Central Role of Oxidative Stress in Age-Related Macular Degeneration: Evidence from a Review of the Molecular Mechanisms and Animal Models
Age-related macular degeneration (AMD) is a common cause of visual impairment in the elderly. There are very limited therapeutic options for AMD with the predominant therapies targeting vascular endothelial growth factor (VEGF) in the retina of patients afflicted with wet AMD. Hence, it is important...
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description | Age-related macular degeneration (AMD) is a common cause of visual impairment in the elderly. There are very limited therapeutic options for AMD with the predominant therapies targeting vascular endothelial growth factor (VEGF) in the retina of patients afflicted with wet AMD. Hence, it is important to remind readers, especially those interested in AMD, about current studies that may help to develop novel therapies for other stages of AMD. This study, therefore, provides a comprehensive review of studies on human specimens as well as rodent models of the disease, to identify and analyze the molecular mechanisms behind AMD development and progression. The evaluation of this information highlights the central role that oxidative damage in the retina plays in contributing to major pathways, including inflammation and angiogenesis, found in the AMD phenotype. Following on the debate of oxidative stress as the earliest injury in the AMD pathogenesis, we demonstrated how the targeting of oxidative stress-associated pathways, such as autophagy and nuclear factor erythroid 2-related factor 2 (Nrf2) signaling, might be the futuristic direction to explore in the search of an effective treatment for AMD, as the dysregulation of these mechanisms is crucial to oxidative injury in the retina. In addition, animal models of AMD have been discussed in great detail, with their strengths and pitfalls included, to assist inform in the selection of suitable models for investigating any of the molecular mechanisms. |
doi_str_mv | 10.1155/2020/7901270 |
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There are very limited therapeutic options for AMD with the predominant therapies targeting vascular endothelial growth factor (VEGF) in the retina of patients afflicted with wet AMD. Hence, it is important to remind readers, especially those interested in AMD, about current studies that may help to develop novel therapies for other stages of AMD. This study, therefore, provides a comprehensive review of studies on human specimens as well as rodent models of the disease, to identify and analyze the molecular mechanisms behind AMD development and progression. The evaluation of this information highlights the central role that oxidative damage in the retina plays in contributing to major pathways, including inflammation and angiogenesis, found in the AMD phenotype. Following on the debate of oxidative stress as the earliest injury in the AMD pathogenesis, we demonstrated how the targeting of oxidative stress-associated pathways, such as autophagy and nuclear factor erythroid 2-related factor 2 (Nrf2) signaling, might be the futuristic direction to explore in the search of an effective treatment for AMD, as the dysregulation of these mechanisms is crucial to oxidative injury in the retina. In addition, animal models of AMD have been discussed in great detail, with their strengths and pitfalls included, to assist inform in the selection of suitable models for investigating any of the molecular mechanisms.</description><identifier>ISSN: 1942-0900</identifier><identifier>EISSN: 1942-0994</identifier><identifier>DOI: 10.1155/2020/7901270</identifier><identifier>PMID: 32104539</identifier><language>eng</language><publisher>Cairo, Egypt: Hindawi Publishing Corporation</publisher><subject>Analysis ; Animals ; Disease Models, Animal ; Health aspects ; Humans ; Lipids ; Macular degeneration ; Macular Degeneration - metabolism ; Metabolites ; NF-E2-Related Factor 2 - metabolism ; Oxidative stress ; Oxidative Stress - physiology ; Physiological aspects ; Retina ; Review ; Vascular endothelial growth factor ; Vascular Endothelial Growth Factor A - metabolism</subject><ispartof>Oxidative medicine and cellular longevity, 2020, Vol.2020 (2020), p.1-19</ispartof><rights>Copyright © 2020 Samuel Abokyi et al.</rights><rights>COPYRIGHT 2020 John Wiley & Sons, Inc.</rights><rights>Copyright © 2020 Samuel Abokyi et al. This is an open access article distributed under the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. http://creativecommons.org/licenses/by/4.0</rights><rights>Copyright © 2020 Samuel Abokyi et al. 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c499t-92002a1b711b52cd5f38384962091b0252b63ade1202f39fb2c569a90e153c113</citedby><cites>FETCH-LOGICAL-c499t-92002a1b711b52cd5f38384962091b0252b63ade1202f39fb2c569a90e153c113</cites><orcidid>0000-0001-8808-1340 ; 0000-0001-7561-9121 ; 0000-0003-2444-360X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7035553/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7035553/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,4010,27900,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32104539$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Monacelli, Fiammetta</contributor><contributor>Fiammetta Monacelli</contributor><creatorcontrib>Tse, Dennis Yan-yin</creatorcontrib><creatorcontrib>Lam, Tim T.</creatorcontrib><creatorcontrib>To, Chi-ho</creatorcontrib><creatorcontrib>Abokyi, Samuel</creatorcontrib><title>Central Role of Oxidative Stress in Age-Related Macular Degeneration: Evidence from a Review of the Molecular Mechanisms and Animal Models</title><title>Oxidative medicine and cellular longevity</title><addtitle>Oxid Med Cell Longev</addtitle><description>Age-related macular degeneration (AMD) is a common cause of visual impairment in the elderly. There are very limited therapeutic options for AMD with the predominant therapies targeting vascular endothelial growth factor (VEGF) in the retina of patients afflicted with wet AMD. Hence, it is important to remind readers, especially those interested in AMD, about current studies that may help to develop novel therapies for other stages of AMD. This study, therefore, provides a comprehensive review of studies on human specimens as well as rodent models of the disease, to identify and analyze the molecular mechanisms behind AMD development and progression. The evaluation of this information highlights the central role that oxidative damage in the retina plays in contributing to major pathways, including inflammation and angiogenesis, found in the AMD phenotype. Following on the debate of oxidative stress as the earliest injury in the AMD pathogenesis, we demonstrated how the targeting of oxidative stress-associated pathways, such as autophagy and nuclear factor erythroid 2-related factor 2 (Nrf2) signaling, might be the futuristic direction to explore in the search of an effective treatment for AMD, as the dysregulation of these mechanisms is crucial to oxidative injury in the retina. In addition, animal models of AMD have been discussed in great detail, with their strengths and pitfalls included, to assist inform in the selection of suitable models for investigating any of the molecular mechanisms.</description><subject>Analysis</subject><subject>Animals</subject><subject>Disease Models, Animal</subject><subject>Health aspects</subject><subject>Humans</subject><subject>Lipids</subject><subject>Macular degeneration</subject><subject>Macular Degeneration - metabolism</subject><subject>Metabolites</subject><subject>NF-E2-Related Factor 2 - metabolism</subject><subject>Oxidative stress</subject><subject>Oxidative Stress - physiology</subject><subject>Physiological aspects</subject><subject>Retina</subject><subject>Review</subject><subject>Vascular endothelial growth factor</subject><subject>Vascular Endothelial Growth Factor A - metabolism</subject><issn>1942-0900</issn><issn>1942-0994</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>RHX</sourceid><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqNkk1v0zAYgCMEYmNw44wscUGCsNd2nNQckKoyPqRVkwqcLcd503pK7GEnHfwFfjWOUjrgxMmW_Ph5P7PsKYXXlApxzoDBeSWBsgruZadUFiwHKYv7xzvASfYoxmuAkrOCPsxOOKNQCC5Ps58rdEPQHdn4DolvydV32-jB7pF8HgLGSKwjyy3mG-z0gA1ZazN2OpB3uEWHIaHevSEXe9ugM0ja4HuiyQb3Fm8n37BDsk7u-dcazU47G_tItGvI0tk-xV77Brv4OHvQ6i7ik8N5ln19f_Fl9TG_vPrwabW8zE0h5ZBLBsA0rStKa8FMI1q-4ItClgwkrYEJVpdcN0hTY1ou25oZUUotAanghlJ-lr2dvTdj3WNj5gaom5ByCT-U11b9_eLsTm39XlXAhRA8CV4cBMF_GzEOqrfRYNdph36MivGyLLmoSkjo83_Qaz8Gl8qbKLrgbAHijtrqDpV1rU9xzSRVy5IlUEI1hX01Uyb4GAO2x5QpqGkV1LQK6rAKCX_2Z5lH-PfsE_ByBnbWNfrW_qcOE4OtvqMZiEJU_BdyQ8N3</recordid><startdate>2020</startdate><enddate>2020</enddate><creator>Tse, Dennis Yan-yin</creator><creator>Lam, Tim T.</creator><creator>To, Chi-ho</creator><creator>Abokyi, Samuel</creator><general>Hindawi Publishing Corporation</general><general>Hindawi</general><general>John Wiley & Sons, Inc</general><general>Hindawi Limited</general><scope>ADJCN</scope><scope>AHFXO</scope><scope>RHU</scope><scope>RHW</scope><scope>RHX</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-8808-1340</orcidid><orcidid>https://orcid.org/0000-0001-7561-9121</orcidid><orcidid>https://orcid.org/0000-0003-2444-360X</orcidid></search><sort><creationdate>2020</creationdate><title>Central Role of Oxidative Stress in Age-Related Macular Degeneration: Evidence from a Review of the Molecular Mechanisms and Animal Models</title><author>Tse, Dennis Yan-yin ; 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There are very limited therapeutic options for AMD with the predominant therapies targeting vascular endothelial growth factor (VEGF) in the retina of patients afflicted with wet AMD. Hence, it is important to remind readers, especially those interested in AMD, about current studies that may help to develop novel therapies for other stages of AMD. This study, therefore, provides a comprehensive review of studies on human specimens as well as rodent models of the disease, to identify and analyze the molecular mechanisms behind AMD development and progression. The evaluation of this information highlights the central role that oxidative damage in the retina plays in contributing to major pathways, including inflammation and angiogenesis, found in the AMD phenotype. Following on the debate of oxidative stress as the earliest injury in the AMD pathogenesis, we demonstrated how the targeting of oxidative stress-associated pathways, such as autophagy and nuclear factor erythroid 2-related factor 2 (Nrf2) signaling, might be the futuristic direction to explore in the search of an effective treatment for AMD, as the dysregulation of these mechanisms is crucial to oxidative injury in the retina. In addition, animal models of AMD have been discussed in great detail, with their strengths and pitfalls included, to assist inform in the selection of suitable models for investigating any of the molecular mechanisms.</abstract><cop>Cairo, Egypt</cop><pub>Hindawi Publishing Corporation</pub><pmid>32104539</pmid><doi>10.1155/2020/7901270</doi><tpages>19</tpages><orcidid>https://orcid.org/0000-0001-8808-1340</orcidid><orcidid>https://orcid.org/0000-0001-7561-9121</orcidid><orcidid>https://orcid.org/0000-0003-2444-360X</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Analysis Animals Disease Models, Animal Health aspects Humans Lipids Macular degeneration Macular Degeneration - metabolism Metabolites NF-E2-Related Factor 2 - metabolism Oxidative stress Oxidative Stress - physiology Physiological aspects Retina Review Vascular endothelial growth factor Vascular Endothelial Growth Factor A - metabolism |
title | Central Role of Oxidative Stress in Age-Related Macular Degeneration: Evidence from a Review of the Molecular Mechanisms and Animal Models |
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