Ameliorative Effects of Peptides Derived from Oyster (Crassostrea gigas) on Immunomodulatory Function and Gut Microbiota Structure in Cyclophosphamide-Treated Mice

Mar Drugs. 2021 Aug 11;19(8):456. doi: 10.3390/md19080456.

Abstract

The intestinal flora is recognized as a significant contributor to the immune system. In this research, the protective effects of oyster peptides on immune regulation and intestinal microbiota were investigated in mice treated with cyclophosphamide. The results showed that oyster peptides restored the indexes of thymus, spleen and liver, stimulated cytokines secretion and promoted the relative mRNA levels of Th1/Th2 cytokines (IL-2, IFN-γ, IL-4 and IL-10). The mRNA levels of Occludin, Claudin-1, ZO-1, and Mucin-2 were up-regulated, and the NF-κB signaling pathway was also activated after oyster peptides administration. Furthermore, oyster peptides treatment reduced the proportion of Firmicutes/Bacteroidetes, increased the relative abundance of Alistipes, Lactobacillus, Rikenell and the content of short-chain fatty acids, and reversed the composition of intestinal microflora similar to that of normal mice. In conclusion, oyster peptides effectively ameliorated cyclophosphamide-induced intestinal damage and modified gut microbiota structure in mice, and might be utilized as a beneficial ingredient in functional foods for immune regulation.

Keywords: cyclophosphamide; gut microbiota; immunomodulatory; oyster (Crassostrea gigas); peptides; short-chain fatty acid.

MeSH terms

  • Animals
  • Aquatic Organisms
  • Cyclophosphamide
  • Cytokines / metabolism
  • Disease Models, Animal
  • Gastroenteritis / chemically induced
  • Gastroenteritis / drug therapy*
  • Gastroenteritis / microbiology
  • Gastrointestinal Microbiome / drug effects
  • Immunologic Factors / pharmacology*
  • Immunomodulation / drug effects
  • Immunosuppressive Agents
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Ostreidae*
  • Peptides / pharmacology*
  • Phytotherapy
  • Specific Pathogen-Free Organisms

Substances

  • Cytokines
  • Immunologic Factors
  • Immunosuppressive Agents
  • Peptides
  • Cyclophosphamide