期刊文献+

外源性脑源性神经营养因子对急性高眼压后大鼠视网膜磷酸化TrkB表达的影响 被引量:4

Expression of phosphorylated-TrkB receptor in rat retina following acute high intraocular pressure pretreated with BDNF
下载PDF
导出
摘要 目的:检测脑源性神经营养因子(BDNF)干预对急性高眼压后大鼠视网膜磷酸化TrkB(p-TrkB)表达变化的影响。方法:成年大鼠随机分为单纯高眼压组、BDNF预处理高眼压组和溶媒预处理高眼压组,BDNF预处理高眼压组和溶媒预处理高眼压组动物左眼于加压前2d分别给予BDNF预处理或溶媒,右眼设为正常对照。各组动物左眼眼压升高至闪光视网膜电图b波消失的临界眼压并维持60min,动物分别存活1、3、7、14d后处死,冷冻切片行p-TrkB的免疫组织化学显色。结果:单纯高眼压组急性高眼压后p-TrkB的表达显著下调;溶媒预处理高眼压组实验结果与单纯急性高眼压组相似;BDNF预处理高眼压组p-TrkB的表达随再灌时间的延长进行性下调,但在各时间点的表达均显著高于单纯高眼压组。结论:外源性BDNF干预部分缓解了急性高眼压后视网膜p-TrkB表达的下调,对急性高眼压后的大鼠视网膜起到一定的保护作用。 Objective: To investigate the expression of p-TrkB in rat retina following acute high intraocular pressure (HIOP) with BDNF pretreatment. Methods : Seventy-two adult rats were randomly divided into acute HIOP group, BDNF pretreated HIOP group and vehicle pretreated HIOP group. The left eyes of rats in BDNF pretreated HIOP group and vehicle pretreated HIOP group were injected with BDNF or vehicle respectively 2 days before HIOP. The intraocular pressure of all left eyes was increased until b wave of flash electroretinogragh (fERG) disappeared and such pressure maintained for 60 minutes. All the right eyes were served as normal control. The rats were sacrificed after a survival of 1, 3, 7 or 14 days. Immunohistochemistry was used to detect the expression of p-TrkB. Results : Compared with the normal control group, the expression of p-TrkB was decreased significantly during reperfusion in the acute HIOP group. The expression of p-TrkB during reperfusion in the vehicle control group was similar to that in the acute HIOP group. In the BDNF pretreated HIOP group, the expression of p-TrkB was also decreased, but significantly higher than that in the acute HIOP group at all time points. Conclusion: Down-regulation of p-TrkB following HIOP was relieved by exogenous BDNF, which may be involved in the protection role of BDNF to the injuried retina following HIOP.
出处 《解剖学杂志》 CAS CSCD 北大核心 2008年第3期368-371,共4页 Chinese Journal of Anatomy
基金 国家自然科学基金(30100098 30570979)
关键词 急性高眼压 脑源性神经营养因子 磷酸化TrkB 视网膜 acute high intraocular pressure brain derived neurotrophic factor phosphorylated TrkB retina
  • 相关文献

参考文献11

  • 1黄菊芳,蒋丽珠,童建斌,陈旦,熊鲲,曾乐平.脑源性神经营养因子预处理后急性高眼压下大鼠视网膜TrkB的表达变化[J].解剖学杂志,2006,29(6):734-737. 被引量:7
  • 2熊鲲,黄菊芳,童建斌,陈旦,潘爱华,罗学港.急性大鼠眼高压诱导的不同缺血/再灌内层视网膜的变化[J].解剖学杂志,2005,28(1):46-49. 被引量:21
  • 3Lom B, Cogen J, Sanchez A L, et al. Local and target-derived brain-derived neurotrophic factor exert opposing effects on the dendritic arborization of retinal ganglion cells in vivo [J]. J Neurosci, 2002,22(17) :7639-7649.
  • 4Mansour-Robaey S, Clarke D B, Wang Y C, et al. Effects of ocular injury and administration of brain-derived neurotrophic factor on survival and regrowth of axotomized retinal ganglion cells [J]. Proc Natl Acad Sci USA, 1994,91(5):1632-1636.
  • 5王慧,刘求理,罗学港,文建亚.脑源性神经营养因子对高眼压后视网膜节细胞的保护作用[J].解剖学研究,2002,24(2):119-122. 被引量:12
  • 6Ikeda K, Tanihara H, Honda Y, et al. BDNF attenuates retinal cell death caused by chemically induced hypoxia in rats[J]. Invest Ophthalmol Vis Sci, 1999,40(9):2130-2140.
  • 7Di Polo A, Aigner L J, Dunn R J, et al. Prolonged delivery of brain-derived neurotrophic factor by adenovirus-infected Muller cells temporarily rescues injured retinal ganglion cells[J]. Proc Natl Acad Sci USA, 1998,95(7) : 3978-3983.
  • 8Cheng L, Sapieha P, Kittlerova P, et al. TrkB gene transfer protects retinal ganglion cells from axotomy-induced death in vivo [J]. J Neurosci, 2002,22(10) :3977-3986.
  • 9Kohler K D, Cellerino A, Guenther E, et al. Expression of Ca^2+ - binding proteins is reduced in retinal neurons of BDNF-knockout mice[J]. Invest Ophthalmol Vis Sci, 2001,42(Suppl):4017.
  • 10Steinbeck J A, Methner A. Translational downregulation of the noncatalytic growth factor receptor TrkB. T1 by ischemic preconditioning of primary neurons [J]. Gene Expr, 2005, 12 (2): 99-106.

二级参考文献37

  • 1[1]Caprioli J. The susceptible optic nerve in glaucoma: Avenues for neuroprotection. Ophthalmic Practice(Asian Edition) 1996,2:144.
  • 2[2]Castillo BJr, delCerro M, Breakefield XO, et al. Retinal ganglion cell survival is promoted by genetically modified astrocytes designed to secrete brain-derived neurotrophic factor (BDNF). Brain Res, 1994,647:30~36.
  • 3[3]Peinado-Ramon P, Salvador M, Perez V, et al. Effects of axotomy and intraocular administration of NT-4、NT-3 and BDNF on the survival of adult rat retinal ganglion cells: a quantitative in vivo study. Invest Ophthalmol Vis Sci,1996,37:489 ~ 500.
  • 4[4]Sawai H, Clarke DB, Kittlerova P, et al. Brain-derived neurotrophic factor and neurotrophin-4/5 stimulate growth of axonal branches from regenerating retinal ganglion cells. J Neurosci, 1996,16:3887~3894.
  • 5[5]Ko M, Hu D, Ritch R, et al. Patterns of retinal ganglion cell survival after brain-derived neurotrophic factor administration in hypertensive eyes of rats. Neurosci Lett, 2001,305:139~142.
  • 6[6]Ko M, Hu D, Ritch R, et al. The combined effect of brainderived neurotrophic factor and a free radical scavenger in experimental glaucoma. Invest Ophthalmol Vis Sci,2000, 41:2967~2971.
  • 7[7]Pease ME, McKinnon SJ, Quigley HA, et al. Obstructed axonal trasport of BDNF and its receptor TrkB in experimental glaucoma. Invest Ophthalmol Vis Sci, 2000,41:764~774.
  • 8[8]Quigley HA, McKinnon SJ, Zack DJ, et al. Retrograde axonal transport of BDNF in retinal ganglion cells is blocked by acute IOP elevation in rats. Invest Ophthalmol Vis Sci,2000,41:3460~3466.
  • 9[9]Kalogeropoulos C, Donati G, Pizzolato GP, et al. Morphology of early retinal lesions after experimental venous occlusion. Klin Monatsbl Augenheilkd, 1996,208:375~376.
  • 10[10]Kerrigan LA, Zack DJ, Quigley HA, et al. TUNEL-positive ganglion cells in human primary open-angle glaucoma. Arch Ophthalmol, 1997,115:1031~1035.

共引文献27

同被引文献66

引证文献4

二级引证文献7

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