Symptom-oriented network pharmacology revealed the mechanism of HuangQi-DanShen herb pair against cerebral ischemia coupled with comprehensive chemical characterization

医学 药理学 MMP9公司 中医药 药品 替代医学 化学 病理 生物化学 下调和上调 基因
作者
Yuetao Liu,Ruoxin Xiang,Wentian Lu,Xuemei Qin
出处
期刊:Journal of Ethnopharmacology [Elsevier BV]
卷期号:318: 116845-116845 被引量:2
标识
DOI:10.1016/j.jep.2023.116845
摘要

In the clinical practice of traditional Chinese medicine, HuangQi-DanShen (HD) is an important drug pair for the treatment of cerebral ischemia (CI). Elucidate the mechanism of HD against CI based on symptom-oriented network pharmacology coupled with comprehensive chemical characterization. UHPLC-Q-Exactive Orbitrap-MS technology was firstly used to obtain the chemical profile of HD constituents. A comprehensive strategy combining in-house library, diagnostic ions, Compound Discover software and network databases was then established to identify its chemical constitutes. Symptomatic treatment is a treatment aimed at relieving or eliminating symptoms which is often characterized as a stop-gap measure due to its inability to cure the disease fundamentally. Nevertheless, symptomatic treatment is an indispensable part of clinical practice and has an important place in medical therapeutics. Therefore, network pharmacology technique were used to elucidate molecular mechanisms from the symptoms of CI. Finally, some literatures were further mined to support our conclusions. A total of 190 ingredients were identified in HD. Symptom-oriented network pharmacology analysis indicated that compounds of HD relieved “blood” through the regulation of ADORA2A, ADORA1, PTPN11, MMP9 and EGFR,. relieved “qi” via the regulation of ADORA2A, EGFR, MMP9 and CA2. The therapeutic effect of HD on “faint” was linked to PTPN11 and MMP9, while the regulation of “dyskinesia” was related to ADORA2A and EGFR, and ADORA1, PTPN11 and MMP9 were associated withe its effect on “speech disorder”. ADORA1, ADORA2A and MMP9 were key to the HD component in treating “visual disturbance”. The approach of symptom-oriented network pharmacology coupled with comprehensive chemical characterization proposed a further orientation for exploring the mechanisms of HD against CI.
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