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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Main Author: Sonali Nashine
Format: Article
Language:English
Published: MDPI AG 2021-09-01
Series:Cells
Subjects:
Online Access:https://www.mdpi.com/2073-4409/10/9/2483
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author Sonali Nashine
author_facet Sonali Nashine
author_sort Sonali Nashine
collection DOAJ
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 doaj.art-636d398d3522491db3dadb48cd27bd712023-11-22T12:26:55ZengMDPI AGCells2073-44092021-09-01109248310.3390/cells10092483Potential Therapeutic Candidates for Age-Related Macular Degeneration (AMD)Sonali Nashine0Department of Ophthalmology, University of California Irvine, Irvine, CA 92697, USAAging 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.https://www.mdpi.com/2073-4409/10/9/2483age-related macular degeneration (AMD)retinaAMD therapeutics
spellingShingle Sonali Nashine
Potential Therapeutic Candidates for Age-Related Macular Degeneration (AMD)
Cells
age-related macular degeneration (AMD)
retina
AMD therapeutics
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 age-related macular degeneration (AMD)
retina
AMD therapeutics
url https://www.mdpi.com/2073-4409/10/9/2483
work_keys_str_mv AT sonalinashine potentialtherapeuticcandidatesforagerelatedmaculardegenerationamd