An Anthocyanin-Rich Extract Obtained from Portuguese Blueberries Maintains Its Efficacy in Reducing Microglia-Driven Neuroinflammation after Simulated Digestion

Nutrients. 2020 Nov 28;12(12):3670. doi: 10.3390/nu12123670.

Abstract

Dietary polyphenols are multi-target compounds that have been considered promising candidates in strategies for the mitigation of neurological diseases, acting particularly through reduction of microglia-driven neuroinflammation. In this study, an anthocyanin-rich extract obtained from Portuguese blueberries was subjected to a simulated gastrointestinal digestion; after chemical characterisation, the potential of both non-digested and digested extracts to combat neuroinflammation was evaluated using a microglia N9 cell line. Although the extracts have markedly different chemical composition, both were efficient in reducing the production of either key inflammatory markers or reactive oxygen species and in enhancing reduced glutathione levels in activated cells. Furthermore, this protection was shown to be related to the suppression of nuclear factor kappa B (NF-kB) activation, and to a signal transducer and activator of transcription 1 (STAT1)-independent mechanism. These results demonstrate that the anthocyanin extract, after simulated digestion, maintains its efficacy against neuroinflammation, and can, therefore, assume a relevant role in prevention of neuroinflammation-related neurological disorders.

Keywords: NF-kB; ROS; STAT1; anthocyanins; in vitro digestion; microglia; neuroinflammation; phenolic acids.

MeSH terms

  • Animals
  • Anthocyanins / chemistry*
  • Blueberry Plants / chemistry*
  • Cell Line
  • Cell Survival / drug effects
  • Fruit / chemistry*
  • Gene Expression Regulation / drug effects
  • Glutathione / metabolism
  • Inflammation / drug therapy*
  • Mice
  • Microglia / drug effects*
  • NF-kappa B / genetics
  • NF-kappa B / metabolism
  • Plant Extracts / chemistry
  • Plant Extracts / pharmacology*
  • STAT1 Transcription Factor / genetics
  • STAT1 Transcription Factor / metabolism
  • Tumor Necrosis Factor-alpha

Substances

  • Anthocyanins
  • NF-kappa B
  • Plant Extracts
  • STAT1 Transcription Factor
  • Stat1 protein, mouse
  • Tumor Necrosis Factor-alpha
  • Glutathione