Notch信号通路
医学
NF-κB
信号转导
槽口1
下调和上调
缺血
药理学
神经学
内科学
神经科学
冲程(发动机)
癌症研究
细胞生物学
炎症
化学
受体
生物
生物化学
基因
工程类
精神科
机械工程
作者
Shuya Li,Xiangjian Zhang,Yongjun Wang,Hui Ji,Yuanyuan Du,Haichao Liu
标识
DOI:10.1007/s10072-012-0948-6
摘要
Gamma-secretase inhibitor, N-[N-(3,5-difluorophenacetyl)-1-alanyl]-S-phenylglycine t-butyl ester (DAPT) suppresses the activation of Notch 1 signaling, which is recognized as the cell fate signaling and may participate in inflammatory processes together with NF-κB pathway that contributes to the brain damage after stroke. DAPT has important pharmacological roles in many diseases. However, little is known about the effect of DAPT on NF-κB during cerebral ischemia. This study investigated the time course expression of Notch 1 and the effects of DAPT on Notch 1 and NF-jB after MCAO. The results showed that Notch 1 signaling was up-regulated at the early stage after MCAO, DAPT down-regulated the expression of Notch 1 and NF-κB and protected brain from damage caused by MCAO. These results may indicate that the downregulation of Notch 1–NF-κB pathway after ischemia by administration of DAPT is a potential mechanism for its protection.
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