Modeling the atrophy of retinal pigment epithelium

Purpose: to develop easy-to make and reproducible models of retinal pigment epithelium atrophy (RPE) and retinal degeneration using two types of solution (0.9 % sodium chloride and bevacizumab) and to evaluate these models using clinical instrumental and pathomorphological studies. Material and meth...

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Main Authors: N. V. Neroeva, V. V. Neroev, P. A. Ilyukhin, A. G. Karmokova, O. A. Losanova, M. V. Ryabina, A. M. Maybogin
Format: Article
Language:Russian
Published: Real Time Ltd 2020-12-01
Series:Российский офтальмологический журнал
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Online Access:https://roj.igb.ru/jour/article/view/520
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author N. V. Neroeva
V. V. Neroev
P. A. Ilyukhin
A. G. Karmokova
O. A. Losanova
M. V. Ryabina
A. M. Maybogin
author_facet N. V. Neroeva
V. V. Neroev
P. A. Ilyukhin
A. G. Karmokova
O. A. Losanova
M. V. Ryabina
A. M. Maybogin
author_sort N. V. Neroeva
collection DOAJ
description Purpose: to develop easy-to make and reproducible models of retinal pigment epithelium atrophy (RPE) and retinal degeneration using two types of solution (0.9 % sodium chloride and bevacizumab) and to evaluate these models using clinical instrumental and pathomorphological studies. Material and methods. To create the two models, we used 60 New Zealand albino rabbits divided into 2 groups of 30 animals each (30 eyes). In group 1, 0.01 ml of 0.9 % sodium chloride solution was delivered into the subretinal space at a distance of 1–1.5 mm downwards from the optic disc forming a subretinal bladder, whilst group 2 received 0.01 ml of bevacizumab solution which contained 0.025 mg of the drug. Optical coherence tomography (OCT) and fundus autofluorescence imaging were performed in live rabbits’ eyes before and after the procedure on the 2nd, 7th, 14th, 24th, and 30th day using Heidelberg Spectralis™ SD-OCT (Heidelberg Engineering, Germany). The enucleated eyes were histologically evaluated 14 and 30 days after RPE atrophy modeling. Results. Two easily reproducible experimental models of RPE atrophy have been developed. Clinical and morphological indications of RPE atrophy are described. Histological analysis revealed a more aggressive action of 0.9% sodium chloride solution on the retina and the choroid as compared with the model obtained with a similarly delivered subretinal angiogenesis inhibitor. Conclusion. The obtained experimental models may be useful in investigating various types of RPE atrophy, including those arising from the use of angiogenesis inhibitors.
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institution Kabale University
issn 2072-0076
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publishDate 2020-12-01
publisher Real Time Ltd
record_format Article
series Российский офтальмологический журнал
spelling doaj-art-315dd1645d8043d793fc8f86cff96c762025-08-20T03:39:53ZrusReal Time LtdРоссийский офтальмологический журнал2072-00762587-57602020-12-01134586310.21516/2072-0076-2020-13-4-58-63317Modeling the atrophy of retinal pigment epitheliumN. V. Neroeva0V. V. Neroev1P. A. Ilyukhin2A. G. Karmokova3O. A. Losanova4M. V. Ryabina5A. M. Maybogin6Helmholtz National Medical Research Center of Eye DiseasesHelmholtz National Medical Research Center of Eye DiseasesHelmholtz National Medical Research Center of Eye DiseasesHelmholtz National Medical Research Center of Eye DiseasesHelmholtz National Medical Research Center of Eye DiseasesHelmholtz National Medical Research Center of Eye DiseasesHelmholtz National Medical Research Center of Eye DiseasesPurpose: to develop easy-to make and reproducible models of retinal pigment epithelium atrophy (RPE) and retinal degeneration using two types of solution (0.9 % sodium chloride and bevacizumab) and to evaluate these models using clinical instrumental and pathomorphological studies. Material and methods. To create the two models, we used 60 New Zealand albino rabbits divided into 2 groups of 30 animals each (30 eyes). In group 1, 0.01 ml of 0.9 % sodium chloride solution was delivered into the subretinal space at a distance of 1–1.5 mm downwards from the optic disc forming a subretinal bladder, whilst group 2 received 0.01 ml of bevacizumab solution which contained 0.025 mg of the drug. Optical coherence tomography (OCT) and fundus autofluorescence imaging were performed in live rabbits’ eyes before and after the procedure on the 2nd, 7th, 14th, 24th, and 30th day using Heidelberg Spectralis™ SD-OCT (Heidelberg Engineering, Germany). The enucleated eyes were histologically evaluated 14 and 30 days after RPE atrophy modeling. Results. Two easily reproducible experimental models of RPE atrophy have been developed. Clinical and morphological indications of RPE atrophy are described. Histological analysis revealed a more aggressive action of 0.9% sodium chloride solution on the retina and the choroid as compared with the model obtained with a similarly delivered subretinal angiogenesis inhibitor. Conclusion. The obtained experimental models may be useful in investigating various types of RPE atrophy, including those arising from the use of angiogenesis inhibitors.https://roj.igb.ru/jour/article/view/520retinal pigment epithelium atrophy0.9 % sodium chloride solutionbevacizumabinhibitors of angiogenesis
spellingShingle N. V. Neroeva
V. V. Neroev
P. A. Ilyukhin
A. G. Karmokova
O. A. Losanova
M. V. Ryabina
A. M. Maybogin
Modeling the atrophy of retinal pigment epithelium
Российский офтальмологический журнал
retinal pigment epithelium atrophy
0.9 % sodium chloride solution
bevacizumab
inhibitors of angiogenesis
title Modeling the atrophy of retinal pigment epithelium
title_full Modeling the atrophy of retinal pigment epithelium
title_fullStr Modeling the atrophy of retinal pigment epithelium
title_full_unstemmed Modeling the atrophy of retinal pigment epithelium
title_short Modeling the atrophy of retinal pigment epithelium
title_sort modeling the atrophy of retinal pigment epithelium
topic retinal pigment epithelium atrophy
0.9 % sodium chloride solution
bevacizumab
inhibitors of angiogenesis
url https://roj.igb.ru/jour/article/view/520
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