Diabetes-Induced Dysfunction of Mitochondria and Stem Cells in Skeletal Muscle and the Nervous System

Int J Mol Sci. 2017 Oct 14;18(10):2147. doi: 10.3390/ijms18102147.

Abstract

Diabetes mellitus is one of the most common metabolic diseases spread all over the world, which results in hyperglycemia caused by the breakdown of insulin secretion or insulin action or both. Diabetes has been reported to disrupt the functions and dynamics of mitochondria, which play a fundamental role in regulating metabolic pathways and are crucial to maintain appropriate energy balance. Similar to mitochondria, the functions and the abilities of stem cells are attenuated under diabetic condition in several tissues. In recent years, several studies have suggested that the regulation of mitochondria functions and dynamics is critical for the precise differentiation of stem cells. Importantly, physical exercise is very useful for preventing the diabetic alteration by improving the functions of both mitochondria and stem cells. In the present review, we provide an overview of the diabetic alterations of mitochondria and stem cells and the preventive effects of physical exercise on diabetes, focused on skeletal muscle and the nervous system. We propose physical exercise as a countermeasure for the dysfunction of mitochondria and stem cells in several target tissues under diabetes complication and to improve the physiological function of patients with diabetes, resulting in their quality of life being maintained.

Keywords: diabetes; exercise; mitochondria; neural stem cells; satellite cells.

Publication types

  • Review

MeSH terms

  • Animals
  • Cell Differentiation
  • Diabetes Mellitus / metabolism*
  • Diabetes Mellitus / prevention & control
  • Energy Metabolism
  • Exercise
  • Humans
  • Mitochondria / metabolism*
  • Mitochondrial Dynamics
  • Muscle, Skeletal / metabolism
  • Neural Stem Cells / cytology
  • Neural Stem Cells / metabolism*
  • Neurogenesis
  • Reactive Oxygen Species / metabolism
  • Satellite Cells, Skeletal Muscle / cytology
  • Satellite Cells, Skeletal Muscle / metabolism*

Substances

  • Reactive Oxygen Species