Systems Pharmacology Dissection of the Integrated Treatment for Cardiovascular and Gastrointestinal Disorders by Traditional Chinese Medicine

被引:57
作者
Zhang, Wenjuan [1 ,2 ]
Tao, Qin [1 ,2 ]
Guo, Zihu [1 ,2 ]
Fu, Yingxue [1 ,2 ]
Chen, Xuetong [1 ,2 ]
Shar, Piar Ali [1 ,2 ]
Shahen, Mohamed [1 ,2 ]
Zhu, Jinglin [3 ]
Xue, Jun [3 ]
Bai, Yaofei [1 ,2 ]
Wu, Ziyin [1 ,2 ]
Wang, Zhenzhong [4 ]
Xiao, Wei [4 ]
Wang, Yonghua [1 ,2 ]
机构
[1] Northwest A&F Univ, Coll Life Sci, Yangling 712100, Shaanxi, Peoples R China
[2] Northwest A&F Univ, Ctr Bioinformat, Yangling 712100, Shaanxi, Peoples R China
[3] Northwest Univ, Coll Life Sci, Xian 710069, Shaanxi, Peoples R China
[4] State Key Lab New Tech Chinese Med Pharmaceut Pro, Lianyungang 222001, Jiangsu, Peoples R China
来源
SCIENTIFIC REPORTS | 2016年 / 6卷
基金
中国国家自然科学基金;
关键词
NITRIC-OXIDE; NETWORK PHARMACOLOGY; ISCHEMIA-REPERFUSION; ADENYLYL-CYCLASE; DRUG DISCOVERY; HEART-FAILURE; ATRIAL-FIBRILLATION; OXIDATIVE STRESS; TANSHINONE-IIA; GASTRIC-CANCER;
D O I
10.1038/srep32400
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Though cardiovascular diseases (CVDs) and gastrointestinal disorders (GIDs) are different diseases associated with different organs, they are highly correlated clinically. Importantly, in Traditional Chinese Medicine (TCM), similar treatment strategies have been applied in both diseases. However, the etiological mechanisms underlying them remain unclear. Here, an integrated systems pharmacology approach is presented for illustrating the molecular correlations between CVDs and GIDs. Firstly, we identified pairs of genes that are associated with CVDs and GIDs and found that these genes are functionally related. Then, the association between 115 heart meridian (HM) herbs and 163 stomach meridian (SM) herbs and their combination application in Chinese patent medicine was investigated, implying that both CVDs and GIDs can be treated by the same strategy. Exemplified by a classical formula Sanhe Decoration (SHD) treating chronic gastritis, we applied systems-based analysis to introduce a drug-target-pathway-organ network that clarifies mechanisms of different diseases being treated by the same strategy. The results indicate that SHD regulated several pathological processes involved in both CVDs and GIDs. We experimentally confirmed the predictions implied by the effect of SHD for myocardial ischemia. The systems pharmacology suggests a novel integrated strategy for rational drug development for complex associated diseases.
引用
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页数:26
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