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糖尿病对血-视网膜屏障超微结构影响的研究进展
引用本文:周媛,崔浩,刘洪涛,张丽琼. 糖尿病对血-视网膜屏障超微结构影响的研究进展[J]. 国际眼科杂志, 2014, 14(7): 1220-1222
作者姓名:周媛  崔浩  刘洪涛  张丽琼
作者单位:中国黑龙江省哈尔滨市,哈尔滨医科大学附属第一医院;中国黑龙江省哈尔滨市,哈尔滨医科大学附属第一医院;中国黑龙江省哈尔滨市,哈尔滨医科大学附属第一医院;中国黑龙江省哈尔滨市,哈尔滨医科大学附属第一医院
基金项目:黑龙江省自然科学基金项目(No.D200949); 黑龙江省教育厅科学技术研究项目(No.11541219); 黑龙江省卫生厅科研项目(No.2007-222); 哈尔滨市科技局资助项目(No.2007RFQXS090)
摘    要:糖尿病视网膜病变(diabeticretinopathy,DR)是全世界最主要的致盲性眼病,也是最严重和最常见的微血管病变之一。糖尿病可造成血一视网膜屏障的损害引起血管源性水肿和神经组织损伤,造成视力下降。内层血-视网膜屏障主要是由视网膜毛细血管内皮细胞的紧密连接构成,此屏障阻碍血液的渗透及内源性物质和外源性物质在视网膜中的自由扩散,使视网膜保持恒定的环境,有效的供应营养物质。糖尿病患者的视网膜中由于细胞因子、生长因子、晚期糖基化终产物、炎症、高血糖症和周细胞丢失的增加,导致视网膜血管内皮细胞通透性增加。本文就糖尿病所引起的血-视网膜屏障超微结构改变进行综述。

关 键 词:糖尿病  血-视网膜内屏障  超微结构
收稿时间:2014-03-11
修稿时间:2014-06-11

Research progress of diabetes on the ultrastructure of blood retina barrier
Yuan Zhou,Hao Cui,Hong-Tao Liu and Li-Qiong Zhang. Research progress of diabetes on the ultrastructure of blood retina barrier[J]. International Eye Science, 2014, 14(7): 1220-1222
Authors:Yuan Zhou  Hao Cui  Hong-Tao Liu  Li-Qiong Zhang
Affiliation:The First Affiliated Hospital of Harbin Medical University, Harbin 150000, Heilongjiang Province, China;The First Affiliated Hospital of Harbin Medical University, Harbin 150000, Heilongjiang Province, China;The First Affiliated Hospital of Harbin Medical University, Harbin 150000, Heilongjiang Province, China;The First Affiliated Hospital of Harbin Medical University, Harbin 150000, Heilongjiang Province, China
Abstract:Diabetic retinopathy is a major cause of blindness all over the world, and it is one of the most serious and common microvascular complications of diabetes. Breakdown of the endothelial blood-retinal barrier(BRB), as occurs in diabetic retinopathy, result in vasogenic edema and neural tissue damage, causing loss of vision. The inner BRB is created by complex tight juctions of retinal capillary endothelial cells, this barrier prevents the free diffusion of substances between the circulating blood and the neural retinal, the inner BRB efficiently supplies nutrients to the retinal and removes endobiotics and xenobiotics from the retina to maintain a constant milieu in the neural retina. The central mechanism of altered inner BRB function is a change in the permeability characteristics of retinal endothelial cells caused by elevated levels of cytokines, growth factors, advanced glycation end products, inflammation, hyperglycema and loss of pericytes. This article reviews the relationship between diabetes and the ultrastructure changes of BRB.
Keywords:diabetic retinopathy   inner blood-retinal barrier   ultrastructure
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