TCM grammar systems: An approach to aid the interpretation of the molecular interactions in Chinese herbal medicine

被引:46
作者
Yan, Jing [1 ]
Wang, Yun [1 ]
Luo, Si-jun [1 ]
Qiao, Yan-jiang [1 ]
机构
[1] Beijing Univ Chinese Med, Sch Chinese Pharm, Beijing 100102, Peoples R China
关键词
Entity grammar systems; Traditional Chinese medicines; Herba Ephedrae Decoction; INTERLEUKIN-12;
D O I
10.1016/j.jep.2011.04.057
中图分类号
Q94 [植物学];
学科分类号
071001 [植物学];
摘要
Ethnopharmacological relevance: Interpreting the molecular interactions in Chinese herbal medicine will help to understand the molecular mechanisms of Traditional Chinese medicines (TCM) and predict the new pharmacological effects of TCM. Yet, we still lack a method which could integrate the concerned pieces of parsed knowledge about TCM. Materials and methods: To solve the problem, a new method named TCM grammar systems was proposed in the present article. The possibility to study the interactions of TCM at the molecular level using TCM grammar systems was explored using Herba Ephedrae Decoction (HED) as an example. Results: A platform was established based on the formalism of TCM grammar systems. The related molecular network of Herba Ephedrae Decoction (HED) can be extracted automatically. The molecular network indicates that Beta2 adrenergic receptor, Glucocorticoid receptor and Interleukin12 are the relatively important targets for the anti-anaphylaxis asthma function of HED. Moreover, the anti-anaphylaxis asthma function of HED is also related with suppressing inflammation process. The results show the feasibility using TCM grammar systems to interpret the molecular mechanism of TCM. Although the results obtained depend on the database absolutely, recombination of existing knowledge in this method provides new insight for interpreting the molecular mechanism of TCM. Conclusions: TCM grammar systems could aid the interpretation of the molecular interactions in TCM to some extent. Moreover, it might be useful to predict the new pharmacological effects of TCM. The method is an in silico technology. In association with the experimental techniques, this method will play an important role in the understanding of the molecular mechanisms of TCM. (C) 2011 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:77 / 84
页数:8
相关论文
共 31 条
[1]
Binding modes of 2,4-diaminoquinazoline and 2,4-diaminopteridine analogs to P. falciparum dihydrofolate reductase enzyme: Molecular Docking Studies [J].
Adane, L. ;
Bharatam, P. V. .
INDIAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2010, 72 (03) :324-333
[2]
High throughput screening of active pharmaceutical ingredients by UPLC [J].
Al-Sayah, Mohammad A. ;
Rizos, Panagiota ;
Antonucci, Vincent ;
Wu, Naijun .
JOURNAL OF SEPARATION SCIENCE, 2008, 31 (12) :2167-2172
[3]
Barton R.H., 2011, EXPERT OPINION DRUG
[4]
Bonizzi G., 2004, TRENDS IMMUNOL, V25, P758
[5]
Eicosanoids in asthma, allergic inflammation, and host defense [J].
Boyce, Joshua A. .
CURRENT MOLECULAR MEDICINE, 2008, 8 (05) :335-349
[6]
Cao, 2006, J 4 MILITARY MED U, V562, P216
[7]
TNF-R1 signaling: A beautiful pathway [J].
Chen, GQ ;
Goeddel, DV .
SCIENCE, 2002, 296 (5573) :1634-1635
[8]
Chen KQ, 2006, CELL MOL IMMUNOL, V3, P163
[9]
Activation of the IκB kinase complex by TRAF6 requires a dimeric ubiquitin-conjugating enzyme complex and a unique polyubiquitin chain [J].
Deng, L ;
Wang, C ;
Spencer, E ;
Yang, LY ;
Braun, A ;
You, JX ;
Slaughter, C ;
Pickart, C ;
Chen, ZJ .
CELL, 2000, 103 (02) :351-361
[10]
Pharmacophore modelling and virtual screening for identification of new aurora-a kinase inhibitors [J].
Deng, Xiao-Qiang ;
Wang, Hui-Yuan ;
Zhao, Ying-Lan ;
Xiang, Ming-Li ;
Jiang, Pei-Du ;
Cao, Zhi-Xing ;
Zheng, Yu-Zhu ;
Luo, Shi-Dong ;
Yu, Luo-Ting ;
Wei, Yu-Quan ;
Yang, Sheng-Yong .
CHEMICAL BIOLOGY & DRUG DESIGN, 2008, 71 (06) :533-539