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Photoprotection by dietary phenolics against melanogenesis induced by UVA through Nrf2-dependent antioxidant responses
Dietary phenolics may play a protective role in UV-mediated skin pigmentation through their antioxidant and UV-absorbing actions. In this study, we investigated whether genetic silencing of Nrf2, regulating the transcription of antioxidant genes, affected melanogenesis in primary human epidermal mel...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4712325/ https://www.ncbi.nlm.nih.gov/pubmed/26765101 http://dx.doi.org/10.1016/j.redox.2015.12.006 |
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author | Chaiprasongsuk, Anyamanee Onkoksoong, Tasanee Pluemsamran, Thanyawan Limsaengurai, Saowalak Panich, Uraiwan |
author_facet | Chaiprasongsuk, Anyamanee Onkoksoong, Tasanee Pluemsamran, Thanyawan Limsaengurai, Saowalak Panich, Uraiwan |
author_sort | Chaiprasongsuk, Anyamanee |
collection | PubMed |
description | Dietary phenolics may play a protective role in UV-mediated skin pigmentation through their antioxidant and UV-absorbing actions. In this study, we investigated whether genetic silencing of Nrf2, regulating the transcription of antioxidant genes, affected melanogenesis in primary human epidermal melanocytes (HEMn) and B16F10 melanoma cells subjected to UVA (8 J/cm(2)) exposure. Then, we explored the antimelanogenic actions of phenolics; caffeic acid (CA) and ferulic acid (FA) providing partial UVA protection; quercetin (QU) and rutin (RU) providing strong UVA protection and; avobenzone (AV), an efficient UVA filter, in association with modulation of Nrf2-mediated antioxidant defenses in response to UVA insults in B16F10 cells. Upon oxidative insults, Nrf2 silencing promoted melanogenesis in both HEMn and B16F10 cells irradiated with UVA. Stimulation of melanogenesis by UVA correlated with increased ROS and oxidative DNA damage (8-OHdG), GSH depletion as well as a transient downregulation of Nrf2 nuclear translocation and of Nrf2-ARE signaling in B16F10 cells. All test compounds exerted antimelanogenic effects with respect to their abilities to reverse UVA-mediated oxidative damage as well as downregulation of Nrf2 activity and its target antioxidants (GCLC, GST and NQO1) in B16F10 cells. In conclusion, defective Nrf2 may promote melanogenesis under UVA irradiation through oxidative stress mechanisms. Compounds with antioxidant and/or UVA absorption properties could protect against UVA-induced melanogenesis through indirect regulatory effect on Nrf2-ARE pathway. |
format | Online Article Text |
id | pubmed-4712325 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-47123252016-02-11 Photoprotection by dietary phenolics against melanogenesis induced by UVA through Nrf2-dependent antioxidant responses Chaiprasongsuk, Anyamanee Onkoksoong, Tasanee Pluemsamran, Thanyawan Limsaengurai, Saowalak Panich, Uraiwan Redox Biol Research Paper Dietary phenolics may play a protective role in UV-mediated skin pigmentation through their antioxidant and UV-absorbing actions. In this study, we investigated whether genetic silencing of Nrf2, regulating the transcription of antioxidant genes, affected melanogenesis in primary human epidermal melanocytes (HEMn) and B16F10 melanoma cells subjected to UVA (8 J/cm(2)) exposure. Then, we explored the antimelanogenic actions of phenolics; caffeic acid (CA) and ferulic acid (FA) providing partial UVA protection; quercetin (QU) and rutin (RU) providing strong UVA protection and; avobenzone (AV), an efficient UVA filter, in association with modulation of Nrf2-mediated antioxidant defenses in response to UVA insults in B16F10 cells. Upon oxidative insults, Nrf2 silencing promoted melanogenesis in both HEMn and B16F10 cells irradiated with UVA. Stimulation of melanogenesis by UVA correlated with increased ROS and oxidative DNA damage (8-OHdG), GSH depletion as well as a transient downregulation of Nrf2 nuclear translocation and of Nrf2-ARE signaling in B16F10 cells. All test compounds exerted antimelanogenic effects with respect to their abilities to reverse UVA-mediated oxidative damage as well as downregulation of Nrf2 activity and its target antioxidants (GCLC, GST and NQO1) in B16F10 cells. In conclusion, defective Nrf2 may promote melanogenesis under UVA irradiation through oxidative stress mechanisms. Compounds with antioxidant and/or UVA absorption properties could protect against UVA-induced melanogenesis through indirect regulatory effect on Nrf2-ARE pathway. Elsevier 2015-12-19 /pmc/articles/PMC4712325/ /pubmed/26765101 http://dx.doi.org/10.1016/j.redox.2015.12.006 Text en © 2016 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Paper Chaiprasongsuk, Anyamanee Onkoksoong, Tasanee Pluemsamran, Thanyawan Limsaengurai, Saowalak Panich, Uraiwan Photoprotection by dietary phenolics against melanogenesis induced by UVA through Nrf2-dependent antioxidant responses |
title | Photoprotection by dietary phenolics against melanogenesis induced by UVA through Nrf2-dependent antioxidant responses |
title_full | Photoprotection by dietary phenolics against melanogenesis induced by UVA through Nrf2-dependent antioxidant responses |
title_fullStr | Photoprotection by dietary phenolics against melanogenesis induced by UVA through Nrf2-dependent antioxidant responses |
title_full_unstemmed | Photoprotection by dietary phenolics against melanogenesis induced by UVA through Nrf2-dependent antioxidant responses |
title_short | Photoprotection by dietary phenolics against melanogenesis induced by UVA through Nrf2-dependent antioxidant responses |
title_sort | photoprotection by dietary phenolics against melanogenesis induced by uva through nrf2-dependent antioxidant responses |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4712325/ https://www.ncbi.nlm.nih.gov/pubmed/26765101 http://dx.doi.org/10.1016/j.redox.2015.12.006 |
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