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中国临床药理学与治疗学 ›› 2015, Vol. 20 ›› Issue (6): 611-615.

• 基础研究 • 上一篇    下一篇

JNK3信号介导亚低温治疗对大鼠脑缺血再灌注损伤的保护作用

田和平,褚正民,金城胜,沈建国   

  1. 嘉兴市第二医院
  • 收稿日期:2014-03-07 修回日期:2015-06-05 出版日期:2015-06-26 发布日期:2015-06-29
  • 通讯作者: 褚正民 E-mail:chuzhengmin@msn.com

Inhibiting JNK3 signals is important molecular mechanism in neuroprotective effect of Hypothermia after ischemia-reperfusion.

  • Received:2014-03-07 Revised:2015-06-05 Online:2015-06-26 Published:2015-06-29

摘要: 目的:探讨JNK3信号通路在亚低温治疗脑缺血再灌注性损伤中的作用及其具体机制。方法:采用四动脉阻断法诱导大鼠全脑缺血,将SD大鼠随机分为假手术组、缺血再灌注对照组、亚低温处理组、SP600125(JNK3抑制剂)处理组及溶剂组;采用亚甲基蓝染色检测大鼠缺血再灌注后海马CA1区神经元的损伤情况;采用免疫印迹法检测脑组织中JNK3及c-jun蛋白的磷酸化水平。结果:亚低温处理组、SP600125(JNK3抑制剂)处理组与缺血再灌注对照组相比海马CA1区神经元损伤明显减轻,蛋白JNK3、c-jun磷酸化水平显著降低(P<0.05)。结论:亚低温治疗通过抑制脑缺血再灌注损伤后JNK3的磷酸化激活参与了对海马CA1 区神经元的保护性作用。

Abstract: Objective To investigate the role of JNK3 on neuroprotective effect of Hypothermia in the CA1 region of the adult rat after ischemia-reperfusion. Method Models with cerebral ischemia-reperfusion were induced using four-vessel occlusion and received 10 min ischemia. Rats were randomly divided into several groups, including sham-operation, ischemia-reperfusion, Hypothermia pretreated ischemia-reperfusion, SP600125 pretreated ischemia-reperfusion and Vehicle pretreated ischemia-reperfusion. Histological assessment of neuronal damage in the CA1 field was performed via Staining with Toluidine blue. Western blotting was operated to detect expression of JNK3 and c-jun. Results In the CA1 field, both groups of Hypothermia pretreated and SP600125 pretreated, not only ischemia-reperfusion injury was alleviated, but also expressions of p-JNK3 and p-c-jun were down-regulated, compared to ischemia-reperfusion only group. Conclusions Hypothermia inhibits post-ischemic cell death in region of CA1 by down-regulated phosphorylation of JNK3 and its downstream effectors.