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Neurovascular unit in diabetic retinopathy: pathophysiological roles and potential therapeutical targets
Diabetic retinopathy (DR), one of the common complications of diabetes, is the leading cause of visual loss in working-age individuals in many industrialized countries. It has been traditionally regarded as a purely microvascular disease in the retina. However, an increasing number of studies have s...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8088070/ https://www.ncbi.nlm.nih.gov/pubmed/33931128 http://dx.doi.org/10.1186/s40662-021-00239-1 |
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author | Nian, Shen Lo, Amy C. Y. Mi, Yajing Ren, Kai Yang, Di |
author_facet | Nian, Shen Lo, Amy C. Y. Mi, Yajing Ren, Kai Yang, Di |
author_sort | Nian, Shen |
collection | PubMed |
description | Diabetic retinopathy (DR), one of the common complications of diabetes, is the leading cause of visual loss in working-age individuals in many industrialized countries. It has been traditionally regarded as a purely microvascular disease in the retina. However, an increasing number of studies have shown that DR is a complex neurovascular disorder that affects not only vascular structure but also neural tissue of the retina. Deterioration of neural retina could precede microvascular abnormalities in the DR, leading to microvascular changes. Furthermore, disruption of interactions among neurons, vascular cells, glia and local immune cells, which collectively form the neurovascular unit, is considered to be associated with the progression of DR early on in the disease. Therefore, it makes sense to develop new therapeutic strategies to prevent or reverse retinal neurodegeneration, neuroinflammation and impaired cell-cell interactions of the neurovascular unit in early stage DR. Here, we present current perspectives on the pathophysiology of DR as a neurovascular disease, especially at the early stage. Potential novel treatments for preventing or reversing neurovascular injuries in DR are discussed as well. |
format | Online Article Text |
id | pubmed-8088070 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-80880702021-05-03 Neurovascular unit in diabetic retinopathy: pathophysiological roles and potential therapeutical targets Nian, Shen Lo, Amy C. Y. Mi, Yajing Ren, Kai Yang, Di Eye Vis (Lond) Review Diabetic retinopathy (DR), one of the common complications of diabetes, is the leading cause of visual loss in working-age individuals in many industrialized countries. It has been traditionally regarded as a purely microvascular disease in the retina. However, an increasing number of studies have shown that DR is a complex neurovascular disorder that affects not only vascular structure but also neural tissue of the retina. Deterioration of neural retina could precede microvascular abnormalities in the DR, leading to microvascular changes. Furthermore, disruption of interactions among neurons, vascular cells, glia and local immune cells, which collectively form the neurovascular unit, is considered to be associated with the progression of DR early on in the disease. Therefore, it makes sense to develop new therapeutic strategies to prevent or reverse retinal neurodegeneration, neuroinflammation and impaired cell-cell interactions of the neurovascular unit in early stage DR. Here, we present current perspectives on the pathophysiology of DR as a neurovascular disease, especially at the early stage. Potential novel treatments for preventing or reversing neurovascular injuries in DR are discussed as well. BioMed Central 2021-05-01 /pmc/articles/PMC8088070/ /pubmed/33931128 http://dx.doi.org/10.1186/s40662-021-00239-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Review Nian, Shen Lo, Amy C. Y. Mi, Yajing Ren, Kai Yang, Di Neurovascular unit in diabetic retinopathy: pathophysiological roles and potential therapeutical targets |
title | Neurovascular unit in diabetic retinopathy: pathophysiological roles and potential therapeutical targets |
title_full | Neurovascular unit in diabetic retinopathy: pathophysiological roles and potential therapeutical targets |
title_fullStr | Neurovascular unit in diabetic retinopathy: pathophysiological roles and potential therapeutical targets |
title_full_unstemmed | Neurovascular unit in diabetic retinopathy: pathophysiological roles and potential therapeutical targets |
title_short | Neurovascular unit in diabetic retinopathy: pathophysiological roles and potential therapeutical targets |
title_sort | neurovascular unit in diabetic retinopathy: pathophysiological roles and potential therapeutical targets |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8088070/ https://www.ncbi.nlm.nih.gov/pubmed/33931128 http://dx.doi.org/10.1186/s40662-021-00239-1 |
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