Apple Polysaccharide inhibits microbial dysbiosis and chronic inflammation and modulates gut permeability in HFD-fed

Sheng Wang1, Qian Li2, Yue Zang1

  • 1China State Institute of Pharmaceutical Industry, Shanghai, 200040, China; State Key Laboratory of New Drug & Pharmaceutial process, Shanghai Institute of Pharmaceutial Industry, Shanghai, 200437, China.

Insights

Apple polysaccharides (AP) combat gut dysbiosis in rats fed a high-fat diet. AP treatment improved gut microbiota, increased beneficial short-chain fatty acids (SCFAs), and reduced inflammation and gut permeability.

Area of Science:

  • Gut Microbiome Research
  • Nutritional Science
  • Inflammation Biology

Background:

  • Chronic diseases are linked to gut dysbiosis, an imbalance in the gut microbiota.
  • Apple consumption is associated with reduced chronic disease risk, but mechanisms are unclear.
  • Apple polysaccharides (AP) are bioactive compounds with potential health benefits.

Purpose of the Study:

  • To investigate the effects of apple polysaccharides (AP) on high-fat diet (HFD)-induced gut dysbiosis in rats.
  • To analyze the impact of AP on gut microbiota composition, short-chain fatty acids (SCFAs), gut permeability, and inflammation.

Main Methods:

  • Rats were fed a high-fat diet (HFD) and treated with AP for 14 weeks.
  • Analysis included gut microbiota composition, SCFA production, plasma lipopolysaccharide-binding protein (LBP), and gut barrier markers (Occludin).
  • Inflammatory markers such as tumor necrosis factor-alpha (TNF-α), MCP-1, CXCL-1, and IL-1β were measured.

Main Results:

  • AP treatment modulated gut microbiota, increasing Bacteroidetes and Lactobacillus while decreasing Firmicutes and Fusobacterium.
  • Significant increases in total SCFAs, particularly acetic and isobutyric acid, were observed.
  • AP alleviated gut permeability and chronic inflammation, evidenced by decreased plasma LBP and modulated inflammatory cytokines.

Conclusions:

  • Apple polysaccharides (AP) effectively inhibit gut dysbiosis and chronic inflammation in a HFD-induced rat model.
  • AP improves gut barrier function by reducing permeability and modulating inflammatory responses.
  • The findings suggest AP exerts health benefits by restoring gut homeostasis and reducing inflammation.