吴茱萸碱
小檗碱
TRPV1型
MAPK/ERK通路
巨噬细胞极化
信号转导
NF-κB
化学
癌症研究
药理学
吴茱萸碱
医学
巨噬细胞
生物化学
受体
体外
瞬时受体电位通道
作者
Guoliang Cui,Manli Wang,Xiaofeng Li,Can Wang,Kinyu Shon,Zhiting Liu,Ren Lang,Xiaoyan Yang,Xiaoman Li,Yuanyuan Wu,Zhiguang Sun
出处
期刊:Phytomedicine
[Elsevier BV]
日期:2024-11-12
卷期号:135: 156251-156251
被引量:16
标识
DOI:10.1016/j.phymed.2024.156251
摘要
We firstly demonstrate that BBR and EVO alleviate GERD, with enhanced synergistic efficacy observed when used in combination. Mechanistically, BBR and EVO activate the TAS2R38 and TRPV1, respectively, leading to downregulation of phosphorylation in MAPK/NF-κB signaling pathways and modulation of macrophage polarization. These findings offer a novel foundation for the clinical application of BBR and EVO in GERD treatment.
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