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A Metabolomic Signature of Acute Caloric Restriction

CONTEXT: The experimental paradigm of acute caloric restriction (CR) followed by refeeding (RF) 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 hund...

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Autores principales: Collet, Tinh-Hai, Sonoyama, Takuhiro, Henning, Elana, Keogh, Julia M., Ingram, Brian, Kelway, Sarah, Guo, Lining, Farooqi, I. Sadaf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Endocrine Society 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5718701/
https://www.ncbi.nlm.nih.gov/pubmed/29029202
http://dx.doi.org/10.1210/jc.2017-01020
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author Collet, Tinh-Hai
Sonoyama, Takuhiro
Henning, Elana
Keogh, Julia M.
Ingram, Brian
Kelway, Sarah
Guo, Lining
Farooqi, I. Sadaf
author_facet Collet, Tinh-Hai
Sonoyama, Takuhiro
Henning, Elana
Keogh, Julia M.
Ingram, Brian
Kelway, Sarah
Guo, Lining
Farooqi, I. Sadaf
author_sort Collet, Tinh-Hai
collection PubMed
description CONTEXT: The experimental paradigm of acute caloric restriction (CR) followed by refeeding (RF) 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 CR. 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 CR (10% of energy requirements) and after 48 hours of ad libitum RF 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 β-fatty acid oxidation. We found an increase in ω-fatty acid oxidation and levels of endocannabinoids, which are known to promote food intake. These changes were reversed with RF. Several plasmalogen phosphatidylethanolamines (endogenous antioxidants) significantly decreased with CR (all P ≤ 0.0007). Additionally, acute CR was associated with an increase in the branched chain amino acids (all P ≤ 1.4 × 10(−7)) and dehydroepiandrosterone sulfate (P = 0.0006). CONCLUSIONS: We identified a distinct metabolomic signature associated with acute CR. Further studies are needed to characterize the mechanisms that mediate these changes and their potential contribution to the adaptive response to dietary restriction.
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spelling pubmed-57187012017-12-21 A Metabolomic Signature of Acute Caloric Restriction Collet, Tinh-Hai Sonoyama, Takuhiro Henning, Elana Keogh, Julia M. Ingram, Brian Kelway, Sarah Guo, Lining Farooqi, I. Sadaf J Clin Endocrinol Metab Clinical Research Articles CONTEXT: The experimental paradigm of acute caloric restriction (CR) followed by refeeding (RF) 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 CR. 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 CR (10% of energy requirements) and after 48 hours of ad libitum RF 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 β-fatty acid oxidation. We found an increase in ω-fatty acid oxidation and levels of endocannabinoids, which are known to promote food intake. These changes were reversed with RF. Several plasmalogen phosphatidylethanolamines (endogenous antioxidants) significantly decreased with CR (all P ≤ 0.0007). Additionally, acute CR was associated with an increase in the branched chain amino acids (all P ≤ 1.4 × 10(−7)) and dehydroepiandrosterone sulfate (P = 0.0006). CONCLUSIONS: We identified a distinct metabolomic signature associated with acute CR. Further studies are needed to characterize the mechanisms that mediate these changes and their potential contribution to the adaptive response to dietary restriction. Endocrine Society 2017-09-28 /pmc/articles/PMC5718701/ /pubmed/29029202 http://dx.doi.org/10.1210/jc.2017-01020 Text en https://creativecommons.org/licenses/by/4.0/ This article has been published under the terms of the Creative Commons Attribution License (CC BY; https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Copyright for this article is retained by the author(s).
spellingShingle Clinical Research Articles
Collet, Tinh-Hai
Sonoyama, Takuhiro
Henning, Elana
Keogh, Julia M.
Ingram, Brian
Kelway, Sarah
Guo, Lining
Farooqi, I. Sadaf
A Metabolomic Signature of Acute Caloric Restriction
title A Metabolomic Signature of Acute Caloric Restriction
title_full A Metabolomic Signature of Acute Caloric Restriction
title_fullStr A Metabolomic Signature of Acute Caloric Restriction
title_full_unstemmed A Metabolomic Signature of Acute Caloric Restriction
title_short A Metabolomic Signature of Acute Caloric Restriction
title_sort metabolomic signature of acute caloric restriction
topic Clinical Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5718701/
https://www.ncbi.nlm.nih.gov/pubmed/29029202
http://dx.doi.org/10.1210/jc.2017-01020
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