2026 Volume 49 Issue 9 Pages 1538-1549
Non‑alcoholic steatohepatitis (NASH) is characterized by hepatic steatosis, inflammation, and fibrosis, yet therapeutic options remain limited. Aberrant activation of stimulator of interferon genes (STING) signaling in macrophages drives hepatic inflammation. Saikosaponin D (SSd), a bioactive triterpenoid saponin from Bupleurum falcatum, exhibits hepatoprotective properties, but its role in modulating STING-mediated macrophage polarization in NASH remains unknown. A NASH mouse model was established in C57BL/6J mice by feeding a methionine-choline-deficient (MCD) diet for 4 weeks, followed by 8 weeks of the MCD diet combined with SSd (10 mg/kg, oral gavage), polyene phosphatidylcholine (177.8 mg/kg, oral gavage), or the STING inhibitor C-176 (15 mg/kg, intraperitoneally). Hepatic injury, inflammation, and fibrosis were assessed by serum biochemistry, enzyme-linked immunosorbent assay, hematoxylin-eosin and Masson staining. Macrophage polarization status was analyzed by flow cytometry, qRT-PCR, and immunofluorescence, while STING pathway activation was quantified by qRT-PCR and Western blot. Molecular docking was performed using AutoDock Vina. SSd significantly attenuated MCD-induced hepatic steatosis, inflammation (reduced tumor necrosis factor-α and interleukin-6), and fibrosis. SSd decreased the proportion of hepatic M1 macrophages (F4/80+CD86+) while increasing M2 macrophages (F4/80+CD206+), alongside diminished colocalization between STING and F4/80. SSd markedly suppressed the expression and phosphorylation of STING, TBK1, IRF3, and nuclear factor-κB (NF-κB) at both the mRNA and protein levels, with efficacy comparable to that of C-176. Molecular docking revealed a strong binding affinity between SSd and STING (−9.9 kcal/mol). Collectively, SSd ameliorates NASH by inhibiting the STING-TBK1-IRF3/NF-κB axis in macrophages and promoting M1-to-M2 polarization, identifying SSd as a promising immunomodulatory therapy for NASH.
