Protective effect of liquiritin against cisplatin-induced liver injury in mice through reduction of inflammation, oxidative stress, apoptosis and inhibition of p38 MAPK/p53 pathway based on network pharmacology and in experimental validation.

ETHNOPHARMACOLOGICAL RELEVANCE: Cisplatin is widely used in chemotherapy, but hepatotoxicity limits its effectiveness. Liquiritin has liver-protective effects, but its mechanisms have not been elucidated in combination with cisplatin for liver-injury treatment in mice.

AIM OF THE STUDY: This investigation explored liquiritin's protective effect against cisplatin-induced liver damage in mice and its mechanisms.

MATERIALS AND

METHODS

Liquiritin's targets and mechanisms were investigated using pharmacological methods. Targets related to liquiritin and hepatotoxicity were identified using online databases, followed by cross-target and mechanism extraction using STRING, Cytoscape, and DAVID databases. 60 Kunming mice in five groups (n = 12) received physiological saline (control group), cisplatin (5 mg/kg), liquiritin (40 mg/kg), liquiritin (20 mg/kg) with cisplatin (5 mg/kg), and liquiritin (40 mg/kg) with cisplatin (5 mg/kg). Mice received oral liquiritin daily for 7 days. Cisplatin was injected intraperitoneally on days 3 and 6. We evaluated liquiritin's effects on liver coefficients, liver-function indices (ALT, AST, ALP), oxidative-stress indices (CAT, SOD, CAT, and GSH), and inflammatory-factor levels (TNF-α and IL-6). Pathological changes were observed with H&E and Masson-trichrome staining, apoptosis was observed with TUNEL staining, and apoptosis-related proteins and the p38 MAPK/p53 pathway were analysed with western blot.

RESULTS

99 targets and 38 pathways were involved in the liquiritin-target pathway network. Liquiritin's key targets included caspase3, Bcl-2, and MAPK1, and it might regulate the MAPK signaling pathway. In vivo validation results, liquiritin had significantly lower liver coefficients. ALT, AST, ALP, MDA, TNF-α, and IL-6 were significantly decreased after liquiritin treatment, while SOD, CAT, and GSH were increased considerably. Liquiritin upregulated Bcl-2 protein expression and suppressed Bax, Caspase-3, c-Caspase-3 and PUMA protein expression, and the p38 MAPK/p53 pathway.

CONCLUSIONS

Liquiritin exerts hepatoprotective effects by modulating the p38 MAPK/p53 pathway, thereby reducing inflammation, oxidative stress, and apoptosis.