期刊文献+

脑缺血再灌注的炎症损伤分子机制及吲哚美辛的保护作用 被引量:6

Effects of indomethacin on inflammatory process induced by focal cerebral ischemia-reperfusion in rats and its mechanism
暂未订购
导出
摘要 目的研究大鼠局灶性脑缺血再灌注炎症损伤的分子机制,并观察吲哚美辛对脑缺血再灌注炎症损伤的保护作用。方法36只雄性SD大鼠随机分为假手术组,模型组,吲哚美辛3、6、9mg/kg组,每组6-8只。应用线栓法制作大鼠局灶性脑缺血再灌注模型,缺血2h再灌注24h后处死动物,以TTC染色法测定脑梗死范围和神经功能缺损情况,并分别采用ELISA、Western blot法检测脑组织中IL-8、IL-1β、TNF-α、髓过氧化物酶(MPO)含量以及细胞间黏附分子1(ICAM-1)、E选择素(E-selectin)的表达。结果吲哚美辛能明显减小模型大鼠的脑梗死范围,减轻神经损伤症状;预先给予吲哚美辛(6、9mg/kg)可降低脑组织中MPO活性及IL-8、IL-1β、TNF-α的水平,并减少ICAM-1、E-selectin的表达(P〈0.05或0.01)。结论吲哚美辛可通过抑制脑缺血再灌注过程中炎症介质的表达和释放,降低脑缺血再灌注所致的炎症损伤。 Objective Cerebral ischernia would rapidly initiate structural and functional damages in brain, including blood-brain barrier disruption, inflammation, and angiogenesis. The purpose of present study is to investigate the effects of indomethacin, an agent that inhibits cyclooxygenase, on the inflammatory reaction after cerebral ischemia-reperfusion in transient middle cerebral artery occlusion (MCAO)rats and its possible mechanism. Methods Adult male SD rats weighed 250-250g were subjected to either sham surgery or middle cerebral artery occlusion (MCAO) for 2h of brain ischemia and 24h reperfusion. After 24h of reperfusion,the size of cerebral infarction and the neurological deficit were determined by the method of TTC (2,3,5-Triphenyltetrazolium Chloride) staining and Longa's score analysis. The contents of IL-8, IL-1β, TNF-α and MPO in brain tissue were assayed by ELISA. The expressions of ICAM-1 ande E-selectin were evaluated with Western-blot. Results It was observed that indomethacin (6 or 9mg/kg i. p pretreatment for 5d, once a day) significantly reduced cerebral infarct volume and ameliorated the neurological deficit (P〈0. 05 or P〈0. 01 vs vehicle group). Pretreatment with indomethacin (6mg/kg or 9mg/kg) for 5 days, the content of IL-8, IL-1β, TNF-α and MPO activity as well as the protein expressions of ICAM-1, E-selectin in brain tissue were significantly decreased as compared with the vehicle group (P〈0. 05 or P〈0. 01). Conclusion Indomethacin have protective effects on cerebral injury through inhibiting the expression and releasing of the inflammatory mediators after cerebral ischemia-reperfusion, which may be an important mechanism for its resisting ischemic and reperfusion injury.
出处 《解放军医学杂志》 CAS CSCD 北大核心 2007年第10期1051-1053,共3页 Medical Journal of Chinese People's Liberation Army
基金 温州市科技计划基金资助项目(Y2004A068)
关键词 白细胞介素1 白细胞介素8 肿瘤坏死因子 胞间黏附分子1 E选择素 吲哚美辛 脑缺血 interleukin-1 interleukin-8 tumor necrosis factor intercellular adhesion molecule-1 E-selectin indomethacin brain ischemia
  • 相关文献

参考文献10

  • 1Feuerstein GZ,Wang X,Barone FC.The role of cytokines in the neuropathology of stroke and neurotrauma.Neuroimmunomodulation,1998,5(3-4):143.
  • 2Meistrell ME,Botchkina GI,Wang H,et al.Tumor necrosis factor is a brain damaging cytokine in cerebral ischemia.Shock,1997,8(5):341.
  • 3李雪梅,贾军红,任维.大鼠脑缺血后神经元中PYK2及p38MAPK的活化及其意义[J].解放军医学杂志,2005,30(6):526-528. 被引量:1
  • 4Wang ZQ,Wu DC,Huang FP,et al.Inhibition of MEK/ERK 1/2 pathway reduces pro-inflammatory cytokine interleukin-1 expression in focal cerebral ischemia.Brain Res,2004,1996(1):55.
  • 5Longa EZ,Weinstein PR,Carlson S,et al.Reversible middle cerebral artery occlusion without craniectomy in rats.Stroke,1989,20(1):84.
  • 6Kim HJ,Tsoy I,Park JM,et al.Anthocyanins from soybean seed coat inhibit the expression of TNF-alpha-induced genes associated with ischemia/reperfusion in endothelial cell by NF-kappa B-dependent pathway and reduce rat myocardial damages incurred by ischemia and reperfusion in vivo.FEBS Lett,2006,580(5):1391.
  • 7Vila N,Castillo J,Davalos A,et al.Proinflammatory cytokines and early neurological worsening in ischemic stroke.Stroke,2000,31(10):2325.
  • 8Kostulas N,Pelidou SH,Kivisakk P,et al.Increased IL-1beta,IL-8,and IL-17 mRNA expression in b1ood mononuclear cells observed in a prospective ischemic stroke study.Stroke,1999,30(10):2174.
  • 9Flex A,Gaetani E,Papaleo P,et al.Proinflammatory genetic profiles in subjects with history of ischemic stroke.Stroke,2004,35(10):2270.
  • 10Chen Y,Ruetzler C,Pandipati S,et al.Mucosal tolerance to E-selectin provides cell-mediated protection against ischemic brain injury.Proc Natl Acad Sci USA,2003,100(25):15107.

二级参考文献6

  • 1Yu H, Li X, Marchetto GS et al. Activation of a novel calcium-dependent protein-tyrosine kinase. Correlation with c-Jun N-terminal kinase but not mitogen-activated protein kinase activation. J Biol Chem, 1996, 271(47):29993
  • 2Sasaki K, Chiba K. Induction of apoptosis in starfish eggs requires spontaneous inactivation of MAPK (extracellular signal-regulated kinase) followed by activation of p38MAPK. Mol Biol Cell, 2004, 15(3):1387
  • 3Longa EZ, Weinstein PR, Carlson S et al. Reversible middle cerebral artery occlusion without craniotomy in rats. Stroke,1989, 20(1):84
  • 4Huang C, Borchers CH, Schaller MD et al. Phosphorylation of paxillin by p38MAPK is involved in the neurite extension of PC-12 cells. J Cell Biol, 2004, 164(4):593
  • 5Koponen S, Keinanen R, Roivainen R et al. Spreading depression induces expression of calcium-independent protein kinase C subspecies in ischaemia-sensitive cortical layers: regulation by N-methyl-D-aspartate receptors and glucocorticoids. Neuroscience,1999, 93(3):985
  • 6Nakahara S, Yone K, Sakou T et al. Induction of apoptosis signal regulating kinase 1 (ASK1) after spinal cord injury in rats: possible involvement of ASK1-JNK and -p38 pathways in neuronal apoptosis. J Neuropathol Exp Neurol,1999, 58(5):442

同被引文献59

引证文献6

二级引证文献43

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