体内
化学
药理学
特应性皮炎
MAPK/ERK通路
NF-κB
p38丝裂原活化蛋白激酶
细胞毒性
磷酸化
体外
细胞因子
信号转导
免疫学
生物化学
医学
生物
生物技术
作者
Cheng Lü,Xiaohua Li,Du Wang,Xiao Zhang,Yanping Li,Chunyan Hu,Zewei Mao,Yi Zhang,Ruirui Wang
标识
DOI:10.1016/j.bioorg.2023.107054
摘要
Atopic dermatitis (AD) is a common inflammatory disease and it is very difficult to treat. In the present work, a series of costunolide derivatives have been prepared, and in vitro and in vivo anti-inflammatory activities have evaluated. The results showed that most derivatives displayed good inhibition of NO generation with low cytotoxicity, and 7d could inhibit the phosphorylation of P38, P65 NF-κB and IκB-α in LPS-induced RAW264.7 model. The in vivo researches showed that 7d could improve skin injury symptoms, decrease Th2-type cytokine levels, inhibit HIS levels, alleviate scratching and repaire the damaged skin barrier through the inhibition of phosphorylation of MAPK and NF-κB signaling pathways on MC903-induced AD model. Therefore, costunolide derivatives may be new potent anti-AD agents for further study.
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