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Superior cervical gangliectomy induces non-exudative age-related macular degeneration in mice
Non-exudative age-related macular degeneration, a prevalent cause of blindness, is a progressive and degenerative disease characterized by alterations in Bruch's membrane, retinal pigment epithelium, and photoreceptors exclusively localized in the macula. Although experimental murine models exi...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5894943/ https://www.ncbi.nlm.nih.gov/pubmed/29361515 http://dx.doi.org/10.1242/dmm.031641 |
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author | Dieguez, Hernán H. Romeo, Horacio E. González Fleitas, María F. Aranda, Marcos L. Milne, Georgia A. Rosenstein, Ruth E. Dorfman, Damián |
author_facet | Dieguez, Hernán H. Romeo, Horacio E. González Fleitas, María F. Aranda, Marcos L. Milne, Georgia A. Rosenstein, Ruth E. Dorfman, Damián |
author_sort | Dieguez, Hernán H. |
collection | PubMed |
description | Non-exudative age-related macular degeneration, a prevalent cause of blindness, is a progressive and degenerative disease characterized by alterations in Bruch's membrane, retinal pigment epithelium, and photoreceptors exclusively localized in the macula. Although experimental murine models exist, the vast majority take a long time to develop retinal alterations and, in general, these alterations are ubiquitous, with many resulting from non-eye-specific genetic manipulations; additionally, most do not always reproduce the hallmarks of human age-related macular degeneration. Choroid vessels receive sympathetic innervation from the superior cervical ganglion, which, together with the parasympathetic system, regulates blood flow into the choroid. Choroid blood flow changes have been involved in age-related macular degeneration development and progression. At present, no experimental models take this factor into account. The aim of this work was to analyze the effect of superior cervical gangliectomy (also known as ganglionectomy) on the choroid, Bruch's membrane, retinal pigment epithelium and retina. Adult male C57BL/6J mice underwent unilateral superior cervical gangliectomy and a contralateral sham procedure. Although superior cervical gangliectomy induced ubiquitous choroid and choriocapillaris changes, it induced Bruch's membrane thickening, loss of retinal pigment epithelium melanin content and retinoid isomerohydrolase, the appearance of drusen-like deposits, and retinal pigment epithelium and photoreceptor atrophy, exclusively localized in the temporal side. Moreover, superior cervical gangliectomy provoked a localized increase in retinal pigment epithelium and photoreceptor apoptosis, and a decline in photoreceptor electroretinographic function. Therefore, superior cervical gangliectomy recapitulated the main features of human non-exudative age-related macular degeneration, and could become a new experimental model of dry age-related macular degeneration, and a useful platform for developing new therapies. |
format | Online Article Text |
id | pubmed-5894943 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-58949432018-04-12 Superior cervical gangliectomy induces non-exudative age-related macular degeneration in mice Dieguez, Hernán H. Romeo, Horacio E. González Fleitas, María F. Aranda, Marcos L. Milne, Georgia A. Rosenstein, Ruth E. Dorfman, Damián Dis Model Mech Research Article Non-exudative age-related macular degeneration, a prevalent cause of blindness, is a progressive and degenerative disease characterized by alterations in Bruch's membrane, retinal pigment epithelium, and photoreceptors exclusively localized in the macula. Although experimental murine models exist, the vast majority take a long time to develop retinal alterations and, in general, these alterations are ubiquitous, with many resulting from non-eye-specific genetic manipulations; additionally, most do not always reproduce the hallmarks of human age-related macular degeneration. Choroid vessels receive sympathetic innervation from the superior cervical ganglion, which, together with the parasympathetic system, regulates blood flow into the choroid. Choroid blood flow changes have been involved in age-related macular degeneration development and progression. At present, no experimental models take this factor into account. The aim of this work was to analyze the effect of superior cervical gangliectomy (also known as ganglionectomy) on the choroid, Bruch's membrane, retinal pigment epithelium and retina. Adult male C57BL/6J mice underwent unilateral superior cervical gangliectomy and a contralateral sham procedure. Although superior cervical gangliectomy induced ubiquitous choroid and choriocapillaris changes, it induced Bruch's membrane thickening, loss of retinal pigment epithelium melanin content and retinoid isomerohydrolase, the appearance of drusen-like deposits, and retinal pigment epithelium and photoreceptor atrophy, exclusively localized in the temporal side. Moreover, superior cervical gangliectomy provoked a localized increase in retinal pigment epithelium and photoreceptor apoptosis, and a decline in photoreceptor electroretinographic function. Therefore, superior cervical gangliectomy recapitulated the main features of human non-exudative age-related macular degeneration, and could become a new experimental model of dry age-related macular degeneration, and a useful platform for developing new therapies. The Company of Biologists Ltd 2018-02-01 /pmc/articles/PMC5894943/ /pubmed/29361515 http://dx.doi.org/10.1242/dmm.031641 Text en © 2018. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/3.0This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Research Article Dieguez, Hernán H. Romeo, Horacio E. González Fleitas, María F. Aranda, Marcos L. Milne, Georgia A. Rosenstein, Ruth E. Dorfman, Damián Superior cervical gangliectomy induces non-exudative age-related macular degeneration in mice |
title | Superior cervical gangliectomy induces non-exudative age-related macular degeneration in mice |
title_full | Superior cervical gangliectomy induces non-exudative age-related macular degeneration in mice |
title_fullStr | Superior cervical gangliectomy induces non-exudative age-related macular degeneration in mice |
title_full_unstemmed | Superior cervical gangliectomy induces non-exudative age-related macular degeneration in mice |
title_short | Superior cervical gangliectomy induces non-exudative age-related macular degeneration in mice |
title_sort | superior cervical gangliectomy induces non-exudative age-related macular degeneration in mice |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5894943/ https://www.ncbi.nlm.nih.gov/pubmed/29361515 http://dx.doi.org/10.1242/dmm.031641 |
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