A dihydrofuro[2,3-b] benzofuran derivative alleviates lipopolysaccharide induced acute lung injury via suppressing MAPK signaling

Introduction: constituents and to evaluate their anti-inflammatory activity and mechanism in a lipopolysaccharide (LPS)-induced acute lung injury (ALI) model. Methods: α expression. The most active molecule, QFM-3m, was tested in LPS-induced murine ALI through histopathology, cytokine assays, and vascular permeability analysis. Mechanistic studies were conducted using transcriptomic and protein analyses of primary macrophages. Results: . Transcriptomic, western blot and molecular docking analysis revealed that QFM-3m selectively suppressed ERK, JNK, and p38 phosphorylation, while NF-κB activation remained unaffected. Conclusion: -inspired scaffolds for inflammatory lung diseases.

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Publication Details

Journal
Frontiers in Pharmacology
Published
2026-04-21
DOI
https://doi.org/10.3389/fphar.2026.1763318
Primary Topic
Natural Compound Pharmacology Studies
Type
article
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article

A dihydrofuro[2,3-b] benzofuran derivative alleviates lipopolysaccharide induced acute lung injury via suppressing MAPK signaling

Yuxi Wang, Zeping Shan, Yuqing Cai, Shenyan Shao et al.
Frontiers in Pharmacology
Natural Compound Pharmacology Studies
article

A dihydrofuro[2,3-b] benzofuran derivative alleviates lipopolysaccharide induced acute lung injury via suppressing MAPK signaling

Yuxi Wang, Zeping Shan, Yuqing Cai, Shenyan Shao, Chengyun Xu, Yuanyuan Yang, Xiaohong Wu, Guimei Wang, Aijing Zhang
article en

Abstract

Introduction: constituents and to evaluate their anti-inflammatory activity and mechanism in a lipopolysaccharide (LPS)-induced acute lung injury (ALI) model. Methods: α expression. The most active molecule, QFM-3m, was tested in LPS-induced murine ALI through histopathology, cytokine assays, and vascular permeability analysis. Mechanistic studies were conducted using transcriptomic and protein analyses of primary macrophages. Results: . Transcriptomic, western blot and molecular docking analysis revealed that QFM-3m selectively suppressed ERK, JNK, and p38 phosphorylation, while NF-κB activation remained unaffected. Conclusion: -inspired scaffolds for inflammatory lung diseases.

Frontiers in PharmacologyVol. 17
Sir Run Run Shaw Hospital (CN), City University (BD), Hangzhou Hospital of Traditional Chinese Medicine (CN), Communication University of Zhejiang (CN)
Good health and well-being
Openalex Percentile: Top 20%
Natural Compound Pharmacology Studies
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