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A Metabolomic Signature of Acute Caloric Restriction

Published version
Peer-reviewed

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Authors

Farooqi, IS 
Collet, TH 
Sonoyama, T 
Henning, E 
Keogh, JM 

Abstract

Context: The experimental paradigm of acute caloric restriction followed by refeeding can be used to study the homeostatic mechanisms that regulate energy homeostasis, which are relevant to understanding the adaptive response to weight loss.

Objective: Metabolomics, the measurement of hundreds of small molecule metabolites, their precursors, derivatives, and degradation products, has emerged as a useful tool for the study of physiology and disease and was used here to study the metabolic response to acute caloric restriction.

Participants, Design and Setting: We used four ultra high performance liquid chromatography-tandem mass spectrometry methods to characterize changes in carbohydrates, lipids, amino acids and steroids in eight normal weight men at baseline, after 48 hours of caloric restriction (CR; 10% of energy requirements) and after 48 hours of ad libitum refeeding in a tightly-controlled environment.

Results: We identified a distinct metabolomic signature associated with acute CR characterized by the expected switch from carbohydrate to fat utilization with increased lipolysis and beta-fatty acid oxidation. We found an increase in omega-fatty acid oxidation and levels of endocannabinoids which are known to promote food intake. These changes were reversed with refeeding. Several plasmalogen phosphatidylethanolamines (endogenous anti-oxidants) significantly decreased with CR (all p≤0.0007). Additionally, 48 acute CR was associated with an increase in the branched chain amino acids (all p≤1.4x10-7) and dehydroepiandrosterone sulfate (p=0.0006).

Conclusions We identified a distinct metabolomic signature associated with acute CR. Further studies are needed to characterise the mechanisms that mediate these changes and their potential contribution to the adaptive response to dietary restriction.

Description

Keywords

Adult, Amino Acids, Antioxidants, Caloric Restriction, Carbohydrate Metabolism, Chromatography, High Pressure Liquid, Dehydroepiandrosterone Sulfate, Endocannabinoids, Energy Metabolism, Fatty Acids, Homeostasis, Humans, Lipid Metabolism, Lipolysis, Male, Metabolomics, Oxidation-Reduction, Steroids, Tandem Mass Spectrometry, Weight Loss

Journal Title

The Journal of Clinical Endocrinology and Metabolism

Conference Name

Journal ISSN

0021-972X
1945-7197

Volume Title

102

Publisher

Oxford University Press
Sponsorship
Wellcome Trust (098497/Z/12/Z)
European Research Council (282374)
Medical Research Council (MC_UU_12012/5)
Medical Research Council (MC_PC_12012)
This work was supported by the Wellcome Trust (to I.S.F.), the NIHR Cambridge Biomedical Research Centre, the European Research Council, the Bernard Wolfe Health Neuroscience Fund (all to I.S.F.), the Swiss National Science Foundation (P3SMP3-155318, PZ00P3-167826, to T.H.C.), and the Uehara Memorial Foundation (to T.S.). This work was supported by the NIHR Rare Diseases Translational Research Collaboration and the NeuroFAST consortium, which is funded by the European Union’s Seventh Framework Programme (FP7/2007-2013) under grant agreement no 245009.