Yang Ting, Ma Tian, Zhang Huanhuan, Niu Zechen, Cai Chunzhou, Cui Dongxiao
Key Laboratory of Shaanxi Administration of Traditional Chinese Medicine for TCM Compatibility, Shaanxi University of Chinese Medicine, Xianyang, China.
Shaanxi University of International Trade & Commerce, Xianyang, China.
Hum Exp Toxicol. 2025 Jan-Dec;44:9603271251369053. doi: 10.1177/09603271251369053. Epub 2025 Aug 13.
IntroductionThis study aimed to investigate the mechanisms underlying Tripterygium glycosides (TG) - induced liver injury, focusing on the role of the STING-TBK1 signaling pathway, and to evaluate the therapeutic potential of inhibiting this axis in mitigating liver damage.MethodsThe study employed two experimental approaches. First, male Balb/c mice were administered TG at doses of 13.5, 40.5, and 135 mg/kg for 3 weeks to assess dose-dependent hepatotoxicity. Liver injury was evaluated through serum ALT/AST levels, hepatic histopathology, and liver index. Immunohistochemical staining and Western blot analysis were used to examine STING expression in liver tissues and THP-1 cells. In the second approach, pharmacological inhibitors of STING and TBK1 were administered to evaluate their protective effects against TG-induced liver injury.ResultsTG induced dose-dependent liver injury and inflammatory infiltration, along with activation of the STING-TBK1 pathway in non-parenchymal cells. Inhibition of this pathway significantly attenuated hepatotoxicity, as evidenced by reduced ALT/AST levels, decreased inflammatory cytokines, and improved histopathological outcomes.DiscussionThese findings demonstrate that the STING-TBK1 axis plays a critical role in mediating TG-induced hepatotoxicity. Pharmacological inhibition of this pathway effectively alleviates TG-induced hepatotoxicity, suggesting its potential as a therapeutic target for drug-induced liver injury.
引言
本研究旨在探讨雷公藤多苷(TG)诱导肝损伤的潜在机制,重点关注STING-TBK1信号通路的作用,并评估抑制该信号轴在减轻肝损伤方面的治疗潜力。
方法
本研究采用了两种实验方法。首先,给雄性Balb/c小鼠分别腹腔注射13.5、40.5和135mg/kg剂量的TG,持续3周,以评估剂量依赖性肝毒性。通过血清ALT/AST水平、肝脏组织病理学和肝脏指数来评估肝损伤。采用免疫组织化学染色和蛋白质免疫印迹分析检测肝脏组织和THP-1细胞中STING的表达。在第二种方法中,给予STING和TBK1的药理学抑制剂,以评估它们对TG诱导的肝损伤的保护作用。
结果
TG诱导剂量依赖性肝损伤和炎症浸润,并激活非实质细胞中的STING-TBK1信号通路。抑制该信号通路可显著减轻肝毒性,表现为ALT/AST水平降低、炎性细胞因子减少以及组织病理学结果改善。
讨论
这些研究结果表明,STING-TBK1信号轴在介导TG诱导的肝毒性中起关键作用。对该信号通路的药理学抑制可有效减轻TG诱导的肝毒性,提示其作为药物性肝损伤治疗靶点的潜力。