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A revised action spectrum for vitamin D synthesis by suberythemal UV radiation exposure in humans in vivo

Action spectra are important biological weighting functions for risk/benefit analyses of ultraviolet (UV) radiation (UVR) exposure. One important human benefit of exposure to terrestrial solar UVB radiation (∼295 to 315 nm) is the cutaneous synthesis of vitamin D(3) that is initiated by the photocon...

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Autores principales: Young, Antony R., Morgan, Kylie A., Harrison, Graham I., Lawrence, Karl P., Petersen, Bibi, Wulf, Hans Christian, Philipsen, Peter A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8501902/
https://www.ncbi.nlm.nih.gov/pubmed/34580202
http://dx.doi.org/10.1073/pnas.2015867118
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author Young, Antony R.
Morgan, Kylie A.
Harrison, Graham I.
Lawrence, Karl P.
Petersen, Bibi
Wulf, Hans Christian
Philipsen, Peter A.
author_facet Young, Antony R.
Morgan, Kylie A.
Harrison, Graham I.
Lawrence, Karl P.
Petersen, Bibi
Wulf, Hans Christian
Philipsen, Peter A.
author_sort Young, Antony R.
collection PubMed
description Action spectra are important biological weighting functions for risk/benefit analyses of ultraviolet (UV) radiation (UVR) exposure. One important human benefit of exposure to terrestrial solar UVB radiation (∼295 to 315 nm) is the cutaneous synthesis of vitamin D(3) that is initiated by the photoconversion of 7-dehydrocholesterol to previtamin D(3). An action spectrum for this process that is followed by other nonphotochemical steps to achieve biologically active vitamin D(3) has been established from ex vivo data and is widely used, although its validity has been questioned. We tested this action spectrum in vivo by full- or partial-body suberythemal irradiation of 75 healthy young volunteers with five different polychromatic UVR spectra on five serial occasions. Serum 25-hydroxyvitamin D(3) [25(OH)D(3)] levels, as the most accurate measure of vitamin D(3) status, were assessed before, during, and after the exposures. These were then used to generate linear dose–response curves that were different for each UVR spectrum. It was established that the previtamin D(3) action spectrum was not valid when related to the serum 25(OH)D(3) levels, as weighting the UVR doses with this action spectrum did not result in a common regression line unless it was adjusted by a blue shift, with 5 nm giving the best fit. Such a blue shift is in accord with the published in vitro action spectra for vitamin D(3) synthesis. Thus, calculations regarding the risk (typically erythema) versus the benefit of exposure to solar UVR based on the ex vivo previtamin D(3) action spectrum require revision.
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spelling pubmed-85019022021-10-26 A revised action spectrum for vitamin D synthesis by suberythemal UV radiation exposure in humans in vivo Young, Antony R. Morgan, Kylie A. Harrison, Graham I. Lawrence, Karl P. Petersen, Bibi Wulf, Hans Christian Philipsen, Peter A. Proc Natl Acad Sci U S A Biological Sciences Action spectra are important biological weighting functions for risk/benefit analyses of ultraviolet (UV) radiation (UVR) exposure. One important human benefit of exposure to terrestrial solar UVB radiation (∼295 to 315 nm) is the cutaneous synthesis of vitamin D(3) that is initiated by the photoconversion of 7-dehydrocholesterol to previtamin D(3). An action spectrum for this process that is followed by other nonphotochemical steps to achieve biologically active vitamin D(3) has been established from ex vivo data and is widely used, although its validity has been questioned. We tested this action spectrum in vivo by full- or partial-body suberythemal irradiation of 75 healthy young volunteers with five different polychromatic UVR spectra on five serial occasions. Serum 25-hydroxyvitamin D(3) [25(OH)D(3)] levels, as the most accurate measure of vitamin D(3) status, were assessed before, during, and after the exposures. These were then used to generate linear dose–response curves that were different for each UVR spectrum. It was established that the previtamin D(3) action spectrum was not valid when related to the serum 25(OH)D(3) levels, as weighting the UVR doses with this action spectrum did not result in a common regression line unless it was adjusted by a blue shift, with 5 nm giving the best fit. Such a blue shift is in accord with the published in vitro action spectra for vitamin D(3) synthesis. Thus, calculations regarding the risk (typically erythema) versus the benefit of exposure to solar UVR based on the ex vivo previtamin D(3) action spectrum require revision. National Academy of Sciences 2021-10-05 2021-09-27 /pmc/articles/PMC8501902/ /pubmed/34580202 http://dx.doi.org/10.1073/pnas.2015867118 Text en Copyright © 2021 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by/4.0/This open access article is distributed under Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Biological Sciences
Young, Antony R.
Morgan, Kylie A.
Harrison, Graham I.
Lawrence, Karl P.
Petersen, Bibi
Wulf, Hans Christian
Philipsen, Peter A.
A revised action spectrum for vitamin D synthesis by suberythemal UV radiation exposure in humans in vivo
title A revised action spectrum for vitamin D synthesis by suberythemal UV radiation exposure in humans in vivo
title_full A revised action spectrum for vitamin D synthesis by suberythemal UV radiation exposure in humans in vivo
title_fullStr A revised action spectrum for vitamin D synthesis by suberythemal UV radiation exposure in humans in vivo
title_full_unstemmed A revised action spectrum for vitamin D synthesis by suberythemal UV radiation exposure in humans in vivo
title_short A revised action spectrum for vitamin D synthesis by suberythemal UV radiation exposure in humans in vivo
title_sort revised action spectrum for vitamin d synthesis by suberythemal uv radiation exposure in humans in vivo
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8501902/
https://www.ncbi.nlm.nih.gov/pubmed/34580202
http://dx.doi.org/10.1073/pnas.2015867118
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