黄芩素
药理学
系统药理学
黄酮类
绿原酸
药效学
沃戈宁
黄芩苷
酒精性肝病
化学
PI3K/AKT/mTOR通路
医学
信号转导
中医药
生物化学
黄芩
药代动力学
高效液相色谱法
肝硬化
药品
色谱法
内科学
替代医学
病理
作者
Yingying Tan,Fanqin Zhang,Xiaotian Fan,Shan Lu,Yingying Liu,Zhishan Wu,Zhihong Huang,Chao Wu,Guoliang Cheng,Bing Li,Jiaqi Huang,Antony Stalin,Wei Zhou,Jiarui Wu
标识
DOI:10.1186/s13020-023-00759-z
摘要
Yinzhihuang granules (YZHG) is a commonly used Chinese patent medicine for the treatment of liver disease. However, the mechanism of YZHG in alcoholic liver disease (ALD) is still unclear.This study combined liquid chromatography-mass spectrometry technology, pharmacodynamics, network pharmacology and molecular docking methods to evaluate the potential mechanism of YZHG in the treatment of ALD.A total of 25 compounds including 4-hydroxyacetophenone, scoparone, geniposide, quercetin, baicalin, baicalein, chlorogenic acid and caffeic acid in YZHG were identified by ultra performance liquid chromatography tandem mass spectrometry (UPLC-MS/MS). The pharmacodynamic investigations indicated that YZHG could improve liver function and the degree of liver tissue lesions, and reduce liver inflammation and oxidative stress in ALD mice. Network pharmacology analysis showed that YZHG treated ALD mainly by regulating inflammation-related signaling pathways such as the PI3K-Akt signaling pathway. The results of the PPI network and molecular docking showed that the targets of SRC, HSP90AA1, STAT3, EGFR and AKT1 could be the key targets of YZHG in the treatment of ALD.This study explored the potential compounds, potential targets and signaling pathways of YZHG in the treatment of ALD, which is helpful to clarify the efficacy and mechanism of YZHG and provide new insights for the clinical application of YZHG.
科研通智能强力驱动
Strongly Powered by AbleSci AI