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Comparative medical characteristics of ZDF‐T2DM rats during the course of development to late stage disease
BACKGROUND: There are few reports on the comparative medical characteristics of type 2 diabetes models in late stage. An analysis of comparative medical characteristics of Zucker diabetic fatty type 2 diabetes mellitus (ZDF‐T2DM) rats during the course of development to late stage disease was perfor...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6388085/ https://www.ncbi.nlm.nih.gov/pubmed/30891566 http://dx.doi.org/10.1002/ame2.12030 |
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author | Pang, Yun‐Li Hu, Jing‐Wen Liu, Guang‐Long Lu, Shuai‐Yao |
author_facet | Pang, Yun‐Li Hu, Jing‐Wen Liu, Guang‐Long Lu, Shuai‐Yao |
author_sort | Pang, Yun‐Li |
collection | PubMed |
description | BACKGROUND: There are few reports on the comparative medical characteristics of type 2 diabetes models in late stage. An analysis of comparative medical characteristics of Zucker diabetic fatty type 2 diabetes mellitus (ZDF‐T2DM) rats during the course of development to late stage disease was performed. METHODS: In this study, ZDF rats were fed with high‐sugar and high‐fat diets to raise the fasting blood glucose, and develop of type 2 diabetes. At the late stage of T2DM, the preliminary comparative medical characteristics of the T2DM model were analyzed through the detection of clinical indicators, histopathology, related cytokine levels, and insulin‐related signaling molecule expression levels. RESULTS: In the T2DM group, the fasting blood glucose was higher than 6.8 mmol/L, the serum insulin, leptin, and adiponectin levels were significantly decreased, and glucose intolerance and insulin resistance were measured as clinical indicators. Regarding pathological indicators, a large number of pancreatic islet cells showed the reduction of insulin secretion, resulting in damaged glycogen synthesis and liver steatosis. At the molecular level, the insulin signal transduction pathway was inhibited by decreasing the insulin receptor substrate 1 (IRS1), insulin receptor substrate 2 (IRS2), phosphatidylinositol 3 kinase (PI3K), and glycogen synthesis kinase 3β (GSK‐3β) expression levels. CONCLUSION: The results show that the ZDF/T2DM rats have typical clinical, histopathological, and molecular characteristics of human T2DM and thus can be used as an effective model for T2DM drug development and treatment of advanced T2DM. |
format | Online Article Text |
id | pubmed-6388085 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-63880852019-03-19 Comparative medical characteristics of ZDF‐T2DM rats during the course of development to late stage disease Pang, Yun‐Li Hu, Jing‐Wen Liu, Guang‐Long Lu, Shuai‐Yao Animal Model Exp Med Original Articles BACKGROUND: There are few reports on the comparative medical characteristics of type 2 diabetes models in late stage. An analysis of comparative medical characteristics of Zucker diabetic fatty type 2 diabetes mellitus (ZDF‐T2DM) rats during the course of development to late stage disease was performed. METHODS: In this study, ZDF rats were fed with high‐sugar and high‐fat diets to raise the fasting blood glucose, and develop of type 2 diabetes. At the late stage of T2DM, the preliminary comparative medical characteristics of the T2DM model were analyzed through the detection of clinical indicators, histopathology, related cytokine levels, and insulin‐related signaling molecule expression levels. RESULTS: In the T2DM group, the fasting blood glucose was higher than 6.8 mmol/L, the serum insulin, leptin, and adiponectin levels were significantly decreased, and glucose intolerance and insulin resistance were measured as clinical indicators. Regarding pathological indicators, a large number of pancreatic islet cells showed the reduction of insulin secretion, resulting in damaged glycogen synthesis and liver steatosis. At the molecular level, the insulin signal transduction pathway was inhibited by decreasing the insulin receptor substrate 1 (IRS1), insulin receptor substrate 2 (IRS2), phosphatidylinositol 3 kinase (PI3K), and glycogen synthesis kinase 3β (GSK‐3β) expression levels. CONCLUSION: The results show that the ZDF/T2DM rats have typical clinical, histopathological, and molecular characteristics of human T2DM and thus can be used as an effective model for T2DM drug development and treatment of advanced T2DM. John Wiley and Sons Inc. 2018-09-25 /pmc/articles/PMC6388085/ /pubmed/30891566 http://dx.doi.org/10.1002/ame2.12030 Text en © 2018 The Authors. Animal Models and Experimental Medicine published by John Wiley & Sons Australia, Ltd on behalf of The Chinese Association for Laboratory Animal Sciences This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Articles Pang, Yun‐Li Hu, Jing‐Wen Liu, Guang‐Long Lu, Shuai‐Yao Comparative medical characteristics of ZDF‐T2DM rats during the course of development to late stage disease |
title | Comparative medical characteristics of ZDF‐T2DM rats during the course of development to late stage disease |
title_full | Comparative medical characteristics of ZDF‐T2DM rats during the course of development to late stage disease |
title_fullStr | Comparative medical characteristics of ZDF‐T2DM rats during the course of development to late stage disease |
title_full_unstemmed | Comparative medical characteristics of ZDF‐T2DM rats during the course of development to late stage disease |
title_short | Comparative medical characteristics of ZDF‐T2DM rats during the course of development to late stage disease |
title_sort | comparative medical characteristics of zdf‐t2dm rats during the course of development to late stage disease |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6388085/ https://www.ncbi.nlm.nih.gov/pubmed/30891566 http://dx.doi.org/10.1002/ame2.12030 |
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