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假性剥脱综合征中的血-房水屏障:通过内源性白蛋白免疫组织化学染色进行评估

Blood-aqueous barrier in pseudoexfoliation syndrome: evaluation by immunohistochemical staining of endogenous albumin.

作者信息

Küchle M, Vinores S A, Mahlow J, Green W R

机构信息

Wilmer Ophthalmological Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.

出版信息

Graefes Arch Clin Exp Ophthalmol. 1996 Jan;234(1):12-8. doi: 10.1007/BF00186513.

Abstract

BACKGROUND

Alterations of the integrity of the blood-aqueous barrier (BAB) are frequent findings in eyes with pseudoexfoliation syndrome (PSX).

METHODS

Immunohistochemical staining for the demonstration of albumin was used to analyze the BAB in 10 eyes with PSX without previous intraocular surgery and in 10 age-matched normal control eyes.

RESULTS

In eyes with PSX, small amounts of albumin were detected along the anterior surface of the iris in 7, in the anterior chamber in 1, along the ciliary epithelium in 4, and in the trabecular meshwork in 9 of 10 eyes. PSX material was also immunoreactive. In the 10 normal control eyes, albumin was detected anterior to the iris stroma in 1 eye, in the anterior chamber in 2 eyes, in the trabecular meshwork in 1 eye, but not internal to the ciliary epithelium.

CONCLUSIONS

Our findings indicate that impairment of the BAB in PSX can be localized at the level of the iris and, less frequently or to a lesser extent, at the level of the ciliary body.

摘要

背景

血-房水屏障(BAB)完整性改变是假性剥脱综合征(PSX)患者眼部常见的表现。

方法

采用免疫组织化学染色法检测白蛋白,分析10只未行过眼内手术的PSX患者眼及10只年龄匹配的正常对照眼的BAB。

结果

在PSX患者眼中,10只眼中有7只在虹膜前表面检测到少量白蛋白,1只在前房,4只在睫状体上皮,9只在小梁网。PSX物质也具有免疫反应性。在10只正常对照眼中,1只在虹膜基质前方、2只在前房、1只在小梁网检测到白蛋白,但在睫状体上皮内未检测到。

结论

我们的研究结果表明,PSX患者的BAB损伤可定位于虹膜水平,较少见或程度较轻的定位于睫状体水平。

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