Meaghan E Beckner, J Philip Karl, Nicholes J Armstrong, Christopher T Carrigan, Marques A Wilson, Hoangha D Pirnstill, Anthony J Karis, Stefan M Pasiakos, James P McClung, Nicholas D Barringer, Lee M Margolis
{"title":"细胞外囊泡代谢组学分析揭示了高强度军事训练期间氧化应激和能量代谢的增强;探索性研究","authors":"Meaghan E Beckner, J Philip Karl, Nicholes J Armstrong, Christopher T Carrigan, Marques A Wilson, Hoangha D Pirnstill, Anthony J Karis, Stefan M Pasiakos, James P McClung, Nicholas D Barringer, Lee M Margolis","doi":"10.1152/physiolgenomics.00155.2025","DOIUrl":null,"url":null,"abstract":"<p><p>Extracellular vesicles (EVs) are small, membrane-bound vesicles that transfer biological content through the extracellular environment. The role of EVs in energy metabolism have primarily focused on EV proteins and microRNAs, with less attention on the metabolic content of EVs. <b>Purpose:</b> This exploratory study assessed changes in the EV metabolome in response to an arduous, 16-day military training exercise. <b>Methods:</b> Forty male Soldiers (21±2 years, 24.8±2.7 kg/m<sup>2</sup>) provided blood from which circulating EVs were isolated, and completed assessments of body composition, and lower body power on days 1 (PRE) and 16 (POST) of a mountain training exercise (MTX). <b>Results:</b> Total daily energy expenditure (TDEE) during the MTX was 4,187±519 kcal·d<sup>-1</sup>. Fat mass (POST-PRE [95%CI]; -0.9[-1.3,-0.6] kg), lean body mass (-1.6[-2.0,-1.2] kg), body fat percentage (-0.7[-1.1,-0.3]%), and lower body power (-133[-204,-63] Watts) decreased from PRE to POST (<i>p</i><0.05). Global metabolite profiling identified 81 metabolites from lipid (81%), energy (5%), cofactor and vitamin (5%), xenobiotic (4%), carbohydrate (2%), amino acid (1%) and nucleotide (1%) pathways in serum-derived EVs. After adjusting for EV concentration, 11 metabolites were different PRE to POST (<i>p</i><0.05, <i>Q</i><0.20), with the largest increases in the oxidative stress-associated metabolites 5-oxoproline and benzoate. Changes in lean body mass were positively associated with changes the energy metabolites citrate (ρ=0.361, <i>p</i>=0.022) and phosphate (ρ=0.369, <i>p</i>=0.019). <b>Conclusion:</b> Findings suggest that EV metabolites change in response to physiological stress and reflect increased oxidative stress, energy metabolism, and fatty acid metabolism, which may provide early indicators of stress adaptations relevant for optimizing training and sustaining military performance.</p>","PeriodicalId":20129,"journal":{"name":"Physiological genomics","volume":" ","pages":""},"PeriodicalIF":2.5000,"publicationDate":"2025-10-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Metabolomic profiling of extracellular vesicles reveals enhanced oxidative stress and energy metabolism during intense military training; an exploratory study.\",\"authors\":\"Meaghan E Beckner, J Philip Karl, Nicholes J Armstrong, Christopher T Carrigan, Marques A Wilson, Hoangha D Pirnstill, Anthony J Karis, Stefan M Pasiakos, James P McClung, Nicholas D Barringer, Lee M Margolis\",\"doi\":\"10.1152/physiolgenomics.00155.2025\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Extracellular vesicles (EVs) are small, membrane-bound vesicles that transfer biological content through the extracellular environment. The role of EVs in energy metabolism have primarily focused on EV proteins and microRNAs, with less attention on the metabolic content of EVs. <b>Purpose:</b> This exploratory study assessed changes in the EV metabolome in response to an arduous, 16-day military training exercise. <b>Methods:</b> Forty male Soldiers (21±2 years, 24.8±2.7 kg/m<sup>2</sup>) provided blood from which circulating EVs were isolated, and completed assessments of body composition, and lower body power on days 1 (PRE) and 16 (POST) of a mountain training exercise (MTX). <b>Results:</b> Total daily energy expenditure (TDEE) during the MTX was 4,187±519 kcal·d<sup>-1</sup>. Fat mass (POST-PRE [95%CI]; -0.9[-1.3,-0.6] kg), lean body mass (-1.6[-2.0,-1.2] kg), body fat percentage (-0.7[-1.1,-0.3]%), and lower body power (-133[-204,-63] Watts) decreased from PRE to POST (<i>p</i><0.05). Global metabolite profiling identified 81 metabolites from lipid (81%), energy (5%), cofactor and vitamin (5%), xenobiotic (4%), carbohydrate (2%), amino acid (1%) and nucleotide (1%) pathways in serum-derived EVs. After adjusting for EV concentration, 11 metabolites were different PRE to POST (<i>p</i><0.05, <i>Q</i><0.20), with the largest increases in the oxidative stress-associated metabolites 5-oxoproline and benzoate. Changes in lean body mass were positively associated with changes the energy metabolites citrate (ρ=0.361, <i>p</i>=0.022) and phosphate (ρ=0.369, <i>p</i>=0.019). <b>Conclusion:</b> Findings suggest that EV metabolites change in response to physiological stress and reflect increased oxidative stress, energy metabolism, and fatty acid metabolism, which may provide early indicators of stress adaptations relevant for optimizing training and sustaining military performance.</p>\",\"PeriodicalId\":20129,\"journal\":{\"name\":\"Physiological genomics\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":2.5000,\"publicationDate\":\"2025-10-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Physiological genomics\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1152/physiolgenomics.00155.2025\",\"RegionNum\":4,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CELL BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Physiological genomics","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1152/physiolgenomics.00155.2025","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
Metabolomic profiling of extracellular vesicles reveals enhanced oxidative stress and energy metabolism during intense military training; an exploratory study.
Extracellular vesicles (EVs) are small, membrane-bound vesicles that transfer biological content through the extracellular environment. The role of EVs in energy metabolism have primarily focused on EV proteins and microRNAs, with less attention on the metabolic content of EVs. Purpose: This exploratory study assessed changes in the EV metabolome in response to an arduous, 16-day military training exercise. Methods: Forty male Soldiers (21±2 years, 24.8±2.7 kg/m2) provided blood from which circulating EVs were isolated, and completed assessments of body composition, and lower body power on days 1 (PRE) and 16 (POST) of a mountain training exercise (MTX). Results: Total daily energy expenditure (TDEE) during the MTX was 4,187±519 kcal·d-1. Fat mass (POST-PRE [95%CI]; -0.9[-1.3,-0.6] kg), lean body mass (-1.6[-2.0,-1.2] kg), body fat percentage (-0.7[-1.1,-0.3]%), and lower body power (-133[-204,-63] Watts) decreased from PRE to POST (p<0.05). Global metabolite profiling identified 81 metabolites from lipid (81%), energy (5%), cofactor and vitamin (5%), xenobiotic (4%), carbohydrate (2%), amino acid (1%) and nucleotide (1%) pathways in serum-derived EVs. After adjusting for EV concentration, 11 metabolites were different PRE to POST (p<0.05, Q<0.20), with the largest increases in the oxidative stress-associated metabolites 5-oxoproline and benzoate. Changes in lean body mass were positively associated with changes the energy metabolites citrate (ρ=0.361, p=0.022) and phosphate (ρ=0.369, p=0.019). Conclusion: Findings suggest that EV metabolites change in response to physiological stress and reflect increased oxidative stress, energy metabolism, and fatty acid metabolism, which may provide early indicators of stress adaptations relevant for optimizing training and sustaining military performance.
期刊介绍:
The Physiological Genomics publishes original papers, reviews and rapid reports in a wide area of research focused on uncovering the links between genes and physiology at all levels of biological organization. Articles on topics ranging from single genes to the whole genome and their links to the physiology of humans, any model organism, organ, tissue or cell are welcome. Areas of interest include complex polygenic traits preferably of importance to human health and gene-function relationships of disease processes. Specifically, the Journal has dedicated Sections focused on genome-wide association studies (GWAS) to function, cardiovascular, renal, metabolic and neurological systems, exercise physiology, pharmacogenomics, clinical, translational and genomics for precision medicine, comparative and statistical genomics and databases. For further details on research themes covered within these Sections, please refer to the descriptions given under each Section.