Article(id=1304415545693066114, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304415531491152712, articleNumber=null, orderNo=null, doi=10.7501/j.issn.0253-2670.2026.09.019, pmid=null, cstr=null, oa=null, hot=0, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1758556800000, receivedDateStr=2025-09-23, revisedDate=null, revisedDateStr=null, acceptedDate=null, acceptedDateStr=null, onlineDate=1788926500961, onlineDateStr=2026-09-09, pubDate=null, pubDateStr=null, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1788926500961, onlineIssueDateStr=2026-09-09, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1788926500961, creator=13701087609, updateTime=1788926500961, updator=13701087609, issue=Issue{id=1304415531491152712, tenantId=1146029695717560320, journalId=1302319053441957962, year='2026', volume='57', issue='9', pageStart='3261', pageEnd='3684', issueExtLink='null', onlineDate='null', pubDate='1778515200000', pubDateStr='2026-05-12', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1788926497576, creator='13701087609', updateTime=1788926796984, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1304416787358049066, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304415531491152712, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1304416787358049067, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304415531491152712, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=3495, endPage=3507, ext={EN=ArticleExt(id=1304415546036999044, articleId=1304415545693066114, tenantId=1146029695717560320, journalId=1302319053441957962, language=EN, title=Analysis on sedative hypnotic mechanism of Ziziphi Spinosae Semen-Ginseng Radix et Rhizoma herb pair based on data mining and network pharmacology, columnId=null, journalTitle=Chinese Traditional and Herbal Drugs, columnName=null, runingTitle=null, highlight=null, articleAbstract=Objective Discovering the ancient and modern Chinese compound prescriptions containing Suanzaoren (Ziziphi Spinosae Semen)-(Renshen) Ginseng Radix et Rhizoma herb pair (ZSS-GRR) and further analyzing the diseases commonly treated by the pairs and their therapeutic mechanisms. Methods Data mining method was applied to collect the compound formulas containing ZSS-GRR and count the commonly treated diseases and pharmacological effects, network pharmacology was applied to predict the mechanism of ZSS-GRR herb pair, and molecular docking technique was used to verify the binding ability of candidate compounds to potential targets, and finally enzyme-linked immunosorbent assay (ELISA) and immunohistochemistry were used to validate the discovered mechanisms of ZSS-GRR for insomnia and nervous system function. Results A total of 596 compound formulations containing the ZSS-GRR were searched. Statistical analysis of the pharmacological effects of these formulations revealed that the ZSS-GRR primarily exerts sedative and hypnotic effects and is commonly used to treat conditions such as insomnia. Network pharmacology analysis indicates that the ZSS-GRR may exert its sedative and hypnotic effects by regulating neuroactive ligand-receptor interactions, gamma-aminobutyric acid (GABA) ergic synapses, and inflammation-related pathways. Molecular docking results suggest that multiple core active components exhibit strong binding affinity with key targets. Experimental results demonstrate that the ZSS-GRR combination can alleviate glutamate-induced damage in SH-SY5Y cells, increase levels of relevant neurotransmitters in rats with an insomnia model, reduce levels of inflammatory factors, and promote the expression of gamma-aminobutyric acid type A receptor subunit alpha 1 (GABRA1) and gamma-aminobutyric acid type A receptor subunit gamma 2 (GABRG2) in the hippocampus and hypothalamus. Conclusion Through the exploration of the commonly treated diseases and the sedative-hypnotic mechanism of ZSS-GRR, the main direction and mechanism of action of ZSS-GRR have been revealed, which provides certain valuable references for the subsequent in-depth research and clinical application of the pair., authors=LU Chunyang, XU Zhijia, LI Xue, MENG Lingkun, ZHANG Hongyin, LI Guangzhe, YAN Mingming, authorsList=LU Chunyang, XU Zhijia, LI Xue, MENG Lingkun, ZHANG Hongyin, LI Guangzhe, YAN Mingming, authorCompany=null, correspAuthors=null, authorNote=null, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=null, pdfFileSize=null, pdfExtLink=null, richHtmlUrl=null, mobilePdfUrl=null, reviewReport=null, pdfFirstPage=null, abstractGraph=null, abstractGraphContent=null, abstractVideo=null, citation=null, cebUrl=null, magXmlContent=null, mapNumber=null, fund=null), CN=ArticleExt(id=1304415545944724355, articleId=1304415545693066114, tenantId=1146029695717560320, journalId=1302319053441957962, language=CN, title=基于数据挖掘和网络药理学探析酸枣仁-人参药对的镇静催眠作用机制, columnId=1304140194819629763, journalTitle=中草药, columnName=数据挖掘与循证医学, runingTitle=null, highlight=null, articleAbstract=目的 挖掘中国古今含酸枣仁-人参药对的复方,并进一步分析药对常治疾病及机制。方法 应用数据挖掘收集含有酸枣仁-人参药对的复方并统计药对常治疾病及药理作用,运用网络药理学预测酸枣仁-人参药对常治疾病机制,并且使用分子对接技术验证候选化合物与潜在靶标的结合能力,最后运用酶联免疫吸附法和免疫组织化学技术验证所发现的酸枣仁-人参药对失眠与神经系统功能的调节机制。结果 检索得到含酸枣仁-人参药对复方596首,经复方药理作用挖掘统计发现酸枣仁-人参药对主要发挥镇静催眠作用,常用于治疗失眠症等疾病。网络药理学分析结果显示,酸枣仁-人参药对可能通过调控神经活性配体-受体相互作用、γ-氨基丁酸(gamma-aminobutyric acid,GABA)能突触及炎症相关通路发挥镇静催眠作用。分子对接结果表明,多种核心活性成分与关键靶点具有较好的结合活性。体内外实验结果显示,酸枣仁-人参药对可改善谷氨酸诱导的SH-SY5Y细胞损伤,提高失眠模型大鼠相关神经递质水平,降低炎症因子水平,并促进海马及下丘脑中γ-氨基丁酸A型受体亚基α1(gamma-aminobutyric acid type A receptor subunit alpha1,GABRA1)和γ-氨基丁酸A型受体亚基γ2(gamma-aminobutyric acid type A receptor subunit gamma 2,GABRG2)的表达。结论 通过对酸枣仁-人参药对常治疾病的挖掘和发挥镇静催眠机制的探索,揭示了酸枣仁-人参药对的主要用药方向及作用机制,为该药对后续的深入研究及临床应用提供了一定的参考。, authors=卢春阳1, 徐志佳1, 李雪1, 孟令鲲1, 张红印1, 李光哲1,2, 严铭铭1,3, authorsList=卢春阳, 徐志佳, 李雪, 孟令鲲, 张红印, 李光哲, 严铭铭, authorCompany=1 长春中医药大学, 吉林 长春 130117;
2 天然植物化妆品和外用制剂吉林省校企联合技术创新实验室, 吉林 长春 130117;
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aliStartDate=null, aliEndDate=null, collectionFlag=false, citedCount=null, citedUrl=null, previewStatus=0, delFlag=0, hasFullText=0, orderTime=1788926500961, fullTextJson=null, articleText=null, reference=张诗嘉.基于数据挖掘分析刘朝霞教授治疗胃食管反流病的用药规律[D].哈尔滨:黑龙江中医药大学,2022.
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中草药 | 数据挖掘与循证医学 2026,57(9): 3495-3507
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中草药 |数据挖掘与循证医学 2026 , 57 (9) : 3495 -3507
基于数据挖掘和网络药理学探析酸枣仁-人参药对的镇静催眠作用机制
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卢春阳1, 徐志佳1, 李雪1, 孟令鲲1, 张红印1, 李光哲1,2, 严铭铭1,3
作者信息
    1 长春中医药大学, 吉林 长春 130117;
    2 天然植物化妆品和外用制剂吉林省校企联合技术创新实验室, 吉林 长春 130117;
    3 吉林省中医药保健食品科技创新中心, 吉林 长春 130117
通讯作者:
李光哲
作者简介:
卢春阳: 卢春阳,硕士研究生,从事天然药物化学及新药开发研究。E-mail:24204892094@stu.ccucm.edu.cn
Analysis on sedative hypnotic mechanism of Ziziphi Spinosae Semen-Ginseng Radix et Rhizoma herb pair based on data mining and network pharmacology
  • LU Chunyang, XU Zhijia, LI Xue, MENG Lingkun, ZHANG Hongyin, LI Guangzhe, YAN Mingming
  • Affiliations
    doi: 10.7501/j.issn.0253-2670.2026.09.019
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    目的 挖掘中国古今含酸枣仁-人参药对的复方,并进一步分析药对常治疾病及机制。方法 应用数据挖掘收集含有酸枣仁-人参药对的复方并统计药对常治疾病及药理作用,运用网络药理学预测酸枣仁-人参药对常治疾病机制,并且使用分子对接技术验证候选化合物与潜在靶标的结合能力,最后运用酶联免疫吸附法和免疫组织化学技术验证所发现的酸枣仁-人参药对失眠与神经系统功能的调节机制。结果 检索得到含酸枣仁-人参药对复方596首,经复方药理作用挖掘统计发现酸枣仁-人参药对主要发挥镇静催眠作用,常用于治疗失眠症等疾病。网络药理学分析结果显示,酸枣仁-人参药对可能通过调控神经活性配体-受体相互作用、γ-氨基丁酸(gamma-aminobutyric acid,GABA)能突触及炎症相关通路发挥镇静催眠作用。分子对接结果表明,多种核心活性成分与关键靶点具有较好的结合活性。体内外实验结果显示,酸枣仁-人参药对可改善谷氨酸诱导的SH-SY5Y细胞损伤,提高失眠模型大鼠相关神经递质水平,降低炎症因子水平,并促进海马及下丘脑中γ-氨基丁酸A型受体亚基α1(gamma-aminobutyric acid type A receptor subunit alpha1,GABRA1)和γ-氨基丁酸A型受体亚基γ2(gamma-aminobutyric acid type A receptor subunit gamma 2,GABRG2)的表达。结论 通过对酸枣仁-人参药对常治疾病的挖掘和发挥镇静催眠机制的探索,揭示了酸枣仁-人参药对的主要用药方向及作用机制,为该药对后续的深入研究及临床应用提供了一定的参考。
    人参  /  酸枣仁  /  药对  /  数据挖掘  /  网络药理学  /  分子对接  /  失眠症
    Objective Discovering the ancient and modern Chinese compound prescriptions containing Suanzaoren (Ziziphi Spinosae Semen)-(Renshen) Ginseng Radix et Rhizoma herb pair (ZSS-GRR) and further analyzing the diseases commonly treated by the pairs and their therapeutic mechanisms. Methods Data mining method was applied to collect the compound formulas containing ZSS-GRR and count the commonly treated diseases and pharmacological effects, network pharmacology was applied to predict the mechanism of ZSS-GRR herb pair, and molecular docking technique was used to verify the binding ability of candidate compounds to potential targets, and finally enzyme-linked immunosorbent assay (ELISA) and immunohistochemistry were used to validate the discovered mechanisms of ZSS-GRR for insomnia and nervous system function. Results A total of 596 compound formulations containing the ZSS-GRR were searched. Statistical analysis of the pharmacological effects of these formulations revealed that the ZSS-GRR primarily exerts sedative and hypnotic effects and is commonly used to treat conditions such as insomnia. Network pharmacology analysis indicates that the ZSS-GRR may exert its sedative and hypnotic effects by regulating neuroactive ligand-receptor interactions, gamma-aminobutyric acid (GABA) ergic synapses, and inflammation-related pathways. Molecular docking results suggest that multiple core active components exhibit strong binding affinity with key targets. Experimental results demonstrate that the ZSS-GRR combination can alleviate glutamate-induced damage in SH-SY5Y cells, increase levels of relevant neurotransmitters in rats with an insomnia model, reduce levels of inflammatory factors, and promote the expression of gamma-aminobutyric acid type A receptor subunit alpha 1 (GABRA1) and gamma-aminobutyric acid type A receptor subunit gamma 2 (GABRG2) in the hippocampus and hypothalamus. Conclusion Through the exploration of the commonly treated diseases and the sedative-hypnotic mechanism of ZSS-GRR, the main direction and mechanism of action of ZSS-GRR have been revealed, which provides certain valuable references for the subsequent in-depth research and clinical application of the pair.
    Ginseng Radix et Rhizoma  /  Ziziphi Spinosae Semen  /  herb pair  /  data mining  /  network pharmacology  /  molecular docking  /  insomnia
    卢春阳, 徐志佳, 李雪, 孟令鲲, 张红印, 李光哲, 严铭铭. 基于数据挖掘和网络药理学探析酸枣仁-人参药对的镇静催眠作用机制. 中草药, 2026 , 57 (9) : 3495 -3507 . DOI: 10.7501/j.issn.0253-2670.2026.09.019
    LU Chunyang, XU Zhijia, LI Xue, MENG Lingkun, ZHANG Hongyin, LI Guangzhe, YAN Mingming. Analysis on sedative hypnotic mechanism of Ziziphi Spinosae Semen-Ginseng Radix et Rhizoma herb pair based on data mining and network pharmacology[J]. Chinese Traditional and Herbal Drugs, 2026 , 57 (9) : 3495 -3507 . DOI: 10.7501/j.issn.0253-2670.2026.09.019

      国家自然科学基金资助项目(82274360);山西省中医药管理局资助项目(2024ZYY2A032);山西省中医药创新团队(zyytd2024020);山西省中药功效物质研究与利用重点实验室资助(202105D121009);经方扶阳山西省重点实验室开放课题研究基金资助(CPSY202501)

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    姚玉静,张书敏,任艳艳,等.酸枣仁提取物、龙眼肉提取物、γ-氨基丁酸和酪蛋白水解物复配制剂改善睡眠功能[J].食品工业科技, 2023, 44(7):406-410.
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    Liu M, Cai Y Y, Li F T, et al. Metabolomics and network pharmacological analysis to explore the mechanism of ginseng treatment for spleen-qi deficiency[J]. J Sep Sci,2022, 45(24):4427-4438.
    Bian Z H, Zhang W M, Tang J Y, et al. Mechanisms underlying the action of Ziziphi Spinosae Semen in the treatment of insomnia:A study involving network pharmacology and experimental validation[J]. Front Pharmacol, 2021, 12:752211.
    徐敬娅,马欣雨,赵佳鹤,等.人参、附子药对配伍及其温阳功效研究概况[J].河北中医, 2022, 44(7):1224-1228.
    王媛.基于“脑肠轴”探讨药对人参-酸枣仁对心脾两虚失眠大鼠的影响[D].沈阳:辽宁中医药大学, 2022.
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    张经北.基于数据挖掘分析古代名医治疗不寐医案中用药规律[D].长春:长春中医药大学, 2023.
    任海琴,孔祥鹏,王颖莉.基于古今方剂数据挖掘的酸枣仁-远志药对配伍特点及外延分析[J].中草药,2022, 53(13):4065-4074.
    中国药典[S].一部. 2025:431.
    冉小峰,胡长鸿.全国中药成药处方集[M].北京:人民卫生出版社, 1962:34-73.
    Ru J L, Li P, Wang J N, et al. TCMSP:A database of systems pharmacology for drug discovery from herbal medicines[J]. J Cheminf, 2014, 6(1):13.
    Xue R C, Fang Z, Zhang M X, et al. TCMID:Traditional Chinese medicine integrative database for herb molecular mechanism analysis[J]. Nucleic Acids Res, 2012, 41(D1):D1089-D1095.
    Upton D H, Liu J, George S M, et al. High-throughput in vitro drug screening and in vivo studies identify fenretinide as a brain-penetrant DMG therapeutic[J]. Neuro Oncol,2025, 27(7):1813-1828.
    Zhang Y Q, Guo Q Y, Li Q Y, et al. Main active constituent identification in Guanxinjing Capsule, a traditional Chinese medicine, for the treatment of coronary heart disease complicated with depression[J]. Acta Pharmacol Sin, 2018, 39(6):975-987.
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    Hua Y, Guo S, Xie H, et al. Ziziphus jujuba Mill. var.spinosa(Bunge)Hu ex H. F. Chou seed ameliorates insomnia in rats by regulating metabolomics and intestinal flora composition[J]. Front Pharmacol, 2021, 12:653767.
    Cui X F, Zhang S M, He L, et al. In vitro biotransformation of Ziziphi Spinosae Semen saponins by gut microbiota from healthy and insomniac groups[J]. Int J Mol Sci, 2025,26(9):4011.
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    K S B, Charmi B, Chunxiao B, et al. RCSB Protein Data Bank(RCSB.org):Delivery of experimentally-determined PDB structures alongside one million computed structure models of proteins from artificial intelligence/machine learning[J]. Nucleic Acids Res, 2022, 51(D1):D488-D508.
    肖凤琴,王欣,刘晖,等.基于熵权法和灰色关联度法优选人参-酸枣仁抗氧化活性最佳配比[J].食品与机械, 2023, 39(6):173-179.
    肖凤琴.人参-酸枣仁药对药效物质基础及对ROT诱导的帕金森模型的神经保护作用研究[D].长春:长春中医药大学, 2023.
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    2026年第57卷第9期
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    doi: 10.7501/j.issn.0253-2670.2026.09.019
    • 接收时间:2025-09-23
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    2种不同金属材料的力学参数

    Family
    属数
    Number of
    genus
    种数
    Number of
    species
    占总种数比例
    Percentage of
    total species (%)

    Genus
    种数
    Number of
    species
    占总种数比例
    Percentage of total
    species (%)
    鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
    小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
    多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
    红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
    小菇属 Mycena 11 5.26
    光柄菇属 Pluteus 5 2.39
    红菇属 Russula 17 8.13
    栓菌属 Trametes 5 2.39
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