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Chronic consumption of a western diet induces robust glial activation in aging mice and in a mouse model of Alzheimer’s disease
Studies have assessed individual components of a western diet, but no study has assessed the long-term, cumulative effects of a western diet on aging and Alzheimer’s disease (AD). Therefore, we have formulated the first western-style diet that mimics the fat, carbohydrate, protein, vitamin and miner...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4757836/ https://www.ncbi.nlm.nih.gov/pubmed/26888450 http://dx.doi.org/10.1038/srep21568 |
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author | Graham, Leah C. Harder, Jeffrey M. Soto, Ileana de Vries, Wilhelmine N. John, Simon W. M. Howell, Gareth R. |
author_facet | Graham, Leah C. Harder, Jeffrey M. Soto, Ileana de Vries, Wilhelmine N. John, Simon W. M. Howell, Gareth R. |
author_sort | Graham, Leah C. |
collection | PubMed |
description | Studies have assessed individual components of a western diet, but no study has assessed the long-term, cumulative effects of a western diet on aging and Alzheimer’s disease (AD). Therefore, we have formulated the first western-style diet that mimics the fat, carbohydrate, protein, vitamin and mineral levels of western diets. This diet was fed to aging C57BL/6J (B6) mice to identify phenotypes that may increase susceptibility to AD, and to APP/PS1 mice, a mouse model of AD, to determine the effects of the diet in AD. Astrocytosis and microglia/monocyte activation were dramatically increased in response to diet and was further increased in APP/PS1 mice fed the western diet. This increase in glial responses was associated with increased plaque burden in the hippocampus. Interestingly, given recent studies highlighting the importance of TREM2 in microglia/monocytes in AD susceptibility and progression, B6 and APP/PS1 mice fed the western diet showed significant increases TREM2+ microglia/monocytes. Therefore, an increase in TREM2+ microglia/monocytes may underlie the increased risk from a western diet to age-related neurodegenerative diseases such as Alzheimer’s disease. This study lays the foundation to fully investigate the impact of a western diet on glial responses in aging and Alzheimer’s disease. |
format | Online Article Text |
id | pubmed-4757836 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-47578362016-02-25 Chronic consumption of a western diet induces robust glial activation in aging mice and in a mouse model of Alzheimer’s disease Graham, Leah C. Harder, Jeffrey M. Soto, Ileana de Vries, Wilhelmine N. John, Simon W. M. Howell, Gareth R. Sci Rep Article Studies have assessed individual components of a western diet, but no study has assessed the long-term, cumulative effects of a western diet on aging and Alzheimer’s disease (AD). Therefore, we have formulated the first western-style diet that mimics the fat, carbohydrate, protein, vitamin and mineral levels of western diets. This diet was fed to aging C57BL/6J (B6) mice to identify phenotypes that may increase susceptibility to AD, and to APP/PS1 mice, a mouse model of AD, to determine the effects of the diet in AD. Astrocytosis and microglia/monocyte activation were dramatically increased in response to diet and was further increased in APP/PS1 mice fed the western diet. This increase in glial responses was associated with increased plaque burden in the hippocampus. Interestingly, given recent studies highlighting the importance of TREM2 in microglia/monocytes in AD susceptibility and progression, B6 and APP/PS1 mice fed the western diet showed significant increases TREM2+ microglia/monocytes. Therefore, an increase in TREM2+ microglia/monocytes may underlie the increased risk from a western diet to age-related neurodegenerative diseases such as Alzheimer’s disease. This study lays the foundation to fully investigate the impact of a western diet on glial responses in aging and Alzheimer’s disease. Nature Publishing Group 2016-02-18 /pmc/articles/PMC4757836/ /pubmed/26888450 http://dx.doi.org/10.1038/srep21568 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Graham, Leah C. Harder, Jeffrey M. Soto, Ileana de Vries, Wilhelmine N. John, Simon W. M. Howell, Gareth R. Chronic consumption of a western diet induces robust glial activation in aging mice and in a mouse model of Alzheimer’s disease |
title | Chronic consumption of a western diet induces robust glial activation in aging mice and in a mouse model of Alzheimer’s disease |
title_full | Chronic consumption of a western diet induces robust glial activation in aging mice and in a mouse model of Alzheimer’s disease |
title_fullStr | Chronic consumption of a western diet induces robust glial activation in aging mice and in a mouse model of Alzheimer’s disease |
title_full_unstemmed | Chronic consumption of a western diet induces robust glial activation in aging mice and in a mouse model of Alzheimer’s disease |
title_short | Chronic consumption of a western diet induces robust glial activation in aging mice and in a mouse model of Alzheimer’s disease |
title_sort | chronic consumption of a western diet induces robust glial activation in aging mice and in a mouse model of alzheimer’s disease |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4757836/ https://www.ncbi.nlm.nih.gov/pubmed/26888450 http://dx.doi.org/10.1038/srep21568 |
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