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Pathological changes in the cellular structures of retina and choroidea in the early stages of alloxan-induced diabetes
AIM: To investigate the temporal sequence of pathological changes in the cellular structures of retina and choroidea in the early stages of diabetes in laboratory animals. METHODS: Experimental type 1 diabetes was modeled by three intraperitoneal injections of an alloxan solution into 30 male nonlin...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6304297/ https://www.ncbi.nlm.nih.gov/pubmed/30588286 http://dx.doi.org/10.4239/wjd.v9.i12.239 |
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author | Danilova, Irina Medvedeva, Svetlana Shmakova, Svetlana Chereshneva, Margarita Sarapultsev, Alexey Sarapultsev, Petr |
author_facet | Danilova, Irina Medvedeva, Svetlana Shmakova, Svetlana Chereshneva, Margarita Sarapultsev, Alexey Sarapultsev, Petr |
author_sort | Danilova, Irina |
collection | PubMed |
description | AIM: To investigate the temporal sequence of pathological changes in the cellular structures of retina and choroidea in the early stages of diabetes in laboratory animals. METHODS: Experimental type 1 diabetes was modeled by three intraperitoneal injections of an alloxan solution into 30 male nonlinear rats at 16 wk of age. The 30(th) and 60(th) days from the final alloxan injection were chosen as the endpoints. Light and electron microscopy and morphometric and immunohistochemical studies were performed on histological slices of eyeballs from experimental animals. RESULTS: Diabetic disturbances progressed to 60 d of the experiment. Thus, in the retina, a partial destruction of photoreceptors accompanied by interstitial edema was observed. The morphometric analysis revealed a reduction in the thickness of the retina. A reduction in the number of blood vessels of the choroid with disturbances of the endothelial cells and the vascular walls and a persistent reduction in the number of melanocytes were observed. The number of proliferating Ki-67 positive cells decreased, and the number of macrophages increased with diabetes development. CONCLUSION: The starting point in the development of destructive changes involves early reduction in the number of melanocytes of the choroidea and alterations in the retinal pigment epithelium. |
format | Online Article Text |
id | pubmed-6304297 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-63042972018-12-26 Pathological changes in the cellular structures of retina and choroidea in the early stages of alloxan-induced diabetes Danilova, Irina Medvedeva, Svetlana Shmakova, Svetlana Chereshneva, Margarita Sarapultsev, Alexey Sarapultsev, Petr World J Diabetes Basic Study AIM: To investigate the temporal sequence of pathological changes in the cellular structures of retina and choroidea in the early stages of diabetes in laboratory animals. METHODS: Experimental type 1 diabetes was modeled by three intraperitoneal injections of an alloxan solution into 30 male nonlinear rats at 16 wk of age. The 30(th) and 60(th) days from the final alloxan injection were chosen as the endpoints. Light and electron microscopy and morphometric and immunohistochemical studies were performed on histological slices of eyeballs from experimental animals. RESULTS: Diabetic disturbances progressed to 60 d of the experiment. Thus, in the retina, a partial destruction of photoreceptors accompanied by interstitial edema was observed. The morphometric analysis revealed a reduction in the thickness of the retina. A reduction in the number of blood vessels of the choroid with disturbances of the endothelial cells and the vascular walls and a persistent reduction in the number of melanocytes were observed. The number of proliferating Ki-67 positive cells decreased, and the number of macrophages increased with diabetes development. CONCLUSION: The starting point in the development of destructive changes involves early reduction in the number of melanocytes of the choroidea and alterations in the retinal pigment epithelium. Baishideng Publishing Group Inc 2018-12-15 2018-12-15 /pmc/articles/PMC6304297/ /pubmed/30588286 http://dx.doi.org/10.4239/wjd.v9.i12.239 Text en ©The Author(s) 2018. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. |
spellingShingle | Basic Study Danilova, Irina Medvedeva, Svetlana Shmakova, Svetlana Chereshneva, Margarita Sarapultsev, Alexey Sarapultsev, Petr Pathological changes in the cellular structures of retina and choroidea in the early stages of alloxan-induced diabetes |
title | Pathological changes in the cellular structures of retina and choroidea in the early stages of alloxan-induced diabetes |
title_full | Pathological changes in the cellular structures of retina and choroidea in the early stages of alloxan-induced diabetes |
title_fullStr | Pathological changes in the cellular structures of retina and choroidea in the early stages of alloxan-induced diabetes |
title_full_unstemmed | Pathological changes in the cellular structures of retina and choroidea in the early stages of alloxan-induced diabetes |
title_short | Pathological changes in the cellular structures of retina and choroidea in the early stages of alloxan-induced diabetes |
title_sort | pathological changes in the cellular structures of retina and choroidea in the early stages of alloxan-induced diabetes |
topic | Basic Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6304297/ https://www.ncbi.nlm.nih.gov/pubmed/30588286 http://dx.doi.org/10.4239/wjd.v9.i12.239 |
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