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视网膜新生血管的药物治疗研究进展 被引量:2

Advance in medicine therapy for retinal neovascularization
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摘要 全身或局部的病变可导致血—视网膜屏障破坏、血液微循环障碍和血管通透性改变,进一步引起视网膜缺氧,乃至水肿,随之视网膜组织对缺氧发生一系列代偿性反应,在各种细胞因子、细胞内外调控机制的共同作用下生成新生血管,目的是补偿缺血缺氧的视网膜。视网膜新生血管相关疾病包括糖尿病性视网膜病变、视网膜静脉周围炎、早产儿视网膜病变等。抑制新生血管生长是治疗这类疾病的关键。本文对抑制视网膜新生血管药物的研究进展作一综述。 The systemic or partial body diseases may cause the damage to the blood-retinal barrier, blood microcirculation and vessel permeability. Furthermore,they lead to retinal anoxia and edema. Then retinal tissue has a series of compensatory response to the anoxia and neovascularization, which aims to nourish the retina that is deficient in blood and oxygen. The diseases related to retinal neovascularization include diabetic retinopathy, retinal periphlebitis, retinopathy of prematurity, etc. The key to treating these diseases is to inhibit the development of the neovascularization. This paper reviewed the progress in medicine therapy for inhibiting retinal neovascularization.
出处 《国际眼科杂志》 CAS 2008年第2期358-360,共3页 International Eye Science
关键词 视网膜新生血管 药物 治疗 retinal neovascularization medicine treat-ment
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  • 1[4]Alexander JP, Samples JR, Acott TS, et al. Growth factor and cytokine modulation of trabecular meshwork matrix metalloproteinase and TIMP expression. Curr Eye Res, 1998,17 ( 3 ): 276 被引量:1
  • 2[5]Di Girolamo N,Verma M J, McCluskey PJ, et al. Increased matrix metalloproteinases in the aqueous humor of patients and experimental animals with uveitis. Curr Eye Res, 1996,15(10): 1060 被引量:1
  • 3[6]Das A, McGuire PG, Eriqat C, et al. Human diabetic neovascular membranes contain high levels of urokinase and metalloproteinase enzymes.Invest Ophthalmol Vis Sci, 1999,40( 3 ): 809 被引量:1
  • 4[7]Russell SR, Hageman GS. Insoluble interphotoreceptor matrix in human vitreous after rhegmatogenous retinal detachment. Am J Ophthalmol,1997,123 ( 3 ): 386 被引量:1
  • 5[8]Fini ME,Girard MT,Matsubara M,et al. Unique regulation of the matrix metalloproteinase, gelatinase B. Invest Ophthalmol Vis Sci, 1995,36 (3):622 被引量:1
  • 6[9]Wiedemann P. Growth factors in retinal diseases: roliferative vitreoretinopathy, proliferative diabetic retinopathy, and retinal degeneration. Surv Ophthalmol, 1992,36 ( 5 ): 373 被引量:1
  • 7[10]Pournaras C J, Miller JW,Gragoudas ES,et al. Systemic hyperoxia decreases vascular endothelial growth factor gene expression in ischemic primate retina. Arch Ophthalmol, 1997,115 ( 12 ): 1553 被引量:1
  • 8[11]Wang H, Keiser JA. Vascular endothelial growth factor upregulates the expression of matrix metalloproteinases in vascular smooth muscle cells: role of flt-1. Circ Res,1998,83(8): 832 被引量:1
  • 9[12]Wojtowicz-Praga S,Torri J,Johnson M ,et al. Phase I trial of Marimastat,a novel matrix metalloproteinase inhibitor, administered orally to patients with advanced lung cancer. J Clin Oncol, 1998,16 ( 6 ): 2150 被引量:1
  • 10[1]Pepper MS,Belin D, Montesano R, et al. Transforming growth factor b-1 modulates basic growth factorinduced proteolytic and angiogenic properties of endothelial cells in vitro. J Cell Biol, 1990, 1 1: 743 被引量:1

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