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大鼠脑挫伤后NTE与COX-2表达随时间的变化 被引量:3

The variation law of NTE and COX-2 with time in rat's brain which has been contused
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摘要 目的观察大鼠脑挫伤后脑组织NTE和COX-2的表达变化,并评价其法医学的意义。方法健康SD大鼠48只,随机分成正常对照组、手术对照组、挫伤组(按挫伤后处死时间再分为1h、12h、1d、3d、7d、14d共6个组)每组6只。以自由落体撞击法制作脑挫裂伤模型;应用免疫组化方法检测COX-2和NTE在脑组织中的表达情况;用SPSS 13.0软件分析COX-2和NTE的表达情况与脑挫伤后存活时间的相关性。结果正常对照组和假手术组NTE和COX-2均呈低水平表达,脑挫伤组伤后NTE和COX-2表达逐渐增强,均于1d达到高峰,至14d时COX-2表达降至正常对照组水平,而NTE仍高于正常对照组水平;挫伤各组与正常对照组比较,除1h组灰度值无统计学差异(P>0.05)外,其余各组均有明显差异(P<0.01)。结论脑挫伤后脑组织NTE和COX-2的表达均呈现先增强后下降的趋势,其表达规律有望为脑挫伤诊断及损伤时间推断提供参考。 Objective To observe the expression of NTE and COX-2 in rat's brain that has been contused, and to evaluate its forensic significance. Methods 48 rats were divided into three groups, control group(6), sham operation group(6), contusion group(36) which were subdivided into lh, 12h, ld, 3d, 7d and 14d groups (6 rats in each group). After the model of brain contusion was set up in rats through freefaHing dart method, the expression of NTE and COX-2 will be observed using immunohistochemieal method. The correlation between the expression of them and the rat's living time after being contused will be analyzed with SPSS 13.0. Results The expression of NTE and COX-2 were in low level in both the control group and the sham operation control group. In contusion group the expression of them were gradually elevated, the peak of both NTE and COX-2 appear at ld, then weakened gradually. The expression of COX- 2 (positive cell number) have dropped to the normal control group at 14d, but NTE (grey scale value) have not. Compared with the normal control group, the 1 h group of NTE showed no obvious statistical significance ( P 〉 0. 05 ), but other groups have obvious statistical significance ( P 〈 0. 01 ). Conclusion The expression of NTE and COX-2 were both elevated after the brain has been contused, and then weakened. And it is expected to provide a reference for diagnosis of brain contusion and dating of wound.
出处 《中国法医学杂志》 CSCD 2014年第1期22-24,29,I0002,共5页 Chinese Journal of Forensic Medicine
基金 张家口市科技攻关项目(0711046D-14) 河北省卫生厅重点科技研究计划(08386)
关键词 法医病理学 脑挫伤 免疫组织化学 神经病靶酯酶 诱导型环氧合酶 forensic pathology brain contusion immunohistoehemical NTE COX-2
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  • 1Chang P A,Chen Y Y,Qin WZ. The role of cell cycledependent neuropathy target esterase in cell proliferation[J].{H}MOLECULAR BIOLOGY REPORTS,2011,(1):123-130.
  • 2Rainier S,Albers J W,Dyck P J. Motor neuron disease due to neuropathy target esterase gene mutation:clinical features of the index families[J].{H}Muscle & Nerve,2011,(1):19-25.
  • 3Feeney D M,Boyeson M G,Linn R T. Responses to cortical injury:Methodology and local effects of contusion in the rat[J].{H}Brain Research,1981.67-77.
  • 4周高举,秦启生.实验性脑挫伤后神经元和星形胶质细胞反应的时间性变化[J].中国法医学杂志,1998,13(1):7-11. 被引量:14
  • 5Pamies D,Reig J A,Vilanova E. Expression of Neuropathy Target Esterase in mouse embryonic stem cells during differentiation[J].{H}ARCHIVES OF TOXICOLOGY,2010,(6):481-491.
  • 6Chang P A,Wu Y J. Neuropathy target esterase:an essential enzyme for neural development and axonal maintenance[J].{H}International Journal of Biochemistry and Cell Biology,2010,(5):573-575.
  • 7Vose S C,Fujioka K,Gulevich A G. Cellular function of neuropathy target esterase in lysophosphatidylcholine action[J].{H}Toxicology and Applied Pharmacology,2008,(3):376-383.
  • 8Dash P K,Mach S A,Moore A N. Regional expression and role of cyclooxygenase2 following experimental traumatic brain injury[J].{H}Journal of Neurotrauma,2000,(1):69-81.
  • 9Strauss K I,Barbe M F,Marshall R M. Prolonged cyclooxygenase2 induction in neurons and glia following traumatic brain injury in the rat[J].{H}Journal of Neurotrauma,2000,(8):695-711.
  • 10Jadhav V,Ostrowski R P,Tong W. Cyclooxygenase2 mediates hyperbaricoxygen preconditioning-induced neuroprotection in the mouse model of surgical brain injury[J].{H}STROKE,2009,(9):3139-3142.

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  • 1吴旭,王保捷,张国华,官大威,汪德文,杨丽,刘长胜.大鼠脑损伤分级自由落体打击模型的建立[J].中国法医学杂志,2005,20(1):1-3. 被引量:35
  • 2李如波,贾静涛,藤谷登,木村博司.实验性脑弥漫性轴索损伤的组织病理学变化[J].中国法医学杂志,2006,21(1):1-4. 被引量:7
  • 3Connell-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.
  • 4Ino 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.
  • 5He 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.
  • 6Zheng 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.
  • 7Dhariwala FA, Rajadhyaksha MS. An unusual mem- ber of the Cdk family: Cdk5[J]. Cell Mol Neurobiol, 2008,28 (3):351-369.
  • 8Rashidian 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.
  • 9Paglini G, COceres A. The role of the Cdk5-p35 kinase in neuronal development[J]. Eur J Biochem, 2001.268 (6), 1528-1533.
  • 10Iwata 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.

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