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Targeting Mitochondrial Oxidative Stress to Mitigate UV-Induced Skin Damage
Unmitigated UV radiation (UVR) induces skin photoaging and multiple forms of cutaneous carcinoma by complex pathways that include those mediated by UV-induced reactive oxygen species (ROS). Upon UVR exposure, a cascade of events is induced that overwhelms the skin’s natural antioxidant defenses and...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6110189/ https://www.ncbi.nlm.nih.gov/pubmed/30177881 http://dx.doi.org/10.3389/fphar.2018.00920 |
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author | Brand, Rhonda M. Wipf, Peter Durham, Austin Epperly, Michael W. Greenberger, Joel S. Falo, Louis D. |
author_facet | Brand, Rhonda M. Wipf, Peter Durham, Austin Epperly, Michael W. Greenberger, Joel S. Falo, Louis D. |
author_sort | Brand, Rhonda M. |
collection | PubMed |
description | Unmitigated UV radiation (UVR) induces skin photoaging and multiple forms of cutaneous carcinoma by complex pathways that include those mediated by UV-induced reactive oxygen species (ROS). Upon UVR exposure, a cascade of events is induced that overwhelms the skin’s natural antioxidant defenses and results in DNA damage, intracellular lipid and protein peroxidation, and the dysregulation of pathways that modulate inflammatory and apoptotic responses. To this end, natural products with potent antioxidant properties have been developed to prevent, mitigate, or reverse this damage with varying degrees of success. Mitochondria are particularly susceptible to ROS and subsequent DNA damage as they are a major intracellular source of oxidants. Therefore, the development of mitochondrially targeted agents to mitigate mitochondrial oxidative stress and resulting DNA damage is a logical approach to prevent and treat UV-induced skin damage. We summarize evidence that some existing natural products may reduce mitochondrial oxidative stress and support for synthetically generated mitochondrial targeted cyclic nitroxides as potential alternatives for the prevention and mitigation of UVR-induced skin damage. |
format | Online Article Text |
id | pubmed-6110189 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-61101892018-09-03 Targeting Mitochondrial Oxidative Stress to Mitigate UV-Induced Skin Damage Brand, Rhonda M. Wipf, Peter Durham, Austin Epperly, Michael W. Greenberger, Joel S. Falo, Louis D. Front Pharmacol Pharmacology Unmitigated UV radiation (UVR) induces skin photoaging and multiple forms of cutaneous carcinoma by complex pathways that include those mediated by UV-induced reactive oxygen species (ROS). Upon UVR exposure, a cascade of events is induced that overwhelms the skin’s natural antioxidant defenses and results in DNA damage, intracellular lipid and protein peroxidation, and the dysregulation of pathways that modulate inflammatory and apoptotic responses. To this end, natural products with potent antioxidant properties have been developed to prevent, mitigate, or reverse this damage with varying degrees of success. Mitochondria are particularly susceptible to ROS and subsequent DNA damage as they are a major intracellular source of oxidants. Therefore, the development of mitochondrially targeted agents to mitigate mitochondrial oxidative stress and resulting DNA damage is a logical approach to prevent and treat UV-induced skin damage. We summarize evidence that some existing natural products may reduce mitochondrial oxidative stress and support for synthetically generated mitochondrial targeted cyclic nitroxides as potential alternatives for the prevention and mitigation of UVR-induced skin damage. Frontiers Media S.A. 2018-08-20 /pmc/articles/PMC6110189/ /pubmed/30177881 http://dx.doi.org/10.3389/fphar.2018.00920 Text en Copyright © 2018 Brand, Wipf, Durham, Epperly, Greenberger and Falo. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pharmacology Brand, Rhonda M. Wipf, Peter Durham, Austin Epperly, Michael W. Greenberger, Joel S. Falo, Louis D. Targeting Mitochondrial Oxidative Stress to Mitigate UV-Induced Skin Damage |
title | Targeting Mitochondrial Oxidative Stress to Mitigate UV-Induced Skin Damage |
title_full | Targeting Mitochondrial Oxidative Stress to Mitigate UV-Induced Skin Damage |
title_fullStr | Targeting Mitochondrial Oxidative Stress to Mitigate UV-Induced Skin Damage |
title_full_unstemmed | Targeting Mitochondrial Oxidative Stress to Mitigate UV-Induced Skin Damage |
title_short | Targeting Mitochondrial Oxidative Stress to Mitigate UV-Induced Skin Damage |
title_sort | targeting mitochondrial oxidative stress to mitigate uv-induced skin damage |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6110189/ https://www.ncbi.nlm.nih.gov/pubmed/30177881 http://dx.doi.org/10.3389/fphar.2018.00920 |
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