Department of Pharmacology, Nanjing General Hospital of Nanjing Military Command, Jiangsu, China.
Stroke. 2013 Jul;44(7):2031-5. doi: 10.1161/STROKEAHA.113.680181. Epub 2013 May 16.
Ischemic postconditioning, a brief episode of ischemia after a prolonged ischemic insult, has been found to reduce the delayed neuronal loss after stroke. However, the mechanisms underlying such endogenous neuroprotective strategy remain obscure. In this study, we try to explore the excitatory postsynaptic signal events associated with neuroprotective effect of ischemic postconditioning.
Global cerebral ischemia was induced for 15 minutes by the 4-vessel occlusion method in male Sprague-Dawley rats. Ischemic postconditioning was conducted 10 minutes later by a single reocclusion for 3 minutes.
A severe global cerebral ischemia after 5 days of reperfusion destroyed almost all hippocampal CA1 pyramidal neurons. A brief ischemic postconditioning robustly reduced the neuronal loss after ischemia. Preadministration of phosphoinositide 3-kinase inhibitor LY294002 blocked the neuroprotection of postconditioning, whereas mitogen-activated protein kinase kinase 1 inhibitor PD98059 had no effect. Ischemic postconditioning significantly increased the Akt phosphorylation (Ser473). In addition, postconditioning not only perturbed the binding of postsynaptic density protein-95 with glutamatergic kainate receptor subunit 2 and mixed lineage kinase 3 but also suppressed the downstream activation of mixed lineage kinase 3, mitogen-activated protein kinase kinase 7, and c-Jun N-terminal kinase 3. LY294002, but not PD98059, abolished the postconditioning-induced decreases in the assembly of glutamatergic kainate receptor subunit 2-postsynaptic density protein-95-mixed lineage kinase 3 complex and in the mixed lineage kinase 3-c-Jun N-terminal kinase 3 signaling. Akt inhibitor IV, a specific Akt inhibitor, showed the same effects as LY294002.
Ischemic postconditioning protects neurons against stroke by attenuating the postsynaptic glutamatergic kainate receptor subunit 2-postsynaptic density protein-95-mixed lineage kinase 3-c-Jun N-terminal kinase 3 signal cascade via phosphoinositide 3-kinase-Akt pathway.
缺血后处理,即长时间缺血后短暂的再灌注,已被证实能减轻卒中后的迟发性神经元损伤。然而,这种内源性神经保护策略的机制仍不清楚。在本研究中,我们试图探索与缺血后处理的神经保护作用相关的兴奋性突触后信号事件。
通过四血管闭塞法诱导雄性 Sprague-Dawley 大鼠 15 分钟的全脑缺血。缺血后处理在 10 分钟后通过单次再闭塞 3 分钟进行。
5 天再灌注后的严重全脑缺血几乎破坏了所有海马 CA1 锥体神经元。短暂的缺血后处理强烈减轻了缺血后的神经元丢失。磷酸肌醇 3-激酶抑制剂 LY294002 阻断了后处理的神经保护作用,而丝裂原活化蛋白激酶激酶 1 抑制剂 PD98059 则没有作用。缺血后处理显著增加了 Akt 的磷酸化(Ser473)。此外,后处理不仅扰乱了突触后密度蛋白 95 与谷氨酸能 kainate 受体亚单位 2 和混合谱系激酶 3 的结合,还抑制了混合谱系激酶 3、丝裂原活化蛋白激酶激酶 7 和 c-Jun N 末端激酶 3 的下游激活。LY294002,但不是 PD98059,消除了后处理诱导的谷氨酸能 kainate 受体亚单位 2-突触后密度蛋白 95-混合谱系激酶 3 复合物组装和混合谱系激酶 3-c-Jun N 末端激酶 3 信号的减少。Akt 抑制剂 IV,一种特异性 Akt 抑制剂,表现出与 LY294002 相同的效果。
缺血后处理通过磷酸肌醇 3-激酶-Akt 途径减弱突触后谷氨酸能 kainate 受体亚单位 2-突触后密度蛋白 95-混合谱系激酶 3-c-Jun N 末端激酶 3 信号级联来保护神经元免受卒中的影响。