Evidence map›Paper›PMID 25825489›Full record

ArticleThe Journal of biological chemistry2015

Nox2 mediates skeletal muscle insulin resistance induced by a high fat diet.

Alvaro Souto Padron de Figueiredo, Adam B Salmon, Francesca Bruno, Fabio Jimenez, Herman G Martinez, Ganesh V Halade, Seema S Ahuja, Robert A Clark, Ralph A DeFronzo, Hanna E Abboud and 1 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed, 1 pooled it
6.4field-weighted citation impact, top 3% 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

52 citing papers in PubMed, 1 synthesis or guideline pooled it, 79 citations in OpenAlex.

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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

11 authors at 3 institutions in 1 country.

Alvaro Souto Padron de FigueiredoFrom the Department of Medicine, University of Texas Health Science Center, San Antonio, Texas 78229-3900.
Adam B SalmonThe Sam and Ann Barshop Institute for Longevity and Aging Studies 15355 Lambda Drive, San Antonio, Texas 78245, and Audie L. Murphy Hospital, South Texas Veterans Health Care System, San Antonio, Texas 78229-3900.
Francesca BrunoFrom the Department of Medicine, University of Texas Health Science Center, San Antonio, Texas 78229-3900.
Fabio JimenezFrom the Department of Medicine, University of Texas Health Science Center, San Antonio, Texas 78229-3900.
Herman G MartinezFrom the Department of Medicine, University of Texas Health Science Center, San Antonio, Texas 78229-3900.
Ganesh V HaladeFrom the Department of Medicine, University of Texas Health Science Center, San Antonio, Texas 78229-3900.
Seema S AhujaFrom the Department of Medicine, University of Texas Health Science Center, San Antonio, Texas 78229-3900, Audie L. Murphy Hospital, South Texas Veterans Health Care System, San Antonio, Texas 78229-3900.
Robert A ClarkFrom the Department of Medicine, University of Texas Health Science Center, San Antonio, Texas 78229-3900, Audie L. Murphy Hospital, South Texas Veterans Health Care System, San Antonio, Texas 78229-3900.
Ralph A DeFronzoFrom the Department of Medicine, University of Texas Health Science Center, San Antonio, Texas 78229-3900, Audie L. Murphy Hospital, South Texas Veterans Health Care System, San Antonio, Texas 78229-3900.
Hanna E AbboudFrom the Department of Medicine, University of Texas Health Science Center, San Antonio, Texas 78229-3900, Audie L. Murphy Hospital, South Texas Veterans Health Care System, San Antonio, Texas 78229-3900.
Amina El JamaliFrom the Department of Medicine, University of Texas Health Science Center, San Antonio, Texas 78229-3900, AkoulouzeBik@uthscsa.edu.
The University of Texas Health Science Center at San Antonio · USSouth Texas Veterans Health Care System · USMurphy Oil Corporation (United States) · US

Funding

TISSUE CULTURE---COREP30CA054174 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Lei Zheng · 1991 to 2026
$59.1M
TRANSGENIC COREP30AG013319 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI PETER J HORNSBY · 1995 to 2026
$30.6M
Institute for Integration of Medicine & Science: A Partnership to Improve HealthUL1TR001120 · NCATS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI CLARK, ROBERT A, HARGREAVES, KENNETH M · 2013 to 2017
$16.5M
ROLE OF CASPASE-2 IN OSTEOCOLAST APOPTOSIS AGE-EePENDENT OSTEOPOROSISP01AG019316 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI HERMAN, BRIAN A. · 2001 to 2011
$11.3M
PATHOBIOLOGY OF OCCLUSIVE VASCULAR DISEASET32HL007446 · NHLBI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Jean Chrisostome Bopassa · 1985 to 2026
$8.9M
Institute for Integration of Medicine & Science: A Partnership to Improve HealthUL1TR000149 · NCATS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI CLARK, ROBERT A · 2012 to 2013
$6.8M
Tubular epithelial cell injuryR01DK033665 · NIDDK · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI GORIN, YVES CLAUDE · 1986 to 2015
$1.3M
Institute for Integration of Medicine & Science: A Partnership to Improve HealthKL2TR000118 · NCATS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI CLARK, ROBERT A · 2012 to 2013
$757k
Role of NADPH oxidase in insulin resistanceK01DK084297 · NIDDK · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI EL JAMALI, AMINA · 2011 to 2013
$393k
NCATS NIH HHS KL2 TR000118NCATS NIH HHS KL2-TR000118NCATS NIH HHS UL1 TR000149NCATS NIH HHS UL1-TR000149NCATS NIH HHS UL1 TR001120NCI NIH HHS P30 CA054174NHLBI NIH HHS T32 HL007446NHLBI NIH HHS T32-HL007446NIA NIH HHS P01 AG019316NIA NIH HHS P30 AG013319NIDDK NIH HHS K01 DK084297NIDDK NIH HHS R01 DK033665NIDDK NIH HHS R01 DK033665-24
6 · The paper itself

Abstract

Inflammation and oxidative stress through the production of reactive oxygen species (ROS) are consistently associated with metabolic syndrome/type 2 diabetes. Although the role of Nox2, a major ROS-generating enzyme, is well described in host defense and inflammation, little is known about its potential role in insulin resistance in skeletal muscle. Insulin resistance induced by a high fat diet was mitigated in Nox2-null mice compared with wild-type mice after 3 or 9 months on the diet. High fat feeding increased Nox2 expression, superoxide production, and impaired insulin signaling in skeletal muscle tissue of wild-type mice but not in Nox2-null mice. Exposure of C2C12 cultured myotubes to either high glucose concentration, palmitate, or H2O2 decreases insulin-induced Akt phosphorylation and glucose uptake. Pretreatment with catalase abrogated these effects, indicating a key role for H2O2 in mediating insulin resistance. Down-regulation of Nox2 in C2C12 cells by shRNA prevented insulin resistance induced by high glucose or palmitate but not H2O2. These data indicate that increased production of ROS in insulin resistance induced by high glucose in skeletal muscle cells is a consequence of Nox2 activation. This is the first report to show that Nox2 is a key mediator of insulin resistance in skeletal muscle.

Indexed as

Diet, High-FatInsulin ResistanceAnimalsApoptosisBlotting, WesternCells, CulturedDown-RegulationGene Expression ProfilingGlucoseHypoglycemic AgentsInsulinMaleMembrane GlycoproteinsMiceMice, KnockoutMuscle Fibers, SkeletalCybb protein, mouseGlucoseHypoglycemic AgentsInsulinMembrane GlycoproteinsNADPH Oxidase 2NADPH OxidasesPalmitatesReactive Oxygen SpeciesRNA, MessengerSweetening AgentsDiabetesInsulin ResistanceNADPH OxidaseReactive Oxygen Species (ROS)Skeletal MuscleSuperoxide Ion

Identifiers

PMID25825489
PMCPMC4505590
OpenAlexW1977875320

What OpenQuestion holds

Textmetadata
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.