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<p>Exercise intensity critically determines health benefits, yet the underlying molecular mechanisms remain incompletely characterized. This study systematically compared the effects of high-intensity interval training (HIIT) versus moderate-intensity continuous training (MICT) swimming on serum lipidomics. In a randomized controlled trial (ChiCTR2400089036, registered on 30/08/2024, <i>n</i> = 42 healthy students), blood samples were collected at baseline, 0-, 15-, and 30-minutes post-exercise, followed by comprehensive lipidomics analysis. HIIT swimming induced 1.49- to 2.87-fold more extensive serum lipid downregulation than MICT, despite matched energy expenditure. We identified five robust intensity-dependent biomarkers: PC32:2, LPA18:2, and three 18:2-containing triacylglycerols (TAGs). Clustering analysis further revealed three distinct hierarchical patterns of lipid dynamic changes. Structurally, HIIT preferentially mobilized shorter-chain, saturated TAGs, and post-exercise lipid recovery dynamics were also intensity-dependent. The recurrent identification of linoleic acid (18:2)-enriched lipids, which negatively correlated with energy metabolites, suggests coordinated substrate channeling toward inflammatory eicosanoid pathways. These findings advance the mechanistic understanding of exercise intensity benefits and provide molecular evidence for intensity-stratified exercise prescription.</p>

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Intensity-dependent lipidomic dynamic regulation following acute swimming exercise

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2026年2月10日

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  • Jiayu Qian,
  • Baile Wu,
  • Zhongxun Ren,
  • Chunxue Tang,
  • Zihan Fan,
  • YanYan Zhang,
  • Lijun Shi

摘要

Exercise intensity critically determines health benefits, yet the underlying molecular mechanisms remain incompletely characterized. This study systematically compared the effects of high-intensity interval training (HIIT) versus moderate-intensity continuous training (MICT) swimming on serum lipidomics. In a randomized controlled trial (ChiCTR2400089036, registered on 30/08/2024, n = 42 healthy students), blood samples were collected at baseline, 0-, 15-, and 30-minutes post-exercise, followed by comprehensive lipidomics analysis. HIIT swimming induced 1.49- to 2.87-fold more extensive serum lipid downregulation than MICT, despite matched energy expenditure. We identified five robust intensity-dependent biomarkers: PC32:2, LPA18:2, and three 18:2-containing triacylglycerols (TAGs). Clustering analysis further revealed three distinct hierarchical patterns of lipid dynamic changes. Structurally, HIIT preferentially mobilized shorter-chain, saturated TAGs, and post-exercise lipid recovery dynamics were also intensity-dependent. The recurrent identification of linoleic acid (18:2)-enriched lipids, which negatively correlated with energy metabolites, suggests coordinated substrate channeling toward inflammatory eicosanoid pathways. These findings advance the mechanistic understanding of exercise intensity benefits and provide molecular evidence for intensity-stratified exercise prescription.