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大鼠脊髓损伤后轴突病理变化与胶质瘢痕的关系 被引量:5

A study on the pathological changes of axons and the relationship between axons and glial scar after spinal cord injury in rat
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摘要 目的观察脊髓损伤(SCI)后轴突变化及其与胶质瘢痕的关系。方法应用Allen’S法建立大鼠脊髓损伤模型,通过行为学评分、免疫荧光及神经束路示踪等观察SCI后轴突的病理变化,及其与胶质瘢痕的关系,并测量胶质瘢痕的厚度。结果SCI后损伤处的轴突呈断裂、扭曲状,SCI后1周损伤轴突呈再生趋势,2周时再生明显,与此相应动物运动功能逐渐恢复,4周时胶质瘢痕形成,再生的轴突被瘢痕阻挡。头尾侧胶质瘢痕厚度(107.00±20.12)μm大于两侧边厚度(69.92±24.37)μm。结论SCI后轴突仍具有再生能力,但被胶质瘢痕所阻挡,瘢痕厚度的测量为将来去除胶质瘢痕提供了实验依据。 Objective To observe the changes of axons and the relationship between axons and glial scar after spinal cord injury (SCI). Methods we established SCI model using Allen's weight-drop injury setting, and observed the pathological changes of axons, the relationship between axons and glial scar with cavity after SCI via behavioral scoring, double immunofluorescence and tract tracing. Then, we quantitated the thickness of glial scar. Results Axons in the lesion site seen to be interrupted and distorted. Nevertheless, axons seemed to begin to regrow at 1 week after SCI, and obvious neuroregeneration appeared at 2 weeks postinjury, which was consistent with the gradual functional recovery of injured rat. At 4 weeks post SCI, glial scar came into being and inhibited axonal regeneration. The thickness of glial scar after quantitating showed to be ( 107.00 ± 20. 12 ) μm in the rostral and caudal region to the lesion, and ( 69.92 ± 24.37) μm in the lateral region. Conclusion The axons remain regenerative capability after SCI, which are inhibited by the glial scar. The thickness of glial scar measured in the study will provide experimental evidence for ablating glial scar in the future.
出处 《中华神经外科杂志》 CSCD 北大核心 2008年第4期304-306,共3页 Chinese Journal of Neurosurgery
基金 国家自然科学基金重点项目(30330220) 面上项目(30471781.30572167)和863计划重大专项(2003AA205030)
关键词 脊髓损伤 轴突 再生 胶质瘢痕 Spinal cord injury Axon,regeneration Glial scar
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  • 1刘暌,王红云,何乐,王忠诚,张亚卓.室管膜细胞在大鼠脊髓损伤后的反应性增生[J].中华神经外科杂志,2004,20(6):476-478. 被引量:5
  • 2Silver J,Miller JH.Regeneration beyond the glial sear.Nat Rev Neurosci,2004,5:146-156
  • 3李晓光 杨朝阳 李云庆 等.应用脊髓重建管修复猴脊髓损伤的研究[J].中国微侵袭神经外科杂志,2004,9:132-132.
  • 4Basso DM,Beattie MS,Bresnahan JC.Graded histological and locomotor outcomes after spinal cord contusion using the NYU Weight-Drop device versus transection.Exp Neurol,1996,139:244-256
  • 5Khan M,Griebel R.Acure spinal cord injury in the rats:comparsion of three experiment techniques.Can Neurol Sci,1983,10:161-163
  • 6Talac R,Friedman JA,Moore MJ,et al.Animal models of spinal cord injury for evalution of tissue engineering treatment strategies.Biomaterials,2004,25:1505-1510
  • 7Rosenzweiga ES,McDonalda JW.Rodent models for treatment of spinal cord injury:research trends and progress toward useful repair.Curr Opin Neurol,2004,17:121-131
  • 8Wallace MC,Tator CH,Lewis AJ.Chronic regenerative changes in the spinal cord after cord compresion injury in rats.Surg Neurol,1987,27:209-219
  • 9Wagner FC,VanGilder JC,Dohrmann GJ.Pathological changes from acute to chronic in experimental spinal cord trauma.J Neurosurg,1978,48:92-98
  • 10Kao CC.Spinal cord cavitation after injury.In:Windle WF,ed.The spinal cord and its reaction to traumatic injury.New York:Marcel Dekker Inc,1980.249-270

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  • 1宋宇锋,YU Zhi-yuan,XIE Min-jie,BU Bi-tao,WITTE OW,WANG Wei.Suppression of Astroglial Scar Formation and Enhanced Axonal Regeneration Associated with Functional Recovery in a Spinal Cord Injury Rat Model by the Cell Cycle Inhibitor Olomoucine[J].神经损伤与功能重建,2006,1(2):74-83. 被引量:21
  • 2周建军,吴国材,胡荣,陈志,张弦,杨慧,林江凯,冯华,卞修武,李云庆,李晓光.大鼠实验性脊髓损伤后胶质瘢痕分布规律研究[J].中华神经外科杂志,2007,23(5):347-350. 被引量:14
  • 3樊沛(综述),贺西京(审校).嗅鞘细胞移植治疗脊髓损伤应用进展[J].美中国际创伤杂志,2007,6(2):54-57. 被引量:4
  • 4McDonald JW, Sadowsky CS. Spinal-cord injury [ J ]. Lancet, 2002, 359 : 417425.
  • 5Becker EB, Bonni A. Cell cycle regulation of neuronal apoptosis in development and disease [ J ~ . Prog Neurobiol, 2004, 72 : 1-25.
  • 6Sgambato A, Cittadin~ A, Faraglia B, et al. Multiple functions of p27 (Kipl) and its alterations in tumor cells: a review [ J]. J Cell Physiol,2000, 183: 18-27.
  • 7Miyazawa K, Himi T, Garcia V, et al. A role for p27/Kipl in the control of cerebellar granule cell precursor proliferation[ J]. J Neurosci,2000, 20 : 5756-5763.
  • 8Carrano AC, Eytan E, Hershko A, et al. SKF2 is required for ubiquitin-mediated degradation of the CDK inhibitor p27 [ J 1 ~ Nat Cell Biol, 1999, 1:193-199.
  • 9Fotovati A, Nakayama K, Nakayama KI. Impaired germ cell development due to compromised cell cycle progression in Skp2-deficient mic, e[ J]. Cell Div, 2006, 1-4.
  • 10Nguyen L, Bess on A, Heng Jl, el al. p27kipl independently promotes neuronal differentiation and migration in the cerebral cortex[ J ]. Genes Dev, 2006, 20 : 1511-1524.

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