期刊文献+

大鼠脑缺血再灌注基质金属蛋白酶9表达在脑水肿形成中的作用 被引量:1

Effect of the expression of matrix metalloproteinase-9 on edema formation in rats after cerebral ischemia-reperfusion
在线阅读 下载PDF
导出
摘要 目的:观察大鼠局灶性脑缺血再灌注后基质金属蛋白酶-9(matrixmet-alloproteinase-9,MMP-9)表达的情况,探讨其在缺血再灌注炎性反应和脑水肿形成中的作用。方法:用线栓法建立大鼠局灶性脑缺血再灌注模型,分别观察再灌注后3,6,24,48h,5dMMP-9的表达情况,并测定脑组织含水量。结果:脑缺血再灌注后MMP-9阳性细胞数明显增加,再灌注24h阳性细胞数为(35.81±6.87)个/切片,较再灌注3h组(1.56±1.15)个/切片明显增加(P<0.05),这种增高趋势持续至再灌注后5d。测定脑缺血再灌注后脑含水量,再灌注24d组为(81.49±0.68)%,较假手术组(78.11±1.36)%明显增加(P<0.01)。脑含水量的变化与MMP-9的表达增高趋势一致。结论:MMP-9参与了缺血再灌注血管源性脑水肿、炎症反应等过程并在损伤的修复中可能有重要作用。 AIM: To investigate the expression of matrix metalloproteinase-9(MMP-9) in r ats after focal ischemia-reperfusion and to explore its effect on the inflammat ory reaction and the edema formation after ischemia-reperfusion. METHODS:Rat model of focal ischemia-reperfusion was established by middle cer ebral artery occlusion with a nylon monofilament suture.The expressions of MMP- 9 were observed at 3,6,24,48 hours and 5 days respectively after reperfusion and the water content of brain tissue was measured. RESULTS:The number of MMP-9 po sitive cells increased significantly after cerebral ischemia reperfusion.The num ber of positive cells of 24-hour reperfusion group[(35.81±6.87)/slice] was sig nificantly higher than that of 3-hour reperfusion group[(1.56±1.15)/slice](P< 0.05).The increasing tendency lasted to the 5th day after reperfusion. The water content of brain in 24-hour group after reperfusion[(81.49±0.68)%]significan tly increased as compared with that of sham-operation group[(78.11±1.36)%](P< 0.01),and the changes of the water content of brain were in accordance with the increasing tendency of the expression of MMP-9. CONCLUSION:MMP-9 takes part in the process of vasogenic brain edema and the i nflammatory reaction,etc. after ischemia reperfusion, and may play an important role in the rahabilitation of the damage.
作者 魏微 张微微
出处 《中国临床康复》 CSCD 2004年第22期4488-4489,i003,共3页 Chinese Journal of Clinical Rehabilitation
基金 国家自然科学基金资助项目(39770753)~~
  • 相关文献

参考文献10

  • 1屠永华,李岚.炎性细胞因子与脑缺血[J].中国临床康复,2003,7(1):49-50. 被引量:26
  • 2[2]Iadecala C,Salkowski CA,Zhang F,et al.The transcription factor inter-feron regulatoryfactor 1 is expressed after cerebral ischemia and contributes to ischemic braininjury.J Exp Med 1999;189(4):719-27
  • 3兰希发,姚文秀,郭阳.大鼠脑缺血再灌注时脑水肿的实验研究[J].中国临床康复,2003,7(22):3042-3043. 被引量:28
  • 4[4]Man Bryce S, Rosenberg GA. Mtrix metalloproteinase in cerebrovascular disease. J Cereb Blood Flow Metabb 1998; 18 (11 ): 1163 -72
  • 5[5]Dijkhuizen RM, Asahi M, Wu O, et al. Rapid breakdown of microvascular barrier and subsequent hemmorrhagic transformation after delayed recombinant tissuePlasminogen activator treatment in a rat embolic stroke model. Stroke 2002; 33(8): 2100
  • 6[6]Montaner J, Molina C, Monasterio J, et al. Matrix metallooproteinase-9 pretreatment level predicts intracranial hemorrhagic complications after thromobolysis in human stroke. Circulation 2003; 107(4): 598
  • 7武雷,杨俊,秦建强.基底膜与周围神经再生[J].中国临床康复,2004,8(10):1922-1924. 被引量:7
  • 8[8]Hamann GF, Okada Y, Fitridge R, et al. Microvascular basal lamina antigens disappear during cerebral ischemia and reperfusion. Stroke 1995; 26:2120 -6
  • 9[9]Romanic AM, White RF, Arleth AJ, et al. Matrix metalloproteinase expression increase after cerebral focal ischemia in rats. Inhibition of matrix metalloproteinnse-9 reduce infarct size. Stroke 1998; 29(8): 1020 - 30
  • 10[10]Zhang ZG, Zhang L, Jiang Q, et al. VEGF enhances angiogenesis and promotes blood-barrier leakage in the iachemic brain. J Clin Invest 2000; 106(7): 829 - 38

二级参考文献52

  • 1王国英,秦建强,胡耀民,钟世镇.Laminin等因子失活后巨噬细胞的行为及对周围神经再生的影响[J].中华显微外科杂志,1995,18(1):30-33. 被引量:7
  • 2秦建强,王国英,胡耀民,钟世镇.Collagen type Ⅳ对周围神经中再生轴突及非神经元细胞的作用和影响[J].神经解剖学杂志,1995,11(3):195-202. 被引量:10
  • 3扬光华.病理学[M]:5版[M].北京:人民卫生出版社,2001.31-7.
  • 4Bunge MB, Williams AK, Wood PM, et al. Comparison of nerve cell and nerve cell plus Schwann cell cultures, with particular emphasis on basal lamina and collagen formation. J Cell Biol 1980 ; 84 ( 1 ) : 184 - 202.
  • 5Clark MB, Bunge MB. Cultured Schwann ceils assemble normal-appearing basal lamina only- when they ensheathe axons. Des, Biol 1989;133 (2): 393 -404.
  • 6Carey DG. Biosynthsis of type collagen by cultured rat Schwann cells. J Cell Biol 1983 ;97(2):473 - 89.
  • 7Obremski VJ. Wood PM, Bunge MB. Fibroblasts promote Schwann cell basal lamina deposition and elongation in the absence of neurons in culture. Dev Biol 1993;160(1):119 -34.
  • 8Chemousov MA, Scherer SS, Stahl RC, et al. p200, a collagen secreted by Schwann cells, is expressed in developing nerves and in adult nerves following axotomy. J Neurosci Res 1999 ; 56 ( 3 ) : 284 - 94.
  • 9Hirata K, Kawabuchi M. Myelin phagocytosis by macrophages and nonmacrophages during Wallerian degeneration. Microsc Res Tech 2002;57(6) :541 - 7.
  • 10La Fleur M, Underwood JL, Rappolee DA, et al. Basement membrance and repair of injury to peripheral nerve: defining a potential role for macrophages, matrix metalloproteinases, and tissue inhibitor of metalloproteinases-1. J Exp Med 1996:184(6):2311 -26.

共引文献58

同被引文献7

  • 1毛春,张苏明,邓小红,张旻,刘洋.一种改进的自体血血栓栓塞性大鼠缺血性脑卒中模型的建立[J].中华老年心脑血管病杂志,2000,2(1):48-50. 被引量:12
  • 2Busch E, Kruger K, Hossmann KA. Improved model of thromboembolic stroke and rt-PA induced reperfusion in the rat. Brain Res 1997; 778 (1): 16- 24
  • 3Spinale FG. Matrix metalloproteinases: regulation and dysregulation in the failing heart. Circ Res 2002; 90(5): 520 - 30
  • 4Galis ZS, Khatri JJ. Matrix metalloproteinases in vascular remodeling and atherogenesis: the good, the bad, and the ugly. Circ Res 2002; 90 (3):251 -62
  • 5Asahi M, Wang X, Mori T, et al. Effects of matrix metalloproteinase-9 gene knock-out on the proteolysis of blood-brain barrier and white matter components after cerebral ischemia. J Neurosci 2001; 21 ( 19 ): 7724 - 32
  • 6Heo JH, Lucero J, Abumiya T, et al. Matrix metalloproteinases increase very early during experimental focal cerebral ischemia. J Cereb Blood Flow Metab 1999; 19(6):624-33
  • 7Liu WH, Chen XM, Fu B. Thrombin stimulates MMP-9 mRNA expression through AP-1 pathway in human mesangial cells. Acta Pharmacol Sin 2000; 21 (7): 641 -5

引证文献1

二级引证文献1

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