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Huanglian Jiedu Decoction Treats Ischemic Stroke by Regulating Pyroptosis: Insights from Multi-Omics and Drug–Target Relationship Analysis

Published:23 May 2025 DOI: 10.3390/ph18060775 PMID: 40573172
Yixiao Gu, Zijin Sun, Tao Li, Xia Ding

Abstract

Background: Ischemic stroke (IS) is a severe condition with limited therapeutic options. Pyroptosis, a type of programmed cell death linked to inflammation, is closely associated with IS-related damage. Studies suggest inflammation aligns with the traditional Chinese medicine (TCM) concept of "fire-heat syndrome". Huanglian Jiedu Decoction (HLJD), a TCM formula known for clearing heat and purging fire, has shown therapeutic effects on IS, potentially by regulating pyroptosis. Study design: Eight-week-old male mice were divided into six groups: sham operation, model, positive drug, and low-, medium-, and high-dose HLJD groups. After a week of adaptive feeding, mice received respective treatments for five days, followed by modeling on the sixth day, with samples collected 23 h post-perfusion. Analyses included multi-omics, physiology, histopathology, virtual drug screening, target affinity assessment, and molecular biology techniques to measure relevant indicators. Results: HLJD effectively mitigated IS-related damage, maintaining neurological function, reducing ischemic levels, protecting cellular morphology, inhibiting neuronal apoptosis, and preserving blood-brain barrier integrity. Bioinformatics of high-throughput omics data revealed significant activation of pyroptosis and related inflammatory pathways in IS. ScRNA-seq identified neutrophils, macrophages, and microglia as key pyroptotic cell types, suggesting potential therapeutic targets. Network pharmacology and molecular docking identified NLRP3 as a critical target, with 6819 ligand-receptor docking results. SPR molecular fishing, LC-MS, molecular dynamics, and affinity measurements identified small molecules with high affinity for NLRP3. Molecular biology techniques confirmed that HLJD regulates pyroptosis via the classical inflammasome signaling pathway and modulates the inflammatory microenvironment. Conclusions: Following IS, pyroptosis in myeloid cells triggers an inflammatory cascade, leading to neural damage. HLJD may inhibit NLRP3 activity, reducing pyroptosis and associated inflammation, and ultimately mitigating damage.

Substances (38)

Materials
Procduct Name CAS Molecular Formula Supplier Price
Rutin 153-18-4 C27H30O16 859 suppliers $6.00-$569.50
Rutin 153-18-4 C27H30O16 859 suppliers $6.00-$569.50
Puerarin 3681-99-0 C21H20O9 732 suppliers $5.00-$2010.40
Puerarin 3681-99-0 C21H20O9 732 suppliers $5.00-$2010.40
Matrine 519-02-8 C15H24N2O 728 suppliers $29.00-$1280.00
Matrine 519-02-8 C15H24N2O 728 suppliers $29.00-$1280.00
Neochlorogenic acid 906-33-2 C16H18O9 299 suppliers $41.00-$1075.00
Neochlorogenic acid 906-33-2 C16H18O9 299 suppliers $41.00-$1075.00
BETA-D-GLUCOPYRANOSIDURONIC ACID 51059-44-0 C22H20O11 295 suppliers $50.00-$1367.50
BETA-D-GLUCOPYRANOSIDURONIC ACID 51059-44-0 C22H20O11 295 suppliers $50.00-$1367.50

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