Vascular endothelial growth factor and diabetic retinopathy: pathophysiological mechanisms and treatment perspectives

被引:234
作者
Caldwelll, RB [1 ]
Bartoli, M
Behzadian, MA
El-Remessy, AEB
Al-Shabrawey, M
Platt, DH
Caldwell, RW
机构
[1] Med Coll Georgia, Vasc Biol Ctr, Dept Cellular Biol & Anat, Dept Ophthalmol, Augusta, GA 30912 USA
[2] Med Coll Georgia, Dept Cellular Biol & Anat, Augusta, GA 30912 USA
[3] Med Coll Georgia, Dept Pharmacol & Toxicol, Augusta, GA 30912 USA
[4] Med Coll Georgia, Dept Ophthalmol, Augusta, GA 30912 USA
[5] Med Coll Georgia, Dept Pathol, Augusta, GA 30912 USA
关键词
diabetic retinopathy; retina; vascular endothelial growth factor; angiogenesis; vascular permeability; reactive oxygen species;
D O I
10.1002/dmrr.415
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Retinal neovascularization and macular edema are central features of diabetic retinopathy, the major cause of blindness in the developed world. Current treatments are limited in their efficacy and are associated with significant adverse effects. Characterization of the molecular and cellular processes involved in vascular growth and permeability has led to the recognition that the angiogenic growth factor and vascular permeability factor vascular endothelial growth factor (VEGF) plays a pivotal role in the retinal microvascular complications of diabetes. Therefore, VEGF represents an exciting target for therapeutic intervention in diabetic retinopathy. This review highlights the current understanding of the mechanisms that regulate VEGF gene expression and mediate its biological effects and how these processes may become altered during diabetes. The cellular and molecular alterations that characterize experimental models of diabetes are considered in relation to the influence of high glucose-mediated oxidative stress on VEGF expression and on the mechanisms of VEGF's actions under hyperglycemic induction. Finally, potential therapeutic strategies for preventing VEGF overexpression or blocking its pathological effects in the diabetic retina are considered. Copyright (C) 2003 John Wiley Sons, Ltd.
引用
收藏
页码:442 / 455
页数:14
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