期刊文献+

脑心通对实验性脑梗死大鼠脑组织IL-6的影响 被引量:5

The effect of Naoxintong on IL-6 expression in the brain tissues of MCAO rats.
下载PDF
导出
摘要 目的:探讨脑心通对实验性脑梗死大鼠脑组织中IL一6水平的影响。方法:参照Longa等方法制成大脑中动脉梗死(MCAO)模型,应用干一湿重法观察脑含水量变化、HE染色观察梗死周围炎性细胞浸润、免疫组化方法观察脑组织中lL一6的表达。研究不同剂量脑心通对脑梗死后大鼠行为学评分.脑含水量及脑组织中炎性细胞因子lL一6表达的影响。结果:脑梗死组织周围炎细胞浸润和IL一6阳性细胞表达于梗死后6h开始增多,48h达高峰,并持续到7d。脑心通治疗组大鼠脑梗死后脑水肿减轻,行为学评分降低,脑组织中IL一6阳性细胞减少,大、中剂量脑心通治疗组效果较为显著。结论:脑心通有抑制炎性细胞因子IL_6的过度表达,保护神经元,减轻脑水肿的作用。 Objective: To investigate the effect of Naoxintong on the expression of IL-6 in brain tissues after the middle cerebral artery occlusion (MCAO) in the brain. Methods: The model was established with the suture-occuluded method to observe the effect of different doses of Naoxintong on the behavior changes and brain water content of MCAO rats. HE dyeing and immunohistochemistry staining were used in the study. Results: After MCAO, inflammatory cells began to infiltrate at 6 h in the brain tissues, and reached its peak at 48h. IL-6 expressed increasingly at 6 h, reached maximum at 48h. and continued to 7d. The brain water content, behavior scores of MCAO rats treated with Naoxintong decreased, and to some extent, the revel of IL-6 was inhibited by the use of Naoxintong. The effect of large dose and medium dose of Naoxintong was obviously. Conclusion; Naoxintong can effectively inhibit the expression of inflammatory cell factor IL-6, reduce brain edema, and decrease the behavior disturbance of MCAO rats.
出处 《脑与神经疾病杂志》 2005年第3期192-195,共4页 Journal of Brain and Nervous Diseases
关键词 脑梗死脑心通 大鼠脑水肿 白细胞介素IL-6 Cerebral infarction Naoxintong Rat Brain edema Interleukin-6
  • 相关文献

参考文献19

  • 1Longa EZ, Weinstein PR, Carlson S, et al. Reversible middle cerebral artery occlusion without craniectomy in Rats [J]. Stoke, 1989.20:84.
  • 2Laing R J,Jakubowski J,Laing RW,et al.Middle cerebral artery occlusion without craniectomy in rats: which method works best?[J].Stoke, 1993,24:294.
  • 3张祥建,刘春燕,祝春华,胡书超,刘瑞春,李春岩.大鼠自体动脉血脑出血动物模型的建立[J].脑与神经疾病杂志,2003,11(6):341-344. 被引量:80
  • 4Toni D, Chamorro A, Kaste M, et al. Acute treatment of ischaemic stroke. European Stroke Initiative [J]. Cerebrovasc Dis, 2004, 17(Suppl 2):30.
  • 5Kappelle L J, Van Der Worp HB. Treatment or prevention of complications of acute ischemic stroke[J].Curr Neurol Neurosci Rep, 2004,4(1): 36.
  • 6Wester P.New treatment modalities for stroke in the near future[J]. Lakartidningen, 2003,6,100(45): 3605.
  • 7Georgiadis D,Michel P,Bogousslavsky J,et al.Treatment of acute stroke an overview [J].Ther Umsch, 2003,60(9):509.
  • 8Jean WC,Spellman SR,Nussbaaum ES,et al.Reperfusion injury after focal cerebral ischemia:the role of inflammation and the therapeutis horizon [J].Neurosurgery, 1998,43:1382~1387.
  • 9Tomita M, Fukunchi Y, et al. Leukocytes, macrophages and secondary brain damage following cerebral ischemia[J].Acta Neuruhir Suppl (wien), 1996, 66:32~37.
  • 10Matsuo Y, Kihara Y, Ikeda M, et al. Role of neutrophils in free radical production during ischemia and reperfusion of the rat brain:Effect of neutrophil depletion on extracellular ascorbyl radical formation [J].J Cereb Blood Flow metab,1995,15:941~952.

二级参考文献32

  • 1[2]Altumbabic M, Peeling J, Bigio MRD, et al. Intracerebral hemorrhage in the rat: effects of hematoma aspiration. Stroke,1998,29:1917~1923
  • 2[3]Sansing LH, Kaznatcheeva EA, Perking CJ, et al. Edema after intracerebral hemorrhage: correlation with coagulation parameters and treatment. J Neurosug, 2003,98(5):985~992
  • 3[6]Hua Y, Schallert T, Keep RF, et al. Behavioral tests after intracerebral hemorrhage in the rat. Stroke,2002,33(10):2478~2484
  • 4[7]Yang GY, Betz AL, Chenevert TL,et al. Experimental intracerebral hemorrhage: relationship between brain edema, blood flow, and blood-brain barrier permeability in rats. J Neurosurg 1994,81(1):93~102
  • 5[8]Lee KR, Betz AL, Kim S, et al. The role of the coagulation cascade in brain edema formation after intracerebral hemorrhage. Acta Neurochir, 1996,138(2):396~401
  • 6[9]Bullock R, Mendelow AD, Teasdale GM, et al. Intracranial hemorrhage induced at arterial pressure in the rat. Part 1 Description of technique, ICP changes and neuropathological findings. Neurol Res, 1984,6:184~188
  • 7[10]Xi GH, Hua Y, Bhasin R et al. Stroke, 2001;32(11):2932~2940
  • 8[11]Longa EZ, Weinstein PR, Carlson S, et al. Reversible middle cerebral artery occlusion without craniotomy in rats. Stroke, 1989;20(1):84~91
  • 9[12]Sondra T. Bland, BA; Schallert T, et al. Early exclusive use of the affected forelimb after moderate transient focal ischemia in rats: function and anatomic outcome.Stroke,2000,31:1144~1164
  • 10[13]Berderson JB, Pitts LH, Tsuji M, et al. Stroke 1986;17:472~6

共引文献156

同被引文献20

引证文献5

二级引证文献35

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