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A ketogenic diet reduces amyloid beta 40 and 42 in a mouse model of Alzheimer's disease

BACKGROUND: Alzheimer's disease (AD) is a progressive neurodegenerative disorder that primarily strikes the elderly. Studies in both humans and animal models have linked the consumption of cholesterol and saturated fats with amyloid-β (Aβ) deposition and development of AD. Yet, these studies di...

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Autores principales: Van der Auwera, Ingrid, Wera, Stefaan, Van Leuven, Fred, Henderson, Samuel T
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1282589/
https://www.ncbi.nlm.nih.gov/pubmed/16229744
http://dx.doi.org/10.1186/1743-7075-2-28
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author Van der Auwera, Ingrid
Wera, Stefaan
Van Leuven, Fred
Henderson, Samuel T
author_facet Van der Auwera, Ingrid
Wera, Stefaan
Van Leuven, Fred
Henderson, Samuel T
author_sort Van der Auwera, Ingrid
collection PubMed
description BACKGROUND: Alzheimer's disease (AD) is a progressive neurodegenerative disorder that primarily strikes the elderly. Studies in both humans and animal models have linked the consumption of cholesterol and saturated fats with amyloid-β (Aβ) deposition and development of AD. Yet, these studies did not examine high fat diets in combination with reduced carbohydrate intake. Here we tested the effect of a high saturated fat/low carbohydrate diet on a transgenic mouse model of AD. RESULTS: Starting at three months of age, two groups of female transgenic mice carrying the "London" APP mutation (APP/V717I) were fed either, a standard diet (SD) composed of high carbohydrate/low fat chow, or a ketogenic diet (KD) composed of very low carbohydrate/high saturated fat chow for 43 days. Animals fed the KD exhibited greatly elevated serum ketone body levels, as measured by β-hydroxybutyrate (3.85 ± 2.6 mM), compared to SD fed animals (0.29 ± 0.06 mM). In addition, animals fed the KD lost body weight (SD 22.2 ± 0.6 g vs. KD 17.5 ± 1.4 g, p = 0.0067). In contrast to earlier studies, the brief KD feeding regime significantly reduced total brain Aβ levels by approximately 25%. Despite changes in ketone levels, body weight, and Aβ levels, the KD diet did not alter behavioral measures. CONCLUSION: Previous studies have suggested that diets rich in cholesterol and saturated fats increased the deposition of Aβ and the risk of developing AD. Here we demonstrate that a diet rich in saturated fats and low in carbohydrates can actually reduce levels of Aβ. Therefore, dietary strategies aimed at reducing Aβ levels should take into account interactions of dietary components and the metabolic outcomes, in particular, levels of carbohydrates, total calories, and presence of ketone bodies should be considered.
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spelling pubmed-12825892005-11-13 A ketogenic diet reduces amyloid beta 40 and 42 in a mouse model of Alzheimer's disease Van der Auwera, Ingrid Wera, Stefaan Van Leuven, Fred Henderson, Samuel T Nutr Metab (Lond) Research BACKGROUND: Alzheimer's disease (AD) is a progressive neurodegenerative disorder that primarily strikes the elderly. Studies in both humans and animal models have linked the consumption of cholesterol and saturated fats with amyloid-β (Aβ) deposition and development of AD. Yet, these studies did not examine high fat diets in combination with reduced carbohydrate intake. Here we tested the effect of a high saturated fat/low carbohydrate diet on a transgenic mouse model of AD. RESULTS: Starting at three months of age, two groups of female transgenic mice carrying the "London" APP mutation (APP/V717I) were fed either, a standard diet (SD) composed of high carbohydrate/low fat chow, or a ketogenic diet (KD) composed of very low carbohydrate/high saturated fat chow for 43 days. Animals fed the KD exhibited greatly elevated serum ketone body levels, as measured by β-hydroxybutyrate (3.85 ± 2.6 mM), compared to SD fed animals (0.29 ± 0.06 mM). In addition, animals fed the KD lost body weight (SD 22.2 ± 0.6 g vs. KD 17.5 ± 1.4 g, p = 0.0067). In contrast to earlier studies, the brief KD feeding regime significantly reduced total brain Aβ levels by approximately 25%. Despite changes in ketone levels, body weight, and Aβ levels, the KD diet did not alter behavioral measures. CONCLUSION: Previous studies have suggested that diets rich in cholesterol and saturated fats increased the deposition of Aβ and the risk of developing AD. Here we demonstrate that a diet rich in saturated fats and low in carbohydrates can actually reduce levels of Aβ. Therefore, dietary strategies aimed at reducing Aβ levels should take into account interactions of dietary components and the metabolic outcomes, in particular, levels of carbohydrates, total calories, and presence of ketone bodies should be considered. BioMed Central 2005-10-17 /pmc/articles/PMC1282589/ /pubmed/16229744 http://dx.doi.org/10.1186/1743-7075-2-28 Text en Copyright © 2005 Van der Auwera et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Van der Auwera, Ingrid
Wera, Stefaan
Van Leuven, Fred
Henderson, Samuel T
A ketogenic diet reduces amyloid beta 40 and 42 in a mouse model of Alzheimer's disease
title A ketogenic diet reduces amyloid beta 40 and 42 in a mouse model of Alzheimer's disease
title_full A ketogenic diet reduces amyloid beta 40 and 42 in a mouse model of Alzheimer's disease
title_fullStr A ketogenic diet reduces amyloid beta 40 and 42 in a mouse model of Alzheimer's disease
title_full_unstemmed A ketogenic diet reduces amyloid beta 40 and 42 in a mouse model of Alzheimer's disease
title_short A ketogenic diet reduces amyloid beta 40 and 42 in a mouse model of Alzheimer's disease
title_sort ketogenic diet reduces amyloid beta 40 and 42 in a mouse model of alzheimer's disease
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1282589/
https://www.ncbi.nlm.nih.gov/pubmed/16229744
http://dx.doi.org/10.1186/1743-7075-2-28
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