Chen Hao, Zhang Zhen, Lu Congcong, Ding Yi, Huang Zhengao, Li Maoqiang, Zhu Liulong
Zhejiang University School of Medicine, Hangzhou First People's Hospital, Hangzhou 310006, China.
Department of Orthopedics, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310006, China.
Int Immunopharmacol. 2025 May 16;155:114604. doi: 10.1016/j.intimp.2025.114604. Epub 2025 Apr 10.
Urolithin A (UA), a metabolite of natural polyphenols produced by the gut microbiota, alleviates the symptoms of rheumatoid arthritis (RA) by inhibiting the inflammatory response. UA alleviates the clinical symptoms of RA by inhibiting the occurrence of an inflammatory response, but the specific regulatory mechanism remains unclear. In this study, we established a CIA model in 8-week-old DBA mice and chose LPS-stimulated NIH/3 T3 cells to explore the effects of UA and attempted to elucidate its potential mechanisms. Our results showed UA significantly reduced arthritis scores, and inhibited inflammation, pannus formation, and cartilage and bone destruction of inflamed joints in CIA mice. In vitro, UA inhibited LPS-induced migration and proliferation, and alleviated NLRP3-mediated pyroptosis, significantly inhibiting the protein expression levels of NLRP3, N-terminal gasdermin D, interleukin-1β, caspase-1, and ASC in NIH/3T3 cells. A mechanistic investigation revealed that LPS enhanced phosphorylation of NF-κB and downregulated that of AMPK, which were categorically counteracted by UA treatment. Therefore, UA represents a new class of promising RA treatments targeting fibroblasts, widening the therapeutic options for RA.
尿石素A(UA)是肠道微生物群产生的天然多酚的代谢产物,通过抑制炎症反应来缓解类风湿性关节炎(RA)的症状。UA通过抑制炎症反应的发生来缓解RA的临床症状,但其具体调节机制仍不清楚。在本研究中,我们在8周龄的DBA小鼠中建立了胶原诱导性关节炎(CIA)模型,并选择脂多糖(LPS)刺激的NIH/3T3细胞来探究UA的作用,并试图阐明其潜在机制。我们的结果显示,UA显著降低了关节炎评分,并抑制了CIA小鼠炎症关节的炎症、血管翳形成以及软骨和骨破坏。在体外,UA抑制LPS诱导的迁移和增殖,并减轻NLRP3介导的细胞焦亡,显著抑制NIH/3T3细胞中NLRP3、N端gasdermin D、白细胞介素-1β、半胱天冬酶-1和凋亡相关斑点样蛋白(ASC)的蛋白表达水平。机制研究表明,LPS增强了核因子κB(NF-κB)的磷酸化并下调了腺苷酸活化蛋白激酶(AMPK)的磷酸化,而UA处理可完全抵消这些作用。因此,UA代表了一类有前景的针对成纤维细胞的RA治疗药物,拓宽了RA的治疗选择。