1. Academic Validation
  2. Ginsenoside F2-Mediated Intestinal Microbiota and Its Metabolite Propionic Acid Positively Impact the Gut-Skin Axis in Atopic Dermatitis Mice

Ginsenoside F2-Mediated Intestinal Microbiota and Its Metabolite Propionic Acid Positively Impact the Gut-Skin Axis in Atopic Dermatitis Mice

  • J Agric Food Chem. 2024 Jan 10;72(1):339-350. doi: 10.1021/acs.jafc.3c06015.
Dongxu Li 1 Zhao-Bo Luo 2 Jun Zhu 1 Jun-Xia Wang 3 Zheng-Yun Jin 3 Shaobo Qi 2 Meiling Jin 4 Lin-Hu Quan 2
Affiliations

Affiliations

  • 1 College of Integration Science, Yanbian University, Yanji 133002, China.
  • 2 Key Laboratory of Natural Medicines of the Changbai Mountain, Ministry of Education, College of Pharmacy, Yanbian University, Yanji 133002, China.
  • 3 Department of Animal Science, College of Agricultural, Yanbian University, Yanji 133002, China.
  • 4 Department of Pharmacology, College of Medicine, Yanbian University, Yanji 133002, China.
Abstract

Atopic dermatitis (AD) is a complex inflammatory skin disease induced by multiple factors. AD can also cause intestinal inflammation and disorders of the gut microbiota. Ginseng is a kind of edible and medicinal plant; its main active components are ginsenosides. Ginsenosides have a variety of anti-inflammatory effects and regulate the gut microbiota; however, their role in AD and the underlying mechanisms are unclear. In this study, we found that intragastric administration of ginsenoside F2 improved AD-like skin symptoms and reduced inflammatory cell infiltration, serum immunoglobulin E levels, and mRNA expression of inflammatory cytokines in AD mice. 16s rRNA Sequencing analysis showed that ginsenoside F2 altered the intestinal microbiota structure and enriched the short-chain fatty acid-producing microbiota in AD mice. Metabolomic analysis revealed that ginsenoside F2 significantly increased the propionic acid (Pa) content of feces and serum in AD mice, which was positively correlated with significant enrichment of Parabacteroides goldsteinii and Lactobacillus plantarum in the intestines. Pa inhibits inflammatory responses in the gut and skin of AD mice through the G-protein-coupled receptor43/NF-κB pathway, thereby improving skin AD symptoms. These results revealed, for the first time, the mechanism by which ginsenoside F2 improves AD through the Pa (a metabolite of intestinal microbiota)-gut-skin axis.

Keywords

atopic dermatitis; ginsenoside F2; gut microbiota; gut−skin axis; propionic acid.

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