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血管内皮生长因子对脊髓神经组织保护作用及c-fos基因的影响 被引量:2

Protective roles and effects of vascular endothelial growth factor on spinal neuronal tissue and c-fos gene
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摘要 目的探讨血管内皮生长因子(vascularendothelialgrowthfactor,VEGF)对脊髓损伤后脊髓神经元凋亡和c-fos基因的影响及保护机制。方法将85只同龄Wistar大鼠,采用Allens的weightdropping(WD)法挫伤大鼠T11节段脊髓,于术后0,15min,1,2,4,8,12,24h经蛛网膜下腔导管各注入VEGF溶液15μL(含VEGF20μg),并与生理盐水组和正常对照组作对照。采用原位末端标记法(TUNEL法)检测脊髓损伤前后发生凋亡的脊髓神经元。采用免疫组化和原位杂交方法检测脊髓损伤前后c-fos基因的变化。结果正常组脊髓前角中未发现凋亡细胞,生理盐水组于伤后2h始出现凋亡神经元。VEGF组与生理盐水组相比较,凋亡神经元明显减少(P<0.01,t=24.25)。c-fos基因表达在正常脊髓组织中呈弱阳性,在生理盐水组中表达明显增加,VEGF组c-fos基因表达比生理盐水组明显减少(P<0.01,t=12.03)。结论脊髓损伤后脊髓神经元凋亡增多和c-fos基因表达显著增多,VEGF能抑制脊髓损伤后脊髓神经元凋亡和c-fos基因表达,从而保护损伤的神经组织。 AIM:To explore the effect and protective mechanism of vascular endothelial growth factor(VEGF) on apoptosis and c fos gene expression in spinal neurons of rats after spinal cord injury (SCI).METHODS: T11 spinal cord segment of 85 Wistar rats were bruised with Allens' weight dropping method. The VEGFtreated group received 15 μL VEGF liquid through the canal of subarachnoid space (20 μg) at once, 15 minutes, 1, 2, 4, 8, 12 and 24 hours after operation, which was compared with saline group and normal control group.Apoptotic neurons were detected by TUNEL staining.The c fos mRNA levels of the rats were determined by in situ hybridization,and immunohistochemical methods.RESULTS: There were no apoptotic neurons in spinal anterior horn of the normal group.The apoptotic neurons were found 2 hours later in the saline group, which were significantly decreased in the VEGF group compared with the saline group(P< 0.01,t=24.25).The c fos gene expression showed weakly positive in normal spinal cord tissue,and showed significantly increased in saline group.c fos gene expression in VEGF group was significantly decreased in VEGF group compared with saline group(P< 0.01, t=12.03).CONCLUSION:Apoptotic neurons and c fos gene expression in rat spinal cord can be markedly enhanced after SCI,VEGF can protect the apoptosis of spinal neurons and c-fos gene expression thereby protecting the injured nervous tissue.
出处 《中国临床康复》 CSCD 2004年第23期4736-4737,i003,共3页 Chinese Journal of Clinical Rehabilitation
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参考文献14

  • 1[1]Senger DR,Van de Water L,Brown LF,et al.Vascular permeability factor(VPF,VEGF)in tumor biology.Cancer Metastasis Rev 1993;12:303-24
  • 2[2]Baumgartner I,Pieczek A,Manor O,et al.Constitutive expression of ph VEGF165 after intramuscular gene transfer promotes collateral vessel development in patients with critical limb ischemia.Circulation 1998;97:1114-23
  • 3刘京升,孙正义,董平,洪光祥.慢性脊髓压迫及减压后骨骼肌细胞凋亡的实验研究[J].中国临床康复,2003,7(26):3568-3569. 被引量:5
  • 4[4]Lu J,Ashwell KW,Waite P.Advances in secondary spinal cord injury:role of apoptosis.Spine 2000;25:1859-66
  • 5[5]Bullitt E.Induction of c-fos-like protein within the lumbar spinal cord and thalamus of the rat following peripheral stimulation.Brain Res 1989;493:391-7
  • 6[6]Kohmura E,Yuguchi T,Yamada K,et al.Expression of c-fos mRNA after cortical ablation in rat brain is modulated by basic fibroblast growth factor and the NMDA receotor isincolved in c-fos expression.Brain Res Mol Brain Res 1995;28:117-21
  • 7[7]Craig CG,White TD.N-methyl-D-aspartate and non-N-methyl-D-aspartate-evoked adenosine release from rat cortical slices:distinct puringergic sources and mechanisms of release.J Neurochem 1993;60:1073-80
  • 8[8]Yakovlev AG,Faden Al.Sequential expression of c-fos protooncogene,TNF-alpha,and dynorphin genes inspinal cord following experimental traumatic injury.Mol Chem Neuropathol 1994;23:179-90
  • 9[9]Murphy TH,De Long MJ,Coyle JT.Enhanced NAD(P)H:quinine reductase activity prevents glutamate toxicity produced by oxidative stress.J Neurochem 1991;56(3):990-5
  • 10王鸿飞,郑连杰,刘用楫.基因治疗脊髓损伤的前瞻性探讨[J].中国临床康复,2003,7(26):3624-3625. 被引量:4

二级参考文献26

  • 1崔雅珍.脊髓损伤的再生与修复[J].中国组织工程研究与临床康复,2001,10(18):60-61. 被引量:8
  • 2柯青,王云甫,何晓阔.脊髓损伤修复的机制探讨和研究[J].中国组织工程研究与临床康复,2001,10(20):96-97. 被引量:1
  • 3郑文济,王洪生,王阳春,赵志,谭振美,李春光.脊髓继发性损伤的实验与临床研究[J].中国临床神经外科杂志,1996,1(1):40-41. 被引量:5
  • 4Watabe K, Ohashi T, Sakamoto T, et al. Rescue of lesioned adult rat spinal motor neurons by adenoviral gene transfer of glial cell line-derived neurotrophic factor. J Neurosci Res 2000; 60(4): 511 -9.
  • 5Cao L, Zheng AC, Ahao YC, et al. Gene therapy of Parkinson disease mode rat by direct injection of plasmid DNA, Lipofection Complex. Human Gene Therapy 1995; 6:1497.
  • 6Tuszynski MH, Peterson PA, Ray J, et al. Fibroblasta gemetically modified to produce nerve growth factor induce robust neuritic in growth after grafting to the spinal croci. EXP Neurol 1994; 126:1.
  • 7Jiao SS, Wiuams P, Safda N, et al. Contransplantion of plasmid transfected myoblasts and myotubes nto rat brains enables high levels of gene expression longetrm. Cell Transpl 1993; 2:185.
  • 8Liu S, Qu Y, Stewart TJ, et al. Embryonic stem cells differentiate into oligodendrocytes and myelinate in culture and after spinal cord transplantation. Proc Natl Acad Sci USA 2000; 97 ( 11 ) : 6126 - 31.
  • 9Tuszynski MH, Meyers, Nakahara Y, et al. Fibroblasts and Schwann cell sgeurola-ophci factors induce robusttt neuritic growth aftor transplantation to the spinal cord. Soc Neurosci Abstr 1994; 20:10.
  • 10关骅.单唾液酸神经节苷脂在脊髓损伤中的应用[J].中国脊柱脊髓杂志,1997,7(4):185-187. 被引量:6

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