Preliminary Exploration of Potential Active Ingredients and Molecular Mechanisms of Yanggan Yishui Granules for Treating Hypertensive Nephropathy Using UPLC-Q-TOF/MS Coupled with Network Pharmacology and Molecular Docking Strategy.
Fan YangKailun ZhangXiaohua DaiWei-Min JiangPublished in: Journal of analytical methods in chemistry (2024)
Hypertensive nephropathy (HN) is a prevalent complication of hypertension and stands as the second primary reason for end-stage renal disease. Research in clinical settings has revealed that Yanggan Yishui Granule (YGYSG) has significant therapeutic effects on HN. However, the material basis and action mechanisms of YGYSG against HN remain unclear. Consequently, this study utilized a comprehensive method integrating ultraperformance liquid chromatography-quadrupole time-of-flight mass spectrometry (UPLC-Q-TOF/MS), network pharmacology, and molecular docking to delineate the active ingredients and potential therapeutic mechanisms of YGYSG for treating HN. Firstly, sixty distinct components were recognized in total as potential active ingredients in YGYSG by UPLC-Q-TOF/MS. Subsequently, the mechanisms of YGYSG against HN were revealed for the first time using network pharmacology. 23 ingredients played key roles in the complete network and were the key active ingredients, which could affect the renin-angiotensin system, fluid shear stress and atherosclerosis, HIF-1 signaling pathway, and AGE-RAGE signaling pathway in diabetic complications by regulating 29 key targets such as TNF, IL6, ALB, EGFR, ACE, and MMP2. YGYSG could treat HN through the suppression of inflammatory response and oxidative stress, attenuating the proliferation of renal vascular smooth muscle cells, lessening glomerular capillary systolic pressure, and ameliorating renal dysfunction and vascular damage through the aforementioned targets and pathways. Molecular docking results revealed that most key active ingredients exhibited a high affinity for binding to the key targets. This study pioneers in clarifying the bioactive compounds and molecular mechanisms of YGYSG against HN and offers scientific reference into the clinical application.
Keyphrases
- molecular docking
- signaling pathway
- blood pressure
- molecular dynamics simulations
- oxidative stress
- simultaneous determination
- liquid chromatography
- inflammatory response
- vascular smooth muscle cells
- end stage renal disease
- mass spectrometry
- chronic kidney disease
- single cell
- tandem mass spectrometry
- pi k akt
- small cell lung cancer
- epithelial mesenchymal transition
- induced apoptosis
- liquid chromatography tandem mass spectrometry
- type diabetes
- dna damage
- cardiovascular disease
- risk factors
- human health
- high performance liquid chromatography
- network analysis
- diabetic rats
- cell proliferation
- ischemia reperfusion injury
- lps induced
- gas chromatography
- heat stress
- heat shock protein