S1PR1型
化学
受体
信号转导
药理学
TRPV1型
医学
生物化学
癌症研究
血管内皮生长因子受体
瞬时受体电位通道
血管内皮生长因子A
血管内皮生长因子
作者
Yisen Huang,Xiangbo Chen,Xiaoqiang Liu,Chanchan Lin,Yubin Wang
标识
DOI:10.1016/j.intimp.2024.111814
摘要
In summary, our investigation revealed that isofraxidin could modulate S1PR1 and regulate the IL-17 signaling pathway, thus ameliorating DSS-induced UC. These findings establish a robust foundation for considering isofraxidin as a prospective therapeutic intervention to treat UC.
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