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Phase modulation of insulin pulses enhances glucose regulation and enables inter-islet synchronization

Insulin is secreted in a pulsatile manner from multiple micro-organs called the islets of Langerhans. The amplitude and phase (shape) of insulin secretion are modulated by numerous factors including glucose. The role of phase modulation in glucose homeostasis is not well understood compared to the o...

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Autores principales: Lee, Boah, Song, Taegeun, Lee, Kayoung, Kim, Jaeyoon, Han, Seungmin, Berggren, Per-Olof, Ryu, Sung Ho, Jo, Junghyo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5325581/
https://www.ncbi.nlm.nih.gov/pubmed/28235104
http://dx.doi.org/10.1371/journal.pone.0172901
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author Lee, Boah
Song, Taegeun
Lee, Kayoung
Kim, Jaeyoon
Han, Seungmin
Berggren, Per-Olof
Ryu, Sung Ho
Jo, Junghyo
author_facet Lee, Boah
Song, Taegeun
Lee, Kayoung
Kim, Jaeyoon
Han, Seungmin
Berggren, Per-Olof
Ryu, Sung Ho
Jo, Junghyo
author_sort Lee, Boah
collection PubMed
description Insulin is secreted in a pulsatile manner from multiple micro-organs called the islets of Langerhans. The amplitude and phase (shape) of insulin secretion are modulated by numerous factors including glucose. The role of phase modulation in glucose homeostasis is not well understood compared to the obvious contribution of amplitude modulation. In the present study, we measured Ca(2+) oscillations in islets as a proxy for insulin pulses, and we observed their frequency and shape changes under constant/alternating glucose stimuli. Here we asked how the phase modulation of insulin pulses contributes to glucose regulation. To directly answer this question, we developed a phenomenological oscillator model that drastically simplifies insulin secretion, but precisely incorporates the observed phase modulation of insulin pulses in response to glucose stimuli. Then, we mathematically modeled how insulin pulses regulate the glucose concentration in the body. The model of insulin oscillation and glucose regulation describes the glucose-insulin feedback loop. The data-based model demonstrates that the existence of phase modulation narrows the range within which the glucose concentration is maintained through the suppression/enhancement of insulin secretion in conjunction with the amplitude modulation of this secretion. The phase modulation is the response of islets to glucose perturbations. When multiple islets are exposed to the same glucose stimuli, they can be entrained to generate synchronous insulin pulses. Thus, we conclude that the phase modulation of insulin pulses is essential for glucose regulation and inter-islet synchronization.
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spelling pubmed-53255812017-03-09 Phase modulation of insulin pulses enhances glucose regulation and enables inter-islet synchronization Lee, Boah Song, Taegeun Lee, Kayoung Kim, Jaeyoon Han, Seungmin Berggren, Per-Olof Ryu, Sung Ho Jo, Junghyo PLoS One Research Article Insulin is secreted in a pulsatile manner from multiple micro-organs called the islets of Langerhans. The amplitude and phase (shape) of insulin secretion are modulated by numerous factors including glucose. The role of phase modulation in glucose homeostasis is not well understood compared to the obvious contribution of amplitude modulation. In the present study, we measured Ca(2+) oscillations in islets as a proxy for insulin pulses, and we observed their frequency and shape changes under constant/alternating glucose stimuli. Here we asked how the phase modulation of insulin pulses contributes to glucose regulation. To directly answer this question, we developed a phenomenological oscillator model that drastically simplifies insulin secretion, but precisely incorporates the observed phase modulation of insulin pulses in response to glucose stimuli. Then, we mathematically modeled how insulin pulses regulate the glucose concentration in the body. The model of insulin oscillation and glucose regulation describes the glucose-insulin feedback loop. The data-based model demonstrates that the existence of phase modulation narrows the range within which the glucose concentration is maintained through the suppression/enhancement of insulin secretion in conjunction with the amplitude modulation of this secretion. The phase modulation is the response of islets to glucose perturbations. When multiple islets are exposed to the same glucose stimuli, they can be entrained to generate synchronous insulin pulses. Thus, we conclude that the phase modulation of insulin pulses is essential for glucose regulation and inter-islet synchronization. Public Library of Science 2017-02-24 /pmc/articles/PMC5325581/ /pubmed/28235104 http://dx.doi.org/10.1371/journal.pone.0172901 Text en © 2017 Lee 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
Lee, Boah
Song, Taegeun
Lee, Kayoung
Kim, Jaeyoon
Han, Seungmin
Berggren, Per-Olof
Ryu, Sung Ho
Jo, Junghyo
Phase modulation of insulin pulses enhances glucose regulation and enables inter-islet synchronization
title Phase modulation of insulin pulses enhances glucose regulation and enables inter-islet synchronization
title_full Phase modulation of insulin pulses enhances glucose regulation and enables inter-islet synchronization
title_fullStr Phase modulation of insulin pulses enhances glucose regulation and enables inter-islet synchronization
title_full_unstemmed Phase modulation of insulin pulses enhances glucose regulation and enables inter-islet synchronization
title_short Phase modulation of insulin pulses enhances glucose regulation and enables inter-islet synchronization
title_sort phase modulation of insulin pulses enhances glucose regulation and enables inter-islet synchronization
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5325581/
https://www.ncbi.nlm.nih.gov/pubmed/28235104
http://dx.doi.org/10.1371/journal.pone.0172901
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