1. 中国中医科学院望京医院
2. 中国中医科学院中医临床基础医学研究所
纸质出版:2016
移动端阅览
[1]杨丽平,程仕萍,张万强,朱嘉,宋庆慧,张平.基于文献的不同核心药对干预骨性关节炎的生物信息学分析[J].中医杂志,2016,57(23):2042-2046.
YANG Liping, CHENG Shiping, ZHANG Wanqiang, et al. Bioinformatic Analysis of Different Core Herb-pairs in Intervening Osteoarthritis Based on Literature[J]. Journal of Traditional Chinese Medicine2016, 57(23): 2042-2046.
[1]杨丽平,程仕萍,张万强,朱嘉,宋庆慧,张平.基于文献的不同核心药对干预骨性关节炎的生物信息学分析[J].中医杂志,2016,57(23):2042-2046. DOI: 10.13288/j.11-2166/r.2016.23.016.
YANG Liping, CHENG Shiping, ZHANG Wanqiang, et al. Bioinformatic Analysis of Different Core Herb-pairs in Intervening Osteoarthritis Based on Literature[J]. Journal of Traditional Chinese Medicine2016, 57(23): 2042-2046. DOI: 10.13288/j.11-2166/r.2016.23.016.
目的探索骨性关节炎(OA)中药配伍应用规律及其治疗OA的可能分子机制。方法检索中国生物医学文献数据库中医药治疗OA的临床研究
采用Access 2003数据库录入纳入复方的名称、组成药物的名称和药性。计算药物的关联关系并据此建立中药配伍复杂网络
选择网络相对中心度较高的前5味药组成治疗OA的核心复方
并将其分为不同的核心药对。查找复方中各药物主要有效成分的人类活性靶蛋白和OA相关基因
并采用IPA分析平台对靶蛋白及OA的生物学通路进行整合分析。结果共纳入复方208首
复杂配伍网络相对中心度较高的前5味中药依次为牛膝(0.83)、当归(0.79)、甘草(0.73)、杜仲(0.71)白芍(0.71)
可分为当归-白芍、白芍-甘草、杜仲-牛膝3组药对。5味中药主要有效成分靶蛋白分别为杜仲32个、牛膝16个、当归30个、白芍36个、甘草16个
OA相关基因共365个。药物靶蛋白和OA基因所形成的分子网络中包含导入基因较多、相关度评分较高的网络数量分别为核心复方8个、当归-白芍6个、白芍-甘草5个、杜仲-牛膝4个、OA 25个。分子网络整合分析显示
各药对均与OA具有共同直接作用的分子
其中CA1、NF-κB1、VDR是当归-白芍、白芍-甘草与OA共有的关键靶点。OA基因相关度最高的10条通路与各药对通路整合分析显示
10条通路中以当归-白芍影响最大
其次是白芍-甘草
杜仲-牛膝最小;药对在各自通路的关键靶点的出现率以当归-白芍最高
其次是白芍-甘草
杜仲-牛膝最低。结论养血柔肝、调和肝脾中药配伍原则对OA有更强的干预作用
其核心药对当归-白芍、白芍-甘草、杜仲-牛膝可能通过不同分子或通路
从细胞增殖、凋亡、机体免疫、代谢等多个方面综合发挥对OA的治疗作用。
Objective To explore the rules of using compatibility herbs and the possible molecular mechanism in treating osteoarthritis( OA). Methods Clinical researches of Chinese medicine treating OA were searched in Chinese Biological Medical Literature Database. The names of included compound prescriptions
the names of herbs and herbs’ nature were inputted in an Access 2003 database. Herbs’ incidence relation was calculated
and based on the results compatibility herbs complex network was built. Top 5 herbs which got high network relative centrality were chosen to composite the core compound prescription for OA
and they were divided into different core herb-pairs. Human active target proteins and OA related genes of herbs main effective components in the compound prescriptions were searched. Confluence analysis of target proteins and biological pathway of OA were made with Ingenuity Pathway Analysis( IPA) platform. Results Totally 208 compound prescriptions were included. Top 5 herbs which got high complex compatibility network relative centrality were Niuxi( Radix Achyranthis Bidentatae
牛膝)( 0. 83)
Danggui( Radix Angelicae Sinensis
当归)( 0. 79)
Gancao( Radix Glycyrrhizae
甘草)( 0. 73)
Duzhong( Cortex Eucommiae
杜仲)( 0. 71) and Baishao( Radix Paeoniae Alba
白芍)( 0. 71)
which could be divided into 3 herb-pairs
Danggui-Baishao
Baishao-Gancao and Duzhong-Niuxi. There were 32 of main effective components target proteins in Duzhong
16 in Niuxi
30 in Danggui
36 in Baishao
and 16 in Gancao. There were 365 genes related to OA in total. There were 8 networks with many import genes and high correlation score in core compound prescriptions
as well as 6 these kind of networks in Danggui-Baishao
5 in Baishao-gancao
4 in Duzhong-Niuxi and 25 in OA. Molecular network confluence analysis showed that all herb-pairs and OA had common direct effect molecules. Among them
CA1
NF-κB1 and VDR were the common key targets of Danggui-Baishao
Baishao-Gancao and OA. Confluence analysis between top 10 pathways with high OA genes association degree and all herb-pairs pathways showed that Danggui-Baishao had the greatest impact among 10 pathways
followed by Baishao-Gancao and then Duzhong-Niuxi.Danggui-Baishao got the highest occurrence rate of herb-pairs in the key target of each pathway. Baishao-Gancao got the second higher
and Duzhong-Niuxi was the lowest. Conclusion The herb compatibility principle of nourishing blood and softening liver
and harmonizing liver and spleen seems have strong intervention on OA. The core herbpairs
such as Danggui-Baishao
Baishao-Gancao
and Duzhong-Niuxi
might treat OA through different molecules or pathways
from many aspects of cell multiplication
apoptosis
organism immunity
metabolism
etc.
0
浏览量
504
下载量
0
CSCD
关联资源
相关文章
相关作者
相关机构
京公网安备11010102007558号