视网膜积液和血-视网膜屏障破裂的机制。

Developments in ophthalmology Pub Date : 2017-01-01 Epub Date: 2017-03-28 DOI:10.1159/000455265
José Cunha-Vaz
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引用次数: 39

摘要

黄斑水肿是人视网膜中央部分的肿胀,它与视网膜厚度增加有关。它可以简单地定义为视网膜组织内液体过量。必须认识到,正常视网膜具有功能性的细胞外空间。关于视网膜的细胞外体积,很少有生理学研究,但有报道的值为大脑的24.8%和小脑的23.6%。人们普遍认为视网膜细胞外空间类似于大脑。人们普遍认为,黄斑水肿和视网膜积液的直接原因是血视网膜屏障(BRB)的破坏。当BRB破裂时,视网膜水肿可以根据毛细血管过滤的基本原理(Starling定律)来解释。因此,影响视网膜水肿形成的主要因素是BRB渗透性、毛细血管静水压力、组织静水压力、组织渗透压和血浆渗透压。视网膜色素上皮的主动转运是清除眼压下视网膜渗水所必需的,也是疾病中防止液体积聚的安全机制。临床评估BRB和视网膜水肿可以通过一种基于oct的方法进行无创评估,该方法可以识别和量化BRB改变的部位,并通过绘制低光学反射率的部位,即视网膜细胞外液的变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mechanisms of Retinal Fluid Accumulation and Blood-Retinal Barrier Breakdown.

Macular edema is the swelling of the central portion of the human retina and it is associated with increased retinal thickness. It can be simply defined as an excess of fluid within the retinal tissue. It must be realized that the normal retina possesses a functional extracellular space. With regard to the extracellular volume of the retina, there have been few physiologic studies, but there are reported values of 24.8% for the cerebrum and 23.6% for the cerebellum. It is accepted that the retinal extracellular space is similar to the brain. It is generally agreed that the proximate cause of macular edema and retinal fluid accumulation is a breakdown of the blood-retinal barrier (BRB). When there is a breakdown of the BRB, retinal edema can be interpreted in terms of basic principles of capillary filtration (Starling's law). Therefore, the main factors influencing retinal edema formation are BRB permeability, capillary hydrostatic pressure, tissue hydrostatic pressure, tissue osmotic pressure, and plasma osmotic pressure. Active transport by the retinal pigment epithelium is necessary to remove water that percolates through the retina from intraocular pressure and is also as a safety mechanism against fluid accumulation in disease. Clinical evaluation of the BRB and retinal edema can be performed noninvasively by using an OCT-based method designated OCT-Leakage, which is capable of identifying and quantifying sites of alteration of the BRB, and by mapping sites of low optical reflectivity, i.e., changes in the retinal extracellular fluid.

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