综述与专论:运动促进健康的分子机制:代谢标志物的多组学解析
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1)北京市体育科学研究所,北京 100075;2)河北师范大学体育学院,石家庄 050024

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Review:Molecular Mechanisms of Exercise in Promoting Health: a Multi-omics Analysis of Metabolic Biomarkers
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1)Beijing Research Institute of Sports Science, Beijing 100075, China;2)College of Physical Education, Hebei Normal University, Shijiazhuang 050024, China

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    摘要:

    运动促进健康的分子机制尚未完全阐明,代谢物作为连接遗传、运动与表型的关键桥梁,通过多组学技术可高通量检测,为机制研究和疾病预测提供重要线索。运动可显著改变体内代谢物谱,如乳酸作为运动强度标志物,可调控脂肪棕色化、血管生成和线粒体功能,丙酮酸与其比值异常则提示线粒体功能障碍,酮体为机体供能且调控脂代谢,或与中枢疲劳相关,肉碱是线粒体代谢枢纽且具有改善体成分、提高认知等功能,丙氨酸通过糖异生和肌肽合成参与能量代谢,肌酸为短时高强度运动供能并具有增肌等健康效应。代谢物在疾病预测中具有重要价值,如糖蛋白乙酰基和酰基肉碱可提升心血管疾病和糖尿病的预测效能。基因组学发现了与最大摄氧量相关的卵泡刺激素受体基因,并由此探索出肌酐等运动代谢标志物;转录组学揭示了运动通过快速调控果糖、胆碱等基因表达影响代谢通路,可改善帕金森病、提高肌肉力量、缓解胰岛素抵抗等;蛋白质组学则发现运动通过特异性调控SLC25A15等代谢相关蛋白的表达水平或磷酸化修饰,影响精氨酸等代谢通路,进而介导运动适应性反应。多组学联用策略可同步解析代谢标志物及其调控机制,但仍面临数据整合不足等挑战。未来需结合动态监测、单细胞/空间组学和AI算法等,构建精准运动模型以实现最大化健康收益。

    Abstract:

    The molecular mechanisms underlying the health-promoting effects of exercise remain to be fully elucidated. As a bridge between genetics, exercise and phenotype, metabolites can be detected in high throughput through metabolomics, offering valuable insights into mechanism elucidation and disease prediction. Metabolic homeostasis is intricately regulated by various factors, including enzyme activity and transporters. Integration of multiple omics technologies such as genomics, transcriptomics, and proteomics enables the comprehensive elucidation of the metabolic network modulated by exercise interventions and facilitates the identification of key metabolic markers. This review summarizes the current research advancements, biological functions, discovery methods, and applications of exercise-induced multi omics metabolic markers, furnishing a theoretical foundation for understanding the mechanisms of exercise-induced health benefits and enabling precision interventions. Relevant literatures from 2000 to 2025 were systematically retrieved from databases including PubMed, CNKI and other databases with the keywords such as “multi-omics”, “metabolic biomarkers”, “exercise”, “health”. Subsequently, the identified literature was meticulously screened to meet the specified criteria and was subsequently incorporated into the study. (1) Exercise induces profound alterations in metabolite levels within the body, with particular emphasis on markers associated with sugar, lipid, and protein metabolism being extensively investigated. As an intensity marker, lactate is implicated in the regulation of fat browning (UCP-1), angiogenesis (VEGF), mitochondrial function (PGC-1α) and metabolic homeostasis (HIF-1α/CES2). Following resistance training, pyruvate levels increase, and an aberrant pyruvate to lactate ratio (approximately 10) may indicate mitochondrial dysfunction. Supplementation with pyruvate has been shown to reduce weight and lipid levels. Ketone bodies regulate metabolism by inhibiting lipolytic enzyme activity and promoting insulin secretion. Plasma ketone body concentrations rise after high-intensity exercise, with levels positively associated with central fatigue. Carnitine levels elevate post-endurance training, and supplementation with carnitine has been linked to increased lean body mass and enhanced cognitive function in older individuals. Serum alanine levels rise following resistance training and, as a precursor of carnosine, supplementation can elevate carnosine concentration by 80%, exerting antioxidant and neuroprotective effects. Creatine, a pivotal molecule in phosphogen energy supply, exhibits a 93% increase in plasma levels post-marathon, with its metabolism intricately related to AMPK activation. (2) Metabolites play a crucial role in disease prediction, particularly in the context of cardiovascular disease where 18 metabolites including glycoprotein acetyl and ketone bodies have been shown to enhance the performance of prediction models. Similarly, in diabetes research, acylcarnitine and other metabolites can improve prediction model efficacy. The combination of multiple metabolites has been found to substantially enhance predictive capabilities for various conditions such as cancer, aging, and other risks, surpassing the predictive power of traditional indicators. (3) Genomics investigations have unveiled the genetic underpinnings of exercise-related metabolites. VO2max, a significant exercise phenotype with heritability estimates ranging from 0.59 to 0.66, exhibits a negative correlation with the susceptibility to diabetes and cardiovascular disease. SNPs associated with VO2max, such as variants in the FSHR gene, are positively linked to serum creatinine levels. Reduced creatinine levels have been associated with an elevated risk of T2DM. These findings suggest that creatinine serves as a potential marker of exercise metabolism. (4) Transcriptomic studies have elucidated the molecular mechanisms by which exercise modulates metabolites. Acute exercise induces rapid alterations in the expression profiles of 9 132 transcripts. Exercise elicits upregulation of genes involved in the fructose/mannose metabolic pathway (such as SORD, PFKFB3), suggesting these metabolites may serve as pivotal mediators in the beneficial effects of exercise on Parkinson’s disease. Altitude training enhances the expression of the PHOSPHO1 gene, which encodes an enzyme facilitating choline synthesis. Choline deficiency has been linked to insulin resistance. Choline supplementation has been shown to augment the effects of resistance training, underscoring the significance of choline as a key marker in exercise-mediated metabolic health promotion. (5) Proteomic analyses have unveiled the key mechanisms through which exercise modulates metabolism. Endurance training induces significant alterations in myofibrillar expression, with 237 slow muscles and 172 fast muscles proteins showing differential regulation, of which 65% are associated with metabolism, including ACSL1 and ECHS1. Various training modalities elicit distinct phosphorylation modifications, exemplified by the negative correlation between LDHA3 phosphorylation and lactate levels. Endurance training upregulates SLC25A15 expression in adipose tissue, enhancing arginine synthesis. The post-exercise elevation of plasma GPLD1 levels mimics the neuroprotective effects of exercise on the brain. These findings present novel targets for investigating exercise-related metabolic markers. The application of multi omics technologies has expedited the identification and mechanistic analysis of both established and novel sports-related metabolic markers like lactate. Integrated multi omics strategies (e.g., genome-metabolome) enable the simultaneous examination of metabolic markers and their regulatory mechanisms, facilitating the discovery of exercise-related genetic markers and pivotal regulatory proteins. However, challenges persist, including inadequate data integration and a lack of standardization. Future endeavors should focus on developing dynamic monitoring tools, integrating state-of-the-art approaches such as single-cell/spatial omics, and leveraging AI algorithms for optimized analysis to construct precise predictive models for maximizing health benefits in exercise.

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张赛,刘阳.综述与专论:运动促进健康的分子机制:代谢标志物的多组学解析[J].生物化学与生物物理进展,2025,52(6):1631-1644 ZHANG Sai, LIU Yang.Review:Molecular Mechanisms of Exercise in Promoting Health: a Multi-omics Analysis of Metabolic Biomarkers[J]. Progress in Biochemistry and Biophysics,2025,52(6):1631-1644

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  • 收稿日期:2025-04-30
  • 最后修改日期:2025-06-16
  • 录用日期:2025-06-04
  • 在线发布日期: 2025-06-27
  • 出版日期: 2025-06-28
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