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三叉神经痛大鼠模型中Cdk5/p35的表达与活性 被引量:2

Expression and activity of Cdk5/p35 in a rat model of trigeminal neuropathic pain
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摘要 目的:探讨Cdk5激活剂p35在三叉神经痛过程中所起的作用。方法:以三叉神经眶下支(ION)的慢性压迫性损伤(CCI)建立的三叉神经痛大鼠模型为研究对象,采用Western印迹、免疫沉降和Cdk5活性分析方法,检测大鼠眶下神经慢性压迫性损伤(CCI-ION)后三叉神经脊束尾核(Vc)组织中Cdk5的活性变化和Cdk5、p35的表达水平。应用SPSS13.0软件包中的两两比较和扩展t检验进行统计学分析。结果:CCI-ION呈时间依赖形式诱导神经损伤侧Vc组织中的p35上调(第1天为1.23±0.15,第3天为1.36±0.12,第7天为1.62±0.17,第14天为1.83±0.16);Cdk5表达在CCI-ION第1天到第14天基本一致,而Cdk5的活性与p35表达具有一致性;CCI-ION第14天,Vc内的Cdk5活性(115.5Kcpm)是CCI-ION第1天Vc内的Cdk5活性(19.0Kcpm)的6倍,各组之间均有显著差异(P<0.01)。结论:Cdk5/p35与三叉神经痛过程中神经元突触变化及神经元可塑性有密切关系。 PURPOSE:To test the hypothesis that Cdk5/p35 plays important roles during trigeminal neuropathic pain.METHODS:Trigeminal neuralgia rat model was established with a chronic constriction injury (CCI) of the infraorbital branch of the trigeminal nerve (ION).The change of Cdk5 activity, expression of Cdk5 and p35 in Vc after CCI-ION were studied by Western blot, immunoprecipitation and Kinase assay.Statistical analysis was performed using SPSS13.0 software package.RESULTS:Western blot showed CCI-ION induced a time-dependent upregulation of p35 primarily within the ipsilateral superficial laminae of Vc (day 1:1.23±0.15, day 3:1.36±0.12, day 7:1.62±0.17, day 14:1.83±0.16).In contrast, the expression of Cdk5 was constant during day 1-14 in Vc after CCI-ION.Cdk5 activity on day 14 in Vc after CCI-ION (115.5 Kcpm) was 6 times as that on day 1 in Vc after CCI-ION (19.0 Kcpm).The difference was significant (P〈0.01).CONCLUSIONS:The results suggest that cdk5/p35 may plays important roles on synaptic reorganization of Vc after CCI-ION, expression of p35 may be a novel regulatory mechanism to control cdk5 activity in Vc after CCI-ION.
出处 《上海口腔医学》 CAS CSCD 2010年第5期545-548,共4页 Shanghai Journal of Stomatology
关键词 三叉神经痛 慢性压迫性损伤 CDK5 P35 Trigeminal neuropathic pain; Chronic constriction injury; Cdk5; p35
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  • 1Alfonso Represa,Yehezkel Ben-Ari.Kindling is associated with the formation of novel mossy fibre synapses in the CA3 region[J]. Experimental Brain Research . 1992 (1)
  • 2MatsushitaM,TomizawaK,LuYF ,etal.Distinctcellulacompartmentofcyclin dependentkinase 5 (Cdk5 )andneuron specificCdk5activatorprotein (p3 5 nck5a)inthedevelopingratcerebellum. Brain Research Bulletin . 1996
  • 3McNamaraJO,MorrisettR,NadlerJV.Recentadvancesinunderstandingmechanismsofthekindlingmodel. Advances in Neurology . 1992
  • 4HirookaK,TomizawaK,MatsuiH ,etal.Developmentalalterationoftheexpressionandkinaseactivityofcyclin dependentkinase 5 (Cdk5 )intheratretina. JNeuochem . 1996
  • 5Lew J,Beaudette K,Litwin CM,et al.Purification and characterization of a novel proline - directed protein kinase from bovine brain. Journal of Biological Chemistry . 1992
  • 6Lew J,Winkfein RJ,Paudel HK,et al.Brain proline-directed protein kinase is a neurofilament kinase which displays high sequence homology to p34cdc2. Journal of Biological Chemistry . 1992
  • 7Lew J,Wang JH.Neuronal cdc2-like kinase. Trends in Biochemical Sciences . 1995
  • 8Babb TL,Kupfer WR,Pretorius JK,et al.Synaptic reorganization by mossy fibers in human epileptic fascia dentata. Neuroscience . 1991
  • 9Moia LJMP,Matsui H,Barros GAM,et al.Immunosuppressants and calcineurin inhibitors, cyclosporin A and FK506, reversibly inhibit epileptogenesis in amygdaloid kindled rat. Brain Research . 1994
  • 10Racine RJ.Modification of seizure activity by electrical stimulation: Ⅱ.Motor seizure. Electroencephalography and Clinical Neurophysiology . 1972

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  • 1周瑸,刘玉光,吴承远.建立大鼠三叉神经痛动物模型[J].山东医药,2005,45(3):21-22. 被引量:5
  • 2Connell-Crowley L, Le Gall M, Vo DJ, et al. The cyclin-dependent kinase Cdk5 controls multiple as- pects of axon patterning in vivo[J]. Curr Biol,2000, 10(10) :599-602.
  • 3Ino H, Ishizuka T, Chiba T, et al. Expression of CDK5 (PSSALRE kinase), a neural cdc2-related pro- tein kinase, in the mature and developing mouse central and peripheral nervous systems[J]. Brain Res, 1994,661 ( 1-2 ) : 196-206.
  • 4He X, Takahashi S, Suzuki H, et al. Hypomyelination phenotype caused by impaired differentiation of oligo- dendrocytes in Emxl-cre mediated Cdk5 conditional knockout mice[J]. Neurochem Res,2011,36 (7) : 1293- 1303.
  • 5Zheng YL, Li BS, Kammgo J, et cd. Cdk5 Modu- lation of mitogen-activated protein kinase signaling regulates neuronal survival[J]. Mol Biol Ce11,2007,18(2):404-413.
  • 6Dhariwala FA, Rajadhyaksha MS. An unusual mem- ber of the Cdk family: Cdk5[J]. Cell Mol Neurobiol, 2008,28 (3):351-369.
  • 7Rashidian J, Rousseaux MW, Venderova K, et al. Essential role of cytoplasmic cdk5 and Prx2 in mul- tiple ischemic injury models, in vivo[J]. J Neurosci, 2009,29 (40) :12497-12505.
  • 8Paglini G, COceres A. The role of the Cdk5-p35 kinase in neuronal development[J]. Eur J Biochem, 2001.268 (6), 1528-1533.
  • 9Iwata A, Browne KD, Chen XH, et al. Traumatic brain injury induces biphasic upregulation of ApoE and ApoJ protein in rats[J]. J Neurosci Res,2005, 82(1 ) : 103-114.
  • 10黄玲,于生元,董钊,姜磊.三叉神经慢性缩窄环术后大鼠行为反应与组织学变化的关系[J].中国疼痛医学杂志,2008,14(5):274-277. 被引量:4

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