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Animal Models Used to Simulate Retinal Artery Occlusion: A Comprehensive Review
PURPOSE: To present an overview of animal models of retinal artery occlusion (RAO). METHODS: Through a systematic literature search in PubMed and Embase, papers describing methods of inducing RAO in animal models were included. The identified methodologic approaches were presented in a narrative syn...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Association for Research in Vision and Ophthalmology
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6701503/ https://www.ncbi.nlm.nih.gov/pubmed/31440422 http://dx.doi.org/10.1167/tvst.8.4.23 |
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author | Vestergaard, Nanna Cehofski, Lasse Jørgensen Honoré, Bent Aasbjerg, Kristian Vorum, Henrik |
author_facet | Vestergaard, Nanna Cehofski, Lasse Jørgensen Honoré, Bent Aasbjerg, Kristian Vorum, Henrik |
author_sort | Vestergaard, Nanna |
collection | PubMed |
description | PURPOSE: To present an overview of animal models of retinal artery occlusion (RAO). METHODS: Through a systematic literature search in PubMed and Embase, papers describing methods of inducing RAO in animal models were included. The identified methodologic approaches were presented in a narrative synthesis and compared with RAO in humans. RESULTS: In total, 83 papers reporting on 88 experiments were included. Six different species were used with rodents and monkeys being the most common, and a minority were performed using cats, dogs, rabbits, or pigs. The anatomy of pigs and monkeys resemble that of humans most closely. The two most frequently used methods were laser-induced occlusion or ligation of the arteries. Other methods included raised intraocular pressure, arterial clamping, administration of vasoconstricting agents, the use of an occluder, embolization, and endovascular approaches to induce occlusion. In general, occlusions lasted for only 30 to 90 minutes, often followed by reperfusion. CONCLUSIONS: Although a broad range of methods have previously been used, they all have limitations. Preferably, the methods should imitate the human disease as closely as possible and avoid damaging other structures. Therefore, monkeys followed by pigs are to be preferred and ligation or clamping may be a suitable model in larger animals as there is a potential to isolate and occlude the retinal artery only. Being less invasive, laser-induced occlusion is another suitable approach. TRANSLATIONAL RELEVANCE: This review aims at assisting researchers in deciding on the most ideal experimental setting, and thereby increase the translational value to human disease. |
format | Online Article Text |
id | pubmed-6701503 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Association for Research in Vision and Ophthalmology |
record_format | MEDLINE/PubMed |
spelling | pubmed-67015032019-08-22 Animal Models Used to Simulate Retinal Artery Occlusion: A Comprehensive Review Vestergaard, Nanna Cehofski, Lasse Jørgensen Honoré, Bent Aasbjerg, Kristian Vorum, Henrik Transl Vis Sci Technol Review PURPOSE: To present an overview of animal models of retinal artery occlusion (RAO). METHODS: Through a systematic literature search in PubMed and Embase, papers describing methods of inducing RAO in animal models were included. The identified methodologic approaches were presented in a narrative synthesis and compared with RAO in humans. RESULTS: In total, 83 papers reporting on 88 experiments were included. Six different species were used with rodents and monkeys being the most common, and a minority were performed using cats, dogs, rabbits, or pigs. The anatomy of pigs and monkeys resemble that of humans most closely. The two most frequently used methods were laser-induced occlusion or ligation of the arteries. Other methods included raised intraocular pressure, arterial clamping, administration of vasoconstricting agents, the use of an occluder, embolization, and endovascular approaches to induce occlusion. In general, occlusions lasted for only 30 to 90 minutes, often followed by reperfusion. CONCLUSIONS: Although a broad range of methods have previously been used, they all have limitations. Preferably, the methods should imitate the human disease as closely as possible and avoid damaging other structures. Therefore, monkeys followed by pigs are to be preferred and ligation or clamping may be a suitable model in larger animals as there is a potential to isolate and occlude the retinal artery only. Being less invasive, laser-induced occlusion is another suitable approach. TRANSLATIONAL RELEVANCE: This review aims at assisting researchers in deciding on the most ideal experimental setting, and thereby increase the translational value to human disease. The Association for Research in Vision and Ophthalmology 2019-08-15 /pmc/articles/PMC6701503/ /pubmed/31440422 http://dx.doi.org/10.1167/tvst.8.4.23 Text en Copyright 2019 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. |
spellingShingle | Review Vestergaard, Nanna Cehofski, Lasse Jørgensen Honoré, Bent Aasbjerg, Kristian Vorum, Henrik Animal Models Used to Simulate Retinal Artery Occlusion: A Comprehensive Review |
title | Animal Models Used to Simulate Retinal Artery Occlusion: A Comprehensive Review |
title_full | Animal Models Used to Simulate Retinal Artery Occlusion: A Comprehensive Review |
title_fullStr | Animal Models Used to Simulate Retinal Artery Occlusion: A Comprehensive Review |
title_full_unstemmed | Animal Models Used to Simulate Retinal Artery Occlusion: A Comprehensive Review |
title_short | Animal Models Used to Simulate Retinal Artery Occlusion: A Comprehensive Review |
title_sort | animal models used to simulate retinal artery occlusion: a comprehensive review |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6701503/ https://www.ncbi.nlm.nih.gov/pubmed/31440422 http://dx.doi.org/10.1167/tvst.8.4.23 |
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