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The Suprachiasmatic Nucleus Controls Circadian Energy Metabolism and Hepatic Insulin Sensitivity
Disturbances in the circadian system are associated with the development of type 2 diabetes mellitus. Here, we studied the direct contribution of the suprachiasmatic nucleus (SCN), the central pacemaker in the circadian system, in the development of insulin resistance. Exclusive bilateral SCN lesion...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Diabetes Association
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3609590/ https://www.ncbi.nlm.nih.gov/pubmed/23274903 http://dx.doi.org/10.2337/db12-0507 |
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author | Coomans, Claudia P. van den Berg, Sjoerd A.A. Lucassen, Eliane A. Houben, Thijs Pronk, Amanda C.M. van der Spek, Rianne D. Kalsbeek, Andries Biermasz, Nienke R. Willems van Dijk, Ko Romijn, Johannes A. Meijer, Johanna H. |
author_facet | Coomans, Claudia P. van den Berg, Sjoerd A.A. Lucassen, Eliane A. Houben, Thijs Pronk, Amanda C.M. van der Spek, Rianne D. Kalsbeek, Andries Biermasz, Nienke R. Willems van Dijk, Ko Romijn, Johannes A. Meijer, Johanna H. |
author_sort | Coomans, Claudia P. |
collection | PubMed |
description | Disturbances in the circadian system are associated with the development of type 2 diabetes mellitus. Here, we studied the direct contribution of the suprachiasmatic nucleus (SCN), the central pacemaker in the circadian system, in the development of insulin resistance. Exclusive bilateral SCN lesions in male C57Bl/6J mice, as verified by immunochemistry, showed a small but significant increase in body weight (+17%), which was accounted for by an increase in fat mass. In contrast, mice with collateral damage to the ventromedial hypothalamus and paraventricular nucleus showed severe obesity and insulin resistance. Mice with exclusive SCN ablation revealed a loss of circadian rhythm in activity, oxygen consumption, and food intake. Hyperinsulinemic–euglycemic clamp analysis 8 weeks after lesioning showed that the glucose infusion rate was significantly lower in SCN lesioned mice compared with sham-operated mice (−63%). Although insulin potently inhibited endogenous glucose production (−84%), this was greatly reduced in SCN lesioned mice (−7%), indicating severe hepatic insulin resistance. Our data show that SCN malfunctioning plays an important role in the disturbance of energy balance and suggest that an absence of central clock activity, in a genetically intact animal, may lead to the development of insulin resistance. |
format | Online Article Text |
id | pubmed-3609590 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | American Diabetes Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-36095902014-04-01 The Suprachiasmatic Nucleus Controls Circadian Energy Metabolism and Hepatic Insulin Sensitivity Coomans, Claudia P. van den Berg, Sjoerd A.A. Lucassen, Eliane A. Houben, Thijs Pronk, Amanda C.M. van der Spek, Rianne D. Kalsbeek, Andries Biermasz, Nienke R. Willems van Dijk, Ko Romijn, Johannes A. Meijer, Johanna H. Diabetes Original Research Disturbances in the circadian system are associated with the development of type 2 diabetes mellitus. Here, we studied the direct contribution of the suprachiasmatic nucleus (SCN), the central pacemaker in the circadian system, in the development of insulin resistance. Exclusive bilateral SCN lesions in male C57Bl/6J mice, as verified by immunochemistry, showed a small but significant increase in body weight (+17%), which was accounted for by an increase in fat mass. In contrast, mice with collateral damage to the ventromedial hypothalamus and paraventricular nucleus showed severe obesity and insulin resistance. Mice with exclusive SCN ablation revealed a loss of circadian rhythm in activity, oxygen consumption, and food intake. Hyperinsulinemic–euglycemic clamp analysis 8 weeks after lesioning showed that the glucose infusion rate was significantly lower in SCN lesioned mice compared with sham-operated mice (−63%). Although insulin potently inhibited endogenous glucose production (−84%), this was greatly reduced in SCN lesioned mice (−7%), indicating severe hepatic insulin resistance. Our data show that SCN malfunctioning plays an important role in the disturbance of energy balance and suggest that an absence of central clock activity, in a genetically intact animal, may lead to the development of insulin resistance. American Diabetes Association 2013-04 2013-03-14 /pmc/articles/PMC3609590/ /pubmed/23274903 http://dx.doi.org/10.2337/db12-0507 Text en © 2013 by the American Diabetes Association. Readers 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. See http://creativecommons.org/licenses/by-nc-nd/3.0/ for details. |
spellingShingle | Original Research Coomans, Claudia P. van den Berg, Sjoerd A.A. Lucassen, Eliane A. Houben, Thijs Pronk, Amanda C.M. van der Spek, Rianne D. Kalsbeek, Andries Biermasz, Nienke R. Willems van Dijk, Ko Romijn, Johannes A. Meijer, Johanna H. The Suprachiasmatic Nucleus Controls Circadian Energy Metabolism and Hepatic Insulin Sensitivity |
title | The Suprachiasmatic Nucleus Controls Circadian Energy Metabolism and Hepatic Insulin Sensitivity |
title_full | The Suprachiasmatic Nucleus Controls Circadian Energy Metabolism and Hepatic Insulin Sensitivity |
title_fullStr | The Suprachiasmatic Nucleus Controls Circadian Energy Metabolism and Hepatic Insulin Sensitivity |
title_full_unstemmed | The Suprachiasmatic Nucleus Controls Circadian Energy Metabolism and Hepatic Insulin Sensitivity |
title_short | The Suprachiasmatic Nucleus Controls Circadian Energy Metabolism and Hepatic Insulin Sensitivity |
title_sort | suprachiasmatic nucleus controls circadian energy metabolism and hepatic insulin sensitivity |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3609590/ https://www.ncbi.nlm.nih.gov/pubmed/23274903 http://dx.doi.org/10.2337/db12-0507 |
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