结肠炎
促炎细胞因子
MAPK/ERK通路
化学
细胞因子
紧密连接
p38丝裂原活化蛋白激酶
细胞生物学
药理学
激酶
一氧化氮
癌症研究
磷酸化
调节器
势垒函数
蛋白激酶A
肠粘膜
信号转导
免疫学
医学
作者
So Yeon Kim,Yoo Kyong Han,Yun Mi Lee,Kyuhyung Jo,Dong-Seon Kim
标识
DOI:10.1016/j.jff.2025.107120
摘要
This study investigated the anti-inflammatory and barrier-protective effects of Spiraea prunifolia var. simpliciflora ethanol extract (SPSE) in lipopolysaccharide-stimulated macrophages and dextran sulfate sodium (DSS)-induced colitis in mice. SPSE suppressed nitric oxide production and down-regulated pro-inflammatory cytokines (TNF-α, IL-6, and IL-1β) by inhibiting phosphorylation of ERK, JNK, and p38 MAPK. In vivo, SPSE alleviated weight loss, colon shortening, and histological damage, accompanied by reduced cytokine expression and MAPK activation in colonic tissue. Moreover, SPSE restored epithelial tight junction proteins, including ZO-1, occludin, and claudin-1, thereby preserving intestinal barrier integrity. Molecular docking suggested that caffeoyl-type constituents of SPSE interact with transforming growth factor β-activated kinase 1 (TAK1), an upstream regulator of MAPK signalling. These findings demonstrate that SPSE mitigates experimental colitis by modulating MAPK signalling and maintaining epithelial integrity, supporting its potential as a functional food ingredient for intestinal health. • ⸱ SPSE suppressed proinflammatory cytokine production in macrophages. • ⸱ SPSE ameliorated DSS-induced colitis and restored colon barrier integrity. • ⸱ SPSE inhibited MAPK signalling and preserved tight junction proteins. • ⸱ SPSE, rich in caffeoyl derivatives, shows potential as a functional food ingredient for IBD management.
科研通智能强力驱动
Strongly Powered by AbleSci AI