Integrated metabolomic and proteomic analyses reveal the regulatory mechanism of H-2-168 against Echinococcus granulosus infection in mice
This study employs integrated metabolomic and proteomic analyses to demonstrate that the harmine derivative H-2-168 alleviates *Echinococcus granulosus*-induced hepatic injury in mice by modulating key metabolic pathways, including tryptophan and sphingolipid metabolism, and regulating a complex network of proteins and metabolites involved in inflammation, oxidative stress, and ferroptosis.