Metabolic Signatures of Exercise in Human Plasma

Gregory D. Lewis(Broad Institute), Laurie Farrell(Massachusetts General Hospital), Malissa J. Wood(Massachusetts General Hospital), M.FuruS. Martinovic(Massachusetts General Hospital), Zoltàn Arany(Beth Israel Deaconess Medical Center), Glenn C. Rowe(Beth Israel Deaconess Medical Center), Amanda Souza(Broad Institute), Susan Cheng(Brigham and Women's Hospital), Elizabeth L. McCabe, Elaine Yang(Broad Institute), Xu Shi(Broad Institute), Rahul C. Deo(Harvard University), Frederick P. Roth(Harvard University), Aarti Asnani(Massachusetts General Hospital), Eugene P. Rhee(Broad Institute), David M. Systrom(Massachusetts General Hospital), Marc J. Semigran(Massachusetts General Hospital), Ramachandran S. Vasan(Boston University), Steven A. Carr(Broad Institute), Thomas J. Wang(Massachusetts General Hospital), Marc S. Sabatine(Brigham and Women's Hospital), Clary B. Clish(Broad Institute), Robert E. Gerszten(Broad Institute)
Science Translational Medicine
May 26, 2010
Cited by 422Open Access
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Abstract

Exercise provides numerous salutary effects, but our understanding of how these occur is limited. To gain a clearer picture of exercise-induced metabolic responses, we have developed comprehensive plasma metabolite signatures by using mass spectrometry to measure >200 metabolites before and after exercise. We identified plasma indicators of glycogenolysis (glucose-6-phosphate), tricarboxylic acid cycle span 2 expansion (succinate, malate, and fumarate), and lipolysis (glycerol), as well as modulators of insulin sensitivity (niacinamide) and fatty acid oxidation (pantothenic acid). Metabolites that were highly correlated with fitness parameters were found in subjects undergoing acute exercise testing and marathon running and in 302 subjects from a longitudinal cohort study. Exercise-induced increases in glycerol were strongly related to fitness levels in normal individuals and were attenuated in subjects with myocardial ischemia. A combination of metabolites that increased in plasma in response to exercise (glycerol, niacinamide, glucose-6-phosphate, pantothenate, and succinate) up-regulated the expression of nur77, a transcriptional regulator of glucose utilization and lipid metabolism genes in skeletal muscle in vitro. Plasma metabolic profiles obtained during exercise provide signatures of exercise performance and cardiovascular disease susceptibility, in addition to highlighting molecular pathways that may modulate the salutary effects of exercise.


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