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

Mikael Flockhart, Lina C Nilsson, Senna Tais, Björn Ekblom, William Apró, Filip J Larsen, Mikael Flockhart, Lina C Nilsson, Senna Tais, Björn Ekblom, William Apró, Filip J Larsen

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.

Conflict of interest statement

Declaration of interests F.J.L. is co-founder of Silicon Valley Exercise Analytics, a company using data science to improve athletic performance. The company had no role in funding, data collection and analysis, or preparation of the manuscript. All other authors declare no conflict of interest.

Copyright © 2021 Elsevier Inc. All rights reserved.

Source: PubMed

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