Glycation with uronic acid-type reducing sugar enhances the anti-inflammatory activity of fish myofibrillar protein via the Maillard reaction

Food Chem. 2023 May 1:407:135162. doi: 10.1016/j.foodchem.2022.135162. Epub 2022 Dec 7.

Abstract

The role of carboxyl group in uronic acid in enhancing the anti-inflammatory activity of fish myofibrillar protein (Mf) was investigated, when lyophilized Mf was reacted with various reducing sugars at 60 °C and 35% relative humidity through the Maillard reaction. After pepsin and trypsin digestion, the anti-inflammatory activity was evaluated by measuring the secretions of tumor necrosis factor-α, interleukin-6, interleukin-1β, and nitric oxide in lipopolysaccharide-stimulated RAW 264.7 macrophage. The anti-inflammatory activity of Mf was not affected by glycation with glucose or galactose, whereas strongly enhanced by glycation with uronic acid-type reducing sugars: glucuronic acid, galacturonic acid, and alginate oligosaccharide. These results indicate that the presence of carboxyl group in reducing sugar is important for enhancing the anti-inflammatory activity of Mf. This study also shows that the enhanced effect could depend upon the number of carboxyl group in bound reducing sugar.

Keywords: Anti-inflammatory activity; Carboxyl group; Fish myofibrillar protein; Glycation; Maillard reaction; Uronic acid.

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / pharmacology
  • Maillard Reaction*
  • Oligosaccharides
  • Sugars*
  • Uronic Acids

Substances

  • Sugars
  • Uronic Acids
  • Oligosaccharides
  • Anti-Inflammatory Agents