Fecal microbiota transplantation protects rotenone-induced Parkinson's disease mice via suppressing inflammation mediated by the lipopolysaccharide-TLR4 signaling pathway through the microbiota-gut-brain axis.
Zhe ZhaoJingwen NingXiu-Qi BaoMeiyu ShangJingwei MaGen LiDan ZhangPublished in: Microbiome (2021)
Our current study demonstrates that FMT treatment can correct the gut microbiota dysbiosis and ameliorate the rotenone-induced PD mouse model, in which suppression of the inflammation mediated by the LPS-TLR4 signaling pathway both in the gut and the brain possibly plays a significant role. Further, we prove that rotenone-induced microbiota dysbiosis is involved in the genesis of PD via the microbiota-gut-brain axis. Video abstract.
Keyphrases
- signaling pathway
- inflammatory response
- high glucose
- toll like receptor
- diabetic rats
- mouse model
- oxidative stress
- resting state
- white matter
- immune response
- pi k akt
- epithelial mesenchymal transition
- functional connectivity
- drug induced
- stem cells
- adipose tissue
- endothelial cells
- mesenchymal stem cells
- skeletal muscle
- type diabetes
- anti inflammatory
- nuclear factor
- subarachnoid hemorrhage