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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...

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Autores principales: Emond, Claude, Multigner, Luc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
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.
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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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AT multignerluc chlordeconedevelopmentofaphysiologicallybasedpharmacokinetictooltosupporthumanhealthrisksassessments