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Insulin-Dependent H(2)O(2) Production Is Higher in Muscle Fibers of Mice Fed with a High-Fat Diet

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 (H(2)O(2)) produced by NADPH oxidase 2 (NOX2) is involved in signaling pathways trigger...

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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3759883/
https://www.ncbi.nlm.nih.gov/pubmed/23899788
http://dx.doi.org/10.3390/ijms140815740
Descripción
Sumario: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 (H(2)O(2)) 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 H(2)O(2) 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 H(2)O(2) release and decreased reduced-to-oxidized glutathione ratio (GSH/GSSG). In addition, p47(phox) and gp91(phox) (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 H(2)O(2) release upon insulin stimulation when compared with control animals, which appears to be mediated by an increase in NOX2 expression.