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眼内新生血管形成。

Intraocular neovascularization.

作者信息

Yoshida A, Yoshida S, Ishibashi T, Inomata H

机构信息

Department of Ophthalmology, Faculty of Medicine, Kyushu University, Fukuoka, Japan.

出版信息

Histol Histopathol. 1999 Oct;14(4):1287-94. doi: 10.14670/HH-14.1287.

Abstract

An important character of the eye is transparency, so intraocular neovascularization, which is fragile and likely to result in hemorrhage, would cause a functional disorder of the eye and contribute to loss of vision associated with such diseases as retinopathy of prematurity, diabetic retinopathy, retinal vein occlusion, and age-related macular degeneration. Recently interest in the mechanisms of intraocular neovascularization has increased, and the mechanisms have been gradually elucidated using several in vitro and in vivo angiogenesis models. Blood vessels in the eye are composed of, and surrounded by, various types of cells that produce multiple factors. Neovascularization is regulated by complex interactions among these angiogenic factors, angiostatic factors, and adhesion molecules, and some of these angiogenesis-related molecules have also been suggested as new targets for novel therapeutic agents of intraocular neo-vascularization. This review focuses on in vivo representative angiogenesis models of the corneal pocket model and the model of oxygen-induced retinopathy, and discusses the role of some angiogenesis-related factors and adhesion molecules in intraocular neovascularization.

摘要

眼睛的一个重要特征是透明性,因此眼内新生血管形成,这种血管脆弱且容易导致出血,会引起眼睛的功能障碍,并导致与诸如早产儿视网膜病变、糖尿病视网膜病变、视网膜静脉阻塞和年龄相关性黄斑变性等疾病相关的视力丧失。最近,人们对眼内新生血管形成的机制的兴趣有所增加,并且已经使用几种体外和体内血管生成模型逐渐阐明了这些机制。眼睛中的血管由多种产生多种因子的细胞组成并被其包围。新生血管形成受这些血管生成因子、血管生成抑制因子和黏附分子之间复杂相互作用的调节,并且这些与血管生成相关的分子中的一些也已被提议作为眼内新生血管形成新型治疗药物的新靶点。本综述重点关注角膜袋模型和氧诱导性视网膜病变模型这两种体内代表性血管生成模型,并讨论一些与血管生成相关的因子和黏附分子在眼内新生血管形成中的作用。

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