Department of Neurosurgery, Ren Ji Hospital, Shanghai Jiao Tong University School of Medicine, China.
Int J Mol Sci. 2010 Jan 12;11(1):140-53. doi: 10.3390/ijms11010140.
Transient forebrain or global ischemia induces cell death in vulnerable CA1 pyramidal neurons. A brief period of ischemia, i.e., ischemic preconditioning, affords CA1 neurons robust protection against a subsequent, more prolonged ischemic challenge. Using the four-vessel occlusion model, we established an ischemic preconditioning model in which rodents were subjected to 3 min of sublethal ischemia 48 h before a 15 min lethal ischemia. We showed that preconditioning attenuated the ischemia-induced neural cell death and DNA fragmentation in the hippocampal CA1 region. RT-PCR and western blot analysis showed that preconditioning prior to an ischemic insult significantly increased ASIC 2a mRNA and protein expression in comparison to the ischemic insult alone (p < 0.01). These findings implicate a new role of ASIC 2a on endogenous neuroprotection from ischemic insult.
短暂性全脑或局部脑缺血会诱导易损 CA1 锥体神经元死亡。短暂的缺血,即缺血预处理,可以为 CA1 神经元提供强大的保护,使其免受随后更持久的缺血挑战。我们使用四血管闭塞模型,在 15 分钟致死性缺血前 48 小时,对啮齿动物进行 3 分钟的亚致死性缺血,建立了一个缺血预处理模型。结果表明,预处理可减轻海马 CA1 区缺血引起的神经细胞死亡和 DNA 片段化。RT-PCR 和 Western blot 分析显示,与单纯缺血损伤相比,缺血预处理显著增加了 ASIC2a mRNA 和蛋白表达(p<0.01)。这些发现提示 ASIC2a 在缺血损伤的内源性神经保护中发挥了新的作用。