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Chlordecone: development of a physiologically based pharmacokinetic tool to support human health risks assessments
Chlordecone (CD; Kepone™) is a carcinogenic organochlorine insecticide with neurological, reproductive, and developmental toxicity that was widely used in the French West Indies (FWI) from 1973 to 1993 to fight banana weevils. Although CD has not been used there for more than 25 years, it still pers...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8921106/ https://www.ncbi.nlm.nih.gov/pubmed/35122515 http://dx.doi.org/10.1007/s00204-022-03231-3 |
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author | Emond, Claude Multigner, Luc |
author_facet | Emond, Claude Multigner, Luc |
author_sort | Emond, Claude |
collection | PubMed |
description | Chlordecone (CD; Kepone™) is a carcinogenic organochlorine insecticide with neurological, reproductive, and developmental toxicity that was widely used in the French West Indies (FWI) from 1973 to 1993 to fight banana weevils. Although CD has not been used there for more than 25 years, it still persists in the environment and has polluted the waterways and soil of current and older banana fields. Today, human exposure to CD in the FWI mainly arises from consuming contaminated foodstuffs. The aims of this study were to develop a physiologically based pharmacokinetic (PBPK) model in the rat and extrapolate it to humans based on available pharmacokinetic data in the literature. A comparison of simulations using the rat model with published experimental datasets showed reasonable predictability for single and repetitive doses, and, thus, it was extrapolated to humans. The human PBPK model, which has seven compartments, is able to simulate the blood concentrations of CD in human populations and estimate the corresponding external dose using the reverse dosimetry approach. The human PBPK model will make it possible to improve quantitative health risk assessments for CD contamination and reassess the current chronic toxicological reference values to protect the FWI population. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00204-022-03231-3. |
format | Online Article Text |
id | pubmed-8921106 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-89211062022-03-17 Chlordecone: development of a physiologically based pharmacokinetic tool to support human health risks assessments Emond, Claude Multigner, Luc Arch Toxicol Toxicokinetics and Metabolism Chlordecone (CD; Kepone™) is a carcinogenic organochlorine insecticide with neurological, reproductive, and developmental toxicity that was widely used in the French West Indies (FWI) from 1973 to 1993 to fight banana weevils. Although CD has not been used there for more than 25 years, it still persists in the environment and has polluted the waterways and soil of current and older banana fields. Today, human exposure to CD in the FWI mainly arises from consuming contaminated foodstuffs. The aims of this study were to develop a physiologically based pharmacokinetic (PBPK) model in the rat and extrapolate it to humans based on available pharmacokinetic data in the literature. A comparison of simulations using the rat model with published experimental datasets showed reasonable predictability for single and repetitive doses, and, thus, it was extrapolated to humans. The human PBPK model, which has seven compartments, is able to simulate the blood concentrations of CD in human populations and estimate the corresponding external dose using the reverse dosimetry approach. The human PBPK model will make it possible to improve quantitative health risk assessments for CD contamination and reassess the current chronic toxicological reference values to protect the FWI population. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00204-022-03231-3. Springer Berlin Heidelberg 2022-02-05 2022 /pmc/articles/PMC8921106/ /pubmed/35122515 http://dx.doi.org/10.1007/s00204-022-03231-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 | Toxicokinetics and Metabolism Emond, Claude Multigner, Luc Chlordecone: development of a physiologically based pharmacokinetic tool to support human health risks assessments |
title | Chlordecone: development of a physiologically based pharmacokinetic tool to support human health risks assessments |
title_full | Chlordecone: development of a physiologically based pharmacokinetic tool to support human health risks assessments |
title_fullStr | Chlordecone: development of a physiologically based pharmacokinetic tool to support human health risks assessments |
title_full_unstemmed | Chlordecone: development of a physiologically based pharmacokinetic tool to support human health risks assessments |
title_short | Chlordecone: development of a physiologically based pharmacokinetic tool to support human health risks assessments |
title_sort | chlordecone: development of a physiologically based pharmacokinetic tool to support human health risks assessments |
topic | Toxicokinetics and Metabolism |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8921106/ https://www.ncbi.nlm.nih.gov/pubmed/35122515 http://dx.doi.org/10.1007/s00204-022-03231-3 |
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