High-Fat Diet-Induced Obesity Aggravates Food Allergy by Intestinal Barrier Destruction and Inflammation

Int Arch Allergy Immunol. 2022;183(1):80-92. doi: 10.1159/000517866. Epub 2021 Aug 5.

Abstract

Introduction: The increase in high-fat diet (HFD)-induced obesity and food allergy leads to an assumption that the 2 are related. This study aims to (1) systematic verification of HFD-induced obesity aggravates food allergy and (2) explore the correlation and molecular mechanisms of HFD-induced obesity promotes food allergy.

Methods: Female BALB/c mice are divided into the control group (control), the ovalbumin (OVA)-sensitized group (OVA), the HFD-induced obesity group (HFD), and HFD-induced allergic obesity group (HFD + OVA).

Results: In vivo data showed that HFD feed enhance clinical symptoms and intestinal mucosa villi shed on allergic mice. Moreover, we found that HFD and OVA irritation enhanced levels of mast cell degranulation and Th2 humoral response. Additionally, Western blot analysis showed the potentiation of peroxisome proliferator-activated receptor γ (PPAR γ) remarkably reduced on intestinal in HFD and OVA group, thereby inhibiting the expression of nuclear factor kappa B (NF-κB)/PPAR γ signal the phosphorylation of NF-κB P65.

Conclusions: Overall, our results suggest that HFD-induced obesity is a potential risk factor for food allergy, which related to intestinal barrier destruction and inflammation through the PPAR γ/NF-κB signaling pathway.

Keywords: Food allergy; Intestinal barrier; Intestinal immunity; Obesity.

MeSH terms

  • Animals
  • Biomarkers
  • Cytokines / metabolism
  • Diet, High-Fat
  • Disease Models, Animal
  • Disease Susceptibility
  • Female
  • Food Hypersensitivity / etiology*
  • Food Hypersensitivity / metabolism*
  • Food Hypersensitivity / pathology
  • Gastroenteritis / etiology*
  • Gastroenteritis / metabolism*
  • Gastroenteritis / pathology
  • Immunohistochemistry
  • Intestinal Mucosa / immunology*
  • Intestinal Mucosa / metabolism*
  • Intestinal Mucosa / pathology
  • Mice
  • NF-kappa B / metabolism
  • Obesity / complications*
  • Obesity / etiology
  • PPAR gamma
  • T-Lymphocyte Subsets / immunology
  • T-Lymphocyte Subsets / metabolism

Substances

  • Biomarkers
  • Cytokines
  • NF-kappa B
  • PPAR gamma