Sustained Endurance Training Leads to Metabolomic Adaptation

Endurance training induces several adaptations in substrate metabolism, especially in relation to glycogen conservation. The study aimed to investigate differences in the metabolism of lipids, lipid-like substances, and amino acids between highly trained and untrained subjects using targeted metabol...

Full description

Bibliographic Details
Main Authors: Astrid Weiss, Katharina Alack, Stephan Klatt, Sven Zukunft, Ralph Schermuly, Torsten Frech, Frank-Christoph Mooren, Karsten Krüger
Format: Article
Language:English
Published: MDPI AG 2022-07-01
Series:Metabolites
Subjects:
Online Access:https://www.mdpi.com/2218-1989/12/7/658
_version_ 1797445232937140224
author Astrid Weiss
Katharina Alack
Stephan Klatt
Sven Zukunft
Ralph Schermuly
Torsten Frech
Frank-Christoph Mooren
Karsten Krüger
author_facet Astrid Weiss
Katharina Alack
Stephan Klatt
Sven Zukunft
Ralph Schermuly
Torsten Frech
Frank-Christoph Mooren
Karsten Krüger
author_sort Astrid Weiss
collection DOAJ
description Endurance training induces several adaptations in substrate metabolism, especially in relation to glycogen conservation. The study aimed to investigate differences in the metabolism of lipids, lipid-like substances, and amino acids between highly trained and untrained subjects using targeted metabolomics. Depending on their maximum relative oxygen uptake (VO<sub>2max</sub>), subjects were categorized as either endurance-trained (ET) or untrained (UT). Resting blood was taken and plasma isolated. It was screened for changes of 345 metabolites, including amino acids and biogenic amines, acylcarnitines, glycerophosphocholines (GPCs), sphingolipids, hexoses, bile acids, and polyunsaturated fatty acids (PUFAs) by using liquid chromatography coupled to tandem mass spectrometry. Acylcarnitine (C14:1, down in ET) and five GPCs (lysoPC a C18:2, up in ET; PC aa C42:0, up in ET; PC ae C38:2, up in ET; PC aa C38:5, down in ET; lysoPC a C26:0, down in ET) were differently regulated in ET compared to UT. TCDCA was down-regulated in athletes, while for three ratios of bile acids CA/CDCA, CA/(GCA+TCA), and DCA/(GDCA+TDCA) an up-regulation was found. TXB2 and 5,6-EET were down-regulated in the ET group and 18S-HEPE, a PUFA, showed higher levels in 18S-HEPE in endurance-trained subjects. For PC ae C38:2, TCDCA, and the ratio of cholic acid to chenodeoxycholic acid, an association with VO<sub>2max</sub> was found. Numerous phospholipids, acylcarnitines, glycerophosphocholines, bile acids, and PUFAs are present in varying concentrations at rest in ET. These results might represent an adaptation of lipid metabolism and account for the lowered cardiovascular risk profile of endurance athletes.
first_indexed 2024-03-09T13:23:47Z
format Article
id doaj.art-d7d99226df384abd91f67ed898531713
institution Directory Open Access Journal
issn 2218-1989
language English
last_indexed 2024-03-09T13:23:47Z
publishDate 2022-07-01
publisher MDPI AG
record_format Article
series Metabolites
spelling doaj.art-d7d99226df384abd91f67ed8985317132023-11-30T21:27:31ZengMDPI AGMetabolites2218-19892022-07-0112765810.3390/metabo12070658Sustained Endurance Training Leads to Metabolomic AdaptationAstrid Weiss0Katharina Alack1Stephan Klatt2Sven Zukunft3Ralph Schermuly4Torsten Frech5Frank-Christoph Mooren6Karsten Krüger7German Center for Lung Research (DZL), Cardio-Pulmonary Institute (CPI), Justus-Liebig-University, 35390 Giessen, GermanyCenter for Translational and Clinical Research Aachen, RWTH Aachen, 52074 Aachen, GermanyInstitute for Vascular Signalling, Centre for Molecular Medicine, Goethe University, 60323 Frankfurt am Main, GermanyInstitute for Vascular Signalling, Centre for Molecular Medicine, Goethe University, 60323 Frankfurt am Main, GermanyGerman Center for Lung Research (DZL), Cardio-Pulmonary Institute (CPI), Justus-Liebig-University, 35390 Giessen, GermanyDepartment of Exercise Physiology and Sports Therapy, Institute of Sports Sciences, Justus-Liebig-University, 35390 Giessen, GermanyFaculty of Health/School of Medicine, Witten/Herdecke University, 58448 Witten, GermanyDepartment of Exercise Physiology and Sports Therapy, Institute of Sports Sciences, Justus-Liebig-University, 35390 Giessen, GermanyEndurance training induces several adaptations in substrate metabolism, especially in relation to glycogen conservation. The study aimed to investigate differences in the metabolism of lipids, lipid-like substances, and amino acids between highly trained and untrained subjects using targeted metabolomics. Depending on their maximum relative oxygen uptake (VO<sub>2max</sub>), subjects were categorized as either endurance-trained (ET) or untrained (UT). Resting blood was taken and plasma isolated. It was screened for changes of 345 metabolites, including amino acids and biogenic amines, acylcarnitines, glycerophosphocholines (GPCs), sphingolipids, hexoses, bile acids, and polyunsaturated fatty acids (PUFAs) by using liquid chromatography coupled to tandem mass spectrometry. Acylcarnitine (C14:1, down in ET) and five GPCs (lysoPC a C18:2, up in ET; PC aa C42:0, up in ET; PC ae C38:2, up in ET; PC aa C38:5, down in ET; lysoPC a C26:0, down in ET) were differently regulated in ET compared to UT. TCDCA was down-regulated in athletes, while for three ratios of bile acids CA/CDCA, CA/(GCA+TCA), and DCA/(GDCA+TDCA) an up-regulation was found. TXB2 and 5,6-EET were down-regulated in the ET group and 18S-HEPE, a PUFA, showed higher levels in 18S-HEPE in endurance-trained subjects. For PC ae C38:2, TCDCA, and the ratio of cholic acid to chenodeoxycholic acid, an association with VO<sub>2max</sub> was found. Numerous phospholipids, acylcarnitines, glycerophosphocholines, bile acids, and PUFAs are present in varying concentrations at rest in ET. These results might represent an adaptation of lipid metabolism and account for the lowered cardiovascular risk profile of endurance athletes.https://www.mdpi.com/2218-1989/12/7/658glycerophosphocholinescardiopulmonary fitnessathletesbile acids
spellingShingle Astrid Weiss
Katharina Alack
Stephan Klatt
Sven Zukunft
Ralph Schermuly
Torsten Frech
Frank-Christoph Mooren
Karsten Krüger
Sustained Endurance Training Leads to Metabolomic Adaptation
Metabolites
glycerophosphocholines
cardiopulmonary fitness
athletes
bile acids
title Sustained Endurance Training Leads to Metabolomic Adaptation
title_full Sustained Endurance Training Leads to Metabolomic Adaptation
title_fullStr Sustained Endurance Training Leads to Metabolomic Adaptation
title_full_unstemmed Sustained Endurance Training Leads to Metabolomic Adaptation
title_short Sustained Endurance Training Leads to Metabolomic Adaptation
title_sort sustained endurance training leads to metabolomic adaptation
topic glycerophosphocholines
cardiopulmonary fitness
athletes
bile acids
url https://www.mdpi.com/2218-1989/12/7/658
work_keys_str_mv AT astridweiss sustainedendurancetrainingleadstometabolomicadaptation
AT katharinaalack sustainedendurancetrainingleadstometabolomicadaptation
AT stephanklatt sustainedendurancetrainingleadstometabolomicadaptation
AT svenzukunft sustainedendurancetrainingleadstometabolomicadaptation
AT ralphschermuly sustainedendurancetrainingleadstometabolomicadaptation
AT torstenfrech sustainedendurancetrainingleadstometabolomicadaptation
AT frankchristophmooren sustainedendurancetrainingleadstometabolomicadaptation
AT karstenkruger sustainedendurancetrainingleadstometabolomicadaptation