Excessive exercise training causes mitochondrial functional impairment and decreases glucose tolerance in healthy volunteers

Cell Metab. 2021 May 4;33(5):957-970.e6. doi: 10.1016/j.cmet.2021.02.017. Epub 2021 Mar 18.

Abstract

Exercise training positively affects metabolic health through increased mitochondrial oxidative capacity and improved glucose regulation and is the first line of treatment in several metabolic diseases. However, the upper limit of the amount of exercise associated with beneficial therapeutic effects has not been clearly identified. Here, we used a training model with a progressively increasing exercise load during an intervention over 4 weeks. We closely followed changes in glucose tolerance, mitochondrial function and dynamics, physical exercise capacity, and whole-body metabolism. Following the week with the highest exercise load, we found a striking reduction in intrinsic mitochondrial function that coincided with a disturbance in glucose tolerance and insulin secretion. We also assessed continuous blood glucose profiles in world-class endurance athletes and found that they had impaired glucose control compared with a matched control group.

Trial registration: ClinicalTrials.gov NCT04753021.

Keywords: athletes; continuous glucose monitoring; exercise; exercise adaptations; glucose tolerance; high-intensity interval training; insulin resistance; metabolic dysfunction; mitochondria; mitochondrial dynamics; mitochondrial dysfunction.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Blood Glucose / analysis
  • Catalase / metabolism
  • Glucose Tolerance Test
  • Glucose Transporter Type 4 / metabolism
  • Glycogen / metabolism
  • Healthy Volunteers
  • Humans
  • Hydrogen Peroxide / metabolism
  • Mitochondria / metabolism*
  • Muscle, Skeletal / metabolism
  • Muscle, Skeletal / pathology
  • NF-E2-Related Factor 2 / metabolism
  • Oxidative Stress
  • Physical Endurance*
  • Superoxide Dismutase / metabolism

Substances

  • Blood Glucose
  • Glucose Transporter Type 4
  • NF-E2-Related Factor 2
  • NFE2L2 protein, human
  • Glycogen
  • Hydrogen Peroxide
  • Catalase
  • Superoxide Dismutase

Associated data

  • ClinicalTrials.gov/NCT04753021