Elucidation of the mechanism of Yiqi Tongluo Granule against cerebral ischemia/reperfusion injury based on a combined strategy of network pharmacology, multi-omics and molecular biology

被引:19
|
作者
Yuan, Yue [1 ,2 ]
Sheng, Peng [3 ]
Ma, Bo [4 ]
Xue, Bingjie [5 ]
Shen, Mengmeng [3 ]
Zhang, Ling [3 ]
Li, Dan [6 ]
Hou, Jincai [6 ]
Ren, Junguo [2 ]
Liu, Jianxun [2 ]
Yan, Bing Chun [3 ]
Jiang, Yunyao [1 ]
机构
[1] Tsinghua Univ, Inst Chinese Mat Med, Sch Pharmaceut Sci, Beijing 100084, Peoples R China
[2] China Acad Chinese Med Sci, Xiyuan Hosp, Beijing Key Lab TCM Pharmacol, Beijing 100730, Peoples R China
[3] Yangzhou Univ, Affiliated Hosp, Inst Translat Med,Key Lab Syndrome Differentiat &, Med Coll,Dept Neurol,Jiangsu Key Lab Integrated Tr, Yangzhou 225001, Peoples R China
[4] Chinese Acad Med Sci & Peking Union Med Coll, Inst Mat Med, Beijing 100730, Peoples R China
[5] Beijing Univ Chinese Med, Dongzhimen Hosp, Beijing 100700, Peoples R China
[6] Shineway Pharmaceut Grp Co Ltd, Shijiazhuang 051430, Peoples R China
基金
中国国家自然科学基金;
关键词
Yiqi Tongluo Granule; Cerebral ischemia; reperfusion injury; Network pharmacology; Transcriptomics; Proteomics; Apoptosis; BLOOD-BRAIN-BARRIER; INDUCED APOPTOSIS; CHINESE MEDICINE; ISCHEMIA; ACTIVATION; TRANSPORT; LIGUSTILIDE; INHIBITION; INFARCTION; DISEASE;
D O I
10.1016/j.phymed.2023.154934
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Background: Ischemic stroke is caused by local lesions of the central nervous system and is a severe cerebrovascular disease. A traditional Chinese medicine, Yiqi Tongluo Granule (YQTL), shows valuable therapeutic effects. However, the substances and mechanisms remain unclear. Purpose: We combined network pharmacology, multi-omics, and molecular biology to elucidate the mechanisms by which YQTL protects against CIRI. Study design: We innovatively created a combined strategy of network pharmacology, transcriptomics, proteomics and molecular biology to study the active ingredients and mechanisms of YQTL. We performed a network pharmacology study of active ingredients absorbed by the brain to explore the targets, biological processes and pathways of YQTL against CIRI. We also conducted further mechanistic analyses at the gene and protein levels using transcriptomics, proteomics, and molecular biology techniques. Results: YQTL significantly decreased the infarction volume percentage and improved the neurological function of mice with CIRI, inhibited hippocampal neuronal death, and suppressed apoptosis. Fifteen active ingredients of YQTL were detected in the brains of rats. Network pharmacology combined with multi-omics revealed that the 15 ingredients regulated 19 pathways via 82 targets. Further analysis suggested that YQTL protected against CIRI via the PI3K-Akt signaling pathway, MAPK signaling pathway, and cAMP signaling pathway. Conclusion: We confirmed that YQTL protected against CIRI by inhibiting nerve cell apoptosis enhanced by the PI3K-Akt signaling pathway.
引用
收藏
页数:17
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