oxygen species (ROS) are linked to insulin resistance and islet dysfunction. Manganese superoxide dismutase (SOD2) is a primary defense against mitochondrial oxidative stress. To test the hypothesis that heterozygous SOD2 deletion impairs glucose-stimulated insulin secretion (GSIS) and insulin action, wild-type (sod2(+/+)) and heterozygous knockout mice (sod2(+/-)) were fed a chow or high-fat (HF) diet, which accelerates ROS production. Hyperglycemic (HG) and hyperinsulinemic-euglycemic (HI) clamps were performed to assess GSIS and insulin action in vivo. GSIS during HG clamps was equal in chow-fed sod2(+/-) and sod2(+/+) but was markedly decreased in HF-fed sod2(+/-). Remarkably, this impairment was not paralleled by reduced HG glucose infusion rate (GIR). Decreased GSIS in HF-fed sod2(+/-) was associated with increased ROS, such as superoxide ion. Surprisingly, insulin action determined by HI clamps did not differ between sod2(+/-) and sod2(+/+) of either diet. Since insulin action was unaffected, we hypothesized that the unchanged HG GIR in HF-fed sod2(+/-) was due to increased glucose effectiveness. Increased GLUT-1, hexokinase II, and phospho-AMPK protein in muscle of HF-fed sod2(+/-) support this hypothesis. We conclude that heterozygous SOD2 deletion in mice, a model that mimics SOD2 changes observed in diabetic humans, impairs GSIS in HF-fed mice without affecting insulin action.

Indexed as

AnimalsBlotting, WesternDiet, High-FatGlucoseInsulinMiceMice, Mutant StrainsMuscle, SkeletalOxidative StressReactive Oxygen SpeciesReverse Transcriptase Polymerase Chain ReactionSuperoxide DismutaseSuperoxide Dismutase 2SuperoxidesGlucoseInsulinReactive Oxygen SpeciesSuperoxide DismutaseSuperoxide Dismutase 2Superoxides

Identifiers

PMID24947366
PMCPMC4207395
OpenAlexW2137880351

What OpenQuestion 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 OpenQuestion graph.