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Distinct arsenic metabolites following seaweed consumption in humans
Seaweeds contain arsenic primarily in the form of arsenosugars, which can be metabolized to a wide range of arsenic compounds. To characterize human exposure to arsenic from seaweed consumption, we determined concentrations of arsenic species in locally available seaweeds, and assessed urinary arsen...
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/PMC5478658/ https://www.ncbi.nlm.nih.gov/pubmed/28634348 http://dx.doi.org/10.1038/s41598-017-03883-7 |
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author | Taylor, Vivien F. Li, Zhigang Sayarath, Vicki Palys, Thomas J. Morse, Kevin R. Scholz-Bright, Rachel A. Karagas, Margaret R. |
author_facet | Taylor, Vivien F. Li, Zhigang Sayarath, Vicki Palys, Thomas J. Morse, Kevin R. Scholz-Bright, Rachel A. Karagas, Margaret R. |
author_sort | Taylor, Vivien F. |
collection | PubMed |
description | Seaweeds contain arsenic primarily in the form of arsenosugars, which can be metabolized to a wide range of arsenic compounds. To characterize human exposure to arsenic from seaweed consumption, we determined concentrations of arsenic species in locally available seaweeds, and assessed urinary arsenic compounds in an experimental feeding study. A total of 11 volunteers consumed 10 g per day of three types of seaweeds (nori, kombu, and wakame) for three days each, while abstaining from rice and seafood following a three-day washout period. Urinary arsenosugars and their metabolites (including dimethyl arsenate (DMA), thio-dimethylarsinoylethanol (thio-DMAE), thio-dimethylarsinoylacetate (thio-DMAA), and thio-DMA) were measured in spot urine samples prior to seaweed consumption, and in 24-hour urine samples while consuming seaweed. Commercial products made from whole seaweed had substantial concentrations of arsenic (12–84 µg/g), dominated by arsenosugars. Intact arsenosugars along with DMA, thio-DMAA, thio-DMAE all increased in urine after ingesting each type of seaweed, and varied between seaweed types and between individuals. Only trace levels of the known toxic metabolite, thio-DMA, were observed, across individuals. Thio-DMAE and thio-DMAA are unique products of arsenosugar breakdown, thus assessment of these compounds may help to identify dietary intake of arsenic from seaweed from other exposure pathways. |
format | Online Article Text |
id | pubmed-5478658 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-54786582017-06-23 Distinct arsenic metabolites following seaweed consumption in humans Taylor, Vivien F. Li, Zhigang Sayarath, Vicki Palys, Thomas J. Morse, Kevin R. Scholz-Bright, Rachel A. Karagas, Margaret R. Sci Rep Article Seaweeds contain arsenic primarily in the form of arsenosugars, which can be metabolized to a wide range of arsenic compounds. To characterize human exposure to arsenic from seaweed consumption, we determined concentrations of arsenic species in locally available seaweeds, and assessed urinary arsenic compounds in an experimental feeding study. A total of 11 volunteers consumed 10 g per day of three types of seaweeds (nori, kombu, and wakame) for three days each, while abstaining from rice and seafood following a three-day washout period. Urinary arsenosugars and their metabolites (including dimethyl arsenate (DMA), thio-dimethylarsinoylethanol (thio-DMAE), thio-dimethylarsinoylacetate (thio-DMAA), and thio-DMA) were measured in spot urine samples prior to seaweed consumption, and in 24-hour urine samples while consuming seaweed. Commercial products made from whole seaweed had substantial concentrations of arsenic (12–84 µg/g), dominated by arsenosugars. Intact arsenosugars along with DMA, thio-DMAA, thio-DMAE all increased in urine after ingesting each type of seaweed, and varied between seaweed types and between individuals. Only trace levels of the known toxic metabolite, thio-DMA, were observed, across individuals. Thio-DMAE and thio-DMAA are unique products of arsenosugar breakdown, thus assessment of these compounds may help to identify dietary intake of arsenic from seaweed from other exposure pathways. Nature Publishing Group UK 2017-06-20 /pmc/articles/PMC5478658/ /pubmed/28634348 http://dx.doi.org/10.1038/s41598-017-03883-7 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 Taylor, Vivien F. Li, Zhigang Sayarath, Vicki Palys, Thomas J. Morse, Kevin R. Scholz-Bright, Rachel A. Karagas, Margaret R. Distinct arsenic metabolites following seaweed consumption in humans |
title | Distinct arsenic metabolites following seaweed consumption in humans |
title_full | Distinct arsenic metabolites following seaweed consumption in humans |
title_fullStr | Distinct arsenic metabolites following seaweed consumption in humans |
title_full_unstemmed | Distinct arsenic metabolites following seaweed consumption in humans |
title_short | Distinct arsenic metabolites following seaweed consumption in humans |
title_sort | distinct arsenic metabolites following seaweed consumption in humans |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5478658/ https://www.ncbi.nlm.nih.gov/pubmed/28634348 http://dx.doi.org/10.1038/s41598-017-03883-7 |
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