Exercise adaptations: molecular mechanisms and potential targets for therapeutic benefit

Nat Rev Endocrinol. 2020 Sep;16(9):495-505. doi: 10.1038/s41574-020-0377-1. Epub 2020 Jul 6.

Abstract

Exercise is fundamental for good health, whereas physical inactivity underpins many chronic diseases of modern society. It is well appreciated that regular exercise improves metabolism and the metabolic phenotype in a number of tissues. The phenotypic alterations observed in skeletal muscle are partly mediated by transcriptional responses that occur following each individual bout of exercise. This adaptive response increases oxidative capacity and influences the function of myokines and extracellular vesicles that signal to other tissues. Our understanding of the epigenetic and transcriptional mechanisms that mediate the skeletal muscle gene expression response to exercise as well as of their upstream signalling pathways has advanced substantially in the past 10 years. With this knowledge also comes the opportunity to design new therapeutic strategies based on the biology of exercise for a variety of chronic conditions where regular exercise might be a challenge. This Review provides an overview of the beneficial adaptive responses to exercise and details the molecular mechanisms involved. The possibility of designing therapeutic interventions based on these molecular mechanisms is addressed, using relevant examples that have exploited this approach.

Publication types

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

MeSH terms

  • AMP-Activated Protein Kinases / metabolism
  • Adaptation, Physiological
  • Animals
  • Chronic Disease / prevention & control*
  • Endocrine Glands / physiology
  • Epigenesis, Genetic
  • Exercise / physiology*
  • Gene Expression
  • Health Promotion*
  • Histone Deacetylases / metabolism
  • Humans
  • Muscle, Skeletal / physiology
  • Physical Conditioning, Animal / physiology
  • Signal Transduction / physiology
  • Transcription, Genetic / physiology

Substances

  • AMP-Activated Protein Kinases
  • Histone Deacetylases