期刊文献+

神经生长因子受体trkA在EAE模型中的表达及PG490的作用 被引量:1

Expression of trkA and role of PG490 on its expression in experimental autoimmune encephalomyelitis models
原文传递
导出
摘要 目的通过测定神经生长因子受体trkA在实验性变态反应性脑脊髓炎(EAE)模型中的含量变化以及探讨PG490在其中的作用和作用途径。方法48只新西兰兔在已建立EAE模型的基础上按随机数字表法分为3组,即模型组、PG490干预组1(首次发病期给予干预)及PG490干预组2(复发期给予干预)。采用ELISA法检测各组动物脑组织中trkA蛋白含量变化,并观察和比较各组临床学评分变化。结果EAE模型发病是呈缓解复发的过程,干预组其平均临床评分均较模型组明显降低,差异有统计学意义(P〈0.05)。PG490干预组1trkA蛋白含量与模型组相比较差异无统计学意义(P〉0.05);PG490干预组2trkA蛋白含量与模型组相比较差异有统计学意义(P〈0.05)。结论PG490能够通过调节神经生长因子受体trkA含量减轻EAE模型的临床症状。 Objective To determine the changes of NGF receptor trkA content and investigate the role and the pathway of PG490 on trkA expression in experimental autoimmune encephalomyelitis (EAE) models. Methods Fourty-eight rabbit models were induced and randomized into model group, PG490 intervention group 1 (giving PG490 at the onset) and PG490 intervention group 2 (giving PG490 at the recurrence). The clinical scores and pathological changes were observed and the expression changes of trkA in the brain tissue were tested by ELISA methods before and after the treatment with PG490. Results The recurrence in the model group was an extremely slow process. The mean clinical scores in the PG490 intervention groups were significantly lower as compared with those in the model group (P〈 0.05). No obvious differences of the trkA content were found between the model group and the PG490 intervention group 1 (P〉0.05); however, significant differences of the trkA content were noted between the model group and the PG490 intervention group 2 (P〈0.05). Conclusion PG490 can improve the clinical symptoms in EAE models by adjusting the trkA content.
出处 《中华神经医学杂志》 CAS CSCD 北大核心 2010年第3期250-252,257,共4页 Chinese Journal of Neuromedicine
基金 基金项目:广东省中医药局科技项目(2007144):广东省自然科学基金(8151018201000036) 广东省科技计划基金(20098030801363)
关键词 神经生长因子受体 实验性变态反应性脑脊髓炎 PG490 Neurotrophic factor receptor Experimental allergic encephalomyelitis PG490
  • 相关文献

参考文献5

二级参考文献36

共引文献57

同被引文献15

  • 1毕晓莹,丁素菊,黎佳思,陶沂,曹莉,张勇.神经干细胞-脑源性神经营养因子基因工程细胞移植对大鼠缺血性脑损伤的治疗作用[J].中华神经科杂志,2007,40(4):275-279. 被引量:3
  • 2Lu B.BDNF and activity-dependent synaptic mod? Lation[J].Learn Mem,2003,10(2):86-98. 被引量:1
  • 3Escobar ML,Figueroa-Guzman Y,Gomez-Palacio-Schjetnan A.In vivo ius?Lar cortex LTP induced by brain-derived neurotrophic factor[J].Brain Res,2003,991(1-2):274-279. 被引量:1
  • 4Halbach OB.Involvement of BDNF in age-dependent alterations in the hippocampus[J].Front Aging Neurosci,2010,13; 2.pii:36. 被引量:1
  • 5Poo MM.Neurotrophins as synaptic mod?Lators[J].Nat Rev Neurosci,2001,2(1):24-32. 被引量:1
  • 6Peng S,Wuu J,Mufson EJ,et al.Precursor form of brain-derived neurotrophic factor and mature brain-derived neurotrophic factor are decreased in the pre-clinical stages of Alzheimer's disease[J].J Neurochem,2005,93(6):1412-1421. 被引量:1
  • 7Michalski B,Fahnestock M.Pro-brain-derived neurotrophic factor is decreased in parietal cortex in Alzheimer's disease[J].Brain Res Mol Brain Res,2003,111(1-2):148-154. 被引量:1
  • 8Tapia-Arancibia L,Rage F,Givalois L,et al.Physiology of BDNF:focus on hypothalamic function[J].Front Neuroendocrinol,2004,25(2):77-107. 被引量:1
  • 9Zuccato C,Cattaneo E.Brain-derived neurotrophic factor in neurodegenerative diseases[J].Nat Rev Neurol,2009,5(6):311-322. 被引量:1
  • 10Laske C,Stransky E,Leyhe T,et al.Stage-dependent BDNF serum concentrations in Alzheimer's disease[J].J Neural Transm,2006,113(9):1217-1224. 被引量:1

引证文献1

二级引证文献9

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