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Reduced insulin action in muscle of high fat diet rats over the diurnal cycle is not associated with defective insulin signaling

OBJECTIVE: Energy metabolism and insulin action follow a diurnal rhythm. It is therefore important that investigations into dysregulation of these pathways are relevant to the physiology of this diurnal rhythm. METHODS: We examined glucose uptake, markers of insulin action, and the phosphorylation o...

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Detalles Bibliográficos
Autores principales: Small, Lewin, Brandon, Amanda E., Parker, Benjamin L., Deshpande, Vinita, Samsudeen, Azrah F., Kowalski, Greg M., Reznick, Jane, Wilks, Donna L., Preston, Elaine, Bruce, Clinton R., James, David E., Turner, Nigel, Cooney, Gregory J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6600078/
https://www.ncbi.nlm.nih.gov/pubmed/31029696
http://dx.doi.org/10.1016/j.molmet.2019.04.006
Descripción
Sumario:OBJECTIVE: Energy metabolism and insulin action follow a diurnal rhythm. It is therefore important that investigations into dysregulation of these pathways are relevant to the physiology of this diurnal rhythm. METHODS: We examined glucose uptake, markers of insulin action, and the phosphorylation of insulin signaling intermediates in muscle of chow and high fat, high sucrose (HFHS) diet-fed rats over the normal diurnal cycle. RESULTS: HFHS animals displayed hyperinsulinemia but had reduced systemic glucose disposal and lower muscle glucose uptake during the feeding period. Analysis of gene expression, enzyme activity, protein abundance and phosphorylation revealed a clear diurnal regulation of substrate oxidation pathways with no difference in Akt signaling in muscle. Transfection of a constitutively active Akt2 into the muscle of HFHS rats did not rescue diet-induced reductions in insulin-stimulated glucose uptake. CONCLUSIONS: These studies suggest that reduced glucose uptake in muscle during the diurnal cycle induced by short-term HFHS-feeding is not the result of reduced insulin signaling.