Significant Modules and Biological Processes between Active Components of Salvia miltiorrhiza Depside Salt and Aspirin.
Yuan LiYanming XieLianxin WangYingying ZhangHao GuYan ChaiPublished in: Evidence-based complementary and alternative medicine : eCAM (2016)
The aim of this study is to examine and compare the similarities and differences between active components of S. miltiorrhiza depside salt and aspirin using perspective of pharmacological molecular networks. Active components of S. miltiorrhiza depside salt and aspirin's related genes were identified via the STITCH4.0 and GeneCards Database. A text search engine (Agilent Literature Search 2.71) and MCODE software were applied to construct network and divide modules, respectively. Finally, 32, 2, and 28 overlapping genes, modules, and pathways were identified between active components of S. miltiorrhiza depside salt and aspirin. A multidimensional framework of drug network showed that two networks reflected commonly in human aortic endothelial cells and atherosclerosis process. Aspirin plays a more important role in metabolism, such as the well-known AA metabolism pathway and other lipid or carbohydrate metabolism pathways. S. miltiorrhiza depside salt still plays a regulatory role in type II diabetes mellitus, insulin resistance, and adipocytokine signaling pathway. Therefore, this study suggests that aspirin combined with S. miltiorrhiza depside salt may be more efficient in treatment of CHD patients, especially those with diabetes mellitus or hyperlipidemia. Further clinical trials to confirm this hypothesis are still needed.
Keyphrases
- low dose
- cardiovascular events
- antiplatelet therapy
- endothelial cells
- clinical trial
- signaling pathway
- insulin resistance
- network analysis
- anti inflammatory drugs
- cardiovascular disease
- end stage renal disease
- systematic review
- acute coronary syndrome
- percutaneous coronary intervention
- adipose tissue
- newly diagnosed
- cell proliferation
- chronic kidney disease
- randomized controlled trial
- epithelial mesenchymal transition
- transcription factor
- oxidative stress
- genome wide
- vascular endothelial growth factor
- left ventricular
- smoking cessation
- glycemic control
- patient reported outcomes
- peritoneal dialysis
- single molecule
- polycystic ovary syndrome
- electronic health record
- phase iii
- study protocol
- open label
- pluripotent stem cells