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Protective effects of epoxypukalide on pancreatic β-cells and glucose metabolism in STZ-induced diabetic mice
Diabetes is a consequence of a decrease on functional β-cell mass. We have recently demonstrated that epoxypukalide (Epoxy) is a natural compound with beneficial effects on primary cultures of rat islets. In this study, we extend our previous investigations to test the hypothesis that Epoxy protects...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4878260/ https://www.ncbi.nlm.nih.gov/pubmed/26406478 http://dx.doi.org/10.1080/19382014.2015.1078053 |
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author | López-Acosta, Jose F Villa-Pérez, Pablo Fernández-Díaz, Cristina M Román, Daniel de Luis Díaz-Marrero, Ana R Cueto, Mercedes Perdomo, Germán Cózar-Castellano, Irene |
author_facet | López-Acosta, Jose F Villa-Pérez, Pablo Fernández-Díaz, Cristina M Román, Daniel de Luis Díaz-Marrero, Ana R Cueto, Mercedes Perdomo, Germán Cózar-Castellano, Irene |
author_sort | López-Acosta, Jose F |
collection | PubMed |
description | Diabetes is a consequence of a decrease on functional β-cell mass. We have recently demonstrated that epoxypukalide (Epoxy) is a natural compound with beneficial effects on primary cultures of rat islets. In this study, we extend our previous investigations to test the hypothesis that Epoxy protects β-cells and improves glucose metabolism in STZ-induced diabetic mice. We used 3-months old male mice that were treated with Epoxy at 200 μg/kg body weight. Glucose intolerance was induced by multiple intraperitoneal low-doses of streptozotocin (STZ) on 5 consecutive days. Glucose homeostasis was evaluated measuring plasma insulin levels and glucose tolerance. Histomorphometry was used to quantify the number of pancreatic β-cells per islet. β-cell proliferation was assessed by BrdU incorporation, and apoptosis by TUNEL staining. Epoxy treatment significantly improved glucose tolerance and plasma insulin levels. These metabolic changes were associated with increased β-cell numbers, as a result of a two-fold increase in β-cell proliferation and a 50% decrease in β-cell death. Our results demonstrate that Epoxy improves whole-body glucose homeostasis by preventing pancreatic β-cell death due to STZ-induced toxicity in STZ-treated mice. |
format | Online Article Text |
id | pubmed-4878260 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-48782602016-06-07 Protective effects of epoxypukalide on pancreatic β-cells and glucose metabolism in STZ-induced diabetic mice López-Acosta, Jose F Villa-Pérez, Pablo Fernández-Díaz, Cristina M Román, Daniel de Luis Díaz-Marrero, Ana R Cueto, Mercedes Perdomo, Germán Cózar-Castellano, Irene Islets Research Paper Diabetes is a consequence of a decrease on functional β-cell mass. We have recently demonstrated that epoxypukalide (Epoxy) is a natural compound with beneficial effects on primary cultures of rat islets. In this study, we extend our previous investigations to test the hypothesis that Epoxy protects β-cells and improves glucose metabolism in STZ-induced diabetic mice. We used 3-months old male mice that were treated with Epoxy at 200 μg/kg body weight. Glucose intolerance was induced by multiple intraperitoneal low-doses of streptozotocin (STZ) on 5 consecutive days. Glucose homeostasis was evaluated measuring plasma insulin levels and glucose tolerance. Histomorphometry was used to quantify the number of pancreatic β-cells per islet. β-cell proliferation was assessed by BrdU incorporation, and apoptosis by TUNEL staining. Epoxy treatment significantly improved glucose tolerance and plasma insulin levels. These metabolic changes were associated with increased β-cell numbers, as a result of a two-fold increase in β-cell proliferation and a 50% decrease in β-cell death. Our results demonstrate that Epoxy improves whole-body glucose homeostasis by preventing pancreatic β-cell death due to STZ-induced toxicity in STZ-treated mice. Taylor & Francis 2015-09-25 /pmc/articles/PMC4878260/ /pubmed/26406478 http://dx.doi.org/10.1080/19382014.2015.1078053 Text en © 2015 The Author(s). Published with license by Taylor & Francis Group, LLC http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted. |
spellingShingle | Research Paper López-Acosta, Jose F Villa-Pérez, Pablo Fernández-Díaz, Cristina M Román, Daniel de Luis Díaz-Marrero, Ana R Cueto, Mercedes Perdomo, Germán Cózar-Castellano, Irene Protective effects of epoxypukalide on pancreatic β-cells and glucose metabolism in STZ-induced diabetic mice |
title | Protective effects of epoxypukalide on pancreatic β-cells and glucose metabolism in STZ-induced diabetic mice |
title_full | Protective effects of epoxypukalide on pancreatic β-cells and glucose metabolism in STZ-induced diabetic mice |
title_fullStr | Protective effects of epoxypukalide on pancreatic β-cells and glucose metabolism in STZ-induced diabetic mice |
title_full_unstemmed | Protective effects of epoxypukalide on pancreatic β-cells and glucose metabolism in STZ-induced diabetic mice |
title_short | Protective effects of epoxypukalide on pancreatic β-cells and glucose metabolism in STZ-induced diabetic mice |
title_sort | protective effects of epoxypukalide on pancreatic β-cells and glucose metabolism in stz-induced diabetic mice |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4878260/ https://www.ncbi.nlm.nih.gov/pubmed/26406478 http://dx.doi.org/10.1080/19382014.2015.1078053 |
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