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Effects of Soy-Based Infant Formula on Weight Gain and Neurodevelopment in an Autism Mouse Model
Mice fed soy-based diets exhibit increased weight gain compared to mice fed casein-based diets, and the effects are more pronounced in a model of fragile X syndrome (FXS; Fmr1(KO)). FXS is a neurodevelopmental disability characterized by intellectual impairment, seizures, autistic behavior, anxiety,...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9025435/ https://www.ncbi.nlm.nih.gov/pubmed/35456030 http://dx.doi.org/10.3390/cells11081350 |
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author | Westmark, Cara J. Filon, Mikolaj J. Maina, Patricia Steinberg, Lauren I. Ikonomidou, Chrysanthy Westmark, Pamela R. |
author_facet | Westmark, Cara J. Filon, Mikolaj J. Maina, Patricia Steinberg, Lauren I. Ikonomidou, Chrysanthy Westmark, Pamela R. |
author_sort | Westmark, Cara J. |
collection | PubMed |
description | Mice fed soy-based diets exhibit increased weight gain compared to mice fed casein-based diets, and the effects are more pronounced in a model of fragile X syndrome (FXS; Fmr1(KO)). FXS is a neurodevelopmental disability characterized by intellectual impairment, seizures, autistic behavior, anxiety, and obesity. Here, we analyzed body weight as a function of mouse age, diet, and genotype to determine the effect of diet (soy, casein, and grain-based) on weight gain. We also assessed plasma protein biomarker expression and behavior in response to diet. Juvenile Fmr1(KO) mice fed a soy protein-based rodent chow throughout gestation and postnatal development exhibit increased weight gain compared to mice fed a casein-based purified ingredient diet or grain-based, low phytoestrogen chow. Adolescent and adult Fmr1(KO) mice fed a soy-based infant formula diet exhibited increased weight gain compared to reference diets. Increased body mass was due to increased lean mass. Wild-type male mice fed soy-based infant formula exhibited increased learning in a passive avoidance paradigm, and Fmr1(KO) male mice had a deficit in nest building. Thus, at the systems level, consumption of soy-based diets increases weight gain and affects behavior. At the molecular level, a soy-based infant formula diet was associated with altered expression of numerous plasma proteins, including the adipose hormone leptin and the β-amyloid degrading enzyme neprilysin. In conclusion, single-source, soy-based diets may contribute to the development of obesity and the exacerbation of neurological phenotypes in developmental disabilities, such as FXS. |
format | Online Article Text |
id | pubmed-9025435 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-90254352022-04-23 Effects of Soy-Based Infant Formula on Weight Gain and Neurodevelopment in an Autism Mouse Model Westmark, Cara J. Filon, Mikolaj J. Maina, Patricia Steinberg, Lauren I. Ikonomidou, Chrysanthy Westmark, Pamela R. Cells Article Mice fed soy-based diets exhibit increased weight gain compared to mice fed casein-based diets, and the effects are more pronounced in a model of fragile X syndrome (FXS; Fmr1(KO)). FXS is a neurodevelopmental disability characterized by intellectual impairment, seizures, autistic behavior, anxiety, and obesity. Here, we analyzed body weight as a function of mouse age, diet, and genotype to determine the effect of diet (soy, casein, and grain-based) on weight gain. We also assessed plasma protein biomarker expression and behavior in response to diet. Juvenile Fmr1(KO) mice fed a soy protein-based rodent chow throughout gestation and postnatal development exhibit increased weight gain compared to mice fed a casein-based purified ingredient diet or grain-based, low phytoestrogen chow. Adolescent and adult Fmr1(KO) mice fed a soy-based infant formula diet exhibited increased weight gain compared to reference diets. Increased body mass was due to increased lean mass. Wild-type male mice fed soy-based infant formula exhibited increased learning in a passive avoidance paradigm, and Fmr1(KO) male mice had a deficit in nest building. Thus, at the systems level, consumption of soy-based diets increases weight gain and affects behavior. At the molecular level, a soy-based infant formula diet was associated with altered expression of numerous plasma proteins, including the adipose hormone leptin and the β-amyloid degrading enzyme neprilysin. In conclusion, single-source, soy-based diets may contribute to the development of obesity and the exacerbation of neurological phenotypes in developmental disabilities, such as FXS. MDPI 2022-04-15 /pmc/articles/PMC9025435/ /pubmed/35456030 http://dx.doi.org/10.3390/cells11081350 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Westmark, Cara J. Filon, Mikolaj J. Maina, Patricia Steinberg, Lauren I. Ikonomidou, Chrysanthy Westmark, Pamela R. Effects of Soy-Based Infant Formula on Weight Gain and Neurodevelopment in an Autism Mouse Model |
title | Effects of Soy-Based Infant Formula on Weight Gain and Neurodevelopment in an Autism Mouse Model |
title_full | Effects of Soy-Based Infant Formula on Weight Gain and Neurodevelopment in an Autism Mouse Model |
title_fullStr | Effects of Soy-Based Infant Formula on Weight Gain and Neurodevelopment in an Autism Mouse Model |
title_full_unstemmed | Effects of Soy-Based Infant Formula on Weight Gain and Neurodevelopment in an Autism Mouse Model |
title_short | Effects of Soy-Based Infant Formula on Weight Gain and Neurodevelopment in an Autism Mouse Model |
title_sort | effects of soy-based infant formula on weight gain and neurodevelopment in an autism mouse model |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9025435/ https://www.ncbi.nlm.nih.gov/pubmed/35456030 http://dx.doi.org/10.3390/cells11081350 |
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