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老年与青壮年脑挫裂伤组织NGF的表达差异及意义 被引量:2

Expression difference and its significance of NGF in the contusive or lacerated brain tissue in the aged and young patients
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摘要 目的研究衰老对脑挫裂伤组织神经生长因子(NGF)基因表达的影响,进一步探讨老年颅脑损伤病人神经功能缺失程度较重的分子生物学机制。方法收集重型颅脑损伤开颅手术中的脑挫裂伤组织,应用免疫组化和医学数码图像分析技术,观察老年组(≥60岁)和青壮年组(19~59岁)病人脑损伤后3~9h脑挫裂伤组织NGF蛋白的表达差异。结果脑损伤后NGF在老年和青壮年脑挫裂伤组织中的表达均明显增强;老年组脑挫裂伤组织中的NGF蛋白表达显著性低于青壮年组(P<0.05)。结论老年人脑挫裂伤后NGF表达水平下降明显,提示其受损神经元的修复和生存能力降低,这可能是老年颅脑损伤病人恢复不良的重要原因之一。 Objective To study the effect of aging on the expression of nerve growth factor (NGF) protein in the contusive or lacerated brain tissue after traumatic brain injury (TBI), and furthering explore the molecular biological mechanism for old patients having more severe neurological deficits. Methods The contusive and lacerated brain tissues 3 to 9 hours after TBI were collected, and the expressions of NGF protein of the aged group (≥ 60 years old) and young group (19 to 59 years old) were analyzed by immunohistochemistry and digital image analysis system, to determine the possible susceptibility differences in the expression of NGF protein between the two groups. Results In the contusive and lacerated brain tissue, the expression of NGF protein was increased after TBI. However, the level of NGF protein in the contusive and lacerated brain tissue was statistically lower in the aged group than in the young group (P〈0.05). Conclusion The expression of NGF after TBI is influenced by age. The lower level expression of NGF in aged patients suggests that the recovery and survival ability of aged neurons is lowered, which might be an important reason for the bad recovery of the aged patients after craniocerebral injury.
出处 《中国微侵袭神经外科杂志》 CAS 2007年第7期315-317,共3页 Chinese Journal of Minimally Invasive Neurosurgery
关键词 颅脑损伤 老年人 神经生长因子 免疫组织化学 craniocerebral trauma aged nerve growth factor irnmunohistochemistry
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参考文献9

  • 1高进喜,卢亦成,江基尧,由振东,何成.幼龄和老龄大鼠液压脑损伤后NGF、Bcl-2、Bax蛋白的表达[J].第二军医大学学报,2003,24(5):496-498. 被引量:7
  • 2SEMKOVA I,KRIEGLSTEIN J.Neuroprotection mediated via neurotrophic factors and induction of neurotrophic factors[J].Brain Res Brain Res Rev,1999,30(2):176-188.
  • 3PUTCHA G V,LE S,FRANK S,et al.JNK-mediated BIM phosphorylation potentiates BAX-dependent apoptosis[J].Neuron,2003,38(6):899-914.
  • 4JARSKOG L F,GILMORE J H.Developmental expression of Bcl-2 protein in human cortex[J].Brain Res Dev Brain Res,2000,119(2):225-230.
  • 5HAMNER S,SKOGLOSA Y,LINDHOLM D.Differential expression of bcl-w and bcl-x messenger RNA in the developing and adult rat nervous system[J].Neuroscience,1999,91(2):673-684.
  • 6高进喜,卢亦成,王如密,王守森.幼龄和老龄大鼠液压颅脑伤后NGFmRNA表达差异[J].中华神经外科疾病研究杂志,2004,3(5):424-427. 被引量:5
  • 7WATSON D J,LONGHI L,LEE E B,et al.Genetically modified NT2N human neuronal cells mediate long-term gene expression as CNS grafts in vivo and improve functional cognitive outcome following experimental traumatic brain injury[J].J Neuropathol Exp Neurol,2003,62(4):368-380.
  • 8LONGHI L,WATSON D J,SAATMAN K E,et al.Ex vivo gene therapy using targeted engraftment of NGF-expressing human NT2N neurons attenuates cognitive deficits following traumatic brain injury in mice[J].J Neurotrauma,2004,21(12):1723-1736.
  • 9高进喜,卢亦成,江基尧.克仑特罗对幼龄和老龄大鼠液压脑损伤后神经生长因子、bcl-2和bax蛋白表达的调节作用[J].中华实验外科杂志,2003,20(8):764-764. 被引量:4

二级参考文献22

  • 1Semkova I, Krieglstein J. Neuroprotection mediated via neurotrophic factors and induction of neurotrophic factors. Brain Res Rev,1999, 30:176-178.
  • 2Sinson G, Perri BR, John Q, et al. Improvement of cognitive deficits and decreased cholinergic neuronal cell loss and apoptotic cell death following neurotrophin infusion after experimental traumatic brain injury. J Neurosurg, 1997, 86 : 511-518.
  • 3Colangeo AM, FoUesa P, Mocchetti I. Differential induction of nerve growth factor and basic fibroblast growth factor mRNA in neonatal and aged rat brain. Mol Brain Res,1998, 53:218-225.
  • 4Sinson G, Perri BR, Trojanowski JQ, et al.Improvement of cognitive deficits and decreased cholinergic neuronal cell loss and apoptotic cell death following neurotrophin infusion after experimental traumatic brain injury [J].J Neurosurg, 1997, 86(3): 511-5
  • 5Strauss S, Otten U, Joggerst B, et al.Increased levels of nerve growth factor (NGF) protein and mRNA and reactive gliosis following kainic acid injection into the rat striatum [J].Neurosci Lett, 1994, 168(1-2): 193-196.
  • 6Culmsee C, Semkova I, Krieglstein J.NGF mediates the neuroprotective effect of the beta2-adrenoceptor agonist clenbuterol in vitro and in vivo: evidence from an NGF-antisense study [J].Neurochem Int, 1999, 35(1): 47-57.
  • 7Masson F, Thicoipe M, Mokni T, et al.Epidemiology of traumatic comas : a prospective population-based study [J].Brain Inj, 2003, 17(4): 279-293.
  • 8Osteen CL, Moore AH, Prins ML, et al.Age-dependency of 45 Calcium accumulation following lateral fluid percussion: acute and delayed patterns [J].J Neurotrauma, 2001, 18(2): 141-162.
  • 9Maughan PH, Scholten KJ, Schmidt RH.Recovery of water maze performance in aged versus young rats after brain injury with the impact acceleration model [J].J Neurotrauma, 2000, 17(12): 1141-1153.
  • 10Semkova I, Krieglstein J.Neuroprotection mediated via neurotrophic factors and induction of neurotrophic factors [J].Brain Res Rev, 1999, 30(2): 176-188.

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