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An Overview of Murine High Fat Diet as a Model for Type 2 Diabetes Mellitus
Type 2 diabetes mellitus (T2DM) is a worldwide epidemic, which by all predictions will only increase. To help in combating the devastating array of phenotypes associated with T2DM a highly reproducible and human disease-similar mouse model is required for researchers. The current options are genetic...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Hindawi Publishing Corporation
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4983380/ https://www.ncbi.nlm.nih.gov/pubmed/27547764 http://dx.doi.org/10.1155/2016/2902351 |
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author | Heydemann, Ahlke |
author_facet | Heydemann, Ahlke |
author_sort | Heydemann, Ahlke |
collection | PubMed |
description | Type 2 diabetes mellitus (T2DM) is a worldwide epidemic, which by all predictions will only increase. To help in combating the devastating array of phenotypes associated with T2DM a highly reproducible and human disease-similar mouse model is required for researchers. The current options are genetic manipulations to cause T2DM symptoms or diet induced obesity and T2DM symptoms. These methods to model human T2DM have their benefits and their detractions. As far as modeling the majority of T2DM cases, HFD establishes the proper etiological, pathological, and treatment options. A limitation of HFD is that it requires months of feeding to achieve the full spectrum of T2DM symptoms and no standard protocol has been established. This paper will attempt to rectify the last limitation and argue for a standard group of HFD protocols and standard analysis procedures. |
format | Online Article Text |
id | pubmed-4983380 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-49833802016-08-21 An Overview of Murine High Fat Diet as a Model for Type 2 Diabetes Mellitus Heydemann, Ahlke J Diabetes Res Review Article Type 2 diabetes mellitus (T2DM) is a worldwide epidemic, which by all predictions will only increase. To help in combating the devastating array of phenotypes associated with T2DM a highly reproducible and human disease-similar mouse model is required for researchers. The current options are genetic manipulations to cause T2DM symptoms or diet induced obesity and T2DM symptoms. These methods to model human T2DM have their benefits and their detractions. As far as modeling the majority of T2DM cases, HFD establishes the proper etiological, pathological, and treatment options. A limitation of HFD is that it requires months of feeding to achieve the full spectrum of T2DM symptoms and no standard protocol has been established. This paper will attempt to rectify the last limitation and argue for a standard group of HFD protocols and standard analysis procedures. Hindawi Publishing Corporation 2016 2016-07-31 /pmc/articles/PMC4983380/ /pubmed/27547764 http://dx.doi.org/10.1155/2016/2902351 Text en Copyright © 2016 Ahlke Heydemann. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Heydemann, Ahlke An Overview of Murine High Fat Diet as a Model for Type 2 Diabetes Mellitus |
title | An Overview of Murine High Fat Diet as a Model for Type 2 Diabetes Mellitus |
title_full | An Overview of Murine High Fat Diet as a Model for Type 2 Diabetes Mellitus |
title_fullStr | An Overview of Murine High Fat Diet as a Model for Type 2 Diabetes Mellitus |
title_full_unstemmed | An Overview of Murine High Fat Diet as a Model for Type 2 Diabetes Mellitus |
title_short | An Overview of Murine High Fat Diet as a Model for Type 2 Diabetes Mellitus |
title_sort | overview of murine high fat diet as a model for type 2 diabetes mellitus |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4983380/ https://www.ncbi.nlm.nih.gov/pubmed/27547764 http://dx.doi.org/10.1155/2016/2902351 |
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