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Potential Therapeutic Candidates for Age-Related Macular Degeneration (AMD)

Aging contributes to the risk of development of ocular diseases including, but not limited to, Age-related Macular Degeneration (AMD) that is a leading cause of blindness in the United States as well as worldwide. Retinal aging, that contributes to AMD pathogenesis, is characterized by accumulation...

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Detalles Bibliográficos
Autor principal: Nashine, Sonali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8464988/
https://www.ncbi.nlm.nih.gov/pubmed/34572131
http://dx.doi.org/10.3390/cells10092483
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author Nashine, Sonali
author_facet Nashine, Sonali
author_sort Nashine, Sonali
collection PubMed
description Aging contributes to the risk of development of ocular diseases including, but not limited to, Age-related Macular Degeneration (AMD) that is a leading cause of blindness in the United States as well as worldwide. Retinal aging, that contributes to AMD pathogenesis, is characterized by accumulation of drusen deposits, alteration in the composition of Bruch’s membrane and extracellular matrix, vascular inflammation and dysregulation, mitochondrial dysfunction, and accumulation of reactive oxygen species (ROS), and subsequent retinal pigment epithelium (RPE) cell senescence. Since there are limited options available for the prophylaxis and treatment of AMD, new therapeutic interventions are constantly being looked into to identify new therapeutic targets for AMD. This review article discusses the potential candidates for AMD therapy and their known mechanisms of cytoprotection in AMD. These target therapeutic candidates include APE/REF-1, MRZ-99030, Ciliary NeuroTrophic Factor (CNTF), RAP1 GTPase, Celecoxib, and SS-31/Elamipretide.
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spelling pubmed-84649882021-09-27 Potential Therapeutic Candidates for Age-Related Macular Degeneration (AMD) Nashine, Sonali Cells Review Aging contributes to the risk of development of ocular diseases including, but not limited to, Age-related Macular Degeneration (AMD) that is a leading cause of blindness in the United States as well as worldwide. Retinal aging, that contributes to AMD pathogenesis, is characterized by accumulation of drusen deposits, alteration in the composition of Bruch’s membrane and extracellular matrix, vascular inflammation and dysregulation, mitochondrial dysfunction, and accumulation of reactive oxygen species (ROS), and subsequent retinal pigment epithelium (RPE) cell senescence. Since there are limited options available for the prophylaxis and treatment of AMD, new therapeutic interventions are constantly being looked into to identify new therapeutic targets for AMD. This review article discusses the potential candidates for AMD therapy and their known mechanisms of cytoprotection in AMD. These target therapeutic candidates include APE/REF-1, MRZ-99030, Ciliary NeuroTrophic Factor (CNTF), RAP1 GTPase, Celecoxib, and SS-31/Elamipretide. MDPI 2021-09-19 /pmc/articles/PMC8464988/ /pubmed/34572131 http://dx.doi.org/10.3390/cells10092483 Text en © 2021 by the author. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Nashine, Sonali
Potential Therapeutic Candidates for Age-Related Macular Degeneration (AMD)
title Potential Therapeutic Candidates for Age-Related Macular Degeneration (AMD)
title_full Potential Therapeutic Candidates for Age-Related Macular Degeneration (AMD)
title_fullStr Potential Therapeutic Candidates for Age-Related Macular Degeneration (AMD)
title_full_unstemmed Potential Therapeutic Candidates for Age-Related Macular Degeneration (AMD)
title_short Potential Therapeutic Candidates for Age-Related Macular Degeneration (AMD)
title_sort potential therapeutic candidates for age-related macular degeneration (amd)
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8464988/
https://www.ncbi.nlm.nih.gov/pubmed/34572131
http://dx.doi.org/10.3390/cells10092483
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