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Insulin and Glucagon: Partners for Life
In August 2016, several leaders in glucagon biology gathered for the European Association for the Study of Diabetes Hagedorn Workshop in Oxford, England. A key point of discussion focused on the need for basal insulin to allow for the therapeutic benefit of glucagon blockade in the treatment of diab...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Endocrine Society
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6061217/ https://www.ncbi.nlm.nih.gov/pubmed/28323959 http://dx.doi.org/10.1210/en.2016-1748 |
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author | Holst, Jens Juul Holland, William Gromada, Jesper Lee, Young Unger, Roger H. Yan, Hai Sloop, Kyle W. Kieffer, Timothy J. Damond, Nicolas Herrera, Pedro L. |
author_facet | Holst, Jens Juul Holland, William Gromada, Jesper Lee, Young Unger, Roger H. Yan, Hai Sloop, Kyle W. Kieffer, Timothy J. Damond, Nicolas Herrera, Pedro L. |
author_sort | Holst, Jens Juul |
collection | PubMed |
description | In August 2016, several leaders in glucagon biology gathered for the European Association for the Study of Diabetes Hagedorn Workshop in Oxford, England. A key point of discussion focused on the need for basal insulin to allow for the therapeutic benefit of glucagon blockade in the treatment of diabetes. Among the most enlightening experimental results presented were findings from studies in which glucagon receptor–deficient mice were administered streptozotocin to destroy pancreatic β cells or had undergone diphtheria toxin–induced β cell ablation. This article summarizes key features of the discussion as a consensus was reached. Agents that antagonize glucagon may be of great benefit for the treatment of diabetes; however, sufficient levels of basal insulin are required for their therapeutic efficacy. |
format | Online Article Text |
id | pubmed-6061217 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Endocrine Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-60612172018-08-07 Insulin and Glucagon: Partners for Life Holst, Jens Juul Holland, William Gromada, Jesper Lee, Young Unger, Roger H. Yan, Hai Sloop, Kyle W. Kieffer, Timothy J. Damond, Nicolas Herrera, Pedro L. Endocrinology Mini-review In August 2016, several leaders in glucagon biology gathered for the European Association for the Study of Diabetes Hagedorn Workshop in Oxford, England. A key point of discussion focused on the need for basal insulin to allow for the therapeutic benefit of glucagon blockade in the treatment of diabetes. Among the most enlightening experimental results presented were findings from studies in which glucagon receptor–deficient mice were administered streptozotocin to destroy pancreatic β cells or had undergone diphtheria toxin–induced β cell ablation. This article summarizes key features of the discussion as a consensus was reached. Agents that antagonize glucagon may be of great benefit for the treatment of diabetes; however, sufficient levels of basal insulin are required for their therapeutic efficacy. Endocrine Society 2017-01-31 /pmc/articles/PMC6061217/ /pubmed/28323959 http://dx.doi.org/10.1210/en.2016-1748 Text en Copyright © 2017 Endocrine Society https://creativecommons.org/licenses/by/4.0/ This article has been published under the terms of the Creative Commons Attribution License (CC BY; https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Mini-review Holst, Jens Juul Holland, William Gromada, Jesper Lee, Young Unger, Roger H. Yan, Hai Sloop, Kyle W. Kieffer, Timothy J. Damond, Nicolas Herrera, Pedro L. Insulin and Glucagon: Partners for Life |
title | Insulin and Glucagon: Partners for Life |
title_full | Insulin and Glucagon: Partners for Life |
title_fullStr | Insulin and Glucagon: Partners for Life |
title_full_unstemmed | Insulin and Glucagon: Partners for Life |
title_short | Insulin and Glucagon: Partners for Life |
title_sort | insulin and glucagon: partners for life |
topic | Mini-review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6061217/ https://www.ncbi.nlm.nih.gov/pubmed/28323959 http://dx.doi.org/10.1210/en.2016-1748 |
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