Department of Physiology and Pathophysiology, School of Basic Medical Sciences, Peking University Health Science Center, Beijing, People's Republic of China.
Biochem Biophys Res Commun. 2013 Jul 12;436(4):655-9. doi: 10.1016/j.bbrc.2013.05.142. Epub 2013 Jun 14.
Cocaine and amphetamine regulated transcript (CART), a neuropeptide, has shown strong neuroprotective effects against cerebral ischemia and reperfusion (I/R) injury in vivo and in vitro. Here, we report a new effect of CART on ER stress which is induced by cerebral I/R in a rat model of middle cerebral artery occlusion (MCAO) or by oxygen and glucose deprivation (OGD) in cultured cortical neurons, as well as a new functionality of BDNF in the neuroprotection by CART against the ER stress in cerebral I/R. The results showed that CART was effective in reducing the neuronal apoptosis and expression of ER stress markers (GRP78, CHOP and cleaved caspase12), and increasing the BDNF expression in I/R injury rat cortex both in vivo and in vitro. In addition, the effects of CART on ischemia-induced neuronal apoptosis and ER stress were suppressed by tyrosine receptor kinase B (TrkB) IgG, whereas the effects of CART on BDNF transcription, synthesis and secretion were abolished by CREB siRNA. This work suggests that CART is functional in inhibiting the cerebral I/R-induced ER stress and neuronal apoptosis by facilitating the transcription, synthesis and secretion of BDNF in a CREB-dependent way.
可卡因和苯丙胺调节转录物 (CART) 是一种神经肽,已显示出对体内和体外脑缺血再灌注 (I/R) 损伤具有很强的神经保护作用。在这里,我们报告了 CART 对脑 I/R 诱导的培养皮质神经元中 ER 应激的新作用,以及 CART 对脑 I/R 中 ER 应激的神经保护作用中 BDNF 的新功能。结果表明,CART 可有效减少神经元凋亡和 ER 应激标志物 (GRP78、CHOP 和 cleaved caspase12) 的表达,并增加 I/R 损伤大鼠皮质中的 BDNF 表达,无论是在体内还是体外。此外,CART 对缺血诱导的神经元凋亡和 ER 应激的作用被酪氨酸受体激酶 B (TrkB) IgG 抑制,而 CART 对 BDNF 转录、合成和分泌的作用被 CREB siRNA 消除。这项工作表明,CART 通过 CREB 依赖性方式促进 BDNF 的转录、合成和分泌,从而在功能上抑制脑 I/R 诱导的 ER 应激和神经元凋亡。