Investigation of the Potential Mechanism of Compound Dragon's Blood Capsule against Myocardial Ischemia Based on Network Pharmacology
- Authors: Su X.1, Xue H.2, Lou Y.3, Lv X.2, Mi X.2, Lu J.2, Chen X.3
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Affiliations:
- Chinese Academy of Medical Sciences, Yunnan Branch, Institute of Medicinal Plant Development
- Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences, Peking Union Medical College
- Chinese Academy of Medical Sciences, Peking Union Medical College, Institute of Medicinal Plant Development
- Issue: Vol 27, No 19 (2024)
- Pages: 2940-2950
- Section: Chemistry
- URL: https://gynecology.orscience.ru/1386-2073/article/view/644569
- DOI: https://doi.org/10.2174/0113862073264485240102064653
- ID: 644569
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Full Text
Abstract
Background:Dragon's blood is widely consumed in China, Vietnam and Laos to promote blood circulation. A Compound Dragon's blood capsule (CDC) is a patented medicine composed of dragons blood, notoginseng, and borneol. This combination is purported to stabilize coronary heart disease and myocardial ischemia. However, the possible mechanisms and the characterization of its drug targets relevance at the systemic level remain unclear.
Aim:The present study aims to reveal the potential mechanisms of CDCs anti-myocardial ischemia effect
Materials and Methods:The potential mechanisms were investigated by network pharmacology and qRT-PCR was used to verify the expression levels of key genes of PI3k-Akt pathway.
Results:S1PR2 and AGTR1 were the common targets, which involved 6 biological processes annotated by KEGG and GO analysis. The qRT-PCR results showed a remarkable increase in the expression of Pi3k, Pdk1, Akt, Mdm2, Bcl2, and mTOR. Results also showed a decline in the expression of P53 and Casp3 after CDC intervention.
Conclusion:CDC has a significant anti-myocardial ischemia effect through the PI3k/Akt pathway, which demonstrates that CDC is a suitable adjuvant to treat CHD and provides a theoretical basis for its further clinical application.
About the authors
Xin Su
Chinese Academy of Medical Sciences, Yunnan Branch, Institute of Medicinal Plant Development
Email: info@benthamscience.net
Hongwei Xue
Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences, Peking Union Medical College
Email: info@benthamscience.net
Yang Lou
Chinese Academy of Medical Sciences, Peking Union Medical College, Institute of Medicinal Plant Development
Email: info@benthamscience.net
Xinkai Lv
Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences, Peking Union Medical College
Email: info@benthamscience.net
Xiao Mi
Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences, Peking Union Medical College
Email: info@benthamscience.net
Juan Lu
Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences, Peking Union Medical College
Author for correspondence.
Email: info@benthamscience.net
Xi Chen
Chinese Academy of Medical Sciences, Peking Union Medical College, Institute of Medicinal Plant Development
Author for correspondence.
Email: info@benthamscience.net
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