期刊文献+

阿司匹林对大鼠脑缺血后VEGF和Survivin表达的影响 被引量:6

Effect of aspirin on expressions of VEGF and survivin Survivin after focal cerebral ischemia/reperfusion in rats
下载PDF
导出
摘要 目的观察大鼠脑缺血-再灌注(CI/RP)后VEGF和Survivin表达规律及阿司匹林(ASA)对其表达的影响,探讨阿司匹林的神经保护机制。方法健康雄性SD大鼠60只,随机分为对照组和ASA组,每组按再灌注时间分为6h、24h、3d、5d和7d,每个亚组6只大鼠。采用改良Zea Longa线栓法制作大脑中动脉阻塞(2h)模型。ASA组于再灌注后即刻及每日清晨腹腔注射ASA(80mg/kg,溶解于1.5ml的10%L-赖氨酸等渗盐水溶液中)1次。对照组在相同时间点注射10%L-赖氨酸1.5ml。采用免疫组织化学方法检测脑组织VEGF和Survivin的表达。结果 CI/RP后,VEGF和Survivin主要在梗死侧缺血中心区及周边区表达,神经元和血管内皮细胞均有表达。VEGF和Survivin的表达趋势是一致的。在梗死中心区,CI/RP后6h即呈强阳性表达,细胞数最多,随后细胞数逐渐减少,7d最少;而在梗死周边区,两者的表达是先逐渐增加,随后逐渐减少,7d最少。ASA能够进一步增加缺血诱导的VEGF和Survivin的表达。结论缺血可诱导大鼠脑梗死侧半球神经元、部分血管内皮细胞内VEGF、Survivin的表达,ASA增加缺血脑组织VEGF和Survivin的表达,可能是其神经保护机制之一。 Objective To observe the expressions of vascular endothelial growth factor(VEGF)and survivin after focal cerebral ischemia/reperfusion(CI/RP)in rats and the effect of aspirin on their expressions.Methods A total of 60 healthy male Sprague-Dawley rats were randomly assigned to the control group and aspirin group(n=30 in each group).Each group was further divided into five subgroups according to the reperfusion time of 6h,24h,3d,5d and 7d after vessel occlusion(n=6 in each subgroup).A model of temporary middle cerebral artery occlusion(2h)was established by suture method.Aspirin(80mg/kg dissolved in 1.5ml 10% L-Lysine normal saline solution)was intraperitoneally injected immediately after reperfusion and once every early morning in the aspirin groups;And 1.5ml 10% L-Lysine was injected intraperitoneally in the control group at the same time points as the aspirin groups.Immunohistochemical methods were used to detect VEGF and Survivin expression of ischemic brain tissues.Results VEGF and Survivin was mainly expressed in the infarct core and the peri-infarct areas of ischemic side.Both neurons and endothelial cells could be expressed them.Expressions of Survivin and VEGF in haved consistency.In the infarct core,the numbers of VEGF-and Survivin-expressing cells were maximum at 6 hours after reperfusion,then decreased gradually,and reached to minimum at 7day 7.In peri-infarct areas,the numbers of VEGF-and Survivin-expressing cells were gradually increased and then reduced,and reached to minimum at on 7day 7.Aspirin could be able to increase the expression of VEGF and Survivin after CI/RP.Conclusion Conclusion Cerebral ischemia may induce the expressions of VEGF and Survivin in neurons and endothelial cells of rats.And the up-regulation of VEGF and Survivin expressions after ischemia may be one of neuroprotective mechanisms of aspirin.
出处 《中风与神经疾病杂志》 CAS CSCD 北大核心 2012年第9期819-823,共5页 Journal of Apoplexy and Nervous Diseases
基金 辽宁省科技攻关项目计划资助课题(2004225003-16)
关键词 脑缺血 血管内皮生长因子 存活素 阿司匹林 Brain ischemia Vascular endothelial growth factor Survivin Aspirin
  • 相关文献

参考文献30

  • 1Sondell M,Lundberg G,Kanje M.Vascular endothelial growth factorhas neurotriphic activity and stimulates axonal growth enhancing cellsurvival and Schwann cell proliferation in the peripheral nervous sys-tem[J].J Neurosci,1999,19(14):5731-5741. 被引量:1
  • 2Louissaint A,Rao S,Leventhal C,et al.Coordinated interaction ofneurogenesis and angiogenesis in the adult songbird brain[J].Neu-ron,2002,34(6):945-960. 被引量:1
  • 3栗世方,王任直,李桂林.血管内皮生长因子治疗脑缺血实验研究进展[J].中国医学科学院学报,2005,27(1):115-119. 被引量:13
  • 4Chiba Y,Sasayama T,Miyake S,et al.Anti-VEGF receptor antagonist(VGA1155)reduces infarction in rat permanent focal brain ischemia[J].Kobe J Med Sci,2008,54(2):E136-146. 被引量:1
  • 5章露易,范彦英,陈忠.VEGF与中枢神经系统疾病的关系[J].浙江大学学报(医学版),2009,38(6):644-648. 被引量:5
  • 6Gerstner ER,Duda DG,di Tomaso E,et al.VEGF inhibitors in thetreatment of cerebral edema in patients with brain cancer[J].Nat RevClin Oncol,2009,6(4):229-236. 被引量:1
  • 7Ambrosini G,Adida C,Altieri DC.A novel anti-apoptosis gene,Sur-vivin,expressed in cancer and lymphoma[J].Nat Med,1997,3(8):917-921. 被引量:1
  • 8Hayashi T,Abe K,Itoyama Y.Reduction of ischemic damage by ap-plication of vascular endothelial growth factor in rat brain after transi-ent ischemia[J].J Cereb Blood Flow Metab,1998,18(8):887-895. 被引量:1
  • 9Pich iule P,Chavez JC,Xu K,et al.Vascular endothelial growth factorup regulation in transient global ischemia induced by cardiac arrestand resuscitation in rat brain[J].Mol Brain Res,1999,74(122):83-87. 被引量:1
  • 10王浩,魏麓云.存活素的研究进展及其与脑缺血的关系[J].实用心脑肺血管病杂志,2006,14(10):769-770. 被引量:6

二级参考文献172

共引文献74

同被引文献56

  • 1徐涛,曲方,周中和,宋福林.阿司匹林对脑缺血-再灌注损伤大鼠神经保护作用的机制[J].中国脑血管病杂志,2006,3(6):267-272. 被引量:8
  • 2Longa EZ,Weinstein PR,CarsonS,et al. Reversible middle cere-bral artery, occlusion without craniotomy in rats [ J ]. Stroke,1989,20:84-90. 被引量:1
  • 3Conway EM, Zwerts F, Eygen VV, et al. Survivin - dependentangiogenesis in ischemic Brain, molecular mechanisms of hypoxi-a - induced up - regulation[ J]. Am J Pathoi,2003(163) :935-946. 被引量:1
  • 4Papapetropoulos A,Fulton D,Mahboubi FC,et al. Angiopoietin - 1inhibits Endothelial cell apoptosis via the Akt/Survivin pathway[J].J Biol Chem,2000(275) :9 102-9 105. 被引量:1
  • 5Danton GH,Dietrich WD.Inflammatory mechanisms after ischemia and stroke[J].J Neuropathol Exp Neurol,2003,62:127-136. 被引量:1
  • 6Kim YS,Kim SS,Cho JJ,et al.Matrix metalloproteinase-3:a novel signaling proteinase from apoptotic neuronal cells that activates microglia[J].J Neurosci,2005,25:3701-3711. 被引量:1
  • 7Weber GF,Zawaideh S,Hikita S,et al.Phosphorylation-dependent interaction of osteopontin with its receptors regulates macrophage migration and activation[J].J Leukoc Biol,2002,72:752-761. 被引量:1
  • 8Attur MG,Dave MN,Stuchin S,et al.Osteopontin:an intrinsic inhibitor of inflammation in cartilage[J].Arthritis Rheum,2001,44:578-84. 被引量:1
  • 9Rosenberg GA,Cunningham LA,Wallace J,et al.Immunohistochemistry of matrix metalloproteinases in reperfusion injury to rat brain:activation of MMP-9 linked to stromelysin-1 and microglia in cell cultures[J].Brain Res,2001,893:104-112. 被引量:1
  • 10Shin T,Ahn M,Kim H,et al.Temporal expression of osteopontin and CD44 in rat brains with experimental cryolesions[J].Brain Res,2005,1041:95-101. 被引量:1

引证文献6

二级引证文献13

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