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Subsequently, bacteria and endotoxins are translocated into the liver through the portal vein, activating the TLR4/NF-B signaling pathway of liver Kupffer cells, and promoting the liver inflammatory cascade and fibrosis development (Jiang and Schnabl, 2020)

Under neuroinflammatory conditions, dysfunctional mitochondria release ROS and damage-associated molecular patterns (DAMPs) (53), activating microglia and astrocytes, and triggering the release of pro-inflammatory cytokines and chemokines (54), thereby exacerbating the damage

(2024).Khor SLQ, Ng KY, Koh RY, Chye SM

Key factors in this process include Myosin19 (Myo19), KIF5B, and Drp1