期刊文献+

MnTBAP对鼠面神经元损伤后凋亡的抑制作用 被引量:1

The inhibitive effect of MnTBAP on apoptosis of facial neurons following transection of facial nerve
下载PDF
导出
摘要 目的:探讨外源性药物锰卟啉(MnTBAP)对面神经元凋亡的抑制作用。方法:制作大鼠面神经切断伤模型,分别于术后1d、3d、7d、14d、28d和42d时,利用免疫组织化学技术检测面神经元cyto-c、caspase-9和caspase-3的表达;利用原位末端标记法(TUNEL法)检测面神经元的凋亡情况。采用SPSS13.0软件包进行组间t检验。结果:术后1d,cyto-c、caspase-9表达水平开始升高,7d时达到高峰;术后3d时,caspase-3表达水平开始升高,TUNEL阳性细胞增多,14d时达到高峰。各时间点表达水平MnTBAP侧较对照侧显著降低(P<0.05)。结论:MnTBAP对损伤的面神经元有明显的抗凋亡作用,是一种有效的神经保护剂。 PURPOSE: The study is to investigate the inhibitive effect of MnTBAP on apoptosis of facial neurons following transection of facial nerve. METHODS: The bilateral facial nerve were exposed and transected. At 1d,3d,7d, 14d,2gd and 42d after operation, the expression of eyto-e,caspase-9 and caspase-3 were detected by immunohistoehemistry. The apoptotie cells of facial neurons were observed by TUNEL staining. Statistical analysis was performed with SPSS 13.0 software package. RESULTS: At ld, the expression of cyto-c, easpase-9 increased after transection and achieved the peak at 7d. At 3d ,the expression of easpase-3 increased and TUNEL-positive cells were observed, they reached the peak at 14d. The positive level in MnTBAP side was significantly lower than that in control side at each time point. There was significant difference between the experimental group and the control group (P〈0.05). CONCLUSION: MnTBAP can effectively inhibit apoptosis of facial neurons and has neuroproteetive effect on facial nerve after transection.Supported by Science Planning Project of Shenyang City(200340).
出处 《中国口腔颌面外科杂志》 CAS 2011年第4期276-280,共5页 China Journal of Oral and Maxillofacial Surgery
基金 沈阳市科学计划项目(200340)~~
关键词 面神经元 MnTBAP 凋亡 Neuron MnTBAP Apoptosis
  • 相关文献

参考文献13

  • 1李龙江,赵洪伟.腮腺区应用解剖特点与术式改良[J].中国实用口腔科杂志,2008,1(3):138-141. 被引量:15
  • 2Millesi H.Progress in peripheral nerve reconstruction[J]. World J SurgA 990,14(6):733-747.
  • 3Lundborg G,Zhao Q,Kanje M,et al.Can sensory and motor collateral sprouting be induced from intact peripheral nerve by end to side anatomosis[J]? J Hand Surg, 1994,19 ( 3 ) :277-282.
  • 4Sakamoto T,Kawazoe Y,Shen JS,et al.Adenoviral gene transfer of GDNF,BDNF and TGF~2,but not CNTF, cardiotrophin-I or IGF1, protects injured adult motoneurons after facial nerve avulsion[J].J Neurosci Res, 2003,72( 1 ):54-64.
  • 5lkeda K,Sakamoto T, Kawazoe Y,et al.Oral administration of a neuroproteetive compound T -588 prevents motoneuron degeneration after facial nerve avulsion in adult rats[J].Amyotroph Lateral Scler Other Motor Neuron Disord,2003A(2 ):74-80.
  • 6Ok-hee P, Kea JL, lm JR, et al. Bax-dependent and- independent death of motoneurons after facial nerve injury in adult nfice[J].Eur J Neurosci,2007.26(6):1421-1432.
  • 7Martin-villaiba A, Herr I ,Jeremiasl 1 ,et aI.CD95 ligand(Fas -- L/ APO -- IL) and tumor necrosis factor-related apoptosis-indueing ligand mediate ischemia-induced apoptosis in neurons [J].J Neurosci, 1999,19( 10):3809-3817.
  • 8Enokido Y, Hatanaka J. Apoptotic cell death occurs on hippocampal neuroma cultured in a high oxygen atmosphere[J]. Neuroscience, 1993,57 (4) : 965-972.
  • 9Day BJ,Fridovich l,Crapo JD.Manganic porphyrins possess catalase activity and protect endothelial cells against hydrogen peroxide- mediated injury[J]. Arch Biochem Biophys,1997,347f2):256-262.
  • 10Lee BLChan PH, Kim GW,et al.Metalloporphyrin-based superoxide dismutase mimic attenuates the nuclear transloeation of apoptosis-inducing factor and the subsequent DNA fragmentation after permanent focal cerebral isehemia in mice[J].Stroke,2005,36 (12):2712-2717.

二级参考文献12

共引文献14

同被引文献21

  • 1HA G K, HUANG Z, PARIKH R, et al. Immunodeficiency impairs re-injury induced reversal of neuronal atrophy: relation to T cell subsets and microglia [J]. Exp Neurol, 2007,208( 1 ):92--99.
  • 2MIGNINI F, GIOVANNETFI F,COCHIONIM,et al. Neu- ropeptide expression and T-lymphocyte recruitment in facial nucleus after facial nerve axotomy[J]. J Craniofac Surg, 2012,23(5):1 479-- 1 483.
  • 3OKHEE P,KEA J L,IMJR,et al. Bax -dependent and independent death of motoneurons after facial nerve injury inadult mice [J].Eur J Neurosci,2007,26 (6):1 421 -- 1 432.
  • 4MARCONDES M C,FURTADO G C,WENSKY A,et al. Immune regulatory mechanisms influence early pathology in spinal cord injury and encephalomyelitis [J]. Am 749-- 1 760. lnspontaneous autolmmune J Pathol,2005,166 (6):1.
  • 5SERPE C J,KOHM A P,HUPPENBAUER C B,et al. Exacerbation of facial motoneuron loss after facial nerve transection in severe combinedimmunodeficient (scid) mice[J ]. J Neurosci, 1999,19( 11 ): 7.
  • 6DEBOY C A, XIN J, BYRAM S C, et al. Immune-mediated neuroprotection of axotomized mouse facial motoneurons is dependent on the IL-4! STATE signaling pathway in CD4+ T cells [ J ]. ExpNeurol, 2006,201 ( 1 ): 212-- 224.
  • 7MINH-Y, CANH A, CRAIG J,et al. CD4+T cell mediated facial motoneuron survival after injury:Distribution pattern of cell death and rescue throughout the extent of the facial motor nucleus [J]. Journal of Neuroimmunology, 2006, 181 ( 1-2):93--99.
  • 8JONES K J,SERPE C I,BYRAM S C,et al. Role of the immune system in the maintenance of mouse facial motoneuron viability after nerveinjury [J]. Brain Behav Immun ,2005,19( 1 ) : 12-- 19.
  • 9MARZO S J, MOELLER C W, SHARMA N,et al. Facial motor nuclei cell loss with intratemporal facial nerve crush injuries in rats [J]. Laryn-goscope,2010,120 (11): 2 264-- 2 269.
  • 10JUNPING X I N, DEREK A, WAINWRIGHT, et al. Phen- otype of CD4+ T cell subsets that develop following mouse facial nerve axotomy [J]. Brain Behavior and Immunity, 2008, ( 22 ) : 528-- 537.

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