Rice bran prevents high-fat diet-induced inflammation and macrophage content in adipose tissue

Maria Luisa Justo1, Carmen Claro1, Maximilian Zeyda2

  • 1Department of Pharmacology, School of Pharmacy, University of Seville, C/Profesor Garcia-Gonzalez 2, 41012, Seville, Spain.

Abstract

Insights

Rice bran extract (RBEE) supplementation in a high-fat diet reduced obesity-related inflammation and insulin resistance in mice. This nutritional strategy improved metabolic health and adipose tissue function, offering a potential alternative for metabolic syndrome.

Area of Science:

  • Nutrition and Metabolism
  • Obesity Research
  • Adipose Tissue Biology

Background:

  • Obesity-induced inflammation primarily stems from white adipose tissue (WAT) dysfunction.
  • Nutritional interventions are emerging as alternatives to pharmacotherapy for obesity-related pathologies.
  • Diet-induced obesity (DIO) in mice serves as a model to study metabolic and inflammatory changes.

Purpose of the Study:

  • To evaluate the efficacy of a rice bran enzymatic extract (RBEE)-supplemented diet.
  • To investigate the prevention of metabolic, biochemical, and functional alterations in adipose tissue and macrophages in DIO mice.
  • To assess the impact of RBEE on obesity-related inflammation and insulin resistance.

Main Methods:

  • C57BL/6J mice were fed a high-fat (HF) diet, or HF supplemented with 1% or 5% RBEE.
  • Serum cardiometabolic parameters, adipocyte size, and gene expression in WAT and liver were analyzed.
  • Macrophage polarization markers and pro-inflammatory biomarkers were assessed.

Main Results:

  • RBEE supplementation significantly reduced insulin resistance and improved dyslipidemia in DIO mice.
  • Adipocyte size and pro-inflammatory markers (IL-6, IL-1β, TNF-α) in WAT were decreased by RBEE.
  • RBEE partially restored serum levels of triglycerides, cholesterol, glucose, insulin, and adiponectin.
  • RBEE modulated macrophage polarization markers (M1/M2) and adiponectin/PPARγ expression in WAT.

Conclusions:

  • RBEE-supplemented diets attenuated insulin resistance, dyslipidemia, and adipose tissue dysfunction in DIO mice.
  • RBEE demonstrated a beneficial effect on adipocyte secretion and macrophage polarization.
  • RBEE shows potential as a nutritional complement for managing metabolic syndrome and its complications.