期刊文献+

脑缺血再灌注后IL-8与微血管炎症损伤关系的实验研究 被引量:16

Experimental Study of IL-8 and Microvascular Inflammatory Damage after Cerebral Ischemia-reperfusion
暂未订购
导出
摘要 目的 探讨白细胞介素 -8( IL-8)在大鼠全脑缺血再灌注 ( ischemia reperfusion,IR)血管内皮细胞损伤过程中的作用。方法 将大鼠随机分为假手术组和脑缺血 3 0 min再灌注 1、3、6、1 2、2 4、48、72 h组 ,动物模型采用全脑缺血模型三血管阻塞法 ,用免疫组化法检测脑组织 IR不同时间点层粘连蛋白表达以标记微血管损伤与修复过程 ,同时用原位杂交方法检测 IL-8m RNA的表达变化。结果  IR后 1 h IL-8m RNA表达出现上调 ,2 4h达高峰。层粘连蛋白在假手术组呈强阳性表达 ,IR后 3 h表达下降 ,2 4~ 48h表达最低 ,72 h表达开始恢复。结论  IR微血管炎症损伤主要发生在早期 ,此过程中 IL-8m RNA表达上调 ,说明 IL-8参与了脑缺血后微血管炎症损伤过程。 Objective To study the role of P-selectin in microvascular inflammtory damage after cerebral ischemia -reperfusion. Methods The rats were randomly divided into the groups as sham operated control group and ischemia-reperfusion 1 h, 3 h, 6 h, 12 h,24 h, 48 h, 72 h groups. The global cerebral ischemia-reperfusion model was formed by occluding three arteries. The expression of laminin was evaluated by immunohistochemical methold, and IL-8 mRNA was detected by in situ hybridization. Results The expression of IL-8 mRNA was increased as early as 1 h after reperfusion and peaked at 24 h after reperfusion. At 72 h after reperfusion, it was still higher than that of sham operated control group. The expression of laminin was strong positive in sham operated control group.At 3 h after reperfusion, the expression of laminin began to decrease, and its lowest level was during 24-48 h. At 72 h, the expression began to reappear. Conclusions The microvascular inflammatory damage appeared in early period after cerebral ischemia-reperfusion. IL-8 was involved in the inflammatory damage of endothelial cell during global cerebral ischmia-reperfusion.
出处 《中国神经免疫学和神经病学杂志》 CAS 2004年第2期87-90,F003,共5页 Chinese Journal of Neuroimmunology and Neurology
关键词 脑缺血再灌注 白细胞介素-8 IL-8 大鼠 IR 微血管炎症 微血管损伤 免疫组化 层粘连蛋白 cerebral ischemia-reperfusion IL-8 Laminin immunohitochemistry endothelial cell in situ hybridization
  • 相关文献

参考文献8

  • 1Wagner S,Tagaya M,koziol JA,et al.Rapid disruption of an astrocyte interaction with the extra-cellular matrix mediated by intergrin alpha 6 beta 4 during cerebral ischemia/reperfusion[J].Stroke,1997,28(4):858-865.
  • 2Yurchenco PD,Schittny JC.Molecular architecture of basement membrane[J].FASEB J,1990,4(6):1577-1590.
  • 3Ruoslahti E.Intergrins[J].J Clin Invest,1991,87:1-5.
  • 4Hamn GF,Okada Y,Fitridge R.Microvacular basal lamina antigens disappear during cerebral ischemia and reperfusion[J].Stroke,1995,26(11): 2120-2126.
  • 5Gross AK,Woodroofe MN.Chemokines induce migration and changes in actin polymerization in adult rat brain microglia and a human fetal microglial cell line in vitro[J].J Neurosci Res,1999,55(1):17-23.
  • 6Matsumoto T,Ikeda K,Mukaida N,et al.Prevention of cerebral edema and infarct incerebral reperfusion injury by an antibody to interleukin-8[J].Laboratory,1997,77(2):119-125.
  • 7Mukaida N,matsumoto T,Yokoi K,et al.Inhibition of neutrophil-mediated acute inflammation injury by an antibody against interleukin-8(IL-8)[J].Inflamm Res,1998,47(suppl 3):151-157.
  • 8Okada Y,Copeland BR,Hamann GF,et al.Integrin αvβ3 is expressed in selected microvessels after focal cerebral ischemia[J].Am J Pathol,1996,149:37-44.

同被引文献169

引证文献16

二级引证文献101

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