The Synergistic Effects of Polysaccharides and Ginsenosides From American Ginseng (Panax quinquefolius L.) Ameliorating Cyclophosphamide-Induced Intestinal Immune Disorders and Gut Barrier Dysfunctions Based on Microbiome-Metabolomics Analysis

Front Immunol. 2021 Apr 22:12:665901. doi: 10.3389/fimmu.2021.665901. eCollection 2021.

Abstract

Cyclophosphamide (CTX), used in cancer chemotherapy, a high dose of which would cause immunosuppressive effect and intestinal mucosa damage. American ginseng (Panax quinquefolius L.) has a long history of functional food use for immunological disorder, colitis, cancer, and so on. This study aimed to illustrate the underlying mechanism of American ginseng's immunomodulatory effect in CTX-induced mice. In this study, all groups of American ginseng (American ginseng polysaccharide [AGP], American ginseng ginsenoside [AGG], co-treated with American ginseng polysaccharide and ginsenoside [AGP_AGG]) have relieve the immune disorder by reversing the lymphocyte subsets ratio in spleen and peripheral blood, as well as stimulating CD4+T cells and IgA-secreting cells in small intestine. These three treatment groups, especially AGP_AGG co-treated group recovered the intestine morphology that up-regulated villus height (VH)/crypt depth (CD) ratio, areas of mucins expression, quantity of goblet cells, and expression of tight junction proteins (ZO-1, occludin). Importantly, the microbiome-metabolomics analysis was applied in this study to illustrate the possible immuno-modulating mechanism. The synergistic effect of polysaccharides and ginsenosides (AGP_AGG group) restored the gut microbiota composition and increased various beneficial mucosa-associated bacterial taxa Clostridiales, Bifidobacterium, and Lachnospiraceae, while decreased harmful bacteria Escherichia-Shigella and Peptococcaceae. Also, AGP_AGG group altered various fecal metabolites such as uric acid, xanthurenic acid, acylcarnitine, 9,10-DHOME, 13-HDoHE, LysoPE15:0, LysoPC 16:0, LysoPI 18:0, and so on, that associated with immunometabolism or protective effect of gut barrier. These results suggest AG, particularly co-treated of polysaccharide and ginsenoside may be used as immunostimulants targeting microbiome-metabolomics axis to prevent CTX-induced side effects in cancer patients.

Keywords: American ginseng; fecal metabolites; gut barrier function; gut microbiota; immunostimulant.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bacteria / classification
  • Bacteria / drug effects
  • Bacteria / growth & development
  • Bacteria / metabolism
  • Cyclophosphamide / adverse effects*
  • Drug Therapy, Combination
  • Feces / chemistry
  • Feces / microbiology
  • Gastrointestinal Microbiome / drug effects*
  • Ginsenosides / pharmacology
  • Ginsenosides / therapeutic use*
  • Immune System Diseases / chemically induced
  • Immune System Diseases / drug therapy
  • Immune System Diseases / metabolism
  • Immune System Diseases / microbiology
  • Immunomodulation / drug effects*
  • Immunosuppressive Agents / adverse effects
  • Intestinal Mucosa / drug effects*
  • Intestinal Mucosa / metabolism
  • Intestinal Mucosa / microbiology
  • Metabolomics
  • Mice
  • Panax / chemistry*
  • Polysaccharides / pharmacology
  • Polysaccharides / therapeutic use*

Substances

  • Ginsenosides
  • Immunosuppressive Agents
  • Polysaccharides
  • Cyclophosphamide