期刊文献+

依达拉奉对大鼠实验性自身免疫性脑脊髓炎的保护作用 被引量:3

Protective Effect of Edaravone on Experimental Autoimmune Encephalomyelitis in Rats
原文传递
导出
摘要 目的:研究依达拉奉对实验性自身免疫性脑脊髓炎(Experimental Autoimmune Encephalomyelitis,EAE)的影响。方法:72只健康成年雌性Wistar大鼠随机分为:正常对照组、EAE组、EAE+小剂量依达拉奉组、EAE+大剂量依达拉奉组(n=18)。正常对照组注射生理盐水,其它组采用自制完全抗原诱导EAE模型。EAE组建模后不做任何处理,EAE+小剂量依达拉奉组、EAE+大剂量依达拉奉组分别在建模后给予依达拉奉4mg/k·d、10mg/k·d。比较各组发病率并行神经功能评分,取脊髓组织行HE染色、iNOS、OPN免疫组织化学染色观察。结果:依达拉奉干预组大鼠较EAE组发病率、神经功能缺损评分均明显降低(P<0.05)。HE结果显示依达拉奉干预组较EAE组炎症反应减少,损伤程度减轻。依达拉奉组iNOS、OPN表达均明显小于EAE组(P<0.05)。大剂量依达拉奉iNOS、OPN表达均低于小剂量依达拉奉组(P<0.05)。结论:依达拉奉对EAE具有保护作用,可能与抑制小神经胶质细胞活化,减轻炎症反应,降低iNOS和OPN表达有关。 Objective:To study the effect of edaravone on experimental autoimmune encephalomyelitis(EAE) in rats.Methods:72 adult healthy female Wistar rats were randomly divided into 4 groups:normal control group,EAE group,EAE group plus low dose edar-avone group,EAE group plus large dose of edaravone group(n = 18).Normal group were subcutaneously injected saline water.The EAE model were established with self-made complete antigen,then the small(4mg/kg o d) and large(10mg/kg o d) doses of edaravone were given according the experimental protocol.The incidence and the scores of neurologic impairment were recorded,also the HE staining,the inducible nitro oxide synthase(iNOS) and Osteopontin(OPN) immunohistochemistry staining were performed and analyzed.Results:After the treatment of edaravon,the incidence and scores of neurologic impairment were significantly decreased(P0.05).HE staining showed that the edaravone group with alleviation of inflammatory reaction and degree of injury.Either low or large-dose edaravone group,the expression of iNOS,OPN was significantly less than the EAE group(P0.05).In large-dose edaravone group,the expres-sion of iNOS and OPN was significantly lower than low-dose edaravone group(P0.05).Conclusion:The results suggested that Edar-avone have protective role on EAE,which maybe related to the inhibition of microgliacyte activation,alleviation of inflammatory reac-tion and reduction of iNOS and OPN expression.
出处 《现代生物医学进展》 CAS 2011年第4期680-683,共4页 Progress in Modern Biomedicine
关键词 实验性自身免疫性脑脊髓炎 依达拉奉 诱导型一氧化氮合酶 骨桥蛋白 大鼠 Experimental autoimmune encephalomyelitis Edaravone Inducible nitro oxide synthase Osteopontin Rat
  • 相关文献

参考文献17

  • 1O'Connor KC, Roy SM, Becker CH, et al. Comprehensive phenotyping in multiple sclerosis: discovery based proteomics and the current understanding of putative biomarkers [J]. Disease Marker, 2006,22(4): 213-225.
  • 2Levine S M, ChakrabartyA. The role of iron in the pathogenesis of experimental allergic encephalomyelitis and multiple sclerosis [J].Ann NY Acad Sei, 2004,1012:252-266.
  • 3Takayasu Y, Nakaki J, Kawasaki T, et al. Edaravone, a radical scavenger, inhibits mitochondrial permeability transition pore in rat brain [J]. J Pharmacol Sci, 2007,103(4):434-437.
  • 4Kotani Y, Ishino K, Osaki S, et al. Efficacy ofMCI-186, a free-radical scavenger and antioxidant, for resuscitation of nonbeating donor hearts[J]. J Thorac Cardiovasc Surg, 2007, 133(6): 1626-1632.
  • 5Mancardi G, Hart BA, Capello E, et al. Restricted immune responses lead to CNS demyelination and axonal damage [J]. J Neuroimmunol, 2000,107(2): 178-183.
  • 6Zhang JF, Stephen H, Sinclair, et al. The Ministry of Science and Technology of the People's Republic of China. Guidance Suggestions for the Care and Use of Laboratory [J] Animals, 2006, 22 (11):2701-2708.
  • 7Banno M, Mizuno T, Kato H,et al. The radical scavenger edaravone prevents oxidative neurotoxicity induced by peroxynitrite and activatedmicroglia[J]. Neuropharmacology, 2005,48 (2) :283-290.
  • 8Sergei V, Gwen S, Tatiana M, et al. Comparison of uric acid and ascorbic acid in protection against EAE [J]. Free Radic Biol Med, 2002,33(10):1363-1371.
  • 9Hooper DC, Scott GS, Zborek A, et al. Uric acid, a peroxynitrite scavenger, inhibits CNS inflammation, blood-CNS barrier permeability changes, and tissue damage in a mouse model of multiple sclerosis [J]. FASEB-J, 2000,14(5):691-698.
  • 10Zhang N, Komine-Kobayashi M, Tanaka R, et al. Edaravone reduces early accumulation of oxidative products and sequential inflammatory responses after transient focal ischemia in mice brain [J]. Stroke, 2005,36 (10):2220-2225.

同被引文献31

引证文献3

二级引证文献6

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