小胶质细胞
细胞凋亡
p38丝裂原活化蛋白激酶
丙戊酸
MAPK/ERK通路
细胞生物学
蛋白激酶A
丝裂原活化蛋白激酶
激酶
化学
药理学
生物
癌症研究
神经科学
免疫学
炎症
生物化学
癫痫
作者
Nanchang Xie,Cui Wang,Y.H. Lin,Hui Li,Lin Chen,Tongxia Zhang,Yong Sun,Yi Zhang,Deling Yin,Chi Zhao-fu
标识
DOI:10.1016/j.neulet.2010.07.004
摘要
Valproic acid (VPA), a widely prescribed drug for seizures and bipolar disorder, induces apoptosis in microglia, but the underlying mechanism by which microglia apoptosis in response to VPA is not yet known. In this study, we found that the mitochondrial pathway played an important role in VPA-induced apoptosis in both BV-2 microglia and mouse primary microglial cells. In addition, VPA increased the level of phospho-p38 mitogen-activated protein kinase (MAPK), but had no effects on phospho-ERK and phospho-JNK MAPKs. Moreover, p38 inhibitor SB203580 strongly inhibited VPA-induced apoptosis and caspase-3 activation. Taken together, our results clearly demonstrated that VPA could induce apoptosis of microglia via p38 MAPK and mitochondrial apoptosis pathway.
科研通智能强力驱动
Strongly Powered by AbleSci AI