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The selective control of glycolysis, gluconeogenesis and glycogenesis by temporal insulin patterns

Insulin governs systemic glucose metabolism, including glycolysis, gluconeogenesis and glycogenesis, through temporal change and absolute concentration. However, how insulin-signalling pathway selectively regulates glycolysis, gluconeogenesis and glycogenesis remains to be elucidated. To address thi...

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Autores principales: Noguchi, Rei, Kubota, Hiroyuki, Yugi, Katsuyuki, Toyoshima, Yu, Komori, Yasunori, Soga, Tomoyoshi, Kuroda, Shinya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: European Molecular Biology Organization 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4039368/
https://www.ncbi.nlm.nih.gov/pubmed/23670537
http://dx.doi.org/10.1038/msb.2013.19
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author Noguchi, Rei
Kubota, Hiroyuki
Yugi, Katsuyuki
Toyoshima, Yu
Komori, Yasunori
Soga, Tomoyoshi
Kuroda, Shinya
author_facet Noguchi, Rei
Kubota, Hiroyuki
Yugi, Katsuyuki
Toyoshima, Yu
Komori, Yasunori
Soga, Tomoyoshi
Kuroda, Shinya
author_sort Noguchi, Rei
collection PubMed
description Insulin governs systemic glucose metabolism, including glycolysis, gluconeogenesis and glycogenesis, through temporal change and absolute concentration. However, how insulin-signalling pathway selectively regulates glycolysis, gluconeogenesis and glycogenesis remains to be elucidated. To address this issue, we experimentally measured metabolites in glucose metabolism in response to insulin. Step stimulation of insulin induced transient response of glycolysis and glycogenesis, and sustained response of gluconeogenesis and extracellular glucose concentration (GLC(ex)). Based on the experimental results, we constructed a simple computational model that characterises response of insulin-signalling-dependent glucose metabolism. The model revealed that the network motifs of glycolysis and glycogenesis pathways constitute a feedforward (FF) with substrate depletion and incoherent feedforward loop (iFFL), respectively, enabling glycolysis and glycogenesis responsive to temporal changes of insulin rather than its absolute concentration. In contrast, the network motifs of gluconeogenesis pathway constituted a FF inhibition, enabling gluconeogenesis responsive to absolute concentration of insulin regardless of its temporal patterns. GLC(ex) was regulated by gluconeogenesis and glycolysis. These results demonstrate the selective control mechanism of glucose metabolism by temporal patterns of insulin.
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spelling pubmed-40393682014-06-02 The selective control of glycolysis, gluconeogenesis and glycogenesis by temporal insulin patterns Noguchi, Rei Kubota, Hiroyuki Yugi, Katsuyuki Toyoshima, Yu Komori, Yasunori Soga, Tomoyoshi Kuroda, Shinya Mol Syst Biol Article Insulin governs systemic glucose metabolism, including glycolysis, gluconeogenesis and glycogenesis, through temporal change and absolute concentration. However, how insulin-signalling pathway selectively regulates glycolysis, gluconeogenesis and glycogenesis remains to be elucidated. To address this issue, we experimentally measured metabolites in glucose metabolism in response to insulin. Step stimulation of insulin induced transient response of glycolysis and glycogenesis, and sustained response of gluconeogenesis and extracellular glucose concentration (GLC(ex)). Based on the experimental results, we constructed a simple computational model that characterises response of insulin-signalling-dependent glucose metabolism. The model revealed that the network motifs of glycolysis and glycogenesis pathways constitute a feedforward (FF) with substrate depletion and incoherent feedforward loop (iFFL), respectively, enabling glycolysis and glycogenesis responsive to temporal changes of insulin rather than its absolute concentration. In contrast, the network motifs of gluconeogenesis pathway constituted a FF inhibition, enabling gluconeogenesis responsive to absolute concentration of insulin regardless of its temporal patterns. GLC(ex) was regulated by gluconeogenesis and glycolysis. These results demonstrate the selective control mechanism of glucose metabolism by temporal patterns of insulin. European Molecular Biology Organization 2013-05-14 /pmc/articles/PMC4039368/ /pubmed/23670537 http://dx.doi.org/10.1038/msb.2013.19 Text en Copyright © 2013, EMBO and Macmillan Publishers Limited https://creativecommons.org/licenses/by-nc-sa/3.0/This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported Licence. To view a copy of this licence visit http://creativecommons.org/licenses/by-nc-sa/3.0/.
spellingShingle Article
Noguchi, Rei
Kubota, Hiroyuki
Yugi, Katsuyuki
Toyoshima, Yu
Komori, Yasunori
Soga, Tomoyoshi
Kuroda, Shinya
The selective control of glycolysis, gluconeogenesis and glycogenesis by temporal insulin patterns
title The selective control of glycolysis, gluconeogenesis and glycogenesis by temporal insulin patterns
title_full The selective control of glycolysis, gluconeogenesis and glycogenesis by temporal insulin patterns
title_fullStr The selective control of glycolysis, gluconeogenesis and glycogenesis by temporal insulin patterns
title_full_unstemmed The selective control of glycolysis, gluconeogenesis and glycogenesis by temporal insulin patterns
title_short The selective control of glycolysis, gluconeogenesis and glycogenesis by temporal insulin patterns
title_sort selective control of glycolysis, gluconeogenesis and glycogenesis by temporal insulin patterns
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4039368/
https://www.ncbi.nlm.nih.gov/pubmed/23670537
http://dx.doi.org/10.1038/msb.2013.19
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