期刊文献+

神经血管关系在早产儿视网膜病中的研究进展 被引量:1

暂未订购
导出
摘要 传统理论认为早产儿视网膜病变(ROP)属于一种纤维血管增殖性疾病,高浓度氧是其主要诱因,发生过程可分为暴露于高氧时的血管闭塞消失期及继发的血管增生期.但实际上它也是视网膜的一种神经变性疾病。ROP早期,甚至在血管并发症出现之前,视网膜神经细胞的改变已经发生.主要为大胶质细胞反应性增生、小胶质细胞激活及神经细胞凋亡的增加。为了调节血流量以适应组织需要,除了受血管内皮细胞的控制外,视网膜血管还受神经和胶质细胞的调节.而脉络膜血管还受自主神经调节。神经和胶质细胞还可产生NO、乳酸盐、花生四烯酸代谢物等来影响血流量。因此.视网膜神经和胶质细胞的损伤不但直接影响视力,还会进一步加重血管病变.继而形成恶性循环.加速ROP的进程。
作者 张素娥
出处 《现代医药卫生》 2009年第18期2810-2811,共2页 Journal of Modern Medicine & Health
  • 相关文献

参考文献17

  • 1Flammer J, Mozaffarieh M. Autoregulation, a balancing act between supply and demand[J].Can J Ophthalmol,2008,43(3):317.
  • 2Poumaras C J, Rungger-Brandle E, Riva CE,et al. Regulation of retinal blood flow in health and disease[J].Prog Retin Eye Res.2008,27 (3):284.
  • 3Michael ID,Edith A,Martin F.Retinal Vascular Development Is Mediated by Endothelial Filopodia, a Preexisting Astrocytic Template and Specific R-Cadherin Adhesion[J].Investigative Ophthalmology and Visual Science ,2002,43:3500.
  • 4赵晓萍,陈燕,姚怡心,李西华,沈淑坤,陆振虞.免疫荧光法检测氧诱导小鼠视网膜的病变[J].现代生物医学进展,2008,8(5):810-813. 被引量:1
  • 5Choi YK,Kim JH,Kim WJ,et al. AKAP12 regulates human bloodretinal barrier formation by downregulation of hypoxia-inducible factor- lalpha[J].Neurosci.2007,27(16) :4472.
  • 6梁文英,蒋犁.血管生长刺激因子与早产儿视网膜病的关系[J].中国实用儿科杂志,2008,23(1):67-69. 被引量:3
  • 7Portillo JA,Van Grol J,Zheng L,et al.CD40 mediates retinal inflammation and neurovaseular degeneration[J].Immunol, 2008,181 ( 12): 8719.
  • 8Downie LE ,Pianta MJ ,Vingrvs AJ.et al.AT1 receptor inhibition prevents astrocyte degeneration and restores vascular growth in oxygeninduced retinopathy[J].Glia,2008,56(10) : 1076.
  • 9王爱玲,吴玲玲.视网膜小胶质细胞与眼科疾病[J].国外医学(眼科学分册),2004,28(6):418-421. 被引量:6
  • 10Matthew RR, Eyal B, Stacey KM. Myeloid progenitors differentiate into microglia and promote vascular repair in a model of ischemic retinopathy[J].Clin Invest, 2006,116(12) : 3266.

二级参考文献53

  • 1罗先琼,柳国胜,赖日权,聂川,吴坤河,田野,夏明翰,康举龄.血管内皮生长因子及其受体在早产儿视网膜病大鼠模型中的表达和作用[J].中华儿科杂志,2004,42(7):511-515. 被引量:16
  • 2石文静,陈超,王玉环,肖虹蕾,周国民.不同吸氧浓度和时间在新生小鼠视网膜病发病中的作用[J].中华儿科杂志,2007,45(1):14-19. 被引量:6
  • 3Navascues J, Moujahid A, Almendros A, et al. Origin of microglia in the quail retina: central-to-peripheral and vitreal-to-scleral migration of microglial precursors during development. J Comp Neurol,1995, 354: 209-228.
  • 4Hageman GS, Luthert PJ, Victor-Chong NH, et al. An integrated hypothesis that considers drusen as biomarkers of immune-mediated processes at the RPE-Bruch's membrane interface in aging and agerelated macular degeneration. Prog Retin Eye Res, 2001, 20:705-
  • 5Wierzba-Bobrowicz T, Schmidt-Sidor B, Gwiazda E, et al. Major histocompatibility complex class Ⅱ expression in the frontal and temporal lobes in the human fetus during development. Folia Neuropathol, 2000, 38: 73-77.
  • 6Chen A, Kumar SM, Sahley CL, et al. Nitric oxide influences injury-induced microglial migration and accumulation in the leech CNS.J Neurosci, 2000 , 20: 1036-1043.
  • 7Kreutzberg GW. Microglia: a sensor for pathological events in the CNS. Trends Neurosci, 1996, 19: 312-318.
  • 8Moore P, El-sherbeny A , Roon P, et al. Apoptosis cell death in the mouse retinal ganglion cell layer is induced in vivo by the excitatory amino acid homocysteine. Exp Eye Res, 2001, 73: 45-57.
  • 9Brownlee M. Biochemistry and molecular cell biology of diabetic complications. Nature, 2001, 414(6865): 813-820.
  • 10Ryu JK, Nagai A, Kim J, et al. Microglial activation and cell death induced by the mitochondrial toxin 3-nitropropionic acid: in vitro and in vivo studies. Neurobiol Dis, 2003 , 12: 121-132.

共引文献16

同被引文献7

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