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

Mol Metab. 2019 Jul:25:107-118. doi: 10.1016/j.molmet.2019.04.006. Epub 2019 Apr 12.

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.

Keywords: Diurnal rhythms; Glucose uptake; Insulin action; Insulin signaling; Phosphoproteomics; Skeletal muscle.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blood Glucose
  • Circadian Rhythm / physiology*
  • Diet, High-Fat / adverse effects*
  • Disease Models, Animal
  • Energy Metabolism
  • Gene Expression
  • Insulin / metabolism*
  • Insulin Resistance / physiology
  • Male
  • Muscle, Skeletal / metabolism*
  • Phosphorylation
  • Proto-Oncogene Proteins c-akt / genetics
  • Proto-Oncogene Proteins c-akt / metabolism
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Wistar
  • Signal Transduction / physiology*

Substances

  • Blood Glucose
  • Insulin
  • RNA, Messenger
  • Akt2 protein, rat
  • Proto-Oncogene Proteins c-akt