FOLLOWUS
1.Department of Clinical Chinese Pharmacy, School of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing(100029), China
2.Xiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing (100091), China
Correspondence to: Prof. WU Jia-rui, E-mail: exogamy@163.com
纸质出版日期:2021-01-01,
网络出版日期:2020-05-22,
录用日期:2019-08-28
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Zi-qi MENG, Jia-rui WU, Ying-li ZHU, 等. Revealing the Common Mechanisms of Scutellarin in Angina Pectoris and Ischemic Stroke Treatment via A Network Pharmacology Approach[J]. Chinese Journal of Integrative Medicine, 2021,27(1):62-69.
Zi-qi MENG, Jia-rui WU, Ying-li ZHU, et al. Revealing the Common Mechanisms of Scutellarin in Angina Pectoris and Ischemic Stroke Treatment via A Network Pharmacology Approach[J]. Chinese Journal of Integrative Medicine, 2021,27(1):62-69.
Zi-qi MENG, Jia-rui WU, Ying-li ZHU, 等. Revealing the Common Mechanisms of Scutellarin in Angina Pectoris and Ischemic Stroke Treatment via A Network Pharmacology Approach[J]. Chinese Journal of Integrative Medicine, 2021,27(1):62-69. DOI: 10.1007/s11655-020-2716-4.
Zi-qi MENG, Jia-rui WU, Ying-li ZHU, et al. Revealing the Common Mechanisms of Scutellarin in Angina Pectoris and Ischemic Stroke Treatment via A Network Pharmacology Approach[J]. Chinese Journal of Integrative Medicine, 2021,27(1):62-69. DOI: 10.1007/s11655-020-2716-4.
Objective:
2
To investigate the shared mechanisms of scutellarin in angina pectoris (AP) and ischemic stroke (IS) treatment.
Methods:
2
A network pharmacology approach was used to detect the potential mechanisms of scutellarin in AP and IS treatment by target prediction
protein-protein interaction (PPI) data collection
network construction
network analysis
and enrichment analysis. Furthermore
molecular docking simulation was employed to analyze the interaction between scutellarin and core targets.
Results:
2
Two networks were established
including a disease-target network and a PPI network of scutellarin targets against AP and IS. Network analysis showed that 14 targets
namely
AKT1
VEGFA
JUN
ALB
MTOR
ESR1
MAPK8
HSP90AA1
NOS3
SERPINE1
FGA
F2
FOXO3
and STAT1
might be the therapeutic targets of scutellarin in AP and IS. Among them
NOS3 and F2 were recognized as the core targets. Additionally
molecular docking simulation confirmed that scutellarin exhibited a relatively high potential for binding to the active sites of NOS3 and F2. Furthermore
enrichment analysis indicated that scutellarin might exert a therapeutic role in both AP and IS by regulating several important pathways
such as coagulation cascades
mitogen-activated protein kinase (MAPK) signaling pathway
phosphatidylinositol 3 kinase (PI3K)/protein kinase B (Akt)/mammalian target of rapamycin (mTOR) signaling pathway
Toll-like receptor signaling pathway
hypoxia inducible factor-1 (HIF-1) signaling pathway
forkhead box O (FoxO) signaling pathway
tumor necrosis factor (TNF) signaling pathway
adipocytokine signaling pathway
insulin signaling pathway
insulin resistance
and estrogen signaling pathway.
Conclusions:
2
The shared underlying mechanisms of scutellarin on AP and IS treatment might be strongly associated with its vasorelaxant
anticoagulant
anti-inflammatory
and antioxidative effects as well as its effect on improving lipid metabolism.
scutellarinangina pectorisischemic strokenetwork pharmacology
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