Neuroinflammation induced by chronic cerebral hypoperfusion (CCH) plays a crucial role in the pathophysiologic mechanisms of
vascular dementia (VD). A growing body of research has found that intestinal microbiota is associated with a variety of
central nervous system disorders and that there is a relationship between intestinal microbiota
dysbiosis and
cognitive dysfunction and inflammatory responses.
Baicalein belongs to the class of
flavonoids and has a variety of biological functions, including anti-inflammatory,
antioxidant and anti-apoptotic.
Baicalein has a significant improvement in memory and learning, and can be used as a potential drug for the protection and treatment of
central nervous system disorders. Whether
baicalein has an ameliorative effect on
cognitive impairment in VD, and whether its mechanism is related to the inhibition of inflammatory response and regulation of intestinal microbiota has not been reported. We used bilateral common carotid artery occlusion (BCCAO) to establish a VD rat model. Morris water maze (MWM) test showed that
baicalein improved
cognitive dysfunction in VD rats. We applied HE staining, immunofluorescence and ELISA to observe that
baicalein treatment significantly improved CCH-induced neuronal damage in the CA1 region of the hippocampus, and reduced glial cell activation and release of pro-inflammatory factors. Western blot showed that
baicalein inhibited the activation of the TLR4/MyD88/NF-κB signaling pathway in VD rats. We applied 16 S
rDNA sequencing to analyze the composition of the intestinal microbiota. The results showed that
baicalein modulated the diversity and composition of the intestinal microbiota, and suppressed the relative abundance of
inflammation-associated microbiota in VD rats. In conclusion, this study found that
baicalein ameliorated
cognitive impairment, attenuated hippocampal inflammatory responses, inhibited the TLR4/MyD88/NF-κB signaling pathway, and modulated intestinal microbiota in VD rats.