Abstract

BackgroundGrowing evidence has strengthened the association of food allergy with neuropsychiatric symptoms such as depression, anxiety, and autism. However, underlying mechanisms by which peripheral allergic responses lead to behavioral dysfunction are yet to be determined. Allergen-activated mast cells may serve as mediators by releasing histamine and other inflammatory factors that could adversely affect brain function. We hypothesized that eliciting food allergy in experimental animals would result in behavioral changes accompanied by mast cell accumulation in the brain. Our hypothesis was tested in a mouse model of milk allergy using bovine milk whey proteins (WP) as the allergen.MethodsMale and female C57BL/6 mice at 4 weeks (young) and 10 months (old) of age underwent 5-week WP sensitization with weekly intragastric administration of 20 mg WP and 10 μg cholera toxin as an adjuvant. Age-matched sham animals were given the vehicle containing only the adjuvant. All animals were orally challenged with 50 mg WP in week 6 and their intrinsic digging behavior was assessed the next day. Animals were sacrificed 3 days after the challenge, and WP-specific serum IgE, intestinal and brain mast cells, glial activation, and epigenetic DNA modification in the brain were examined.ResultsWP-sensitized males showed significantly less digging activity than the sham males in both age groups while no apparent difference was observed in females. Mast cells and their activities were evident in the intestines in an age- and sex-dependent manner. Brain mast cells were predominantly located in the region between the lateral midbrain and medial hippocampus, and their number increased in the WP-sensitized young, but not old, male brains. Noticeable differences in for 5-hydroxymethylcytosine immunoreactivity were observed in WP mice of both age groups in the amygdala, suggesting epigenetic regulation. Increased microglial Iba1 immunoreactivity and perivascular astrocytes hypertrophy were also observed in the WP-sensitized old male mice.ConclusionsOur results demonstrated that food allergy induced behavioral abnormality, increases in the number of mast cells, epigenetic DNA modification in the brain, microgliosis, and astrocyte hypertrophy in a sex- and age-dependent manner, providing a potential mechanism by which peripheral allergic responses evoke behavioral dysfunction.

Highlights

  • Growing evidence has strengthened the association of food allergy with neuropsychiatric symptoms such as depression, anxiety, and autism

  • Our results demonstrated that food allergy induced behavioral abnormality, increases in the number of mast cells, epigenetic DNA modification in the brain, microgliosis, and astrocyte hypertrophy in a sex- and age-dependent manner, providing a potential mechanism by which peripheral allergic responses evoke behavioral dysfunction

  • whey proteins (WP)-sensitized male mice exhibited decreased digging activity following an oral antigen challenge Digging activity is thought to reflect rodent burrowing behavior [27, 31]. To test whether this instinctive behavior would be affected by WP-sensitization, all animals were orally challenged with 50 mg of WP at week 6, and their digging activity was observed the following day

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Summary

Introduction

Growing evidence has strengthened the association of food allergy with neuropsychiatric symptoms such as depression, anxiety, and autism. Food allergy has been linked to abnormal psychosocial behavior and mood disorders, such as depression [2, 3], anxiety [3,4,5,6], attention-deficit hyperactivity disorder [2, 3, 6, 7], and autism [7,8,9]. Allergen recognition by the membraneassociated IgE leads to rapid degranulation of mast cells to release histamine, proteases, cytokines, and other inflammatory molecules into the circulation. These peripheral inflammatory molecules reach the brain and affect its cells and their functions, serving as peripheryderived neuroinflammatory mediators [12,13,14]

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