Apple peel polyphenol alleviates antibiotic-induced intestinal dysbiosis by modulating tight junction proteins, the TLR4/NF-κB pathway and intestinal flora

Food Funct. 2023 Jul 17;14(14):6678-6689. doi: 10.1039/d3fo01358h.

Abstract

The intestine and its flora have established a strong link with each other and co-evolved to become a micro-ecological system that plays an important role in human health. Plant polyphenols have attracted a great deal of attention as potential interventions to regulate the intestinal microecology. In this study, we investigated the effects of apple peel polyphenol (APP) on the intestinal ecology by establishing an intestinal ecological dysregulation model using lincomycin hydrochloride-induced Balb/c mice. The results showed that APP enhanced the mechanical barrier function of mice by upregulating the expression of the tight junction proteins at the transcriptional and translational levels. In terms of the immune barrier, APP downregulated the protein and mRNA expression of TLR4 and NF-κB. As for the biological barrier, APP promoted the growth of beneficial bacteria as well as increasing the diversity of intestinal flora. In addition, APP treatment significantly increased the contents of short-chain fatty acids in mice. In conclusion, APP can alleviate intestinal inflammation and epithelial damage as well as inducing potentially beneficial changes in the intestinal microbiota, which helps to reveal the potential mechanisms of host-microbial interactions and polyphenol regulation of intestinal ecology.

MeSH terms

  • Animals
  • Anti-Bacterial Agents / pharmacology
  • Dysbiosis / chemically induced
  • Dysbiosis / drug therapy
  • Dysbiosis / genetics
  • Gastrointestinal Microbiome*
  • Humans
  • Malus* / metabolism
  • Mice
  • NF-kappa B / genetics
  • Polyphenols / pharmacology
  • Tight Junction Proteins / metabolism
  • Toll-Like Receptor 4 / genetics

Substances

  • NF-kappa B
  • Anti-Bacterial Agents
  • Toll-Like Receptor 4
  • Tight Junction Proteins
  • Polyphenols
  • TLR4 protein, human