[1]姜海慧 张化为 姜祎 宋小妹 黄文丽 许洪波 邓翀.基于网络药理学预测山茱萸抗肝损伤的作用机制[J].陕西中医药大学学报,2022,(04):133-143.[doi:10.13424/j.cnki.jsctcm.2022.04.029]
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基于网络药理学预测山茱萸抗肝损伤的作用机制
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《陕西中医药大学学报》[ISSN:2096-1340/CN:61-1501/R]

卷:
期数:
2022年04期
页码:
133-143
栏目:
论著
出版日期:
2022-07-20

文章信息/Info

文章编号:
2096-1340(2022)04-0133-11
作者:
姜海慧 张化为 姜祎 宋小妹 黄文丽 许洪波 邓翀
陕西中医药大学/陕西省秦岭中草药应用开发工程技术研究中心/ 陕西省中药基础与新药研究重点实验室,陕西 咸阳 712046
关键词:
关键词:山茱萸肝损伤网络药理作用机制分子对接
分类号:
R285
DOI:
10.13424/j.cnki.jsctcm.2022.04.029
文献标志码:
A
摘要:
摘 要:目的 通过网络药理学和分子对接的方法预测山茱萸抗肝损伤的作用机制。方法 从多个数据库挖掘山茱萸活性成分及相关作用靶点;利用GeneCards和OMIM数据库查询与肝损伤相关靶点。通过venny获取山茱萸抗肝损伤的潜在靶点,通过R进行GO与KEGG分析,构建蛋白蛋白相互作用(PPI)网络和活性成分成分相关靶点的可视化网络,并筛选出核心靶点。最后采用DiscoverStudio 2016分子对接进行验证。结果 共查询到235个山茱萸候选成分,筛选了32种有效成分且与肝损伤相关靶标有PIK3R1、MAPK1、TP53、HSP90AA1等333个,GO与KEGG分析得到其机制与response to molecule of bacterial origin、vascular process in circulatory system、response to lipopolysaccharide等生物过程和AGERAGE signaling pathway in diabetic complications、PI3KAkt signaling pathway等信号通路相关。分子对接结果显示山茱萸活性成分与潜在的核心靶点有良好的结合活性。结论 该研究从靶点、通路、分子对接多方面验证了山茱萸抗肝损伤有着抗炎、抗氧化等潜在功效,为进一步的临床研究提供了科学依据。

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备注/Memo

备注/Memo:
基金项目:陕西省教育厅重点科研计划项目(18JS028);陕西中医药大学学科创新团队项目(2019-YL12)
更新日期/Last Update: 2022-07-25