Literature DB >> 35779734

How to analyse and account for interactions in mixture toxicity with toxicokinetic-toxicodynamic models.

Sylvain Bart1, Stephen Short2, Tjalling Jager3, Emily J Eagles4, Alex Robinson4, Claire Badder2, Elma Lahive4, David J Spurgeon4, Roman Ashauer5.   

Abstract

The assessment of chemical mixture toxicity is one of the major challenges in ecotoxicology. Chemicals can interact, leading to more or less effects than expected, commonly named synergism and antagonism respectively. The classic ad hoc approach for the assessment of mixture effects is based on dose-response curves at a single time point, and is limited to identifying a mixture interaction but cannot provide predictions for untested exposure durations, nor for scenarios where exposure varies in time. We here propose a new approach using toxicokinetic-toxicodynamic modelling: The General Unified Threshold model of Survival (GUTS) framework, recently extended for mixture toxicity assessment. We designed a dedicated mechanistic interaction module coupled with the GUTS mixture model to i) identify interactions, ii) test hypotheses to identify which chemical is likely responsible for the interaction, and finally iii) simulate and predict the effect of synergistic and antagonistic mixtures. We tested the modelling approach experimentally with two species (Enchytraeus crypticus and Mamestra brassicae) exposed to different potentially synergistic mixtures (composed of: prochloraz, imidacloprid, cypermethrin, azoxystrobin, chlorothalonil, and chlorpyrifos). Furthermore, we also tested the model with previously published experimental data on two other species (Bombus terrestris and Daphnia magna) exposed to pesticide mixtures (clothianidin, propiconazole, dimethoate, imidacloprid and thiacloprid) found to be synergistic or antagonistic with the classic approach. The results showed an accurate simulation of synergistic and antagonistic effects for the different tested species and mixtures. This modelling approach can identify interactions accounting for the entire time of exposure, and not only at one time point as in the classic approach, and provides predictions of the mixture effect for untested mixture exposure scenarios, including those with time-variable mixture composition.
Copyright © 2022 The Authors. Published by Elsevier B.V. All rights reserved.

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Keywords:  Acute toxicity; Effect modelling; Mixture hazard; Survival assay; TKTD modelling

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Year:  2022        PMID: 35779734     DOI: 10.1016/j.scitotenv.2022.157048

Source DB:  PubMed          Journal:  Sci Total Environ        ISSN: 0048-9697            Impact factor:   10.753


  1 in total

1.  Acute, chronic, and genotoxic studies on the protopine total alkaloids of the Macleaya cordata (willd.) R. Br. in rodents.

Authors:  Zhen Dong; Shu-Sheng Tang; Xiao-Lan Ma; Bin Tan; Zhao-Shan Tang; Chang-Hong Li; Zi-Hui Yang; Jian-Guo Zeng
Journal:  Front Pharmacol       Date:  2022-09-28       Impact factor: 5.988

  1 in total

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