Compositional Analysis and Network Pharmacological Strategy for the Treatment of Diabetic Kidney Disease by Shengjiang Powder Based on UHPLC-Q-TOF-MS

被引:0
|
作者
Yin, Yongzhi [1 ,2 ]
Yang, Lu [2 ]
Zhang, Ke [1 ]
Yu, Silin [2 ,3 ]
Liao, Jinfa [1 ,2 ]
Wang, Jinhui [1 ,3 ]
机构
[1] Shihezi Univ, Coll Pharm, Key Lab Xinjiang Phytomed Resource & Utilizat, Minist Educ, Shihezi 832002, Peoples R China
[2] Xinjiang Acad Forestry, Key Lab Forest Resources & Utilizat Xinjiang, Natl Forestry & Grassland Adm, Urumqi 830052, Peoples R China
[3] Harbin Med Univ, Coll Pharm, Harbin, Peoples R China
基金
中国国家自然科学基金;
关键词
Diabetic kidney disease; key active ingredient; molecular docking; network pharmacology; Shengjiang powder;
D O I
10.1177/1934578X241277543
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Objective: Shengjiang Powder (SJP) is a traditional Chinese medicine compound formula commonly used in the treatment of diabetic kidney disease (DKD). However, its material basis and mechanism of action are still unclear. Methods: In this study, the aqueous extract of SJP was obtained by aqueous decoction method, and the in vivo and in vitro constituents of SJP were analysed by ultra-high performance liquid chromatography coupled with quadrupole time-of-flight mass spectrometry (UHPLC-Q-TOF-MS), and a network pharmacological strategy was established in conjunction with molecular docking in order to investigate the mechanism of action of SJP in the treatment of DKD. Results: The results identified 162 components, of which 28 could be absorbed into the blood and exert therapeutic effects in vivo. The main active ingredients were CT-1, CT-2, CT-7, BJC-2, and BJC-5, and the main targets in vivo were related to AKT1, MAPK1, MAPK3, MAPK8, and MAPK14, which could exert their therapeutic effects through the PI3K-Akt signaling pathway, Insulin resistance, and AGE-RAGE signaling pathway in diabetic complications, etc Conclusion: The present study adopts a comprehensive analytical strategy to reveal the pharmacodynamic material basis and mechanism of action of SJP in the treatment of DKD, and to provide a scientific basis for its clinical application.
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收藏
页数:17
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