Yu Xuecheng, Shi Kun, Wu Bin, Gao Zengxiang, Tu Jiyuan, Cao Yan, Chen Linlin, Cao Guosheng
College of Pharmacy, Hubei University of Chinese Medicine, Wuhan, 430065, People's Republic of China.
Hubei Shizhen Laboratory, Wuhan, 430065, People's Republic of China.
Curr Comput Aided Drug Des. 2024 Apr 15. doi: 10.2174/0115734099292513240404091734.
Shenfu injection was derived from the classical Chinese medicine formula 'Shenfu decoction', which was widely used in the treatment of cardiovascular and cerebrovascular diseases in clinical practice.
Predict the main active ingredients, core targets, and related signaling pathways of Shenfu injection in the treatment of ischemic stroke.
Databases were used to collect the active ingredients and target information of Shenfu injection; GO and KEGG pathway enrichment analyses were performed using the David database. The effects of Shenfu injection on core targets were verified using molecular docking and in vivo experiments.
The predicted results identified 44 active ingredients and 635 targets in Shenfu injection, among which 418 targets, including TNF, IL-6, MAPK1, and MAPK14, were potential targets for the treatment of ischemic stroke. Molecular docking revealed that the active ingredients had good binding to IL-6, MAPK1, and MAPK14. In vivo experiments demonstrated that Shenfu injection significantly improved the pathological damage due to ischemic stroke, promoted the expression of tight junction proteins, and inhibited MMP-2 and MMP-9 expressions, thereby reducing BBB permeability. Animal experiments revealed that Shenfu injection could inhibit p38、JNK and ERK phosphorylation.
Mechanism of Shenfu injection in treating ischemic stroke may be via inhibition of the inflammatory factors levels and protecting the BBB, thereby warranting subsequent studies and highlighting its potential as a reference for new drug development.
参附注射液源自经典中药方剂“参附汤”,在临床实践中广泛用于治疗心脑血管疾病。
预测参附注射液治疗缺血性脑卒中的主要活性成分、核心靶点及相关信号通路。
利用数据库收集参附注射液的活性成分和靶点信息;使用David数据库进行基因本体(GO)和京都基因与基因组百科全书(KEGG)通路富集分析。通过分子对接和体内实验验证参附注射液对核心靶点的作用。
预测结果确定参附注射液中有44种活性成分和635个靶点,其中包括肿瘤坏死因子(TNF)、白细胞介素-6(IL-6)、丝裂原活化蛋白激酶1(MAPK1)和丝裂原活化蛋白激酶14(MAPK14)等418个靶点是治疗缺血性脑卒中的潜在靶点。分子对接显示活性成分与IL-6、MAPK1和MAPK14具有良好的结合。体内实验表明参附注射液可显著改善缺血性脑卒中所致的病理损伤,促进紧密连接蛋白的表达,并抑制基质金属蛋白酶-2(MMP-2)和基质金属蛋白酶-9(MMP-9)的表达,从而降低血脑屏障通透性。动物实验显示参附注射液可抑制p38、JNK和ERK的磷酸化。
参附注射液治疗缺血性脑卒中的机制可能是通过抑制炎症因子水平和保护血脑屏障,从而值得后续研究,并突出其作为新药开发参考的潜力。