The blood serum metabolome profile after different phases of a 4‐km cycling time trial: Secondary analysis of a randomized controlled trial

Author:

Azevedo Rafael A.12ORCID,Cruz Ramon13,Silva‐Cavalcante Marcos D.14,Lima‐Silva Adriano E.5,Bertuzzi Romulo1

Affiliation:

1. School of Physical Education and Sport Endurance Sports Research Group (GEDAE‐USP) University of Sao Paulo Sao Paulo Brazil

2. Faculdade de Medicina FMUSP Applied Physiology and Nutrition Research Group ‐ Center of Lifestyle Medicine Universidade de São Paulo Sao Paulo Brazil

3. Department of Physical Education Sports Center Federal University of Santa Catarina Florianopolis Santa Catarina Brazil

4. Faculty of Nutrition Post‐graduate Program in Nutrition Federal University of Alagoas Maceió Alagoas Brazil

5. Human Performance Research Group Federal University of Technology – Parana Parana Brazil

Abstract

AbstractIt has been assumed that exercise intensity variation throughout a cycling time trial (TT) occurs in alignment of various metabolic changes to prevent premature task failure. However, this assumption is based on target metabolite responses, which limits our understanding of the complex interconnection of metabolic responses during exercise. The current study characterized the metabolomic profile, an untargeted metabolic analysis, after specific phases of a cycling 4‐km TT. Eleven male cyclists performed three separated TTs in a crossover counterbalanced design, which were interrupted at the end of the fast‐start (FS, 600 ± 205 m), even‐pace (EP, 3600 ± 190 m), or end‐spurt (ES, 4000 m) phases. Blood samples were taken before any exercise and 5 min after exercise cessation, and the metabolomic profile characterization was performed using Nuclear Magnetic Resonance metabolomics. Power output (PO) was also continually recorded. There were higher PO values during the FS and ES compared to the EP (all p < 0.05), which were accompanied by distinct metabolomic profiles. FS showed high metabolite expression in TCA cycle and its related pathways (e.g., glutamate, citric acid, and valine metabolism); whereas, the EP elicited changes associated with antioxidant effects and oxygen delivery adjustment. Finally, ES was related to pathways involved in NAD turnover and serotonin metabolism. These findings suggest that the specific phases of a cycling TT are accompanied by distinct metabolomic profiles, providing novel insights regarding the relevance of specific metabolic pathways on the process of exercise intensity regulation.

Funder

Fundação de Amparo à Pesquisa do Estado de São Paulo

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

Publisher

Wiley

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