An Integrative Workflow Combining Machine Learning and GNPS to Identify Key Anti‐Inflammatory Constituents in Honey‐Processed Ephedrae Herba ( Ephedra sinica Stapf)

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Authors: Hengyang Li, Qi An, Bing Guo, Xinyao Lu, Yuguang Zheng, Long Guo, Dan Zhang
Cited by: 0
References: 20

Abstract

Ephedrae Herba (EH), a traditional Chinese medicine long used for asthma treatment, is commonly processed with honey to yield honey-processed Ephedrae Herba (HEH), a form believed to enhance therapeutic efficacy. This study developed an integrated approach combining bioactivity evaluation, mass spectrometry, and machine learning to identify the key anti-inflammatory constituents of HEH. HEH extract was separated into five fractions using column chromatography. Anti-inflammatory activity was assessed in lipopolysaccharides (LPS)-induced RAW 264.7 macrophages, with Fr C demonstrating the strongest inhibition of nitric oxide (NO), tumor necrosis factor-α (TNF-α), interleukin-1β (IL-1β), and IL-6 production. UPLC-quadrupole time-of-flight mass spectrometer (Q-TOF-MS) and Global Natural Products Social Molecular Networking (GNPS)-based molecular networking enabled the tentative identification of 150 compounds in Fr C. Using the machine learning model (InflamNat) and molecular docking, 14 compounds were predicted to show anti-inflammatory potential. Four high-priority compounds were selected based on docking scores and experimentally validated. Each significantly suppressed the release of NO and pro-inflammatory cytokines (p < 0.01). These results indicate that the enhanced anti-inflammatory activity of HEH is attributable to its flavonoid and alkaloid components, providing a chemical basis for its traditional use in inflammatory diseases such as asthma. Our findings not only clarify the material basis of HEH's but also demonstrate a powerful analytical strategy for rapidly identifying bioactive compounds in processed herbal medicines.

Fields of Study & Subjects

Traditional Chinese Medicine Analysis Phytochemistry and Biological Activities Computational Drug Discovery Methods

Publication details

Journal / source
Chemistry & Biodiversity
Volume
23
Issue
3
Pages
e03767–e03767
Publication date
1 March 2026
Language
EN