Skip to main content

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

Citation
Small, L., et al. “Reduced Insulin Action In Muscle Of High Fat Diet Rats Over The Diurnal Cycle Is Not Associated With Defective Insulin Signaling.”. Molecular Metabolism, pp. 107-118.
Center University of Michigan
Author Lewin Small, Amanda E Brandon, Benjamin L Parker, Vinita Deshpande, Azrah F Samsudeen, Greg M Kowalski, Jane Reznick, Donna L Wilks, Elaine Preston, Clinton R Bruce, David E James, Nigel Turner, Gregory J Cooney
Keywords Diurnal rhythms, Glucose uptake, Insulin action, Insulin Signaling, Phosphoproteomics, Skeletal muscle
Abstract

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.

Year of Publication
2019
Journal
Molecular metabolism
Volume
25
Number of Pages
107-118
Date Published
12/2019
ISSN Number
2212-8778
DOI
10.1016/j.molmet.2019.04.006
Alternate Journal
Mol Metab
PMID
31029696
PMCID
PMC6600078
Download citation