Direct Action of Non-Digestible Oligosaccharides against a Leaky Gut

Nutrients. 2022 Nov 7;14(21):4699. doi: 10.3390/nu14214699.

Abstract

The epithelial monolayer is the primary determinant of mucosal barrier function, and tight junction (TJ) complexes seal the paracellular space between the adjacent epithelial cells and represent the main "gate-keepers" of the paracellular route. Impaired TJ functionality results in increased permeation of the "pro-inflammatory" luminal contents to the circulation that induces local and systemic inflammatory and immune responses, ultimately triggering and/or perpetuating (chronic) systemic inflammatory disorders. Increased gut leakiness is associated with intestinal and systemic disease states such as inflammatory bowel disease and neurodegenerative diseases such as Parkinson's disease. Modulation of TJ dynamics is an appealing strategy aiming at inflammatory conditions associated with compromised intestinal epithelial function. Recently there has been a growing interest in nutraceuticals, particularly in non-digestible oligosaccharides (NDOs). NDOs confer innumerable health benefits via microbiome-shaping and gut microbiota-related immune responses, including enhancement of epithelial barrier integrity. Emerging evidence supports that NDOs also exert health-beneficial effects on microbiota independently via direct interactions with intestinal epithelial and immune cells. Among these valuable features, NDOs promote barrier function by directly regulating TJs via AMPK-, PKC-, MAPK-, and TLR-associated pathways. This review provides a comprehensive overview of the epithelial barrier-protective effects of different NDOs with a special focus on their microbiota-independent modulation of TJs.

Keywords: TEER; commensal microbiota; intestinal epithelial barrier; leaky gut; non-digestible oligosaccharides; paracellular permeability; tight junctions.

Publication types

  • Review

MeSH terms

  • Epithelial Cells
  • Gastrointestinal Microbiome*
  • Humans
  • Inflammatory Bowel Diseases* / metabolism
  • Intestinal Mucosa / metabolism
  • Oligosaccharides / metabolism
  • Oligosaccharides / pharmacology
  • Permeability
  • Tight Junctions / metabolism

Substances

  • Oligosaccharides

Grants and funding

This research received no external funding.