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Insulin-Dependent H2O2 Production Is Higher in Muscle Fibers of Mice Fed with a High-Fat Diet.

Authors :
Espinosa, Alejandra
Campos, Cristian
Díaz-Vegas, Alexis
Galgani, José E.
Juretic, Nevenka
Osorio-Fuentealba, César
Bucarey, José L.
Tapia, Gladys
Valenzuela, Rodrigo
Contreras-Ferrat, Ariel
Llanos, Paola
Jaimovich, Enrique
Source :
International Journal of Molecular Sciences. Aug2013, Vol. 14 Issue 8, p15740-15754. 15p. 5 Diagrams.
Publication Year :
2013

Abstract

Insulin resistance is defined as a reduced ability of insulin to stimulate glucose utilization. C57BL/6 mice fed with a high-fat diet (HFD) are a model of insulin resistance. In skeletal muscle, hydrogen peroxide (H2O2) produced by NADPH oxidase 2 (NOX2) is involved in signaling pathways triggered by insulin. We evaluated oxidative status in skeletal muscle fibers from insulin-resistant and control mice by determining H2O2 generation (HyPer probe), reduced-to-oxidized glutathione ratio and NOX2 expression. After eight weeks of HFD, insulin-dependent glucose uptake was impaired in skeletal muscle fibers when compared with control muscle fibers. Insulin-resistant mice showed increased insulin-stimulated H2O2 release and decreased reduced-to-oxidized glutathione ratio (GSH/GSSG). In addition, p47phox and gp91phox (NOX2 subunits) mRNA levels were also high (~3-fold in HFD mice compared to controls), while protein levels were 6.8- and 1.6-fold higher, respectively. Using apocynin (NOX2 inhibitor) during the HFD feeding period, the oxidative intracellular environment was diminished and skeletal muscle insulin-dependent glucose uptake restored. Our results indicate that insulin-resistant mice have increased H2O2 release upon insulin stimulation when compared with control animals, which appears to be mediated by an increase in NOX2 expression. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
16616596
Volume :
14
Issue :
8
Database :
Academic Search Index
Journal :
International Journal of Molecular Sciences
Publication Type :
Academic Journal
Accession number :
89942133
Full Text :
https://doi.org/10.3390/ijms140815740