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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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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. |
format | Online Article Text |
id | pubmed-4849781 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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