Bioactive Lipids of Cardiorespiratory Fitness Insights From Exercise Models in Humans, Mice, and Burmese Pythons

BACKGROUND: Cardiorespiratory fitness, commonly measured as peak oxygen consumption (peak VO 2 , is a strong predictor of cardiovascular health. Circulating lipids have been linked to exercise responses and metabolic adaptation, but the bioactive lipid species associated with objectively measured aerobic capacity and their dynamic regulation during exercise remain incompletely defined. METHODS: We performed directed, nontargeted liquid chromatography–mass spectrometry profiling of circulating bioactive lipids in adults undergoing clinically indicated cardiopulmonary exercise testing, relating resting lipid levels and acute exercise-induced lipid changes to peak VO 2 . We then examined fitness-associated lipid species across complementary models of physiological stress, including marathon running, chronic voluntary wheel running in mice, and the postprandial Burmese python model. RESULTS: Among 1896 detected lipid species in the primary human cohort, 47 were associated with peak VO 2 after false-discovery rate correction, including 16 metabolites with known molecular identities. Higher levels of several eicosanoids and free fatty acids were associated with greater peak VO 2 , including docosahexaenoic acid, arachidic acid, and 12,13-dihydroxy-9Z-octadecenoic acid. In paired rest and peak exercise samples, 37 of 47 fitness-associated lipid species changed acutely with exercise. Among metabolites with known identities, exercise-induced changes in 12,13-dihydroxy-9Z-octadecenoic acid, 8-hydroxyicosa-9,11,14-trienoic acid, 11,12-epoxy-5Z,8Z,14Z-eicosatrienoic acid, and 8,9-dihydroxy-5Z,11Z,14Z-eicosatrienoic acid were associated with peak VO 2 . In marathon runners, 43 of 47 fitness-associated lipid species changed after prolonged endurance exercise. Exploratory animal analyses demonstrated overlapping lipid regulation in chronic voluntary wheel-running mice and in the postprandial Burmese python model. CONCLUSIONS: Circulating bioactive lipids, particularly eicosanoids and free fatty acids, are associated with human cardiorespiratory fitness and are dynamically regulated during exercise. Overlapping lipid responses across complementary human and animal models identify candidate lipid pathways that may merit future mechanistic study.

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Publication Details

Journal
Circulation Genomic and Precision Medicine
Published
2026-10-07
DOI
https://doi.org/10.1161/circgen.126.005720
Primary Topic
Cardiovascular and exercise physiology
Type
article
Field-Weighted Citation Impact
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article

Bioactive Lipids of Cardiorespiratory Fitness Insights From Exercise Models in Humans, Mice, and Burmese Pythons

Jennifer E. Ho, Amit Choudhary, Nima Saeidi, Susan C. Cheng et al.
Circulation Genomic and Precision Medicine
Cardiovascular and exercise physiology
article

Bioactive Lipids of Cardiorespiratory Fitness Insights From Exercise Models in Humans, Mice, and Burmese Pythons

Jennifer E. Ho, Amit Choudhary, Nima Saeidi, Susan C. Cheng, Gregory D. Lewis, Emily S. Lau, James Sawalla Guseh, Anthony Rosenzweig, Shahrooz Zarbafian, Athar Roshandelpoor, Alexandra Kuznetsov, Mona Alotaibi, Mohit Jain
article en

Abstract

BACKGROUND: Cardiorespiratory fitness, commonly measured as peak oxygen consumption (peak VO 2 , is a strong predictor of cardiovascular health. Circulating lipids have been linked to exercise responses and metabolic adaptation, but the bioactive lipid species associated with objectively measured aerobic capacity and their dynamic regulation during exercise remain incompletely defined. METHODS: We performed directed, nontargeted liquid chromatography–mass spectrometry profiling of circulating bioactive lipids in adults undergoing clinically indicated cardiopulmonary exercise testing, relating resting lipid levels and acute exercise-induced lipid changes to peak VO 2 . We then examined fitness-associated lipid species across complementary models of physiological stress, including marathon running, chronic voluntary wheel running in mice, and the postprandial Burmese python model. RESULTS: Among 1896 detected lipid species in the primary human cohort, 47 were associated with peak VO 2 after false-discovery rate correction, including 16 metabolites with known molecular identities. Higher levels of several eicosanoids and free fatty acids were associated with greater peak VO 2 , including docosahexaenoic acid, arachidic acid, and 12,13-dihydroxy-9Z-octadecenoic acid. In paired rest and peak exercise samples, 37 of 47 fitness-associated lipid species changed acutely with exercise. Among metabolites with known identities, exercise-induced changes in 12,13-dihydroxy-9Z-octadecenoic acid, 8-hydroxyicosa-9,11,14-trienoic acid, 11,12-epoxy-5Z,8Z,14Z-eicosatrienoic acid, and 8,9-dihydroxy-5Z,11Z,14Z-eicosatrienoic acid were associated with peak VO 2 . In marathon runners, 43 of 47 fitness-associated lipid species changed after prolonged endurance exercise. Exploratory animal analyses demonstrated overlapping lipid regulation in chronic voluntary wheel-running mice and in the postprandial Burmese python model. CONCLUSIONS: Circulating bioactive lipids, particularly eicosanoids and free fatty acids, are associated with human cardiorespiratory fitness and are dynamically regulated during exercise. Overlapping lipid responses across complementary human and animal models identify candidate lipid pathways that may merit future mechanistic study.

Circulation Genomic and Precision Medicine
Broad Institute (US), Cedars-Sinai Medical Center (US), Google (United States) (US), Beth Israel Deaconess Medical Center (US), Shriners Hospitals for Children - Erie (US), University of California System (US), University of California San Diego (US), Massachusetts General Hospital (US), Shriners Hospitals for Children - Boston (US), Cedars-Sinai Smidt Heart Institute (US), Harvard Stem Cell Institute (US)
Openalex Percentile: Top 7%
Cardiovascular and exercise physiology
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