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The fate of methylmercury through the formation of bismethylmercury sulfide as an intermediate in mice
A previous study by our group indicated that methylmercury (MeHg) is biotransformed to bismethylmercury sulfide [(MeHg)(2)S)] by interaction with reactive sulfur species (RSS) produced in the body. In the present study, we explored the transformation of MeHg to (MeHg)(2)S in the gut and the subseque...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8413320/ https://www.ncbi.nlm.nih.gov/pubmed/34475444 http://dx.doi.org/10.1038/s41598-021-96579-y |
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author | Abiko, Yumi Katayama, Yusuke Zhao, Wenyang Horai, Sawako Sakurai, Kenji Kumagai, Yoshito |
author_facet | Abiko, Yumi Katayama, Yusuke Zhao, Wenyang Horai, Sawako Sakurai, Kenji Kumagai, Yoshito |
author_sort | Abiko, Yumi |
collection | PubMed |
description | A previous study by our group indicated that methylmercury (MeHg) is biotransformed to bismethylmercury sulfide [(MeHg)(2)S)] by interaction with reactive sulfur species (RSS) produced in the body. In the present study, we explored the transformation of MeHg to (MeHg)(2)S in the gut and the subsequent fate of (MeHg)(2)S in vitro and in vivo. An ex vivo experiment suggested the possibility of the extracellular transformation of MeHg to (MeHg)(2)S in the distal colon, and accordingly, the MeHg sulfur adduct was detected in the intestinal contents and feces of mice administered MeHg, suggesting that (MeHg)(2)S is formed through reactions between MeHg and RSS in the gut. In a cell-free system, we found that (MeHg)(2)S undergoes degradation in a time-dependent manner, resulting in the formation of mercury sulfide and dimethylmercury (DMeHg), as determined by X-ray diffraction and gas chromatography/mass spectrometry, respectively. We also identified DMeHg in the expiration after the intraperitoneal administration of (MeHg)(2)S to mice. Thus, our present study identified a new fate of MeHg through (MeHg)(2)S as an intermediate, which leads to conversion of volatile DMeHg in the body. |
format | Online Article Text |
id | pubmed-8413320 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-84133202021-09-07 The fate of methylmercury through the formation of bismethylmercury sulfide as an intermediate in mice Abiko, Yumi Katayama, Yusuke Zhao, Wenyang Horai, Sawako Sakurai, Kenji Kumagai, Yoshito Sci Rep Article A previous study by our group indicated that methylmercury (MeHg) is biotransformed to bismethylmercury sulfide [(MeHg)(2)S)] by interaction with reactive sulfur species (RSS) produced in the body. In the present study, we explored the transformation of MeHg to (MeHg)(2)S in the gut and the subsequent fate of (MeHg)(2)S in vitro and in vivo. An ex vivo experiment suggested the possibility of the extracellular transformation of MeHg to (MeHg)(2)S in the distal colon, and accordingly, the MeHg sulfur adduct was detected in the intestinal contents and feces of mice administered MeHg, suggesting that (MeHg)(2)S is formed through reactions between MeHg and RSS in the gut. In a cell-free system, we found that (MeHg)(2)S undergoes degradation in a time-dependent manner, resulting in the formation of mercury sulfide and dimethylmercury (DMeHg), as determined by X-ray diffraction and gas chromatography/mass spectrometry, respectively. We also identified DMeHg in the expiration after the intraperitoneal administration of (MeHg)(2)S to mice. Thus, our present study identified a new fate of MeHg through (MeHg)(2)S as an intermediate, which leads to conversion of volatile DMeHg in the body. Nature Publishing Group UK 2021-09-02 /pmc/articles/PMC8413320/ /pubmed/34475444 http://dx.doi.org/10.1038/s41598-021-96579-y Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Abiko, Yumi Katayama, Yusuke Zhao, Wenyang Horai, Sawako Sakurai, Kenji Kumagai, Yoshito The fate of methylmercury through the formation of bismethylmercury sulfide as an intermediate in mice |
title | The fate of methylmercury through the formation of bismethylmercury sulfide as an intermediate in mice |
title_full | The fate of methylmercury through the formation of bismethylmercury sulfide as an intermediate in mice |
title_fullStr | The fate of methylmercury through the formation of bismethylmercury sulfide as an intermediate in mice |
title_full_unstemmed | The fate of methylmercury through the formation of bismethylmercury sulfide as an intermediate in mice |
title_short | The fate of methylmercury through the formation of bismethylmercury sulfide as an intermediate in mice |
title_sort | fate of methylmercury through the formation of bismethylmercury sulfide as an intermediate in mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8413320/ https://www.ncbi.nlm.nih.gov/pubmed/34475444 http://dx.doi.org/10.1038/s41598-021-96579-y |
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