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Protective Effect of the Aqueous Extract of Deschampsia antarctica (EDAFENCE(®)) on Skin Cells against Blue Light Emitted from Digital Devices

Skin is being increasingly exposed to artificial blue light due to the extensive use of electronic devices. This, together with recent observations reporting that blue light—also known as high-energy visible light—can exert cytotoxic effects associated with oxidative stress and promote hyperpigmenta...

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Autores principales: Lorrio, Silvia, Rodríguez-Luna, Azahara, Delgado-Wicke, Pablo, Mascaraque, Marta, Gallego, María, Pérez-Davó, Azahara, González, Salvador, Juarranz, Ángeles
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7038134/
https://www.ncbi.nlm.nih.gov/pubmed/32024276
http://dx.doi.org/10.3390/ijms21030988
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author Lorrio, Silvia
Rodríguez-Luna, Azahara
Delgado-Wicke, Pablo
Mascaraque, Marta
Gallego, María
Pérez-Davó, Azahara
González, Salvador
Juarranz, Ángeles
author_facet Lorrio, Silvia
Rodríguez-Luna, Azahara
Delgado-Wicke, Pablo
Mascaraque, Marta
Gallego, María
Pérez-Davó, Azahara
González, Salvador
Juarranz, Ángeles
author_sort Lorrio, Silvia
collection PubMed
description Skin is being increasingly exposed to artificial blue light due to the extensive use of electronic devices. This, together with recent observations reporting that blue light—also known as high-energy visible light—can exert cytotoxic effects associated with oxidative stress and promote hyperpigmentation, has sparked interest in blue light and its potential harmful effects on skin. The photoprotective properties of new extracts of different botanicals with antioxidant activity are therefore being studied. Deschampsia antarctica (Edafence(®), EDA), a natural aqueous extract, has shown keratinocyte and fibroblast cell protection effects against ultraviolet radiation and dioxin toxicity. In this regard, we studied the protective capacity of EDA against the deleterious effects of artificial blue light irradiation in human dermal fibroblasts (HDF) and melanocytes. We analyzed the impact of EDA on viability, cell morphology, oxidative stress, melanogenic signaling pathway activation and hyperpigmentation in HDF and melanocytes subjected to artificial blue light irradiation. Our results show that EDA protects against cell damage caused by artificial blue light, decreasing oxidative stress, melanogenic signaling pathway activation and hyperpigmentation caused by blue light irradiation. All these findings suggest that EDA might help prevent skin damage produced by artificial blue light exposure from screen of electronic devices.
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spelling pubmed-70381342020-03-10 Protective Effect of the Aqueous Extract of Deschampsia antarctica (EDAFENCE(®)) on Skin Cells against Blue Light Emitted from Digital Devices Lorrio, Silvia Rodríguez-Luna, Azahara Delgado-Wicke, Pablo Mascaraque, Marta Gallego, María Pérez-Davó, Azahara González, Salvador Juarranz, Ángeles Int J Mol Sci Article Skin is being increasingly exposed to artificial blue light due to the extensive use of electronic devices. This, together with recent observations reporting that blue light—also known as high-energy visible light—can exert cytotoxic effects associated with oxidative stress and promote hyperpigmentation, has sparked interest in blue light and its potential harmful effects on skin. The photoprotective properties of new extracts of different botanicals with antioxidant activity are therefore being studied. Deschampsia antarctica (Edafence(®), EDA), a natural aqueous extract, has shown keratinocyte and fibroblast cell protection effects against ultraviolet radiation and dioxin toxicity. In this regard, we studied the protective capacity of EDA against the deleterious effects of artificial blue light irradiation in human dermal fibroblasts (HDF) and melanocytes. We analyzed the impact of EDA on viability, cell morphology, oxidative stress, melanogenic signaling pathway activation and hyperpigmentation in HDF and melanocytes subjected to artificial blue light irradiation. Our results show that EDA protects against cell damage caused by artificial blue light, decreasing oxidative stress, melanogenic signaling pathway activation and hyperpigmentation caused by blue light irradiation. All these findings suggest that EDA might help prevent skin damage produced by artificial blue light exposure from screen of electronic devices. MDPI 2020-02-02 /pmc/articles/PMC7038134/ /pubmed/32024276 http://dx.doi.org/10.3390/ijms21030988 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Lorrio, Silvia
Rodríguez-Luna, Azahara
Delgado-Wicke, Pablo
Mascaraque, Marta
Gallego, María
Pérez-Davó, Azahara
González, Salvador
Juarranz, Ángeles
Protective Effect of the Aqueous Extract of Deschampsia antarctica (EDAFENCE(®)) on Skin Cells against Blue Light Emitted from Digital Devices
title Protective Effect of the Aqueous Extract of Deschampsia antarctica (EDAFENCE(®)) on Skin Cells against Blue Light Emitted from Digital Devices
title_full Protective Effect of the Aqueous Extract of Deschampsia antarctica (EDAFENCE(®)) on Skin Cells against Blue Light Emitted from Digital Devices
title_fullStr Protective Effect of the Aqueous Extract of Deschampsia antarctica (EDAFENCE(®)) on Skin Cells against Blue Light Emitted from Digital Devices
title_full_unstemmed Protective Effect of the Aqueous Extract of Deschampsia antarctica (EDAFENCE(®)) on Skin Cells against Blue Light Emitted from Digital Devices
title_short Protective Effect of the Aqueous Extract of Deschampsia antarctica (EDAFENCE(®)) on Skin Cells against Blue Light Emitted from Digital Devices
title_sort protective effect of the aqueous extract of deschampsia antarctica (edafence(®)) on skin cells against blue light emitted from digital devices
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7038134/
https://www.ncbi.nlm.nih.gov/pubmed/32024276
http://dx.doi.org/10.3390/ijms21030988
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