期刊文献+

基质金属蛋白酶和组织型纤溶酶原激活剂在脑卒中后脑损伤中的作用 被引量:1

Role of Matrix Metalloproteinases and Tissue-type Plasminogen Activator in Brain Injury after Stroke
下载PDF
导出
摘要 基质金属蛋白酶(MMPs)有降解脑血管基膜,促进中性粒细胞和炎性因子迁移的作用,这与脑卒中后急性期脑损伤有关。而在脑卒中恢复期,MMPs在细胞外基质的修复和神经血管重构中起重要作用。组织型纤溶酶原激活剂(t-PA)对脑损伤有一定保护作用,但在脑缺血和炎性因子作用下可以上调MMPs表达,不仅加重脑损伤,同时也是采用t-PA溶栓治疗后发生出血转化的主要机制。现就MMPs和t-PA在脑卒中后脑损伤中的作用及与此相关的药物研究予以综述。 Matrix metalloproteinases (MMPs)can degrade cerebral vascular basement membrane andpromote the migration of neutrophils and inflammatory cytokines, which are deleterious actions m acute stroke. However, MMPs may play beneficial roles during stroke recovery. MMPs may mediate neurovascular remodeling and repair the extracellular matrix. Tissue-type plasminogen activator(t-PA) has a protective effect on brain injury, but under the action of cerebral ischemia and inflammatory cytokines, it can up-regulate the expression of MMPs ,which not only aggravates the brain damage, but also is the main mechanism of hemor- rhage transformation after thrombolytic therapy by t-PA. Here is to make a review on the role of MMPs and t- PA in brain iniurv after stroke and the related drug studies.
出处 《医学综述》 2012年第17期2732-2736,共5页 Medical Recapitulate
基金 国家自然科学基金(81072801) 北京市自然科学基金(7093129)
关键词 基质金属蛋白酶 组织型纤溶酶原激活剂 脑卒中后脑损伤 作用机制 药物研究 Matrix metalloproteinases Tissue-type plasminogen activator Brain injury after stroke Mechanism Drug research
  • 相关文献

参考文献41

  • 1RoseU A, Lo EH. Multiphasic roles for matrix metalloproteinases af- ter stroke [ J ]. Curr Opin Pharmaco1,2008,8 ( 1 ) : 82-89.
  • 2MF,et al. Lithium upregulates vascular endo- Guo S, Arai K, Stins in brain endothelial cells and astrocytes [ J ]. thelial growth factor Stroke ,2009,40( 2 ) :652-655.
  • 3许宏伟,杨期东,刘晓英,肖波,唐北沙,赵真.MMP-2/9与脑出血后脑水肿的关系探讨[J].中风与神经疾病杂志,2004,21(4):295-297. 被引量:38
  • 4Xue M, Fan Y, Liu S, et al. Contributions of multiple proteases to neurotoxicity in a mouse model of intracerebral haemorrhage [ J ]. Brain ,2009,132 ( Pt 1 ) :26-36.
  • 5Planas AM, 5o16 S, Justicia C. Expression and activation of matrix metalloproteinase-2 and-9 in rat brain after transient focal cerebral ischemia [ J ]. Neurobiol Dis,2001,8 (5) :834-846.
  • 6Jiang X.Ntmura S, Nagata I. Matnx'metallopmteinase inhibitor KB-R7785 attenuates brain damage resulting from permanent focalcerebral ischemia in mice [ J ]. Neurosci Lett, 2001,305 ( 1 ) : 41-44.
  • 7Heo JH, Lucero J, Abumiya T, et al. Matrix metalloproteinases in- crease very early during experimental focal cerebral ischemia[ J]. J Cereb Blood Flow Metab, 1999,19(6) :624-633.
  • 8Romanic AM, White RF, Arleth A J, et al. Matrix metalloproteinase expression increases after cerebral focal ischemia in rats:inhibition of matrix metalloproteinase-9 reduces infarct size [ J ]. Stroke, 1998,29(5) :1020-1030.
  • 9徐群,张毅,苏敏,沈沸,苗玲.缺血再灌注大鼠脑内基质金属蛋白酶的动态变化[J].上海第二医科大学学报,2004,24(10):814-817. 被引量:8
  • 10Gasche Y, Fujimura M, Morita-Fujimura Y, et al. Early appearance of activated matrix metalloproteinase-9 after focal cerebral ischemia in mice:a possible role in blood-brain barrier dysfunction [ J ]. J Cereb Blood Flow M etab, 1999,19 (9) :1020-1028.

二级参考文献59

  • 1黎杏群,贺双腾,罗团连,何泽云,张花先,彭泽春,梁清华,何纲,唐涛.脑溢安对出血性中风大鼠脑缺血损伤的保护作用研究[J].医学研究通讯,2005,34(2):28-29. 被引量:1
  • 2方琪,董万利,许丽珍.凝血酶对脑组织毒性损伤机制及水蛭素、尼莫地平干预作用的研究[J].临床神经病学杂志,2005,18(5):350-353. 被引量:9
  • 3Southgate KM,Davies M,Booth RF,Newby AC.Involvement of extracellular-matrix-degrading metalloproteinases in rabbit aortic smooth-muscle cell proliferation.Biochem J.1992,288:93–99.
  • 4Faxon DP,Sanborn TA,Weber VJ,Haudenschild C,Gottsman SB,McGovern WA,Ryan TJ.Restenosis following transluminal angioplasty in experimental atherosclerosis.Arteriosclerosis.1984,4:189–195.
  • 5Morice MC,Serruys PW,Sousa JE,Fajadet J,Ban Hayashi E,Perin M,Rogers C,Karnovsky MJ,Edelman ER.Inhibition of experimental neointimal hyperplasia and thrombosis depends on the type of vascular injury and the site of drug administration.Circulation.1993,88:1215–1221.
  • 6Thyberg J,Blomgren K,Hedin U,Dryjski M.Phenotypic modulation of smooth muscle cells during the formation of neointimal thickenings in the rat carotid artery after balloon injury:an electron-microscopic and stereological study.Cell Tissue Res.1995,281:421–433.
  • 7Nguyen M,He B,Karaplis A.Nuclear forms of parathyroid hormonerelated Liu MW,Roubin GS,King SB III.Restenosis after coronary angioplasty:potential biologic determinants and role of intimal hyperplasia.Circulation.1989,79:1374–1387.
  • 8Hall KL,Harding JW,Hosick HL.Isolation and characterization of clonal vascular smooth muscle cell lines from spontaneously hypertensive and normotensive rat aortas.In Vitro Cell Dev Biol.1991,27:791–798.
  • 9Toyoshima H,Hunter T.p27,a novel inhibitor of G1 cyclin-Cdk protein kinase activity,is related to p21.Cell.1994,78:67–74.
  • 10Belknap JK,Grieshaber NA,Schwartz PE,Orton EC,Reidy MA,Majack RA.Tropoelastin gene expression in individual vascular smooth muscle cells:relationship to DNA synthesis during vascular development and after arterial injury.Circ Res 1996,78:388-94.

共引文献62

同被引文献14

二级引证文献3

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