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HepatoDyn: A Dynamic Model of Hepatocyte Metabolism That Integrates (13)C Isotopomer Data

The liver performs many essential metabolic functions, which can be studied using computational models of hepatocytes. Here we present HepatoDyn, a highly detailed dynamic model of hepatocyte metabolism. HepatoDyn includes a large metabolic network, highly detailed kinetic laws, and is capable of dy...

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Autores principales: Foguet, Carles, Marin, Silvia, Selivanov, Vitaly A., Fanchon, Eric, Lee, Wai-Nang Paul, Guinovart, Joan J., de Atauri, Pedro, Cascante, Marta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4849781/
https://www.ncbi.nlm.nih.gov/pubmed/27124774
http://dx.doi.org/10.1371/journal.pcbi.1004899
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author Foguet, Carles
Marin, Silvia
Selivanov, Vitaly A.
Fanchon, Eric
Lee, Wai-Nang Paul
Guinovart, Joan J.
de Atauri, Pedro
Cascante, Marta
author_facet Foguet, Carles
Marin, Silvia
Selivanov, Vitaly A.
Fanchon, Eric
Lee, Wai-Nang Paul
Guinovart, Joan J.
de Atauri, Pedro
Cascante, Marta
author_sort Foguet, Carles
collection PubMed
description The liver performs many essential metabolic functions, which can be studied using computational models of hepatocytes. Here we present HepatoDyn, a highly detailed dynamic model of hepatocyte metabolism. HepatoDyn includes a large metabolic network, highly detailed kinetic laws, and is capable of dynamically simulating the redox and energy metabolism of hepatocytes. Furthermore, the model was coupled to the module for isotopic label propagation of the software package IsoDyn, allowing HepatoDyn to integrate data derived from (13)C based experiments. As an example of dynamical simulations applied to hepatocytes, we studied the effects of high fructose concentrations on hepatocyte metabolism by integrating data from experiments in which rat hepatocytes were incubated with 20 mM glucose supplemented with either 3 mM or 20 mM fructose. These experiments showed that glycogen accumulation was significantly lower in hepatocytes incubated with medium supplemented with 20 mM fructose than in hepatocytes incubated with medium supplemented with 3 mM fructose. Through the integration of extracellular fluxes and (13)C enrichment measurements, HepatoDyn predicted that this phenomenon can be attributed to a depletion of cytosolic ATP and phosphate induced by high fructose concentrations in the medium.
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spelling pubmed-48497812016-05-07 HepatoDyn: A Dynamic Model of Hepatocyte Metabolism That Integrates (13)C Isotopomer Data Foguet, Carles Marin, Silvia Selivanov, Vitaly A. Fanchon, Eric Lee, Wai-Nang Paul Guinovart, Joan J. de Atauri, Pedro Cascante, Marta PLoS Comput Biol Research Article The liver performs many essential metabolic functions, which can be studied using computational models of hepatocytes. Here we present HepatoDyn, a highly detailed dynamic model of hepatocyte metabolism. HepatoDyn includes a large metabolic network, highly detailed kinetic laws, and is capable of dynamically simulating the redox and energy metabolism of hepatocytes. Furthermore, the model was coupled to the module for isotopic label propagation of the software package IsoDyn, allowing HepatoDyn to integrate data derived from (13)C based experiments. As an example of dynamical simulations applied to hepatocytes, we studied the effects of high fructose concentrations on hepatocyte metabolism by integrating data from experiments in which rat hepatocytes were incubated with 20 mM glucose supplemented with either 3 mM or 20 mM fructose. These experiments showed that glycogen accumulation was significantly lower in hepatocytes incubated with medium supplemented with 20 mM fructose than in hepatocytes incubated with medium supplemented with 3 mM fructose. Through the integration of extracellular fluxes and (13)C enrichment measurements, HepatoDyn predicted that this phenomenon can be attributed to a depletion of cytosolic ATP and phosphate induced by high fructose concentrations in the medium. Public Library of Science 2016-04-28 /pmc/articles/PMC4849781/ /pubmed/27124774 http://dx.doi.org/10.1371/journal.pcbi.1004899 Text en © 2016 Foguet 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Foguet, Carles
Marin, Silvia
Selivanov, Vitaly A.
Fanchon, Eric
Lee, Wai-Nang Paul
Guinovart, Joan J.
de Atauri, Pedro
Cascante, Marta
HepatoDyn: A Dynamic Model of Hepatocyte Metabolism That Integrates (13)C Isotopomer Data
title HepatoDyn: A Dynamic Model of Hepatocyte Metabolism That Integrates (13)C Isotopomer Data
title_full HepatoDyn: A Dynamic Model of Hepatocyte Metabolism That Integrates (13)C Isotopomer Data
title_fullStr HepatoDyn: A Dynamic Model of Hepatocyte Metabolism That Integrates (13)C Isotopomer Data
title_full_unstemmed HepatoDyn: A Dynamic Model of Hepatocyte Metabolism That Integrates (13)C Isotopomer Data
title_short HepatoDyn: A Dynamic Model of Hepatocyte Metabolism That Integrates (13)C Isotopomer Data
title_sort hepatodyn: a dynamic model of hepatocyte metabolism that integrates (13)c isotopomer data
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4849781/
https://www.ncbi.nlm.nih.gov/pubmed/27124774
http://dx.doi.org/10.1371/journal.pcbi.1004899
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