Physiological extremes of the human blood metabolome: A metabolomics analysis of highly glycolytic, oxidative, and anabolic athletes.


Journal

Physiological reports
ISSN: 2051-817X
Titre abrégé: Physiol Rep
Pays: United States
ID NLM: 101607800

Informations de publication

Date de publication:
06 2021
Historique:
revised: 01 05 2021
received: 27 01 2021
accepted: 04 05 2021
entrez: 21 6 2021
pubmed: 22 6 2021
medline: 29 1 2022
Statut: ppublish

Résumé

Human metabolism is highly variable. At one end of the spectrum, defects of enzymes, transporters, and metabolic regulation result in metabolic diseases such as diabetes mellitus or inborn errors of metabolism. At the other end of the spectrum, favorable genetics and years of training combine to result in physiologically extreme forms of metabolism in athletes. Here, we investigated how the highly glycolytic metabolism of sprinters, highly oxidative metabolism of endurance athletes, and highly anabolic metabolism of natural bodybuilders affect their serum metabolome at rest and after a bout of exercise to exhaustion. We used targeted mass spectrometry-based metabolomics to measure the serum concentrations of 151 metabolites and 43 metabolite ratios or sums in 15 competitive male athletes (6 endurance athletes, 5 sprinters, and 4 natural bodybuilders) and 4 untrained control subjects at fasted rest and 5 minutes after a maximum graded bicycle test to exhaustion. The analysis of all 194 metabolite concentrations, ratios and sums revealed that natural bodybuilders and endurance athletes had overall different metabolite profiles, whereas sprinters and untrained controls were more similar. Specifically, natural bodybuilders had 1.5 to 1.8-fold higher concentrations of specific phosphatidylcholines and lower levels of branched chain amino acids than all other subjects. Endurance athletes had 1.4-fold higher levels of a metabolite ratio showing the activity of carnitine-palmitoyl-transferase I and 1.4-fold lower levels of various alkyl-acyl-phosphatidylcholines. When we compared the effect of exercise between groups, endurance athletes showed 1.3-fold higher increases of hexose and of tetradecenoylcarnitine (C14:1). In summary, physiologically extreme metabolic capacities of endurance athletes and natural bodybuilders are associated with unique blood metabolite concentrations, ratios, and sums at rest and after exercise. Our results suggest that long-term specific training, along with genetics and other athlete-specific factors systematically change metabolite concentrations at rest and after exercise.

Identifiants

pubmed: 34152092
doi: 10.14814/phy2.14885
pmc: PMC8215680
doi:

Substances chimiques

Blood Proteins 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e14885

Subventions

Organisme : NIA NIH HHS
ID : U19 AG063744
Pays : United States
Organisme : NIA NIH HHS
ID : RF1 AG059093
Pays : United States
Organisme : NIA NIH HHS
ID : U01 AG061359
Pays : United States
Organisme : NIA NIH HHS
ID : RF1 AG057452
Pays : United States
Organisme : NIA NIH HHS
ID : RF1 AG058942
Pays : United States

Informations de copyright

© 2021 The Authors. Physiological Reports published by Wiley Periodicals LLC on behalf of The Physiological Society and the American Physiological Society.

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Auteurs

Daniela Schranner (D)

Exercise Biology, Department of Sport and Health Sciences, Technische Universität München, Munich, Germany.

Martin Schönfelder (M)

Exercise Biology, Department of Sport and Health Sciences, Technische Universität München, Munich, Germany.

Werner Römisch-Margl (W)

Institute of Computational Biology, Helmholtz Zentrum München, Neuherberg, Germany.

Johannes Scherr (J)

University Center for Prevention and Sports Medicine, University Hospital Balgrist, Universität Zürich, Zurich, Switzerland.

Jürgen Schlegel (J)

Department of Neuropathology, Institute of Pathology, Technische Universität München, Munich, Germany.

Otto Zelger (O)

Department of Prevention and Sports Medicine, Technische Universität München, Munich, Germany.

Annett Riermeier (A)

Exercise Biology, Department of Sport and Health Sciences, Technische Universität München, Munich, Germany.

Stephanie Kaps (S)

Exercise Biology, Department of Sport and Health Sciences, Technische Universität München, Munich, Germany.

Cornelia Prehn (C)

Research Unit Molecular Endocrinology and Metabolism, Helmholtz Zentrum München, Neuherberg, Germany.

Jerzy Adamski (J)

Research Unit Molecular Endocrinology and Metabolism, Helmholtz Zentrum München, Neuherberg, Germany.
German Center for Diabetes Research, Neuherberg, Germany.
Chair of Experimental Genetics, Technische Universität München, Freising-Weihenstephan, Germany.
Department of Biochemistry, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.

Quirin Söhnlein (Q)

Exercise Biology, Department of Sport and Health Sciences, Technische Universität München, Munich, Germany.

Fabian Stöcker (F)

Teaching and Educational Lab, Department of Sport and Health Sciences, Technische Universität München, Munich, Germany.

Florian Kreuzpointner (F)

Prevention Center, Department of Sport and Health Sciences, Technische Universität München, Munich, Germany.

Martin Halle (M)

Department of Prevention and Sports Medicine, Technische Universität München, Munich, Germany.

Gabi Kastenmüller (G)

Institute of Computational Biology, Helmholtz Zentrum München, Neuherberg, Germany.
German Center for Diabetes Research, Neuherberg, Germany.

Henning Wackerhage (H)

Exercise Biology, Department of Sport and Health Sciences, Technische Universität München, Munich, Germany.

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