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国家专利中药复方治疗细菌性痢疾的用药规律及作用机制
Medication rules and mechanisms of national patent Traditional Chinese Medicine compounds for the treatment of bacillary dysentery

广西医学 页码:668-680

作者机构:熊常州,在读博士研究生,住院医师,研究方向为中医药防治脾胃病。

基金信息:国家自然科学基金(82360959);广西自然科学基金(2024GXNSFDA010021,2024GXNSFBA010160);广西中医药大学研究生教育创新计划项目(YCBZ2025183)

DOI:10.11675/j.issn.0253⁃4304.2026.05.11

  • 中文简介
  • 英文简介
  • 参考文献

目的 探讨国家专利中药复方治疗细菌性痢疾的用药规律及作用机制。方法 检索中国专利公布公告网建库至2025年1月10日授权的治疗细菌性痢疾的中药复方专利。运用Microsoft Excel 2019软件、古今医案云平台(V2.3.9)及中医传承计算平台(V3.5)对所涉及中药复方专利药物的使用频次、性味归经及功效进行分析,并采用关联规则分析、聚类分析挖掘其用药及组方规律。选取核心药物组合,通过网络药理学方法筛选有效活性成分作用靶点及疾病相关靶点,构建蛋白-蛋白相互作用网络及核心药物组合-活性成分-靶点网络,进行基因本体论功能富集分析及京都基因与基因组百科全书通路富集分析,并开展分子对接验证。结果 共纳入92项治疗细菌性痢疾的中药复方专利,涉及中药308味,总使用频次1 004次。高频药物(使用频次≥10次)共24味,以黄连、甘草、木香、白头翁、马齿苋等为核心药物;药性以寒性、温性、平性为主,药味以苦味、辛味、甘味为主,主要归胃经、脾经、肝经及大肠经;药物功效以清热解毒、清热燥湿、凉血止血为主。关联规则分析结果显示,核心组方为马齿苋、白头翁、木香、黄柏、黄连、秦皮;聚类分析得到5类不同治疗侧重的药物组合,并与芍药汤、白头翁汤、异功散、达原饮等经典名方相似。网络药理学分析结果表明,核心药物组合白头翁-黄柏-木香的主要活性成分(黄柏苷、菜蓟苦素、小檗碱、苦楝酮、β⁃谷甾醇)可作用于TNF、GAPDH、ALB、AKT1、TLR4等核心靶点,调控糖尿病并发症中的AGE/RAGE信号通路、趋化因子信号通路、Toll样受体信号通路及HIF⁃1信号通路。分子对接结果显示,主要活性成分与核心靶点蛋白之间具有良好的结合活性,其中苦楝酮与GAPDH、ALB的结合能力最强。结论 治疗细菌性痢疾的国家专利中药复方以“清热燥湿、解毒止痢”为核心治则,其核心药物组合白头翁-黄柏-木香通过多成分、多靶点、多通路协同作用,构建起抑制炎症反应、抗菌及修复肠道黏膜的综合效应网络,从而发挥治疗细菌性痢疾的作用。

Objective To investigate the medication rules and mechanism of national patent Traditional Chinese Medicine compounds for the treatment of bacillary dysentery. Methods Patent of Traditional Chinese Medicine compounds for the treatment of bacillary dysentery authorized in China Patent Publication Bulletin Network from the establishment of the database to January 10, 2025 were retrieved. The Microsoft Excel 2019, the Ancient and Modern Medical Records Cloud Platform (V2.3.9), and the Traditional Chinese Medicine Inheritance Computing Platform (V3.5) were adopted to analyze the frequency of use, property, flavor, meridian entry, and efficacy of the involved patent Traditional Chinese Medicine compounds, and association rule analysis and cluster analysis were employed to explore the medication and prescription rules. The core drug combinations were selected, and network pharmacology method was applied to screen effect targets of effectively active components and disease⁃related targets. A protein⁃protein interaction network and a core drug combination⁃active component⁃target network were constructed. Gene Ontology functional enrichment analysis and Kyoto Encyclopedia of Genes and Genomes pathway enrichment analysis were performed, followed by molecular docking validation. Results A total of 92 patent Traditional Chinese Medicine compounds for the treatment of bacillary dysentery were enrolled, involving 308 flavors of Traditional Chinese Medicine, with a total frequency of use of 1004 times. There were 24 flavors of high⁃frequency drugs with the frequency of use ≥10 times, with Coptidis rhizoma, Glycyrrhizae radix et rhizoma, Aucklandiae radix, Pulsatillae radix, and Portulacae herba as the core drugs. The drug properties were mainly cold, warm, and moderate. The primary flavors were bitter, acrid, and sweet. These drugs mainly belonged to the stomach, spleen, liver, and large intestine meridians. Their main efficacy of drugs were clearing heat and toxic materials, clearing heat and removing dampness, and removing heat from blood to stop bleeding. The results of association rule analysis revealed that the core prescriptions consisted of Portulacae herba, Pulsatillae radix, Aucklandiae radix, Phellodendri chinensis cortex, Coptidis rhizoma, and Fraxini cortex. Cluster analysis yielded five categories of drug combinations with different therapeutic focuses, which indicated similarities to classic famous prescriptions such as Shaoyao Decoction, Baitouweng Decoction, Yigong Powder, and Dayuan Decoction. Network pharmacology analysis demonstrated that the main active components of the core drug combination (Pulsatillae radix⁃Phellodendri chinensis cortex⁃Aucklandiae radix), namely phellamarin, cynaropicrin, berberine, kulinone, and β⁃sitosterol, acted on core targets such as TNF, GAPDH, ALB, AKT1, and TLR4, regulating the AGE/RAGE signaling pathway, chemokine signaling pathway, Toll⁃like receptor signaling pathway, and HIF⁃1 signaling pathway in the complications of diabetes mellitus. Molecular docking results interpreted good binding affinity between the main active components and the core target proteins, with kulinone exhibiting the strongest binding ability to GAPDH and ALB. Conclusion National patent Traditional Chinese Medicine compounds for the treatment of bacillary dysentery take “clearing heat and removing dampness, clearing toxic materials and stopping dysentery” as its core therapeutic principle. Its core drug combination (Pulsatillae radix⁃Phellodendri chinensis cortex⁃Aucklandiae radix) constructs comprehensive effective network of inhibiting inflammatory responses, antibiosis, and repairing intestinal mucosa through synergistic effect of multiple components, multiple targets, and multiple pathways, thereby exerting effect for treating bacillary dysentery. 

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