College of Traditional Chinese Medicine and Health Service, Shanxi Datong University, Datong, China.
Department of Chinese Medicine, Medical School, Hubei Minzu University, Enshi, China.
Hereditas. 2024 Apr 3;161(1):12. doi: 10.1186/s41065-024-00316-0.
The Huanglian-Hongqu herb pair (HH) is a carefully crafted traditional Chinese herbal compound designed to address disorders related to glucose and lipid metabolism. Its primary application lies in treating hyperlipidemia and fatty liver conditions. This study explored the potential mechanism of HH in treating non-alcoholic fatty liver disease (NAFLD) through network pharmacology, molecular docking, and in vivo animal experiments. Ultrahigh performanceliquid chromatography-quadrupole/orbitrapmass spectrometry (UPLC-Q-TOF-MS) was employed to identify the chemical composition of HH. Network pharmacology was used to analyze the related signaling pathways affected by HH. Subsequently, the prediction was verified by animal experiment. Finally, we identified 29 components within HH. Network pharmacology unveiled interactions between HH and 153 NAFLD-related targets, highlighting HH's potential to alleviate NAFLD through NF-κB signaling pathway. Molecular docking analyses illuminated the binding interactions between HH components and key regulatory proteins, including NF-κB, NLRP3, ASC, and Caspase-1. In vivo experiments demonstrated that HH alleviated NAFLD by reducing serum and liver lipid levels, improving liver function, and lowering inflammatory cytokine levels in the serum. Moreover, HH administration downregulated mRNA and protein levels of the NF-κB/NLRP3 pathway. In conclusion, our findings demonstrated that HH has potential therapeutic benefits in ameliorating NAFLD by targeting the NF-κB/NLRP3 pathway, facilitating the broader application of HH in the field of NAFLD.
黄连-虎杖药对(HH)是一种精心设计的中草药复方,旨在治疗与葡萄糖和脂质代谢相关的疾病。其主要应用在于治疗高脂血症和脂肪肝。本研究通过网络药理学、分子对接和体内动物实验探讨了 HH 治疗非酒精性脂肪性肝病(NAFLD)的潜在机制。采用超高效液相色谱-四极杆/轨道阱质谱(UPLC-Q-TOF-MS)鉴定 HH 的化学成分。利用网络药理学分析 HH 影响的相关信号通路。随后,通过动物实验验证预测。最后,我们确定了 HH 中的 29 个成分。网络药理学揭示了 HH 与 153 个 NAFLD 相关靶点之间的相互作用,表明 HH 有可能通过 NF-κB 信号通路缓解 NAFLD。分子对接分析阐明了 HH 成分与关键调节蛋白(包括 NF-κB、NLRP3、ASC 和 Caspase-1)之间的结合相互作用。体内实验表明,HH 通过降低血清和肝脏脂质水平、改善肝功能和降低血清中炎症细胞因子水平来缓解 NAFLD。此外,HH 给药可下调 NF-κB/NLRP3 通路的 mRNA 和蛋白水平。总之,我们的研究结果表明,HH 通过靶向 NF-κB/NLRP3 通路在改善 NAFLD 方面具有潜在的治疗益处,为 HH 在 NAFLD 领域的广泛应用提供了依据。