Ji Yichun, Si Wenwen, Zeng Juan, Huang Liqiao, Huang Zifeng, Zhao Lijun, Liu Jiahui, Zhu Meiling, Kuang Weihong
Shenzhen Bao'an Traditional Chinese Medicine Hospital, Guangzhou University of Chinese Medicine, Shenzhen, 518133, China.
Shenzhou Hospital of Integrated Traditional Chinese and Western Medicine, Guangzhou University of Chinese Medicine, Shenzhen, 518104, China.
J Ethnopharmacol. 2021 Oct 28;279:114305. doi: 10.1016/j.jep.2021.114305. Epub 2021 Jun 12.
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.
To determine the protective effect of NDD on D-galactosamine/lipopolysaccharide (D-GalN/LPS)-induced ALF and explore the underlying mechanisms.
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 of serum biochemical analysis, liver histopathology, and cell viability showed that NDD effectively 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.
Our findings indicate that NDD exerts hepatoprotective activity by evoking the reprogramming of GSH metabolism, and thereby, inhibiting ferroptosis.
牛角地黄解毒汤(NDD)是一种综合的中药方剂,一直被用作治疗急性肝衰竭(ALF)的治疗药物。然而,其作用机制仍不清楚。
确定NDD对D-半乳糖胺/脂多糖(D-GalN/LPS)诱导的急性肝衰竭的保护作用,并探讨其潜在机制。
我们通过高效液相色谱法(HPLC)对NDD指纹图谱进行了表征,并在Sprague-Dawley大鼠和LO2细胞中建立了D-GalN/LPS诱导的急性肝衰竭模型。接下来,我们在体内和体外测量了NDD的保护和抗铁死亡作用。为了进一步研究NDD作用的分子机制,我们使用液相色谱-串联质谱法(LC-MS/MS)对肝组织进行了代谢组学分析。
血清生化分析、肝脏组织病理学和细胞活力结果表明,NDD有效缓解了肝损伤。它通过增强GPX4活性减少了不稳定铁的积累并减轻了脂质过氧化。线粒体形态表明NDD通过抗铁死亡活性发挥其肝脏保护作用。代谢组学分析表明,NDD治疗增加了半胱氨酸水平,降低了谷氨酸水平,并改善了D-GalN/LPS诱导的谷胱甘肽(GSH)水平降低。还原型(GSH)和氧化型(GSSG)谷胱甘肽的细胞内水平结果与代谢组学分析结果一致。
我们的研究结果表明,NDD通过引发谷胱甘肽代谢的重编程,从而抑制铁死亡,发挥肝脏保护活性。