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Establishment of an experimental ferret ocular hypertension model for the analysis of central visual pathway damage
Glaucoma optic neuropathy (GON) is a condition where pathogenic intraocular pressure (IOP) results in axonal damage following retinal ganglion cell (RGC) death, and further results in secondary damage of the lateral geniculate nucleus (LGN). Therapeutic targets for glaucoma thus focus on both the LG...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4194439/ https://www.ncbi.nlm.nih.gov/pubmed/25308730 http://dx.doi.org/10.1038/srep06501 |
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author | Fujishiro, Takashi Kawasaki, Hiroshi Aihara, Makoto Saeki, Tadashiro Ymagishi, Reiko Atarashi, Takuya Mayama, Chihiro Araie, Makoto |
author_facet | Fujishiro, Takashi Kawasaki, Hiroshi Aihara, Makoto Saeki, Tadashiro Ymagishi, Reiko Atarashi, Takuya Mayama, Chihiro Araie, Makoto |
author_sort | Fujishiro, Takashi |
collection | PubMed |
description | Glaucoma optic neuropathy (GON) is a condition where pathogenic intraocular pressure (IOP) results in axonal damage following retinal ganglion cell (RGC) death, and further results in secondary damage of the lateral geniculate nucleus (LGN). Therapeutic targets for glaucoma thus focus on both the LGN and RGC. However, the temporal and spatial patterns of degeneration and the mechanism of LGN damage have not been fully elucidated. Suitable and convenient ocular hypertension (OH) animal models with binocular vision comparable to that of monkeys are strongly needed. The ferret is relatively small mammal with binocular vision like humans – here we report on its suitability for investigating LGN. We developed a new method to elevate IOP by injection of cultured conjunctival cells into the anterior chamber to obstruct aqueous outflow. Histologically, cultured conjunctival cells successfully proliferated to occlude the angle, and IOP was elevated for 13 weeks after injection. Macroscopically, the size of the eye gradually expanded. Subsequent enlargement of optic nerve head cupping and atrophic damage of LGN projected from the OH eye were clearly observed by anterograde staining with cholera toxin B. We believe the ferret may be a promising OH model to investigate secondary degeneration of central nervous system including LGN. |
format | Online Article Text |
id | pubmed-4194439 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-41944392014-10-21 Establishment of an experimental ferret ocular hypertension model for the analysis of central visual pathway damage Fujishiro, Takashi Kawasaki, Hiroshi Aihara, Makoto Saeki, Tadashiro Ymagishi, Reiko Atarashi, Takuya Mayama, Chihiro Araie, Makoto Sci Rep Article Glaucoma optic neuropathy (GON) is a condition where pathogenic intraocular pressure (IOP) results in axonal damage following retinal ganglion cell (RGC) death, and further results in secondary damage of the lateral geniculate nucleus (LGN). Therapeutic targets for glaucoma thus focus on both the LGN and RGC. However, the temporal and spatial patterns of degeneration and the mechanism of LGN damage have not been fully elucidated. Suitable and convenient ocular hypertension (OH) animal models with binocular vision comparable to that of monkeys are strongly needed. The ferret is relatively small mammal with binocular vision like humans – here we report on its suitability for investigating LGN. We developed a new method to elevate IOP by injection of cultured conjunctival cells into the anterior chamber to obstruct aqueous outflow. Histologically, cultured conjunctival cells successfully proliferated to occlude the angle, and IOP was elevated for 13 weeks after injection. Macroscopically, the size of the eye gradually expanded. Subsequent enlargement of optic nerve head cupping and atrophic damage of LGN projected from the OH eye were clearly observed by anterograde staining with cholera toxin B. We believe the ferret may be a promising OH model to investigate secondary degeneration of central nervous system including LGN. Nature Publishing Group 2014-10-13 /pmc/articles/PMC4194439/ /pubmed/25308730 http://dx.doi.org/10.1038/srep06501 Text en Copyright © 2014, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Fujishiro, Takashi Kawasaki, Hiroshi Aihara, Makoto Saeki, Tadashiro Ymagishi, Reiko Atarashi, Takuya Mayama, Chihiro Araie, Makoto Establishment of an experimental ferret ocular hypertension model for the analysis of central visual pathway damage |
title | Establishment of an experimental ferret ocular hypertension model for the analysis of central visual pathway damage |
title_full | Establishment of an experimental ferret ocular hypertension model for the analysis of central visual pathway damage |
title_fullStr | Establishment of an experimental ferret ocular hypertension model for the analysis of central visual pathway damage |
title_full_unstemmed | Establishment of an experimental ferret ocular hypertension model for the analysis of central visual pathway damage |
title_short | Establishment of an experimental ferret ocular hypertension model for the analysis of central visual pathway damage |
title_sort | establishment of an experimental ferret ocular hypertension model for the analysis of central visual pathway damage |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4194439/ https://www.ncbi.nlm.nih.gov/pubmed/25308730 http://dx.doi.org/10.1038/srep06501 |
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