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Translational Preclinical Pharmacologic Disease Models for Ophthalmic Drug Development
Preclinical models of human diseases are critical to our understanding of disease etiology, pathology, and progression and enable the development of effective treatments. An ideal model of human disease should capture anatomical features and pathophysiological mechanisms, mimic the progression patte...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6394514/ https://www.ncbi.nlm.nih.gov/pubmed/30805711 http://dx.doi.org/10.1007/s11095-019-2588-5 |
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author | Shah, Mihir Cabrera-Ghayouri, Sara Christie, Lori-Ann Held, Katherine S. Viswanath, Veena |
author_facet | Shah, Mihir Cabrera-Ghayouri, Sara Christie, Lori-Ann Held, Katherine S. Viswanath, Veena |
author_sort | Shah, Mihir |
collection | PubMed |
description | Preclinical models of human diseases are critical to our understanding of disease etiology, pathology, and progression and enable the development of effective treatments. An ideal model of human disease should capture anatomical features and pathophysiological mechanisms, mimic the progression pattern, and should be amenable to evaluating translational endpoints and treatment approaches. Preclinical animal models have been developed for a variety of human ophthalmological diseases to mirror disease mechanisms, location of the affected region in the eye and severity. These models offer clues to aid in our fundamental understanding of disease pathogenesis and enable progression of new therapies to clinical development by providing an opportunity to gain proof of concept (POC). Here, we review preclinical animal models associated with development of new therapies for diseases of the ocular surface, glaucoma, presbyopia, and retinal diseases, including diabetic retinopathy and age-related macular degeneration (AMD). We have focused on summarizing the models critical to new drug development and described the translational features of the models that contributed to our understanding of disease pathogenesis and establishment of preclinical POC. |
format | Online Article Text |
id | pubmed-6394514 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-63945142019-03-15 Translational Preclinical Pharmacologic Disease Models for Ophthalmic Drug Development Shah, Mihir Cabrera-Ghayouri, Sara Christie, Lori-Ann Held, Katherine S. Viswanath, Veena Pharm Res Expert Review Preclinical models of human diseases are critical to our understanding of disease etiology, pathology, and progression and enable the development of effective treatments. An ideal model of human disease should capture anatomical features and pathophysiological mechanisms, mimic the progression pattern, and should be amenable to evaluating translational endpoints and treatment approaches. Preclinical animal models have been developed for a variety of human ophthalmological diseases to mirror disease mechanisms, location of the affected region in the eye and severity. These models offer clues to aid in our fundamental understanding of disease pathogenesis and enable progression of new therapies to clinical development by providing an opportunity to gain proof of concept (POC). Here, we review preclinical animal models associated with development of new therapies for diseases of the ocular surface, glaucoma, presbyopia, and retinal diseases, including diabetic retinopathy and age-related macular degeneration (AMD). We have focused on summarizing the models critical to new drug development and described the translational features of the models that contributed to our understanding of disease pathogenesis and establishment of preclinical POC. Springer US 2019-02-25 2019 /pmc/articles/PMC6394514/ /pubmed/30805711 http://dx.doi.org/10.1007/s11095-019-2588-5 Text en © The Author(s) 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Expert Review Shah, Mihir Cabrera-Ghayouri, Sara Christie, Lori-Ann Held, Katherine S. Viswanath, Veena Translational Preclinical Pharmacologic Disease Models for Ophthalmic Drug Development |
title | Translational Preclinical Pharmacologic Disease Models for Ophthalmic Drug Development |
title_full | Translational Preclinical Pharmacologic Disease Models for Ophthalmic Drug Development |
title_fullStr | Translational Preclinical Pharmacologic Disease Models for Ophthalmic Drug Development |
title_full_unstemmed | Translational Preclinical Pharmacologic Disease Models for Ophthalmic Drug Development |
title_short | Translational Preclinical Pharmacologic Disease Models for Ophthalmic Drug Development |
title_sort | translational preclinical pharmacologic disease models for ophthalmic drug development |
topic | Expert Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6394514/ https://www.ncbi.nlm.nih.gov/pubmed/30805711 http://dx.doi.org/10.1007/s11095-019-2588-5 |
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