Tussilagone mitigates sepsis-induced acute lung injury in mice by suppressing RIPK1 expression

作者：Jie Gu, Yachen Cai, Jiangwen Yin, Mengjie Zhang, Jun Chen, Hongjun Miao · 发表于：Hereditas · 年份：2026 · DOI：10.1186/s41065-026-00678-7 · 研究领域：Plant Toxicity and Pharmacological Properties、Plant-based Medicinal Research、Pharmacological Effects of Natural Compounds

OBJECTIVE: Sepsis is a severe condition characterized by life-threatening organ dysfunction resulting from an excessive host response to infection. Among the affected organs, the lungs are particularly susceptible during the progression of sepsis. Tussilagone (TS), a sesquiterpenoid compound derived from the flowers of Tussilago farfara, has been explored for its potential therapeutic effects on sepsis-induced lung injury. This study used both in vitro and in vivo experimental approaches, complemented by network pharmacology analyses, to verify the mechanisms and molecular targets underlying the effects of TS. METHODS: TS was administered to mice with sepsis-induced lung injury and to lung epithelial cells stimulated with lipopolysaccharide (LPS) to assess its therapeutic potential. Inflammatory factor levels in mouse serum, lung tissue, and cells were assessed. Western blot analysis was used to determine the expression of NF-κB p65 and MyD88 in lung tissues. Potential molecular TS targets were identified, with receptor-interacting serine/threonine-protein kinase 1 (RIPK1) selected for further investigation using the Traditional Chinese Medicine Systems Pharmacology Database and Analysis Platform. Additionally, the study explored if TS exerts its protective effects against lung injury in septic mice through targeted regulation of RIPK1. RESULTS: TS inhibited the NF-κB p65 and MyD88 signaling pathways, reducing the release of inflammatory factors and a mitigation of lung injur...