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Gestational ketogenic diet programs brain structure and susceptibility to depression & anxiety in the adult mouse offspring
INTRODUCTION: The ketogenic diet (KD) has seen an increase in popularity for clinical and non-clinical purposes, leading to rise in concern about the diet's impact on following generations. The KD is known to have a neurological effect, suggesting that exposure to it during prenatal brain devel...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BlackWell Publishing Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4309881/ https://www.ncbi.nlm.nih.gov/pubmed/25642385 http://dx.doi.org/10.1002/brb3.300 |
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author | Sussman, Dafna Germann, Jurgen Henkelman, Mark |
author_facet | Sussman, Dafna Germann, Jurgen Henkelman, Mark |
author_sort | Sussman, Dafna |
collection | PubMed |
description | INTRODUCTION: The ketogenic diet (KD) has seen an increase in popularity for clinical and non-clinical purposes, leading to rise in concern about the diet's impact on following generations. The KD is known to have a neurological effect, suggesting that exposure to it during prenatal brain development may alter neuro-anatomy. Studies have also indicated that the KD has an anti-depressant effect on the consumer. However, it is unclear whether any neuro-anatomical and/or behavioral changes would occur in the offspring and persist into adulthood. METHODS: To fill this knowledge gap we assessed the brain morphology and behavior of 8-week-old young-adult CD-1 mice, who were exposed to the KD in utero, and were fed only a standard-diet (SD) in postnatal life. Standardized neuro-behavior tests included the Open-Field, Forced-Swim, and Exercise Wheel tests, and were followed by post-mortem Magnetic Resonance Imaging (MRI) to assess brain anatomy. RESULTS: The adult KD offspring exhibit reduced susceptibility to anxiety and depression, and elevated physical activity level when compared with controls exposed to the SD both in utero and postnatally. Many neuro-anatomical differences exist between the KD offspring and controls, including, for example, a cerebellar volumetric enlargement by 4.8%, a hypothalamic reduction by 1.39%, and a corpus callosum reduction by 4.77%, as computed relative to total brain volume. CONCLUSIONS: These results suggest that prenatal exposure to the KD programs the offspring neuro-anatomy and influences their behavior in adulthood. |
format | Online Article Text |
id | pubmed-4309881 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BlackWell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-43098812015-01-30 Gestational ketogenic diet programs brain structure and susceptibility to depression & anxiety in the adult mouse offspring Sussman, Dafna Germann, Jurgen Henkelman, Mark Brain Behav Original Research INTRODUCTION: The ketogenic diet (KD) has seen an increase in popularity for clinical and non-clinical purposes, leading to rise in concern about the diet's impact on following generations. The KD is known to have a neurological effect, suggesting that exposure to it during prenatal brain development may alter neuro-anatomy. Studies have also indicated that the KD has an anti-depressant effect on the consumer. However, it is unclear whether any neuro-anatomical and/or behavioral changes would occur in the offspring and persist into adulthood. METHODS: To fill this knowledge gap we assessed the brain morphology and behavior of 8-week-old young-adult CD-1 mice, who were exposed to the KD in utero, and were fed only a standard-diet (SD) in postnatal life. Standardized neuro-behavior tests included the Open-Field, Forced-Swim, and Exercise Wheel tests, and were followed by post-mortem Magnetic Resonance Imaging (MRI) to assess brain anatomy. RESULTS: The adult KD offspring exhibit reduced susceptibility to anxiety and depression, and elevated physical activity level when compared with controls exposed to the SD both in utero and postnatally. Many neuro-anatomical differences exist between the KD offspring and controls, including, for example, a cerebellar volumetric enlargement by 4.8%, a hypothalamic reduction by 1.39%, and a corpus callosum reduction by 4.77%, as computed relative to total brain volume. CONCLUSIONS: These results suggest that prenatal exposure to the KD programs the offspring neuro-anatomy and influences their behavior in adulthood. BlackWell Publishing Ltd 2015-02 2014-12-29 /pmc/articles/PMC4309881/ /pubmed/25642385 http://dx.doi.org/10.1002/brb3.300 Text en © 2014 The Authors. Brain and Behavior published by Wiley Periodicals, Inc. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Sussman, Dafna Germann, Jurgen Henkelman, Mark Gestational ketogenic diet programs brain structure and susceptibility to depression & anxiety in the adult mouse offspring |
title | Gestational ketogenic diet programs brain structure and susceptibility to depression & anxiety in the adult mouse offspring |
title_full | Gestational ketogenic diet programs brain structure and susceptibility to depression & anxiety in the adult mouse offspring |
title_fullStr | Gestational ketogenic diet programs brain structure and susceptibility to depression & anxiety in the adult mouse offspring |
title_full_unstemmed | Gestational ketogenic diet programs brain structure and susceptibility to depression & anxiety in the adult mouse offspring |
title_short | Gestational ketogenic diet programs brain structure and susceptibility to depression & anxiety in the adult mouse offspring |
title_sort | gestational ketogenic diet programs brain structure and susceptibility to depression & anxiety in the adult mouse offspring |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4309881/ https://www.ncbi.nlm.nih.gov/pubmed/25642385 http://dx.doi.org/10.1002/brb3.300 |
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