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Investigation of corneal endothelial changes post selective laser trabeculoplasty
Author(s) -
Leahy Kate E,
Madigan Michele C,
Sarris Maria,
Watson Stephanie L,
McCluskey Peter,
White Andrew JR
Publication year - 2018
Publication title -
clinical and experimental ophthalmology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.3
H-Index - 74
eISSN - 1442-9071
pISSN - 1442-6404
DOI - 10.1111/ceo.13172
Subject(s) - immunostaining , medicine , haematoxylin , ophthalmology , staining , cornea , tight junction , endothelium , pathology , endothelial stem cell , immunohistochemistry , chemistry , microbiology and biotechnology , biology , in vitro , biochemistry
Importance Transient corneal endothelial changes are routinely noted on slit‐lamp examination immediately following selective laser trabeculoplasty (SLT). Background To determine the mechanism of transient corneal endothelial changes observed following SLT. Design University laboratory‐based observational study. Samples Ten corneas from six human cadaveric donors. Methods Corneas were treated with SLT, direct laser or peroxide, or used as controls. Haematoxylin and eosin staining and immunolabelling for zonula occludens‐1 (ZO‐1) and beta‐catenin were performed. Main Outcome Measures Histological appearance; ZO‐1 and beta‐catenin immunostaining. Results There were no differences in histological features between SLT‐treated and control corneas. Corneas treated with SLT or peroxide showed reduced and less regular ZO‐1 immunofluorescence along cell membranes compared with ZO‐1 expression in controls. These changes were generalized across the endothelium. There was no effect on the ZO‐1 immunostaining after direct laser. There was no difference in beta‐catenin immunostaining patterns between control, SLT and peroxide‐treated corneas. Conclusions and Relevance Altered ZO‐1 immunostaining may represent disassembly of tight junctions between corneal endothelial cells. The similarity of our findings between SLT‐treated and peroxide‐treated corneas suggests that both conditions trigger changes at the level of endothelial tight junctions, perhaps triggered by liberation of free radicals as previously proposed.