Table 5.
Compounds | Models | Mechanisms | Administration | Ref. |
---|---|---|---|---|
Berberine | PD patients | Improving the disorder of intestinal flora and suppressing the expression of inflammatory factors | oral | [69] |
Curcumin | APP/PS1 mice as AD model | Altering the relative abundances of bacterial taxa | i.g. | [70] |
Gastrodin | D-galactose-induced AD mice | Changing the gut microbiome composition | i.g. | [71] |
Ginkgolide B | D-galactose and aluminum chloride-induced AD mice | Reconstructing gut microbiota by reversing the decreased abundance of Lactobacillus and the increased abundance of Bacteroidales, Muribaculaceae, and Alloprevotella | i.g. | [72] |
Ginsenoside Rg1 | Aβ25–35-induced tree shrews as AD model | Changing the abundance of gut microbiota and increasing lactobacillaceae | i.g. | [73] |
Salidroside | SAMP8 mice as AD model | Improving the gut barrier integrity and modifying the gut microbiota | i.g. | [66] |
Silibinin and silymarin | APP/PS1 mice as AD model | Regulating the microbiota diversity and abundance of several key bacterial species associated with AD | i.g. | [65] |
i.g. for intragastric administration, oral for drugs mixed in the diet.