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Ocular toxicity of intravitreal golimumab in a rabbit model

BACKGROUND/AIM: To investigate the effect of intravitreal golimumab on rabbit retina histopathology. MATERIALS AND METHODS: Sixteen albino New Zealand rabbits were divided into three groups. The right eye of each rabbit in groups I, II, and III received a single intravitreal injection of 5 mg/0.05 m...

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Autores principales: DURMAZ ENGİN, Ceren, CİLAKER MIÇILI, Serap, YILMAZ, Osman, BAĞRIYANIK, Alper, ERGÜR, Bekir Uğur, ÖNEN, Fatoş, SAATCİ, Ali Osman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Scientific and Technological Research Council of Turkey 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7379407/
https://www.ncbi.nlm.nih.gov/pubmed/32151118
http://dx.doi.org/10.3906/sag-1911-11
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author DURMAZ ENGİN, Ceren
CİLAKER MIÇILI, Serap
YILMAZ, Osman
BAĞRIYANIK, Alper
ERGÜR, Bekir Uğur
ÖNEN, Fatoş
SAATCİ, Ali Osman
author_facet DURMAZ ENGİN, Ceren
CİLAKER MIÇILI, Serap
YILMAZ, Osman
BAĞRIYANIK, Alper
ERGÜR, Bekir Uğur
ÖNEN, Fatoş
SAATCİ, Ali Osman
author_sort DURMAZ ENGİN, Ceren
collection PubMed
description BACKGROUND/AIM: To investigate the effect of intravitreal golimumab on rabbit retina histopathology. MATERIALS AND METHODS: Sixteen albino New Zealand rabbits were divided into three groups. The right eye of each rabbit in groups I, II, and III received a single intravitreal injection of 5 mg/0.05 mL (6 eyes), 10 mg/0.1 mL (6 eyes), or 20 mg/0.2 mL (4 eyes) golimumab, while left eyes served as controls with the same volume of a balanced salt solution injection. All animals were examined using slit-lamp biomicroscopy and indirect ophthalmoscopy before and after intravitreal injection and at days 1 and 7. Animals were euthanized on day 7 and the eyes were enucleated for immunohistochemistry evaluation and electron microscopic examination of the retinas. RESULTS: For groups I, II, and III, the number of cells in the outer nuclear layer and the inner nuclear layer was decreased compared to those in the control groups. In group I, the percentage of caspase-3 staining of the outer nuclear layer was significantly higher than that in the control. For groups II and III, TUNEL and caspase-3 staining percentages in the outer and inner nuclear layers were found to be significantly higher than those for the control groups. In the ganglion cell layer, for groups I, II, and III, neither TUNEL nor caspase-3 staining percentages showed any significant difference between two groups. No significant dose-dependent relationship was found for increasing doses of golimumab in all layers. Myelin figures and karyorrhexis in the photoreceptor cells were prominent in electron microscopy of the golimumab-injected eyes. CONCLUSION: Golimumab caused apoptosis in both photoreceptors and bipolar cells of the rabbit retina. Potential retinal toxicity of intravitreal golimumab should be considered if an intravitreal administration is planned.
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spelling pubmed-73794072020-07-27 Ocular toxicity of intravitreal golimumab in a rabbit model DURMAZ ENGİN, Ceren CİLAKER MIÇILI, Serap YILMAZ, Osman BAĞRIYANIK, Alper ERGÜR, Bekir Uğur ÖNEN, Fatoş SAATCİ, Ali Osman Turk J Med Sci Article BACKGROUND/AIM: To investigate the effect of intravitreal golimumab on rabbit retina histopathology. MATERIALS AND METHODS: Sixteen albino New Zealand rabbits were divided into three groups. The right eye of each rabbit in groups I, II, and III received a single intravitreal injection of 5 mg/0.05 mL (6 eyes), 10 mg/0.1 mL (6 eyes), or 20 mg/0.2 mL (4 eyes) golimumab, while left eyes served as controls with the same volume of a balanced salt solution injection. All animals were examined using slit-lamp biomicroscopy and indirect ophthalmoscopy before and after intravitreal injection and at days 1 and 7. Animals were euthanized on day 7 and the eyes were enucleated for immunohistochemistry evaluation and electron microscopic examination of the retinas. RESULTS: For groups I, II, and III, the number of cells in the outer nuclear layer and the inner nuclear layer was decreased compared to those in the control groups. In group I, the percentage of caspase-3 staining of the outer nuclear layer was significantly higher than that in the control. For groups II and III, TUNEL and caspase-3 staining percentages in the outer and inner nuclear layers were found to be significantly higher than those for the control groups. In the ganglion cell layer, for groups I, II, and III, neither TUNEL nor caspase-3 staining percentages showed any significant difference between two groups. No significant dose-dependent relationship was found for increasing doses of golimumab in all layers. Myelin figures and karyorrhexis in the photoreceptor cells were prominent in electron microscopy of the golimumab-injected eyes. CONCLUSION: Golimumab caused apoptosis in both photoreceptors and bipolar cells of the rabbit retina. Potential retinal toxicity of intravitreal golimumab should be considered if an intravitreal administration is planned. The Scientific and Technological Research Council of Turkey 2020-06-23 /pmc/articles/PMC7379407/ /pubmed/32151118 http://dx.doi.org/10.3906/sag-1911-11 Text en Copyright © 2020 The Author(s) This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Article
DURMAZ ENGİN, Ceren
CİLAKER MIÇILI, Serap
YILMAZ, Osman
BAĞRIYANIK, Alper
ERGÜR, Bekir Uğur
ÖNEN, Fatoş
SAATCİ, Ali Osman
Ocular toxicity of intravitreal golimumab in a rabbit model
title Ocular toxicity of intravitreal golimumab in a rabbit model
title_full Ocular toxicity of intravitreal golimumab in a rabbit model
title_fullStr Ocular toxicity of intravitreal golimumab in a rabbit model
title_full_unstemmed Ocular toxicity of intravitreal golimumab in a rabbit model
title_short Ocular toxicity of intravitreal golimumab in a rabbit model
title_sort ocular toxicity of intravitreal golimumab in a rabbit model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7379407/
https://www.ncbi.nlm.nih.gov/pubmed/32151118
http://dx.doi.org/10.3906/sag-1911-11
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