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Type 2 diabetes model TSOD mouse is exposed to oxidative stress at young age
Tsumura Suzuki Obese Diabetes (TSOD) mouse, a model of obese type 2 diabetes, older than around 11 weeks of age develops diabetic phenotypes. Previous studies have indicated that the development of diabetes is partly due to three loci associated with body weight and glucose homeostasis. However, lit...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
the Society for Free Radical Research Japan
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4227832/ https://www.ncbi.nlm.nih.gov/pubmed/25411529 http://dx.doi.org/10.3164/jcbn.14-73 |
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author | Murotomi, Kazutoshi Umeno, Aya Yasunaga, Mayu Shichiri, Mototada Ishida, Noriko Abe, Hiroko Yoshida, Yasukazu Nakajima, Yoshihiro |
author_facet | Murotomi, Kazutoshi Umeno, Aya Yasunaga, Mayu Shichiri, Mototada Ishida, Noriko Abe, Hiroko Yoshida, Yasukazu Nakajima, Yoshihiro |
author_sort | Murotomi, Kazutoshi |
collection | PubMed |
description | Tsumura Suzuki Obese Diabetes (TSOD) mouse, a model of obese type 2 diabetes, older than around 11 weeks of age develops diabetic phenotypes. Previous studies have indicated that the development of diabetes is partly due to three loci associated with body weight and glucose homeostasis. However, little is known about the initial events triggering the development of the diabetic phenotypes in TSOD mouse. Here, we investigated the alteration of diabetes-related parameters, including the levels of blood glucose and inflammatory cytokines, and the oxidative stress status, in young TSOD mice. TSOD mice at 5 weeks of age showed increases in body weight and plasma total cholesterol level, but not hyperglycemia or impaired glucose tolerance, compared with age-matched control Tsumura Suzuki Non-Obese (TSNO) mice. Plasma tumor necrosis factor (TNF)-α and interleukin (IL)-6 were not detected in TSOD mice at 5 weeks of age. However, plasma total hydroxyoctadecadienoic acid (tHODE), a biomarker of oxidative stress, was increased in TSOD mice relative to TSNO mice at same age. The results demonstrated that young TSOD mice are exposed to oxidative stress before developing the diabetic phenotypes, and suggested that oxidative stress is an initial event triggering the development of diabetes in TSOD mice. |
format | Online Article Text |
id | pubmed-4227832 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | the Society for Free Radical Research Japan |
record_format | MEDLINE/PubMed |
spelling | pubmed-42278322014-11-19 Type 2 diabetes model TSOD mouse is exposed to oxidative stress at young age Murotomi, Kazutoshi Umeno, Aya Yasunaga, Mayu Shichiri, Mototada Ishida, Noriko Abe, Hiroko Yoshida, Yasukazu Nakajima, Yoshihiro J Clin Biochem Nutr Original Article Tsumura Suzuki Obese Diabetes (TSOD) mouse, a model of obese type 2 diabetes, older than around 11 weeks of age develops diabetic phenotypes. Previous studies have indicated that the development of diabetes is partly due to three loci associated with body weight and glucose homeostasis. However, little is known about the initial events triggering the development of the diabetic phenotypes in TSOD mouse. Here, we investigated the alteration of diabetes-related parameters, including the levels of blood glucose and inflammatory cytokines, and the oxidative stress status, in young TSOD mice. TSOD mice at 5 weeks of age showed increases in body weight and plasma total cholesterol level, but not hyperglycemia or impaired glucose tolerance, compared with age-matched control Tsumura Suzuki Non-Obese (TSNO) mice. Plasma tumor necrosis factor (TNF)-α and interleukin (IL)-6 were not detected in TSOD mice at 5 weeks of age. However, plasma total hydroxyoctadecadienoic acid (tHODE), a biomarker of oxidative stress, was increased in TSOD mice relative to TSNO mice at same age. The results demonstrated that young TSOD mice are exposed to oxidative stress before developing the diabetic phenotypes, and suggested that oxidative stress is an initial event triggering the development of diabetes in TSOD mice. the Society for Free Radical Research Japan 2014-11 2014-08-27 /pmc/articles/PMC4227832/ /pubmed/25411529 http://dx.doi.org/10.3164/jcbn.14-73 Text en Copyright © 2014 JCBN This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Murotomi, Kazutoshi Umeno, Aya Yasunaga, Mayu Shichiri, Mototada Ishida, Noriko Abe, Hiroko Yoshida, Yasukazu Nakajima, Yoshihiro Type 2 diabetes model TSOD mouse is exposed to oxidative stress at young age |
title | Type 2 diabetes model TSOD mouse is exposed to oxidative stress at young age |
title_full | Type 2 diabetes model TSOD mouse is exposed to oxidative stress at young age |
title_fullStr | Type 2 diabetes model TSOD mouse is exposed to oxidative stress at young age |
title_full_unstemmed | Type 2 diabetes model TSOD mouse is exposed to oxidative stress at young age |
title_short | Type 2 diabetes model TSOD mouse is exposed to oxidative stress at young age |
title_sort | type 2 diabetes model tsod mouse is exposed to oxidative stress at young age |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4227832/ https://www.ncbi.nlm.nih.gov/pubmed/25411529 http://dx.doi.org/10.3164/jcbn.14-73 |
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