Cargando…

Natural Isotopic Signatures of Variations in Body Nitrogen Fluxes: A Compartmental Model Analysis

Body tissues are generally (15)N-enriched over the diet, with a discrimination factor (Δ(15)N) that varies among tissues and individuals as a function of their nutritional and physiopathological condition. However, both (15)N bioaccumulation and intra- and inter-individual Δ(15)N variations are stil...

Descripción completa

Detalles Bibliográficos
Autores principales: Poupin, Nathalie, Mariotti, François, Huneau, Jean-François, Hermier, Dominique, Fouillet, Hélène
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4183419/
https://www.ncbi.nlm.nih.gov/pubmed/25275306
http://dx.doi.org/10.1371/journal.pcbi.1003865
_version_ 1782337684569587712
author Poupin, Nathalie
Mariotti, François
Huneau, Jean-François
Hermier, Dominique
Fouillet, Hélène
author_facet Poupin, Nathalie
Mariotti, François
Huneau, Jean-François
Hermier, Dominique
Fouillet, Hélène
author_sort Poupin, Nathalie
collection PubMed
description Body tissues are generally (15)N-enriched over the diet, with a discrimination factor (Δ(15)N) that varies among tissues and individuals as a function of their nutritional and physiopathological condition. However, both (15)N bioaccumulation and intra- and inter-individual Δ(15)N variations are still poorly understood, so that theoretical models are required to understand their underlying mechanisms. Using experimental Δ(15)N measurements in rats, we developed a multi-compartmental model that provides the first detailed representation of the complex functioning of the body's Δ(15)N system, by explicitly linking the sizes and Δ(15)N values of 21 nitrogen pools to the rates and isotope effects of 49 nitrogen metabolic fluxes. We have shown that (i) besides urea production, several metabolic pathways (e.g., protein synthesis, amino acid intracellular metabolism, urea recycling and intestinal absorption or secretion) are most probably associated with isotope fractionation and together contribute to (15)N accumulation in tissues, (ii) the Δ(15)N of a tissue at steady-state is not affected by variations of its P turnover rate, but can vary according to the relative orientation of tissue free amino acids towards oxidation vs. protein synthesis, (iii) at the whole-body level, Δ(15)N variations result from variations in the body partitioning of nitrogen fluxes (e.g., urea production, urea recycling and amino acid exchanges), with or without changes in nitrogen balance, (iv) any deviation from the optimal amino acid intake, in terms of both quality and quantity, causes a global rise in tissue Δ(15)N, and (v) Δ(15)N variations differ between tissues depending on the metabolic changes involved, which can therefore be identified using simultaneous multi-tissue Δ(15)N measurements. This work provides proof of concept that Δ(15)N measurements constitute a new promising tool to investigate how metabolic fluxes are nutritionally or physiopathologically reorganized or altered. The existence of such natural and interpretable isotopic biomarkers promises interesting applications in nutrition and health.
format Online
Article
Text
id pubmed-4183419
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-41834192014-10-07 Natural Isotopic Signatures of Variations in Body Nitrogen Fluxes: A Compartmental Model Analysis Poupin, Nathalie Mariotti, François Huneau, Jean-François Hermier, Dominique Fouillet, Hélène PLoS Comput Biol Research Article Body tissues are generally (15)N-enriched over the diet, with a discrimination factor (Δ(15)N) that varies among tissues and individuals as a function of their nutritional and physiopathological condition. However, both (15)N bioaccumulation and intra- and inter-individual Δ(15)N variations are still poorly understood, so that theoretical models are required to understand their underlying mechanisms. Using experimental Δ(15)N measurements in rats, we developed a multi-compartmental model that provides the first detailed representation of the complex functioning of the body's Δ(15)N system, by explicitly linking the sizes and Δ(15)N values of 21 nitrogen pools to the rates and isotope effects of 49 nitrogen metabolic fluxes. We have shown that (i) besides urea production, several metabolic pathways (e.g., protein synthesis, amino acid intracellular metabolism, urea recycling and intestinal absorption or secretion) are most probably associated with isotope fractionation and together contribute to (15)N accumulation in tissues, (ii) the Δ(15)N of a tissue at steady-state is not affected by variations of its P turnover rate, but can vary according to the relative orientation of tissue free amino acids towards oxidation vs. protein synthesis, (iii) at the whole-body level, Δ(15)N variations result from variations in the body partitioning of nitrogen fluxes (e.g., urea production, urea recycling and amino acid exchanges), with or without changes in nitrogen balance, (iv) any deviation from the optimal amino acid intake, in terms of both quality and quantity, causes a global rise in tissue Δ(15)N, and (v) Δ(15)N variations differ between tissues depending on the metabolic changes involved, which can therefore be identified using simultaneous multi-tissue Δ(15)N measurements. This work provides proof of concept that Δ(15)N measurements constitute a new promising tool to investigate how metabolic fluxes are nutritionally or physiopathologically reorganized or altered. The existence of such natural and interpretable isotopic biomarkers promises interesting applications in nutrition and health. Public Library of Science 2014-10-02 /pmc/articles/PMC4183419/ /pubmed/25275306 http://dx.doi.org/10.1371/journal.pcbi.1003865 Text en © 2014 Poupin et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Poupin, Nathalie
Mariotti, François
Huneau, Jean-François
Hermier, Dominique
Fouillet, Hélène
Natural Isotopic Signatures of Variations in Body Nitrogen Fluxes: A Compartmental Model Analysis
title Natural Isotopic Signatures of Variations in Body Nitrogen Fluxes: A Compartmental Model Analysis
title_full Natural Isotopic Signatures of Variations in Body Nitrogen Fluxes: A Compartmental Model Analysis
title_fullStr Natural Isotopic Signatures of Variations in Body Nitrogen Fluxes: A Compartmental Model Analysis
title_full_unstemmed Natural Isotopic Signatures of Variations in Body Nitrogen Fluxes: A Compartmental Model Analysis
title_short Natural Isotopic Signatures of Variations in Body Nitrogen Fluxes: A Compartmental Model Analysis
title_sort natural isotopic signatures of variations in body nitrogen fluxes: a compartmental model analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4183419/
https://www.ncbi.nlm.nih.gov/pubmed/25275306
http://dx.doi.org/10.1371/journal.pcbi.1003865
work_keys_str_mv AT poupinnathalie naturalisotopicsignaturesofvariationsinbodynitrogenfluxesacompartmentalmodelanalysis
AT mariottifrancois naturalisotopicsignaturesofvariationsinbodynitrogenfluxesacompartmentalmodelanalysis
AT huneaujeanfrancois naturalisotopicsignaturesofvariationsinbodynitrogenfluxesacompartmentalmodelanalysis
AT hermierdominique naturalisotopicsignaturesofvariationsinbodynitrogenfluxesacompartmentalmodelanalysis
AT fouillethelene naturalisotopicsignaturesofvariationsinbodynitrogenfluxesacompartmentalmodelanalysis