Huanglian-Hongqu herb pair improves nonalcoholic fatty liver disease via NF-κB/NLRP3 pathway in mice: network pharmacology, molecular docking and experimental validation

IF 2.7 3区 生物学 Hereditas Pub Date : 2024-04-03 DOI:10.1186/s41065-024-00316-0
Zheng Wang, Hairong Qiu, Yang Yang, Yueyu Zhang, Taiguo Mou, Xiaobo Zhang, Yong Zhang
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Abstract

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.
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黄连-红曲配伍草药通过NF-κB/NLRP3通路改善小鼠非酒精性脂肪肝:网络药理学、分子对接和实验验证
黄连-红曲配伍草药(HH)是一种精心制作的传统中药复方,旨在治疗与葡萄糖和脂质代谢有关的疾病。其主要应用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 治疗非酒精性脂肪肝(NAFLD)的潜在机制。采用超高效液相色谱-四极杆/比质谱(UPLC-Q-TOF-MS)鉴定了HH的化学成分。利用网络药理学分析了受 HH 影响的相关信号通路。随后,通过动物实验验证了预测结果。最后,我们确定了 HH 中的 29 种成分。网络药理学揭示了HH与153个非酒精性脂肪肝相关靶点之间的相互作用,突出了HH通过NF-κB信号通路缓解非酒精性脂肪肝的潜力。分子对接分析揭示了HH成分与NF-κB、NLRP3、ASC和Caspase-1等关键调控蛋白之间的结合相互作用。体内实验表明,HH能降低血清和肝脏脂质水平,改善肝功能,降低血清中炎症细胞因子的水平,从而缓解非酒精性脂肪肝。此外,服用 HH 还能降低 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,在改善非酒精性脂肪肝方面具有潜在的治疗效果,从而促进了HH在非酒精性脂肪肝领域的广泛应用。
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来源期刊
Hereditas
Hereditas Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.80
自引率
3.70%
发文量
0
期刊介绍: For almost a century, Hereditas has published original cutting-edge research and reviews. As the Official journal of the Mendelian Society of Lund, the journal welcomes research from across all areas of genetics and genomics. Topics of interest include human and medical genetics, animal and plant genetics, microbial genetics, agriculture and bioinformatics.
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