期刊文献+

预防性应用氟桂利嗪对实验性脑缺血模型神经细胞的保护 被引量:6

Effect of preventative sibelium in protecting nerve cell against injuries induced by acute stroke
下载PDF
导出
摘要 目的观察预防性应用氟桂利嗪(商品名西比灵)对实验性脑缺血再灌注细胞凋亡及神经细胞损伤的保护作用。方法取沙土鼠按随机数字表法分为4组:假手术组,缺血再灌注组,西比灵预防组,西比灵治疗组。采用加闭双侧颈总动脉法复制沙土鼠脑缺血再灌注模型。假手术组除不夹闭颈总动脉外,其余操作与其他组相同;西比灵预防组于脑缺血再灌注前后各3d给予西比灵10mg/kg,1次/d,连续6次;西比灵治疗组于脑缺血再灌注术后给予西比灵10mg/kg,1次/d,连续3次;术后3d处死动物取材,光、电镜观察神经细胞形态,测脑组织超氧化物歧化酶(SOD)活力,原位末端缺中翻译标记法检测凋亡细胞。结果预防性应用西比灵组与其他3组相比,细胞缺血性形态损伤明显减轻,脑组织SOD活力明显增高犤(31.0±5.8)Nu/mg犦(P<0.01),凋亡细胞表达明显受抑制(40.6±3.3)个(P<0.05)。结论预防性应用西比灵能明显减轻缺血再灌注对神经细胞的损伤。 Aim To observe the preventive effects of sibelium (SBL) in protecting experimental cerebral ischemia reperfusion cell against apoptosis and injuries as an experimental support of SBL in extensive clinical application.Methods Thirty two gerbils were equally divided into four groups at random: sham operation group(group A), ischemia reperfusion group (group B), SBL prevention group (SBL were used before and after ischemia reperfusion, group C) and SBL treatment group (SBL were used only after ischemia reperfusion, group D). Cerebral ischemia replicas of the gerbils were made by clamping closed bilateral common carotid artery in the group B, C and D except group A. Every animal of the SBL prevention group received SBL of 10 mg/kg once a day for three days before and after ischemia reperfusion respectively, and the duration of treatment was six days. In the SBL treatment group, every animal received SBL of 10 mg/kg once a day for three days after the ischemia reperfusion only. All the animals were killed at three days after operation. The section preparations were observed by optical microscope. The nerve cell structures of the ultra thin section were observed by electron microscope. And the superoxide dismutase (SOD) activity of the cerebral tissues and cell apoptosis were measured.Results The activity of SOD in the SBL prevention group was (39.8± 4.8)NU/ mg, significantly lower than that of the sham operation group[(2.3± 6.0)NU/mg], but significantly higher than that of the ischemia reperfusion group(31.0± 5.8)NU/mg]0.05),buthigherthanthatoftheshamoperationgroup(25.7±4.2).ConclusionSBLpreventsnervecellinjuryinducedbyischemiareperfu-sionsignificantly.
出处 《中国临床康复》 CSCD 2003年第19期2652-2653,共2页 Chinese Journal of Clinical Rehabilitation
关键词 氟桂利嗪 实验 脑缺血 动物模型 神经细胞保护 再灌注损伤 西比灵 预防性用药 cerebrovasculardisorders/drugtherapy reperfusioninjury/drugtherapy apoptosis superoxidedismutase flunarizine
  • 相关文献

参考文献3

二级参考文献7

共引文献24

同被引文献38

  • 1[3]Espanol MT, Litt L, Hasegava K, et al. Fructose-1, 6-bisphosphate preserves adenosine triphosphate but not intracellular pH during hypoxia in respiring neonatal rat brain slices. Anesthesiology 1998; 88 (22): 461 - 72
  • 2[4]Bowersox SS, Singh T, Luther RR. Selective blockade of N-type voltage-sensitive calcium channels protects against brain injury after transient focal cerebral ischemia in rat. Brain Res 1997;747 (2): 343 -7
  • 3[6]Iadecola C.Bright and dark sides of nitric oxide in ischemic brain injury Trend Neurosci 1997;20(3):132-9
  • 4[8]Cardenas A, Hurtado O, Leza JC, et al. Fructose-l, 6-bisphosphate inhibits the expression of inducible nitric oxide synthase caused by oxygen-glucose deprivation through the inhibition of glutamate release in rat forebrain slices. Naunyn Schmiedebergs Arch Pharmacol 2000; 362(3): 208 - 12
  • 5[2]Gomes FC, Paulin D, Moura Neto V. Glial fibrillary acidic protein (GFAP): modulation by growth factors and its implication in astrocyte differentiation. Braz J Med Biol Res 1999;32(5): 619 -31
  • 6[3]Zea Longa E, Weinstein PR, Carlson S, et al. Reversible middle cerebral artery occlusion without craniectomy in rats. Stroke 1989; 20( 1 ): 84 - 91
  • 7[5]Westenbroek RE, Bausch SB, Lin RC, et al. upregulation of L-type Ca2 + channels in reactive astrocytes after brain injury, hypomyelination and ischemia. J Neurosci1998; 18(7): 2321 -34
  • 8[7]Tumer R, Tjian R. Leucine repeats and adjacent DNA bind domain mediate the formation of functional c-Fos-c-Jun heterodimers. Science 1989;51:1689 -94
  • 9[8]Laping NJ, Teter B, Nichols NR, et al. glial fibrillary acidic protein: regulation by hormones, cytokines, and growth factors. Brain Pathol 1994; 1:259 - 75
  • 10[9]Morgan JI, Curren T. Immediate-early genes; ten years on. Trends Neurosci 1995;18(2):66-7

引证文献6

二级引证文献23

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