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Effects of Soy-Based Infant Formula on Weight Gain and Neurodevelopment in an Autism Mouse Model.

Authors :
Westmark CJ
Filon MJ
Maina P
Steinberg LI
Ikonomidou C
Westmark PR
Source :
Cells [Cells] 2022 Apr 15; Vol. 11 (8). Date of Electronic Publication: 2022 Apr 15.
Publication Year :
2022

Abstract

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 <superscript>KO</superscript> ). 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 <superscript>KO</superscript> 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 <superscript>KO</superscript> 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 <superscript>KO</superscript> 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.

Details

Language :
English
ISSN :
2073-4409
Volume :
11
Issue :
8
Database :
MEDLINE
Journal :
Cells
Publication Type :
Academic Journal
Accession number :
35456030
Full Text :
https://doi.org/10.3390/cells11081350