Niujiaodihuang Detoxify Decoction inhibits ferroptosis by enhancing glutathione synthesis in acute liver failure models

被引:26
作者
Ji, Yichun [1 ]
Si, Wenwen [2 ]
Zeng, Juan [3 ]
Huang, Liqiao [4 ]
Huang, Zifeng [2 ]
Zhao, Lijun [2 ]
Liu, Jiahui [5 ]
Zhu, Meiling [2 ]
Kuang, Weihong [4 ]
机构
[1] Guangzhou Univ Chinese Med, Shenzhen Baoan Tradit Chinese Med Hosp, Shenzhen 518133, Peoples R China
[2] Guangzhou Univ Chinese Med, Shenzhou Hosp Integrated Tradit Chinese & Western, Shenzhen 518104, Peoples R China
[3] Guangzhou Univ Chinese Med, Affiliated Hosp 1, Dept Gastroenterol, Guangzhou 510405, Peoples R China
[4] Guangdong Med Univ, Sch Pharm, Dongguan 524023, Peoples R China
[5] Sun Yat Sen Univ, Affiliated Hosp 1, Dept Tradit Chinese Med, Guangzhou 510405, Peoples R China
基金
中国国家自然科学基金;
关键词
Niujiaodihuang detoxify decoction; Acute liver failure; Ferroptosis; GSH metabolism; MECHANISMS; PROTECTS;
D O I
10.1016/j.jep.2021.114305
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Ethnopharmacological relevance: Niujiaodihuang Detoxify Decoction (NDD) is an integrated traditional Chinese medicine prescription that has been used as a therapeutic agent for the treatment of acute liver failure (ALF). However, the mechanisms underlying its action remain unclear. Aim of the study: To determine the protective effect of NDD on D-galactosamine/lipopolysaccharide (D-GalN/ LPS)-induced ALF and explore the underlying mechanisms. Materials and methods: We characterized the NDD fingerprint by HPLC and established D-GalN/LPS-induced ALF models in Sprague-Dawley rats and LO2 cells. Next, we measured the protective and antiferroptotic effects of NDD in vivo and in vitro. To further investigate the molecular mechanisms underlying the effects of NDD, we performed metabolomic analysis of the liver tissue using LC-MS/MS. Results: Results of serum biochemical analysis, liver histopathology, and cell viability showed that NDD effec-tively relieved the liver injury. It reduced the accumulation of labile iron and alleviated lipid peroxidation by enhancing GPX4 activity. The mitochondrial morphology indicated that NDD exerted its hepatoprotective effect through an antiferroptotic activity. Metabolomic analysis showed that NDD treatment increased the levels of cysteine, decreased those of glutamate, and ameliorated the D-GalN/LPS-induced reduction in the levels of glutathione (GSH). The results for intracellular levels of reduced (GSH) and oxidized (GSSG) glutathione were consistent with those of metabolomic analysis. Conclusion: Our findings indicate that NDD exerts hepatoprotective activity by evoking the reprogramming of GSH metabolism, and thereby, inhibiting ferroptosis.
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页数:13
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