天然产物研究与开发 ›› 2025, Vol. 37 ›› Issue (2): 346-360.doi: 10.16333/j.1001-6880.2025.2.017 cstr: 32307.14.1001-6880.2025.2.017

• 数据研究 • 上一篇    下一篇

基于网络药理学及实验验证探究二月兰籽水提物对非酒精性脂肪性肝炎大鼠的治疗作用和机制

苏 芮1,裴海鸾1,3,田 骄1,王 晶1*,王志斌2*   

  1. 1北京中医药大学中药学院中药药理学教研室,北京 102488;2北京中研同仁堂医药研发有限公司;3北京同仁堂股份有限公司科学研究所,北京 100079
  • 出版日期:2025-02-28 发布日期:2025-02-28
  • 基金资助:

    国家科技重大专项(2018ZX09201-011)

Study on the therapeutic effects and mechanism of Orychophragmus violaceus (L.) O.E.Schulz seeds in non-alcoholic steatohepatitis rats based on network pharmacology and experimental verification

SU Rui1,PEI Hai-luan1,3,TIAN Jiao1,WANG Jing1*,WANG Zhi-bin2*   

  1. 1Department of Chinese Medicine Pharmacology,School of Chinese Materia Medica,Beijing University of Chinese Medicine,Beijing 102488,China;2Beijing Zhongyan Tongrentang Pharmaceutical R & D Co.,Ltd.;3Beijing Tongrentang Corporation Scientific Research Institute,Beijing 100079,China

  • Online:2025-02-28 Published:2025-02-28

摘要:

探究二月兰籽水提物(water extract of Orychophragmus violaceus (L.) O.E.Schulz seeds,OVSWE)治疗非酒精性脂肪性肝炎(nonalcoholic steatohepatitis,NASH)治疗作用及作用机制。采用中国知网(China National Knowledge Infrastructure,CNKI)检索并获取OVSWE活性成分,使用疾病数据库以获取NASH的相关基因。提取OVSWE和NASH的交集靶点,进一步对“药物-潜在活性成分-潜在靶点”网络进行可视化展示。将交集靶点导入STRING数据库以构建蛋白-蛋白相互作用网络;然后进行GO功能和KEGG通路富集分析并可视化,再用Autodock软件实现分子对接模型的构建。最后通过动物实验对网络药理学预测的靶点及通路进行实验验证。网络药理学分析显示OVSWE治疗NASH的核心靶点有丝氨酸/苏氨酸蛋白激酶1(Akt serine/threonine kinase 1,AKT1)及磷酸肌醇3激酶调节亚基1(phosphoinositide-3-kinase regulatory subunit 1,PIK3R1)等,核心成分有诸葛菜碱A、诸葛菜素B及诸葛菜素C;OVSWE治疗NASH与胰岛素抵抗(insulin resistance,IR)、脂质代谢等相关信号通路关系密切。分子对接结果显示OVSWE中的核心成分与核心靶点AKT1对接良好。OVSWE治疗高脂高糖饮食联合CCl4诱导NASH大鼠动物实验结果中,通过苏木精-伊红染色(hematoxylin-eosin staining,HE)及天狼猩红染色可观察到OVSWE可缓解肝脏脂质堆积和损伤;生化法检测发现,OVSWE可显著降低肝组织甘油三酯(triglycerides,TG)及低密度脂蛋白胆固醇(low-density lipoprotein cholesterol,LDL-C)含量(P< 0.05或P< 0.01);大鼠血清葡萄糖(glucose,GLU)、游离脂肪酸(free fatty acid,FFA)、空腹胰岛素含量及IR指数亦显著降低(P< 0.05或P< 0.01)。非靶向脂质组学分析表明经OVSWE干预后,NASH大鼠多种脂质差异物回调,对其通路富集发现脂质代谢紊乱主要表现在鞘脂代谢及甘油磷脂代谢通路。Western blot结果显示,OVSWE可显著增加肝组织胰岛素受体(insulin receptor,InsR)和p-AKT/AKT蛋白表达水平(P< 0.05或P< 0.01)。以上发现表明,OVSWE对高脂高糖饮食联合CCl4诱导的NASH大鼠的治疗可能是通过激活InsR/PI3K/AKT信号通路,改善IR,调节脂质代谢来实现。

关键词: 非酒精性脂肪性肝炎, 二月兰籽, 网络药理学, 脂质代谢, 胰岛素抵抗

Abstract:

To explore the therapeutic effects and mechanism of water extract of Orychophragmus violaceus (L.) O.E.Schulz seeds (OVSWE) on the treatment of nonalcoholic steatohepatitis (NASH).The China National Knowledge Infrastructure (CNKI) was used to retrieve and obtain the water-soluble active ingredients of OVSWE.This study used diverse disease databases to obtain genes information related to NASH.And this study extracted the intersection targets of OVSWE and NASH,further visualized the network of "drugs-potential active ingredients-potential targets".This study imported intersection targets into the STRING database to construct a protein-protein interaction network;performed GO function and KEGG pathway enrichment analysis and visualization,and then used Autodock software to construct molecular docking models.Finally,the targets and pathways predicted by network pharmacology were experimentally validated through animal experiments.The analysis of network pharmacology showed that the core targets of OVSWE was Akt serine/threonine kinase 1(AKT1) and phosphoinositide-3-kinase regulatory subunit 1(PIK3R1),etc;the core components were schizophylline A,schizophyllin B and schizophyllin C,the treatment of OVSWE is closely related to insulin resistance (IR) and lipid metabolism signal pathway.Molecular docking results suggested that the core ingredient in OVSWE have strong binding ability to target AKT1.The NASH rat model was induced with high-fat and high-sugar diet combined with CCl4.Hematoxylin-eosin staining(HE) and Sirius red staining showed that OVSWE could alleviate liver lipid accumulation and damage.Biochemical tests showed that OVSWE could significantly reduce the content of triglycerides (TG) and low-density lipoprotein cholesterol (LDL-C) in liver tissue (P< 0.05 or P< 0.01).Serum glucose (GLU),free fatty acid (FFA),fasting insulin content and IR index were also significantly decreased (P< 0.05 or P< 0.01).Not targeting lipid omics analysis showed that OVSWE could regulate a variety of lipid differentials.The enrichment of their pathways showed that the disorders of lipid metabolism mainly focused on the sphigolipid metabolism and glycerol phospholipid metabolism in NASH rats.Western blot showed that OVSWE could significantly increase insulin receptor(InsR) and P-Akt/AKT protein expression levels in liver tissue (P< 0.05 or P< 0.01).These findings suggested that the therapeutic mechanism of the OVSWE on NASH rats induced by the high-fat and high-sugar diet combined with CCl4 might be related to its activation of the InsR/PI3K/AKT signaling pathway,improvement of IR,regulation of lipid metabolism and reduction of inflammatory response.

Key words:

nonalcoholic steatohepatitis, Orychophragmus violaceus (L.) O.E.Schulz seeds, network pharmacology, Lipid metabolism, insulin resistance

中图分类号:  R965