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Dynamic Metabolic Changes Driven by Exercise Intensity in Acute Swimming.
Chunxue Tang1, Baile Wu1, Yuxiao Deng1
1Department of Exercise Physiology, Beijing Sport University, Beijing, CHINA.
Medicine and Science in Sports and Exercise
|July 2, 2025
Summary
This study created an intensity-specific swimming exercise model using wearable devices. N-acetylvaline (NAV) emerged as a potential biomarker, with the metabolome atlas revealing intensity-driven changes in energy metabolism and emotional regulation pathways.
Area of Science:
- Exercise Physiology
- Metabolomics
- Biomarker Discovery
Background:
- Understanding physiological responses to exercise intensity is crucial for personalized training.
- High-throughput omics technologies offer novel insights into exercise-induced metabolic changes.
Purpose of the Study:
- To establish an intensity-specific human acute swimming exercise model.
- To create a swimming metabolome atlas to understand physiological responses.
- To identify commonalities and differences in metabolic responses under varying exercise intensities.
Main Methods:
- 42 healthy young adults were divided into moderate-intensity continuous training (MICT) and high-intensity interval training (HIIT) groups.
- Blood samples were collected at multiple time points for metabolomics and lipidomics analysis.
- Wearable devices monitored physiological parameters during acute swimming exercise.
Main Results:
- HIIT group exhibited higher average speeds and maximum heart rates than MICT.
- 209 metabolites significantly changed post-exercise, with 5 showing intensity-dependent characteristics.
- N-acetylvaline (NAV) strongly correlated with lactic acid, suggesting potential as an intensity biomarker.
- Both MICT and HIIT upregulated the TCA cycle, with distinct patterns in amino acid and lipid metabolism.
Conclusions:
- An intensity-specific acute swimming model was successfully established.
- N-acetylvaline (NAV) shows promise as a novel exercise intensity biomarker.
- The swimming metabolome atlas elucidates intensity-dependent substrate utilization and recovery, particularly in emotional regulation and lipid metabolism.
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