Guan Jia-Wei, Xu Yu, Yu Wei, Wei Li-Hua, Xue Rui, Yu Hang, Fan Jing-Min, Wang Hong-Zheng, Abulizi Abudumijiti, Chen Wen, Han Bo
School of Pharmacy/Key Laboratory of Xinjiang Phytomedicine Resource and Utilization, Ministry of Education, Shihezi University, Shihezi, 832002, People's Republic of China.
Anal Bioanal Chem. 2023 Apr;415(9):1641-1655. doi: 10.1007/s00216-023-04565-2. Epub 2023 Jan 31.
Erhuangquzhi granules (EQG) have been clinically proven to be effective in nonalcoholic steatohepatitis (NASH) treatment. However, the active components and molecular mechanisms remain unknown. This study aimed to screen active components targeting tumor necrosis factor α (TNF-α) in EQG for the treatment of NASH by a surface plasmon resonance (SPR) biosensor-based active ingredient recognition system (SPR-AIRS). The amine-coupling method was used to immobilize recombinant TNF-α protein on an SPR chip, the specificity of the TNF-α-immobilized chip was validated, and nine medicinal herbs in EQG were prescreened. Nuciferine (NF), lirinidine (ID), and O-nornuciferine (NNF) from lotus leaves were found and identified as TNF-α ligands by UPLC‒MS/MS, and the affinity constants of NF, ID, and NNF to TNF-α were determined by SPR experiments (Kd = 61.19, 31.02, and 20.71 µM, respectively). NF, ID, and NNF inhibited TNF-α-induced apoptosis in L929 cells, the levels of secreted IL-6 and IL-1β were reduced, and the phosphorylation of IKKβ and IκB was inhibited in lipopolysaccharide (LPS)-stimulated RAW264.7 cells. In conclusion, a class of new active small-molecule TNF-α inhibitors was discovered, which also provides a valuable reference for the material basis and mechanism of EQG action in NASH treatment.
二黄祛脂颗粒(EQG)已被临床证明对非酒精性脂肪性肝炎(NASH)的治疗有效。然而,其活性成分和分子机制仍不清楚。本研究旨在通过基于表面等离子体共振(SPR)生物传感器的活性成分识别系统(SPR-AIRS)筛选EQG中靶向肿瘤坏死因子α(TNF-α)的活性成分,用于治疗NASH。采用胺偶联法将重组TNF-α蛋白固定在SPR芯片上,验证了固定有TNF-α的芯片的特异性,并对EQG中的九种草药进行了预筛选。通过超高效液相色谱-串联质谱(UPLC-MS/MS)从荷叶中发现并鉴定出荷叶碱(NF)、去氢荷叶碱(ID)和O-去甲荷叶碱(NNF)为TNF-α配体,并通过SPR实验测定了NF、ID和NNF与TNF-α的亲和常数(Kd分别为61.19、31.02和20.71 μM)。NF、ID和NNF抑制TNF-α诱导的L929细胞凋亡,降低脂多糖(LPS)刺激的RAW264.7细胞中分泌的IL-6和IL-1β水平,并抑制IKKβ和IκB的磷酸化。总之,发现了一类新型活性小分子TNF-α抑制剂,这也为EQG治疗NASH的物质基础和作用机制提供了有价值的参考。