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Ultraviolet Radiation-Induced Production of Nitric Oxide:A multi-cell and multi-donor analysis
Increasing evidence regarding positive effects of exposure to sunlight has led to suggestions that current advice may be overly weighted in favour of avoidance. UV-A has been reported to lower blood pressure, possibly through nitric oxide (NO) production in skin. Here, we set out to investigate effe...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5593895/ https://www.ncbi.nlm.nih.gov/pubmed/28894213 http://dx.doi.org/10.1038/s41598-017-11567-5 |
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author | Holliman, Graham Lowe, Donna Cohen, Howard Felton, Sarah Raj, Ken |
author_facet | Holliman, Graham Lowe, Donna Cohen, Howard Felton, Sarah Raj, Ken |
author_sort | Holliman, Graham |
collection | PubMed |
description | Increasing evidence regarding positive effects of exposure to sunlight has led to suggestions that current advice may be overly weighted in favour of avoidance. UV-A has been reported to lower blood pressure, possibly through nitric oxide (NO) production in skin. Here, we set out to investigate effects of UV-A and solar-simulated radiation on the potential source of dermal NO, the effective doses and wavelengths, the responsiveness of different human skin cells, the magnitude of inter-individual differences and the potential influence of age. We utilised isogenic keratinocytes, microvascular endothelial cells, melanocytes and fibroblasts isolated from 36 human skins ranging from neonates to 86 years old. We show that keratinocytes and microvascular endothelial cells show greatest NO release following biologically relevant doses of UV-A. This was consistent across multiple neonatal donors and the effect is maintained in adult keratinocytes. Our observations are consistent with a bi-phasic mechanism by which UV-A can trigger vasodilatory effects. Analyses of NO-production spectra adds further evidence that nitrites in skin cells are the source of UV-mediated NO release. These potentially positive effects of ultraviolet radiation lend support for objective assessment of environmental influence on human health and the idea of “healthy sun exposure”. |
format | Online Article Text |
id | pubmed-5593895 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55938952017-09-13 Ultraviolet Radiation-Induced Production of Nitric Oxide:A multi-cell and multi-donor analysis Holliman, Graham Lowe, Donna Cohen, Howard Felton, Sarah Raj, Ken Sci Rep Article Increasing evidence regarding positive effects of exposure to sunlight has led to suggestions that current advice may be overly weighted in favour of avoidance. UV-A has been reported to lower blood pressure, possibly through nitric oxide (NO) production in skin. Here, we set out to investigate effects of UV-A and solar-simulated radiation on the potential source of dermal NO, the effective doses and wavelengths, the responsiveness of different human skin cells, the magnitude of inter-individual differences and the potential influence of age. We utilised isogenic keratinocytes, microvascular endothelial cells, melanocytes and fibroblasts isolated from 36 human skins ranging from neonates to 86 years old. We show that keratinocytes and microvascular endothelial cells show greatest NO release following biologically relevant doses of UV-A. This was consistent across multiple neonatal donors and the effect is maintained in adult keratinocytes. Our observations are consistent with a bi-phasic mechanism by which UV-A can trigger vasodilatory effects. Analyses of NO-production spectra adds further evidence that nitrites in skin cells are the source of UV-mediated NO release. These potentially positive effects of ultraviolet radiation lend support for objective assessment of environmental influence on human health and the idea of “healthy sun exposure”. Nature Publishing Group UK 2017-09-11 /pmc/articles/PMC5593895/ /pubmed/28894213 http://dx.doi.org/10.1038/s41598-017-11567-5 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Holliman, Graham Lowe, Donna Cohen, Howard Felton, Sarah Raj, Ken Ultraviolet Radiation-Induced Production of Nitric Oxide:A multi-cell and multi-donor analysis |
title | Ultraviolet Radiation-Induced Production of Nitric Oxide:A multi-cell and multi-donor analysis |
title_full | Ultraviolet Radiation-Induced Production of Nitric Oxide:A multi-cell and multi-donor analysis |
title_fullStr | Ultraviolet Radiation-Induced Production of Nitric Oxide:A multi-cell and multi-donor analysis |
title_full_unstemmed | Ultraviolet Radiation-Induced Production of Nitric Oxide:A multi-cell and multi-donor analysis |
title_short | Ultraviolet Radiation-Induced Production of Nitric Oxide:A multi-cell and multi-donor analysis |
title_sort | ultraviolet radiation-induced production of nitric oxide:a multi-cell and multi-donor analysis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5593895/ https://www.ncbi.nlm.nih.gov/pubmed/28894213 http://dx.doi.org/10.1038/s41598-017-11567-5 |
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