Evidence map›Paper›PMID 26266089›Full record

ArticleMolecular metabolism2015

Knockout of STAT3 in skeletal muscle does not prevent high-fat diet-induced insulin resistance.

Amanda T White, Samuel A LaBarge, Carrie E McCurdy, Simon Schenk

Open access · goldAbstract read
In one paragraph

Article in Molecular metabolism, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

21 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Antimicrobial Peptide LCN2 Inhibited UropathogenicInternational journal of molecular sciences · 2022
    Article
  7. Article
  8. Article
  9. Stat3 activation induces insulin resistance via a muscle-specific E3 ubiquitin ligase Fbxo40.American journal of physiology. Endocrinology and metabolism · 2020
    Article
  10. Article
  11. Germline or inducible knockout of p300 or CBP in skeletal muscle does not alter insulin sensitivity.American journal of physiology. Endocrinology and metabolism · 2019
    Article
  12. Article
  13. Article
  14. Induced Cre-mediated knockdown of Brca1 in skeletal muscle reduces mitochondrial respiration and prevents glucose intolerance in adult mice on a high-fat diet.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2018
    Article
  15. Review
  16. Article
  17. Skeletal muscle inflammation and insulin resistance in obesity.The Journal of clinical investigation · 2017
    Review
  18. STAT3 in the systemic inflammation of cancer cachexia.Seminars in cell & developmental biology · 2016
    Review
  19. Review
  20. 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

4 authors at 2 institutions in 1 country.

Amanda T WhiteDepartment of Orthopaedic Surgery, University of California San Diego, La Jolla, CA, USA ; Biomedical Sciences Graduate Program, University of California San Diego, La Jolla, CA, USA.
Samuel A LaBargeDepartment of Orthopaedic Surgery, University of California San Diego, La Jolla, CA, USA.
Carrie E McCurdyDepartment of Human Physiology, University of Oregon, Eugene, OR, USA.
Simon SchenkDepartment of Orthopaedic Surgery, University of California San Diego, La Jolla, CA, USA ; Biomedical Sciences Graduate Program, University of California San Diego, La Jolla, CA, USA.
University of California, San Diego · USUniversity of Oregon · US

Funding

Transgenic & Knock-out MouseP30DK063491 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Andrea L Hevener · 2003 to 2026
$40.4M
GRADUATE TRAINING IN CELLULAR &MOLECULAR PHARMACOLOGYT32GM007752 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI BROWN, JOAN HELLER, HANDEL, TRACY M · 1985 to 2023
$13.5M
National Center for Muscle Rehabilitation ResearchR24HD050837 · NICHD · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI LIEBER, RICHARD L., WARD, SAMUEL RICHARD · 2005 to 2014
$7.2M
San Diego Skeletal Muscle Research CenterP30AR061303 · NIAMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI CHEN, JU · 2011 to 2015
$3.3M
Role of STAT3 in muscle stem cell activationR01AR064873 · NIAMS · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI SACCO, ALESSANDRA · 2014 to 2018
$2.1M
SIRT1 and muscle insulin sensitivityR01AG043120 · NIA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI SCHENK, SIMON · 2012 to 2016
$1.6M
Role of PIK3R1 in Adipose Tissue Insulin Resistance and Inflammation in ObesityR01DK095926 · NIDDK · UNIVERSITY OF OREGON · PI MCCURDY, CARRIE E · 2014 to 2018
$1.5M
Muscle Triglyceride Metabolism Core CenterP30AR058878 · NIAMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI LIEBER, RICHARD L. · 2009 to 2010
$925k
NIAMS NIH HHS P30 AR058878NIAMS NIH HHS P30 AR061303NIAMS NIH HHS R01 AR064873NIA NIH HHS R01 AG043120NICHD NIH HHS R24 HD050837NIDDK NIH HHS P30 DK063491NIDDK NIH HHS R01 DK095926NIGMS NIH HHS T32 GM007752
6 · The paper itself

Abstract

objectiveIncreased signal transducer and activator of transcription 3 (STAT3) signaling has been implicated in the development of skeletal muscle insulin resistance, though its contribution, in vivo, remains to be fully defined. Therefore, the aim of this study was to determine whether knockout of skeletal muscle STAT3 would prevent high-fat diet (HFD)-induced insulin resistance.

methodsWe used Cre-LoxP methodology to generate mice with muscle-specific knockout (KO) of STAT3 (mKO). Beginning at 10 weeks of age, mKO mice and their wildtype/floxed (WT) littermates either continued consuming a low fat, control diet (CON; 10% of calories from fat) or were switched to a HFD (60% of calories from fat) for 20 days. We measured body composition, energy expenditure, oral glucose tolerance and in vivo insulin action using hyperinsulinemic-euglycemic clamps. We also measured insulin sensitivity in isolated soleus and extensor digitorum longus muscles using the 2-deoxy-glucose (2DOG) uptake technique.

resultsSTAT3 protein expression was reduced ∼75-100% in muscle from mKO vs. WT mice. Fat mass and body fat percentage did not differ between WT and mKO mice on CON and were increased equally by HFD. There were also no genotype differences in energy expenditure or whole-body fat oxidation. As determined, in vivo (hyperinsulinemic-euglycemic clamps) and ex vivo (2DOG uptake), skeletal muscle insulin sensitivity did not differ between CON-fed mice, and was impaired similarly by HFD.

conclusionsThese results demonstrate that STAT3 activation does not underlie the development of HFD-induced skeletal muscle insulin resistance.

Indexed as

2DOG, 2-deoxyglucoseAdgre1, adhesion G protein-coupled receptor E1AT, adipose tissueClampCON, normal chow, control dietCre-LoxPEDL, extensor digitorum longusGA, gastrocnemiusGIR, glucose infusion rateGlucose homeostasisHFD, high-fat dietHGP, hepatic glucose productionHYP-EUG, hyperinsulinemic-euglycemicIL, interleukinIn vivoIS-GDR, insulin-stimulated glucose disposal rateKO, knockoutMCK, muscle creatine kinasemKO, muscle-specific knockout of STAT3ObesitySTAT3STAT3, signal transducer and activator of transcription 3T2D, type 2 diabetesWT, wild-type

Identifiers

PMID26266089
PMCPMC4529495
OpenAlexW1580772264

What OpenQuestion holds

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LicenceCC BY-NC-ND
Read underepoch 390

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.