期刊文献+

MAPK家族在沙土鼠前脑缺血再灌注期间海马神经元表达的动态变化 被引量:3

Dynamiccbanges and expressions of mitogen-activated protein kinase superfamily during forebrain ischemia-reperfusion in gerbil's hippocampus
在线阅读 下载PDF
导出
摘要 目的:探讨MAPK家族三成员在脑缺血再灌注期间其于海马不同亚区神经元的表达及活性变化。方法:采用沙土鼠双侧颈总动脉阻断缺血再灌注损伤模型。随机分为假手术组(SH)、3min缺血组(IA)及5min缺血组(IS);各组根据再灌注15 min、2 h、4 h、6 h、1 d、3 d、5 d及7 d又分8个亚组(n=8)。在预定时间点行免疫组化法测定海马各亚区MAPK蛋白及其磷酸化水平。结果:三组海马三区ERK、JNK及p38三种蛋白的总体水平在缺血后再灌注期间未发生改变。IS组磷酸化ERK(p-ERK)在缺血后CA3/DG区颗粒细胞及神经元树突上表达,而在CA1区几无表达;磷酸化JNK(p-JNK)在缺血后再灌注7 d内CA3区神经元均有少量表达,在CA1区表达量多并有二次表达高峰(2 h和1 d);磷酸化p-38(p-p38)缺血后再灌注期间的表达区域与p-JNK相似,有一次表达高峰(2 h)。IA组三激酶磷酸化水平均较IS组明显减少(P<0.05),表达规律相同。结论:脑缺血再灌注可导致MAPK三成员在海马各亚区差异性表达,此特征可能与MAPK的作用相关。 Objective:To explore the changes and expressions of mitogen-activated protein kinase (WAPK) superfamily during forebrain ischemia-reperfusion in gerbil's hippocampus. Methods: Forebrain ischemia was induced by occlusion of bilateral common carotid arteries. Gerbils were randomly divided into sham group (SH), 3 minutes ischemia group(IA) and 5 minutes ischemia group (IS). The gerbils were reperfused in 15 min, 2h, 4h, 6h, ld, 3d, 5d and 7d in each group following ischemia(n=8). The expression of MAPK in hippocampus was detected by SABC immunocytochemieal technique. Results: The immunoreactivity of ERK, JNK and p38 in three regions of hippocampus had no changes whether with ischemia or not, but the levels of their phosphorylation and expression regions had obviously altered after ischemia between two ischemia groups. Phosph-ERK(p-ERK) was only expressed in neurofibrils and granules of CA3/DG regions, p-ERK wasn't expressed in CA1 region. The high levels of p-ERK and prolonged expressional time were observed in CA3/DG regions in IS group. Phosph+JNK (p-JNK) was appeared little in CA3 region and was not changed during 7 days after ischomia, but high levels of D-JNI( and activation biphasely (2 h and ld after reperfusion) in CA1 region were observed in group IS. The regions and intracellular distribution of phospho-p38(p-p38) were resemble with that of p-JNK, but it had only one phase increasing (2 h after reperfusion). The level of three kinases in group IA were less than that in group IS, but regularity of expression resemble with that in group IS. Conclusion: The characteristic of three MAPK kinases expression shows variability in different hippocampal regions which correlate with their effects during ischemia-reperfusion.
出处 《温州医学院学报》 CAS 2006年第5期407-410,共4页 Journal of Wenzhou Medical College
基金 浙江省自然科学基金资助项目(Y205200) 江苏省教育厅科研基金资助项目(04KJB3200144)
关键词 MAPK 脑缺血 沙土鼠 海马 神经元 MAPK cerebral ischemia gerbil hippocampal neuron
  • 相关文献

参考文献10

  • 1Chang L,Karin M. Mammalian MAP kinase signalling cascades[J]. Nature,2001,410(6824):37-40.
  • 2Abe J,Baines CP,Berk BC. Role of mitogen-activated protein kinases in ischemia and reperfusion injury: the good and the bad[J]. Circ Res,2000,86(6):607-609.
  • 3Xia Z,Dickens M,Raingeaud J,et al. Opposing Effects of ERK and JNK-p38 MAP kinases on apoptosis[J]. Science,1995,270(5240): 1326-1331.
  • 4Gu Z,Jiang Q,Zhang G,et al. Diophosphorylation of extracellular signal regulated kinases and c-jun N-terminal protein kinases in brain ischemic tolerance in rat[J]. Brain Res,2000,860(1-2): 157-160.
  • 5李军,曹红,曾邦雄,曾因明.MAPK级联反应与缺血性脑损伤[J].国外医学(麻醉学与复苏分册),2002,23(4):232-235. 被引量:15
  • 6Levine S,Sohn D. Cerebral ischemia in infant and adult gerbils:relation to incomplete circle of Willis[J]. Arch Pathol,1969,87(3):315-317.
  • 7Pawson T,Scott JD. Signalling through scaffold,anchoring,and adaptor proteins[J]. Science,1997,278(5346):2075-2080.
  • 8Hu BR,Liu CL,Park DJ.Alteration of MAP kinase pathways after transient forebrain ischemia[J]. J Cereb Blood Flow Metab,2000,20(7): 1089-1095.
  • 9Sugino T, Nozaki K,Takagi Y, et al. Activation of mitogenactivated protein kinases after transient forebrain ischemia in gerbil hippocampus[J]. J Neurosci,2000,20( 12):4506-4515.
  • 10Huser M,Luckett J,Chiloeches A,et al. MEK kinase activity is not necessary for Raf-1 function[J]. EMBO J,2001,20(8):1940-1951.

二级参考文献2

共引文献14

同被引文献30

引证文献3

二级引证文献51

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部