TABLE 1.
Diseases | Compounds/extracts | Subject | Gender | Period | Main gut microbiota analysis | Mechanism | References |
---|---|---|---|---|---|---|---|
Obesity | Ginsenoside Rb1 | Mice | Both Genders | 4 weeks | The abundance of Clostridia and Lactococcus lactis increased | Enhance the production of acetate and butyrate contents of all SCFA | Hasebe et al. (2016) |
Obesity | Ginsenoside Rb1 | Mice | Male | 8 weeks | The relative abundance of Firmicutes phylum increased and the relative abundance of Bacteroidetes phylum improved | Reduce the overall diversity of the gut microbiota in feces and change the microbial composition | Bai et al. (2021) |
Obesity | Panax notoginseng saponins | Mice | Male | 7 Weeks | The abundance of Akkermansia muciniphila and Parabacteroides distasonis increased | Activate leptin AMPK/STAT3 signaling pathway to promote BAT thermogenesis and beige adipocyte reconstruction | Xu et al. (2020b) |
Obesity induced colitis | Ginsenoside Rk3 | Mice | Male | 8 weeks | The relative abundance of Actinomycetes and Clostridiathat, Parabacteroides, Lactobacillus, Butyricicoccus and Clostridium increased, while that of Akkermansia, Acetobacter, Enterobacter, and Anaerotruncus decreased | Inhibit TLR4/NF-κB signaling pathway, and improve the metabolic imbalance of intestinal flora, as well as significantly reduce the ratio of Firmicum/Bacteroide and relieve the inflammatory cascade | Chen et al. (2021) |
Diabetes | Ginsenoside T19 | Mice | Male | 6 weeks | The value of Firmicutes/Bacteroidetes decreased and the relative abundance of the Lachnospiraceae family remarkably raised | Lower the levels of blood glucose and lipid, alleviate insulin resistance via AMPK and PI3K Pathways | Xu et al. (2020a) |
Diabetes | Ginsenoside Rg5 | Mice | Male | 4 weeks | The abundance of Firmicutes and Verrucomicrobia decreased at the phylum level, and the abundance of Bacteroidetes and Proteobacteria increased | Repair intestinal barrier function and relieve metabolic endotoxemia-related inflammatory pathways | Wei et al. (2020) |
Diabetes | Ginsenoside Rb1+ Ginseng polysaccharides (GP) | Rats | Male | 30 days | The abundance of β-D-glucosidase producing probiotics Bifidobacteria spp. Bacteroides spp. and Lactobacillus spp. showed no significant change | Regulate intestinal flora, improve fecal β - D-glucosidase activity, and improve the conversion rate of ginsenoside Rb1 to CK | Li et al. (2018a) |
NAFLD | Ginsenoside Rg1 + Rb1 + Rg3 | Human | Both Genders | 4 weeks | The abundance of Lactobacillus significantly increased | Improve liver enzymes (alanine aminotransferase) and fatigue score by modulating gut microbiota | Hong et al. (2020) |
NAFLD | Ginsenoside extract | Mice | Male | 12 weeks | The abundance of Bacteroidetes significantly increased and the ratio of Firmicutes to Bacteroidetes down-regulated | Enhance the gut barrier function, restore the energy balance, and alleviate metabolic inflammation by gut microbiota regulation | Liang et al. (2021) |
Note: Human studies in the table were randomized controlled clinical trials.