Proteomic analysis of skeletal muscle in insulin-resistant mice: response to 6-week aerobic exercise

PLoS One. 2013;8(1):e53887. doi: 10.1371/journal.pone.0053887. Epub 2013 Jan 9.

Abstract

Aerobic exercise has beneficial effects on both weight control and skeletal muscle insulin sensitivity through a number of specific signaling proteins. To investigate the targets by which exercise exerts its effects on insulin resistance, an approach of proteomic screen was applied to detect the potential different protein expressions from skeletal muscle of insulin-resistant mice after prolonged aerobic exercise training and their sedentary controls. Eighteen C57BL/6 mice were divided into two groups: 6 mice were fed normal chow (NC) and 12 mice were fed high-fat diet (HFD) for 10 weeks to produce an IR model. The model group was then subdivided into HFD sedentary control (HC, n = 6) and HFD exercise groups (HE, n = 6). Mice in HE group underwent 6 weeks of treadmill running. After 6 weeks, mice were sacrificed and skeletal muscle was dissected. Total protein (n = 6, each group) was extracted and followed by citrate synthase, 2D proteome profile analysis and immunoblot. Fifteen protein spots were altered between the NC and HC groups and 23 protein spots were changed between the HC and HE groups significantly. The results provided an array of changes in protein abundance in exercise-trained skeletal muscle and also provided the basis for a new hypothesis regarding the mechanism of exercise ameliorating insulin resistance.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blood Glucose
  • Diet, High-Fat
  • Energy Metabolism
  • Insulin / metabolism
  • Insulin Resistance / genetics
  • Insulin Resistance / physiology*
  • Mice
  • Muscle, Skeletal / metabolism*
  • Physical Conditioning, Animal*
  • Proteins* / metabolism
  • Proteins* / physiology
  • Proteomics

Substances

  • Blood Glucose
  • Insulin
  • Proteins

Grants and funding

This work was supported by grants from the National Natural Science Foundation of China (NSFC) 30871213 (to LF), 31100856 (to YMN), Tianjin Municipal Science and Technology Commission 09JCZDJC17400 (to LF) and 09ZCZDSF04500 (to WYN). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.