期刊文献+

3种大鼠实验性自身免疫性脑脊髓炎模型的差异 被引量:4

Comparison of Difference of Experimental Autoimmune Encephalomyelitis Model in Three Strains of Rats
下载PDF
导出
摘要 目的比较3种大鼠实验性自身免疫性脑脊髓炎模型的差异。方法采用皮下注射豚鼠脊髓匀浆+完全福氏佐剂,并辅以注射百日咳疫苗,诱导制备SD大鼠、Wistar大鼠和Lewis大鼠EAE模型,比较3组大鼠EAE的神经症状及中枢神经不同部位病理学变化。结果与Lewis大鼠相比,SD大鼠和Wistar大鼠潜伏期均延长(P<0.05),达峰时间相应推迟(P<0.05),神经症状以Lewis大鼠最严重,其次为SD大鼠(P<0.05);病理结果显示,3组大鼠CNS均以脑干病理改变最为严重,其次颈髓,而大脑病变最轻;CNS各部位的炎症改变,以Lewis大鼠最明显,而Wistar大鼠最轻。结论 SD大鼠与Lewis大鼠EAE比较,疾病发生率接近,中枢炎症病理改变相似,两者均以脑干炎症变化最严重,故SD大鼠是国内适合制备EAE模型的实验动物。 Objective To compare the difference of experimental autoimmune encephalomyelitis (EAE) model in three strains of rats. Methods SD rats,Wistar rats and Lewis rats were induced to establish EAE model by subcutaneously injecting emulsified spinal cord homogenate of guinea -pig(GPSCH) with complete Freud adjuvant(CFA) and subcutaneously injecting Bordetella pertussis vaccine. The clinical scores and pathological changes of central nervous system were compared among the three strains of rats. Results Compared with Lewis rats, the latency of EAE in SD rats and Wistar rats were longer (P 〈 0.05) ,and peak time of EAE in SD rats and Wistar rats were delayed ( P 〈 0.05 ). The maximal clinical score in Lewis rats was highest, then those in SD rats was higher. The pathological results showed that brainstem in three strains of rats suffered the most severe lesions among all parts of CNS,then cervical cord,but cerebrum had the slightest nervous damage. Conclusion EAE in SD rats has almost similar incidence to EAE in Lewis rats, and inflammatory response and pathological changes of EAE are most serious in the brainstem in SD rats and Lewis rats. Therefor we concluded that SD rats are ideal animals for establishing EAE in China.
出处 《医学研究杂志》 2013年第2期34-37,共4页 Journal of Medical Research
基金 国家自然科学基金资助项目(81070960) 温州市科技局基金资助项目(Y20090285)
关键词 实验性自身免疫性脑脊髓炎 动物模型 SD大鼠 WISTAR大鼠 LEWIS大鼠 Experimental autoimmune encephalomyelitis Animal model SD rats Wistar rats Lewis rats
  • 相关文献

参考文献10

  • 1朱英标,李晓莉,童巧文,夏念格,姚苏琴,郦铮铮,郑荣远.SD大鼠和Wistar大鼠实验性自身免疫性脑脊髓炎发病情况比较[J].中国实验动物学报,2009,17(3):166-171. 被引量:4
  • 2朱振国,郑荣远,李剑敏,韩钊.Lewis大鼠实验性变态反应性脑脊髓炎动物模型的建立及百日咳疫苗的影响[J].医学研究杂志,2008,37(7):21-24. 被引量:1
  • 3Correa JO,Aarestrup BJ,Aarestrup FM. Effect of thalidomide and pentoxifylline on experimental autoimmune encephalomyelitis (EAE)[J].Experimental Neurology,2010,(01):15-23.
  • 4Yin JX,Tu JL,Lin HJ. Centrally administered pertussis toxin inhibits microglia migration to the spinal cord and prevents dissemination of disease in an EAE mouse model[J].PLoS One,2010,(08):e12400.
  • 5郑建筝,高聪,谢富华,蒲蜀湘,陈盛强.SD大鼠实验性变态反应性脑脊髓炎模型的建立[J].实用诊断与治疗杂志,2006,20(7):469-472. 被引量:10
  • 6邱伟文,郑荣远,韩钊,吴赛珍,卢晔芬,章圣辉,韩义香.左旋咪唑对实验性自身免疫性脑脊髓炎大鼠脊髓内CD4、CD8、CD28和CD152表达的影响[J].中国神经免疫学和神经病学杂志,2007,14(2):65-68. 被引量:3
  • 7Fabis M J,Scott GS,Kean RB. Loss of blood-brain barrier integrity in the s pinal cord is common to experimental allergic encephalomyelitis in knockout mouse models[J].Proceedings of the National Academy of Sciences(USA),2007,(13):5656-5661.doi:10.1073/pnas.0701252104.
  • 8Schellenberg AE,Buist R,Yong VW. Magnetic resonance imaging of blood spinal cord barrier disruption in mice with experimental autoimmune encephalomyelitis[J].Magnetic Resonance in Medicine,2007,(02):298-305.doi:10.1002/mrm.21289.
  • 9Pfeiffer F,Schafer J,Lyck R. Claudin-1 induced sealing of blood-brain barrier tight junctions ameliorates chronic experimental autoimmune encephalomyelitis[J].Acta Neuropathologica,2011,(05):601-614.
  • 10Bennett J,Basivireddy J,Kollar A. Blood-brain barrier disruption and enhanced vascular permeability in the multiple sclerosis model EAE[J].Journal of Neuroimmunology,2010,(1-2):180-191.

二级参考文献53

共引文献14

同被引文献44

  • 1张增强,刘振华,谢惠芳,程卫华.二次免疫诱导大鼠实验性自身免疫性脑脊髓炎动物模型的建立[J].广东医学,2005,26(8):1056-1058. 被引量:1
  • 2徐玉,刘瑞春,王颖,赵平平,王秀丽,刘静,郭力.Wistar大鼠实验性自身免疫性脑脊髓炎模型的建立[J].脑与神经疾病杂志,2007,15(6):415-417. 被引量:15
  • 3Kirk SL,Karlik SJ.VEGF and vascular changes in chronic neuroinflammation[J].J Autoimmun,2003,21(4):353-363.
  • 4Hooper DC,Spitsin S,Kean RB,et al.Uric acid,a natural scavenger of peroxynitrite,in experimental allergic encephalomyelitis and multiple sclerosis[J].Proc Natl Acad Sci USA,1998,95(2):675-680.
  • 5Amedei A,Prisco D,D'Elios MM.Multiple sclerosis:the role of cytokines in pathogenesis and in therapies[J].Int J Mol Sci,2012,13(10):13438-13460.
  • 6Hamann I,Zipp F,Infante-Duarte C.Therapeutic targeting of chemokine signaling in Multiple Sclerosis[J].J Neurol Sci,2008,274(1-2):31-38.
  • 7Comabella M,Khoury SJ.Immunopathogenesis of multiple sclerosis[J].Clin Immunol,2012,142(1):2-8.
  • 8Proescholdt MA,Jacobson S,Tresser N,et al.Vascular endothelial growth factor is expressed in multiple sclerosis plaques and can induce inflammatory lesions in experimental allergic encephalomyelitis rats[J].J Neuropathol Exp Neurol,2002,61(10):914-925.
  • 9Argaw AT,Asp L,Zhang J,et al.Astrocyte-derived VEGF-A drives blood-brain barrier disruption in CNS inflammatory disease[J].J Clin Invest,2012,122(7):2454-2468.
  • 10O'Connor RA,Prendergast CT,Sabatos CA,et al.Cutting edge:Th1cells facilitate the entry of Th17 cells to the central nervous system during experimental autoimmune encephalomyelitis[J].J Immunol,2008,181(6):3750-3754.

引证文献4

二级引证文献8

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部