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Wistar大鼠实验性变态反应性脑脊髓炎的模型建立 被引量:19

The establishment of multiple clinical processes on experimental allergic encephalonlyelitis model of Wistar rat
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摘要 目的:建立Wistar大鼠多病程实验性变态反应性脑脊髓炎(EAE)的动物模型,并进行病理学研究,为多发性硬化(MS)的研究提供实验依据。方法:以豚鼠全脊髓匀浆(GPSCH)为抗原免疫Wistar大鼠建立EAE的动物模型,并在光镜下观察不同发病类型EAE的病理改变。结果:根据病理和临床表现可将Wistar大鼠EAE模型分为5种发病形式:急性型、缓解-复发型、持续进展型、良性型和隐匿型。光镜下可见不同发病时期的EAE的病理改变有所不同,但都以血管"袖套"状改变、脑室周围及白质脱髓鞘改变为主,伴有神经元肿胀变性。结论:首次建立了Wistar大鼠多病程EAE,是研究多发性硬化的理想动物模型。 Objective: To investigate establishing the multiple clinical processes model and pathological characteristics of EAE model , and to provide the experimental value for reseaching MS. Method: The animal model was established in Wistar rat by immunization with complete Freund adjuvant and GPSCH , the pathological changes of EAE were studied with the aid of light microscopy. Results: We can divide the EAE into five types by pathological changes and clinical manifestation: acute EAE, relapsing-remitting EAE,persistent progress EAE, benign form EAE and delitescence EAE. Every type mainly showed congestion and inflammatory cuff of small blood vessels, disintegration and disappear of myelin sheath and degeneration of neurons, especially in spinal cord. Conclusion: Multiple clinical processes on EAE model of Wistar rat were established for the first time , it is an ideal animal model in studying MS in our country.
出处 《脑与神经疾病杂志》 2004年第6期425-428,共4页 Journal of Brain and Nervous Diseases
关键词 EAE WISTAR大鼠 实验性变态反应性脑脊髓炎 动物模型 病理改变 多发性硬化 病程 变性 光镜 神经元 experimental allergic encephalomyelitis multiple sclerosis animal model
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参考文献12

  • 1胡学强,陆正齐,饶从志,吴金浪,吴义芳.实验性变应性猴脑脊髓炎的超微结构改变[J].中华神经科杂志,1998,31(6):333-335. 被引量:9
  • 2宋春杰,尹岭,王鲁宁,朱克.髓鞘蛋白脂质蛋白多肽_(139-151)诱发实验性自身免疫性脑脊髓炎小鼠模型[J].中国神经免疫学和神经病学杂志,2001,8(3):142-144. 被引量:17
  • 3曹翠丽,王惠,马常升,杨天祝.实验性变态反应性脑脊髓炎大鼠模型的建立[J].解剖学杂志,2001,24(1):77-81. 被引量:33
  • 4Nikki CO, Brien C, Brett C et al. Inhibition of nitric oxide synthase initiates relapsing remitting experimental autoimmune encephalomyelitis in rats, yet nitric oxide appears to be essential for clinical expression of disease. J Immunol, 2001,167(10):590
  • 5Legge KL, Min B, Bell JJ, et al. Coupling of peripheral tolerance to endogenous interleukin 10 promotes effective modulation of myelin-activated T cells and ameliorates experimental allergic encephalomyelitis. J Exp Med. 2000;191(12):2039
  • 6Giok K, Kuniko K, Naoyuki T, et al. Persistent expression of experimental autoimmune encephalomyelitis (EAE)-specific Vβ8.2 TCR spectrarype in the central nervous system of rats with chronic relapsing EAE. J Immunol, 1998,161(12):6993
  • 7Maatta JA, Eralinna JP, Roytta M, et al. Physical state of the neuroantigen in adjuvant emulsions determines encephalitogenic status in the BALB/c mouse. J Immunol Method. 1996,190:133
  • 8Fulumitsu H, Talase YS, Watanabe R. Neuropathology of autoimmune encephalomyelitis modified by retroviral infection. Neurophathology, 2002,22(4):280
  • 9Bert A, Sandra A. The use of animal models to investigate the pathogenesis of neuroinflammatory disorders of the central nervous system. Curr Opin Neurol. 2003;16(3):375
  • 10彭聿平,邱一华,程纯,戴丽,黄慧伟.不同种系动物诱导实验性变态反应性脑脊髓炎模型的研究[J].南通医学院学报,2000,20(1):22-23. 被引量:8

二级参考文献23

  • 1常雅萍,姜顺爱,杨贵贞.杏仁核在实验性变态反应性脑脊髓炎模型鼠的免疫调节效应[J].中国免疫学杂志,1993,9(4):222-222. 被引量:1
  • 2林嘉友.实验性变态反应性脑脊髓炎小鼠模型[J].中国免疫学杂志,1994,10(1):39-40. 被引量:12
  • 3[1]Raine CS.Biology of disease. Analysis of autoimmune demyelination:its impact upon multiple sclerosis,Lab Invest,1984;50:608-635
  • 4[2]Zamvil SS,Mitchell DJ,Moore AC,et al. T-cell epitope of the autoantigen myelin basic protein that induces encephalomyelitis. Nature,1986;324(6094):258-260
  • 5[3]Swanborg RH. Experimental autoimmune encephalomyelitis in rodents as a model for human demyelinating disease. Clin Immunol Immunopathol,1995;77:4-13
  • 6[4]Martin R,McFarland HF,McFarlin DE. Immunological aspects of demyelinating diseases. Annu Rev Immunol,1992;10:153-187
  • 7[5]Fujinaml RS,Paterson PY. Induction of experimental allergic encephalomyelitis in sucking Lewis rats:role of age and type of sensitizing neuroantigen. J Immunol, 1977;119:1634-1638
  • 8[6]Voskuhl RR, Pitchekian-Halabi H, MacKenzie-Graham A. et al.Gender differences in autoimmune demyelination in the mouse:implications for multiple sclerosis. Ann Neurol,1996;39:724-733
  • 9[7]Griffin AC,Whitacre CC. Sex and strain differences in the circadian rhythm fluctuation of endocrine and irmune function in the rat:implications for rodert models of autoimmune disease. J Neuroimmunol,1991;35:53-64
  • 10[8]Maatta JA,Eralinna JP,Roytta M.et al. Physical state of the neuroantigen in adjuvant emulsions determines encephalitogenic status in the BALB/c mouse. J Immunol Method,1996;190:133-141

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