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Development of a Novel Zebrafish Model for Type 2 Diabetes Mellitus

Obesity is a major cause of type 2 diabetes mellitus (T2DM) in mammals. We have previously established a zebrafish model of diet-induced obesity (DIO zebrafish) by overfeeding Artemia. Here we created DIO zebrafish using a different method to induce T2DM. Zebrafish were overfed a commercially availa...

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Autores principales: Zang, Liqing, Shimada, Yasuhito, Nishimura, Norihiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5431185/
https://www.ncbi.nlm.nih.gov/pubmed/28469250
http://dx.doi.org/10.1038/s41598-017-01432-w
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author Zang, Liqing
Shimada, Yasuhito
Nishimura, Norihiro
author_facet Zang, Liqing
Shimada, Yasuhito
Nishimura, Norihiro
author_sort Zang, Liqing
collection PubMed
description Obesity is a major cause of type 2 diabetes mellitus (T2DM) in mammals. We have previously established a zebrafish model of diet-induced obesity (DIO zebrafish) by overfeeding Artemia. Here we created DIO zebrafish using a different method to induce T2DM. Zebrafish were overfed a commercially available fish food using an automated feeding system. We monitored the fasting blood glucose levels in the normal-fed group (one feed/day) and overfed group (six feeds/day) over an 8-week period. The fasting blood glucose level was significantly increased in DIO zebrafish compared with that of normal-fed zebrafish. Intraperitoneal and oral glucose tolerance tests showed impaired glucose tolerance by overfeeding. Insulin production, which was determined indirectly by measuring the EGFP signal strength in overfed Tg(−1.0ins:EGFP) (sc1) zebrafish, was increased in DIO zebrafish. The anti-diabetic drugs metformin and glimepiride ameliorated hyperglycaemia in the overfed group, suggesting that this zebrafish can be used as a model of human T2DM. Finally, we conducted RNA deep sequencing and found that the gene expression profiling of liver-pancreas revealed pathways common to human T2DM. In summary, we developed a zebrafish model of T2DM that shows promise as a platform for mechanistic and therapeutic studies of diet-induced glucose intolerance and insulin resistance.
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spelling pubmed-54311852017-05-16 Development of a Novel Zebrafish Model for Type 2 Diabetes Mellitus Zang, Liqing Shimada, Yasuhito Nishimura, Norihiro Sci Rep Article Obesity is a major cause of type 2 diabetes mellitus (T2DM) in mammals. We have previously established a zebrafish model of diet-induced obesity (DIO zebrafish) by overfeeding Artemia. Here we created DIO zebrafish using a different method to induce T2DM. Zebrafish were overfed a commercially available fish food using an automated feeding system. We monitored the fasting blood glucose levels in the normal-fed group (one feed/day) and overfed group (six feeds/day) over an 8-week period. The fasting blood glucose level was significantly increased in DIO zebrafish compared with that of normal-fed zebrafish. Intraperitoneal and oral glucose tolerance tests showed impaired glucose tolerance by overfeeding. Insulin production, which was determined indirectly by measuring the EGFP signal strength in overfed Tg(−1.0ins:EGFP) (sc1) zebrafish, was increased in DIO zebrafish. The anti-diabetic drugs metformin and glimepiride ameliorated hyperglycaemia in the overfed group, suggesting that this zebrafish can be used as a model of human T2DM. Finally, we conducted RNA deep sequencing and found that the gene expression profiling of liver-pancreas revealed pathways common to human T2DM. In summary, we developed a zebrafish model of T2DM that shows promise as a platform for mechanistic and therapeutic studies of diet-induced glucose intolerance and insulin resistance. Nature Publishing Group UK 2017-05-03 /pmc/articles/PMC5431185/ /pubmed/28469250 http://dx.doi.org/10.1038/s41598-017-01432-w Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Zang, Liqing
Shimada, Yasuhito
Nishimura, Norihiro
Development of a Novel Zebrafish Model for Type 2 Diabetes Mellitus
title Development of a Novel Zebrafish Model for Type 2 Diabetes Mellitus
title_full Development of a Novel Zebrafish Model for Type 2 Diabetes Mellitus
title_fullStr Development of a Novel Zebrafish Model for Type 2 Diabetes Mellitus
title_full_unstemmed Development of a Novel Zebrafish Model for Type 2 Diabetes Mellitus
title_short Development of a Novel Zebrafish Model for Type 2 Diabetes Mellitus
title_sort development of a novel zebrafish model for type 2 diabetes mellitus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5431185/
https://www.ncbi.nlm.nih.gov/pubmed/28469250
http://dx.doi.org/10.1038/s41598-017-01432-w
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