Resistance training for diabetes prevention and therapy: experimental findings and molecular mechanisms

Biomed Res Int. 2013:2013:805217. doi: 10.1155/2013/805217. Epub 2013 Dec 22.

Abstract

Type 2 diabetes mellitus (T2D) is characterized by insulin resistance, impaired glycogen synthesis, lipid accumulation, and impaired mitochondrial function. Exercise training has received increasing recognition as a cornerstone in the prevention and treatment of T2D. Emerging research suggests that resistance training (RT) has the power to combat metabolic dysfunction in patients with T2D and seems to be an effective measure to improve overall metabolic health and reduce metabolic risk factors in diabetic patients. However, there is limited mechanistic insight into how these adaptations occur. This review provides an overview of the intervention data on the impact of RT on glucose metabolism. In addition, the molecular mechanisms that lead to adaptation in skeletal muscle in response to RT and that are associated with possible beneficial metabolic responses are discussed. Some of the beneficial adaptations exerted by RT include increased GLUT4 translocation in skeletal muscle, increased insulin sensitivity and hence restored metabolic flexibility. Increased energy expenditure and excess postexercise oxygen consumption in response to RT may be other beneficial effects. RT is increasingly establishing itself as an effective measure to improve overall metabolic health and reduce metabolic risk factors in diabetic patients.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Diabetes Mellitus, Type 2 / metabolism*
  • Diabetes Mellitus, Type 2 / pathology
  • Diabetes Mellitus, Type 2 / prevention & control
  • Exercise*
  • Glucose / metabolism*
  • Glucose Transporter Type 4 / metabolism
  • Glycogen / metabolism
  • Humans
  • Insulin Resistance
  • Muscles / metabolism
  • Oxygen / metabolism
  • Resistance Training*

Substances

  • Glucose Transporter Type 4
  • SLC2A4 protein, human
  • Glycogen
  • Glucose
  • Oxygen