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Closing in on the Mechanisms of Pulsatile Insulin Secretion
Insulin secretion from pancreatic islet β-cells occurs in a pulsatile fashion, with a typical period of ∼5 min. The basis of this pulsatility in mouse islets has been investigated for more than four decades, and the various theories have been described as either qualitative or mathematical models. I...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Diabetes Association
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5828455/ https://www.ncbi.nlm.nih.gov/pubmed/29463575 http://dx.doi.org/10.2337/dbi17-0004 |
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author | Bertram, Richard Satin, Leslie S. Sherman, Arthur S. |
author_facet | Bertram, Richard Satin, Leslie S. Sherman, Arthur S. |
author_sort | Bertram, Richard |
collection | PubMed |
description | Insulin secretion from pancreatic islet β-cells occurs in a pulsatile fashion, with a typical period of ∼5 min. The basis of this pulsatility in mouse islets has been investigated for more than four decades, and the various theories have been described as either qualitative or mathematical models. In many cases the models differ in their mechanisms for rhythmogenesis, as well as other less important details. In this Perspective, we describe two main classes of models: those in which oscillations in the intracellular Ca(2+) concentration drive oscillations in metabolism, and those in which intrinsic metabolic oscillations drive oscillations in Ca(2+) concentration and electrical activity. We then discuss nine canonical experimental findings that provide key insights into the mechanism of islet oscillations and list the models that can account for each finding. Finally, we describe a new model that integrates features from multiple earlier models and is thus called the Integrated Oscillator Model. In this model, intracellular Ca(2+) acts on the glycolytic pathway in the generation of oscillations, and it is thus a hybrid of the two main classes of models. It alone among models proposed to date can explain all nine key experimental findings, and it serves as a good starting point for future studies of pulsatile insulin secretion from human islets. |
format | Online Article Text |
id | pubmed-5828455 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Diabetes Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-58284552019-03-01 Closing in on the Mechanisms of Pulsatile Insulin Secretion Bertram, Richard Satin, Leslie S. Sherman, Arthur S. Diabetes Perspectives in Diabetes Insulin secretion from pancreatic islet β-cells occurs in a pulsatile fashion, with a typical period of ∼5 min. The basis of this pulsatility in mouse islets has been investigated for more than four decades, and the various theories have been described as either qualitative or mathematical models. In many cases the models differ in their mechanisms for rhythmogenesis, as well as other less important details. In this Perspective, we describe two main classes of models: those in which oscillations in the intracellular Ca(2+) concentration drive oscillations in metabolism, and those in which intrinsic metabolic oscillations drive oscillations in Ca(2+) concentration and electrical activity. We then discuss nine canonical experimental findings that provide key insights into the mechanism of islet oscillations and list the models that can account for each finding. Finally, we describe a new model that integrates features from multiple earlier models and is thus called the Integrated Oscillator Model. In this model, intracellular Ca(2+) acts on the glycolytic pathway in the generation of oscillations, and it is thus a hybrid of the two main classes of models. It alone among models proposed to date can explain all nine key experimental findings, and it serves as a good starting point for future studies of pulsatile insulin secretion from human islets. American Diabetes Association 2018-03 2017-02-14 /pmc/articles/PMC5828455/ /pubmed/29463575 http://dx.doi.org/10.2337/dbi17-0004 Text en © 2018 by the American Diabetes Association. http://www.diabetesjournals.org/content/licenseReaders may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. More information is available at http://www.diabetesjournals.org/content/license. |
spellingShingle | Perspectives in Diabetes Bertram, Richard Satin, Leslie S. Sherman, Arthur S. Closing in on the Mechanisms of Pulsatile Insulin Secretion |
title | Closing in on the Mechanisms of Pulsatile Insulin Secretion |
title_full | Closing in on the Mechanisms of Pulsatile Insulin Secretion |
title_fullStr | Closing in on the Mechanisms of Pulsatile Insulin Secretion |
title_full_unstemmed | Closing in on the Mechanisms of Pulsatile Insulin Secretion |
title_short | Closing in on the Mechanisms of Pulsatile Insulin Secretion |
title_sort | closing in on the mechanisms of pulsatile insulin secretion |
topic | Perspectives in Diabetes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5828455/ https://www.ncbi.nlm.nih.gov/pubmed/29463575 http://dx.doi.org/10.2337/dbi17-0004 |
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