Hydroxysafflor Yellow A Protects Against Cerebral Ischemia–Reperfusion Injury by Anti-apoptotic Effect Through PI3K/Akt/GSK3β Pathway in Rat

被引:24
作者
Lin Chen
Yanxiao Xiang
Lingjun Kong
Xiumei Zhang
Baozhu Sun
Xinbing Wei
Huiqing Liu
机构
[1] Shandong University School of Medicine,Department of Pharmacology
[2] Shandong University,Department of Anesthesiology, Qilu Hospital
来源
Neurochemical Research | 2013年 / 38卷
关键词
Hydroxysafflor yellow A; Ischemia–reperfusion; Apoptosis; PI3K/Akt/GSK3β pathway;
D O I
暂无
中图分类号
学科分类号
摘要
Hydroxysafflor yellow A (HSYA) is the major active chemical component of the flower of the safflower plant, Carthamus tinctorius L. Previously, its neuroprotection against cerebral ischemia–reperfusion (I/R) injury was reported by anti-oxidant action and suppression of thrombin generation. Here, we investigate the role of HSYA in cerebral I/R-mediated apoptosis and possible signaling pathways. Male Wistar rats were subjected to transient middle cerebral artery occlusion for 2 h, followed by 24 h reperfusion. HSYA was administered via tail-vein injection just 15 min after occlusion. The number of apoptotic cells was measured by TUNEL assay, apoptosis-related proteins Bcl-2, Bax and the phosphorylation levels of Akt and GSK3β in ischemic penumbra were assayed by western blot. The results showed that administration of HSYA at the doses of 4 and 8 mg/kg significantly inhibited the apoptosis by decreasing the number of apoptotic cells and increasing the Bcl-2/Bax ratio in rats subjected to I/R injury. Simultaneously, HSYA treatment markedly increased the phosphorylations of Akt and GSK3β. Blockade of PI3K activity by wortmannin dramatically abolished its anti-apoptotic effect and lowered both Akt and GSK3β phosphorylation levels. Taken together, these results suggest that HSYA protects against cerebral I/R injury partly by reducing apoptosis via PI3K/Akt/GSK3β signaling pathway.
引用
收藏
页码:2268 / 2275
页数:7
相关论文
共 181 条
[1]  
Dirnagl U(1999)Pathobiology of ischaemic stroke: an integrated view Trends Neurosci 22 391-397
[2]  
Iadecola C(2009)Apoptotic mechanisms after cerebral ischemia Stroke 40 e331-e339
[3]  
Moskowitz MA(2011)The Akt/GSK-3beta pathway mediates flurbiprofen-induced neuroprotection against focal cerebral ischemia/reperfusion injury in rats Biochem Biophys Res Commun 409 808-813
[4]  
Broughton BR(2012)Losartan, an angiotensin II type 1 receptor blocker, ameliorates cerebral ischemia–reperfusion injury via PI3K/Akt-mediated eNOS phosphorylation Brain Res Bull 89 65-70
[5]  
Reutens DC(2013)Leptin attenuates cerebral ischemia injury through the promotion of energy metabolism via the PI3K/Akt pathway J Cereb Blood Flow Metab 33 567-574
[6]  
Sobey CG(2001)Evidence of phosphorylation of Akt and neuronal survival after transient focal cerebral ischemia in mice J Cereb Blood Flow Metab 21 1442-1450
[7]  
Sun B(2002)The phosphoinositide 3-kinase pathway Science 296 1655-1657
[8]  
Chen L(2005)Toll-like receptor-mediated cytokine production is differentially regulated by glycogen synthase kinase 3 Nat Immunol 6 777-784
[9]  
Wei X(2004)The glamour and gloom of glycogen synthase kinase-3 Trends Biochem Sci 29 95-102
[10]  
Xiang Y(2006)The paradoxical pro- and anti-apoptotic actions of GSK3 in the intrinsic and extrinsic apoptosis signaling pathways Prog Neurobiol 79 173-189