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A mathematical model of the impact of insulin secretion dynamics on selective hepatic insulin resistance

Physiological insulin secretion exhibits various temporal patterns, the dysregulation of which is involved in diabetes development. We analyzed the impact of first-phase and pulsatile insulin release on glucose and lipid control with various hepatic insulin signaling networks. The mathematical model...

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Autores principales: Zhao, Gang, Wirth, Dagmar, Schmitz, Ingo, Meyer-Hermann, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5678123/
https://www.ncbi.nlm.nih.gov/pubmed/29118381
http://dx.doi.org/10.1038/s41467-017-01627-9
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author Zhao, Gang
Wirth, Dagmar
Schmitz, Ingo
Meyer-Hermann, Michael
author_facet Zhao, Gang
Wirth, Dagmar
Schmitz, Ingo
Meyer-Hermann, Michael
author_sort Zhao, Gang
collection PubMed
description Physiological insulin secretion exhibits various temporal patterns, the dysregulation of which is involved in diabetes development. We analyzed the impact of first-phase and pulsatile insulin release on glucose and lipid control with various hepatic insulin signaling networks. The mathematical model suggests that atypical protein kinase C (aPKC) undergoes a bistable switch-on and switch-off, under the control of insulin receptor substrate 2 (IRS2). The activation of IRS1 and IRS2 is temporally separated due to the inhibition of IRS1 by aPKC. The model further shows that the timing of aPKC switch-off is delayed by reduced first-phase insulin and reduced amplitude of insulin pulses. Based on these findings, we propose a sequential model of postprandial hepatic control of glucose and lipid by insulin, according to which delayed aPKC switch-off contributes to selective hepatic insulin resistance, which is a long-standing paradox in the field.
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spelling pubmed-56781232017-11-15 A mathematical model of the impact of insulin secretion dynamics on selective hepatic insulin resistance Zhao, Gang Wirth, Dagmar Schmitz, Ingo Meyer-Hermann, Michael Nat Commun Article Physiological insulin secretion exhibits various temporal patterns, the dysregulation of which is involved in diabetes development. We analyzed the impact of first-phase and pulsatile insulin release on glucose and lipid control with various hepatic insulin signaling networks. The mathematical model suggests that atypical protein kinase C (aPKC) undergoes a bistable switch-on and switch-off, under the control of insulin receptor substrate 2 (IRS2). The activation of IRS1 and IRS2 is temporally separated due to the inhibition of IRS1 by aPKC. The model further shows that the timing of aPKC switch-off is delayed by reduced first-phase insulin and reduced amplitude of insulin pulses. Based on these findings, we propose a sequential model of postprandial hepatic control of glucose and lipid by insulin, according to which delayed aPKC switch-off contributes to selective hepatic insulin resistance, which is a long-standing paradox in the field. Nature Publishing Group UK 2017-11-08 /pmc/articles/PMC5678123/ /pubmed/29118381 http://dx.doi.org/10.1038/s41467-017-01627-9 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Zhao, Gang
Wirth, Dagmar
Schmitz, Ingo
Meyer-Hermann, Michael
A mathematical model of the impact of insulin secretion dynamics on selective hepatic insulin resistance
title A mathematical model of the impact of insulin secretion dynamics on selective hepatic insulin resistance
title_full A mathematical model of the impact of insulin secretion dynamics on selective hepatic insulin resistance
title_fullStr A mathematical model of the impact of insulin secretion dynamics on selective hepatic insulin resistance
title_full_unstemmed A mathematical model of the impact of insulin secretion dynamics on selective hepatic insulin resistance
title_short A mathematical model of the impact of insulin secretion dynamics on selective hepatic insulin resistance
title_sort mathematical model of the impact of insulin secretion dynamics on selective hepatic insulin resistance
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5678123/
https://www.ncbi.nlm.nih.gov/pubmed/29118381
http://dx.doi.org/10.1038/s41467-017-01627-9
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