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High-throughput characterization of chemical-associated embryonic behavioral changes predicts teratogenic outcomes

New strategies are needed to address the data gap between the bioactivity of chemicals in the environment versus existing hazard information. We address whether a high-throughput screening (HTS) system using a vertebrate organism (embryonic zebrafish) can characterize chemical-elicited behavioral re...

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Autores principales: Reif, David M., Truong, Lisa, Mandrell, David, Marvel, Skylar, Zhang, Guozhu, Tanguay, Robert L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4701642/
https://www.ncbi.nlm.nih.gov/pubmed/26126630
http://dx.doi.org/10.1007/s00204-015-1554-1
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author Reif, David M.
Truong, Lisa
Mandrell, David
Marvel, Skylar
Zhang, Guozhu
Tanguay, Robert L.
author_facet Reif, David M.
Truong, Lisa
Mandrell, David
Marvel, Skylar
Zhang, Guozhu
Tanguay, Robert L.
author_sort Reif, David M.
collection PubMed
description New strategies are needed to address the data gap between the bioactivity of chemicals in the environment versus existing hazard information. We address whether a high-throughput screening (HTS) system using a vertebrate organism (embryonic zebrafish) can characterize chemical-elicited behavioral responses at an early, 24 hours post-fertilization (hpf) stage that predict teratogenic consequences at a later developmental stage. The system was used to generate full concentration–response behavioral profiles at 24 hpf across 1060 ToxCast™ chemicals. Detailed, morphological evaluation of all individuals was performed as experimental follow-up at 5 days post-fertilization (dpf). Chemicals eliciting behavioral responses were also mapped against external HTS in vitro results to identify specific molecular targets and neurosignalling pathways. We found that, as an integrative measure of normal development, significant alterations in movement highlighted active chemicals representing several modes of action. These early behavioral responses were predictive for 17 specific developmental abnormalities and mortality measured at 5 dpf, often at lower (i.e., more potent) concentrations than those at which morphological effects were observed. Therefore, this system can provide rapid characterization of chemical-elicited behavioral responses at an early developmental stage that are predictive of observable adverse effects later in life. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00204-015-1554-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-47016422016-06-01 High-throughput characterization of chemical-associated embryonic behavioral changes predicts teratogenic outcomes Reif, David M. Truong, Lisa Mandrell, David Marvel, Skylar Zhang, Guozhu Tanguay, Robert L. Arch Toxicol Reproductive Toxicology New strategies are needed to address the data gap between the bioactivity of chemicals in the environment versus existing hazard information. We address whether a high-throughput screening (HTS) system using a vertebrate organism (embryonic zebrafish) can characterize chemical-elicited behavioral responses at an early, 24 hours post-fertilization (hpf) stage that predict teratogenic consequences at a later developmental stage. The system was used to generate full concentration–response behavioral profiles at 24 hpf across 1060 ToxCast™ chemicals. Detailed, morphological evaluation of all individuals was performed as experimental follow-up at 5 days post-fertilization (dpf). Chemicals eliciting behavioral responses were also mapped against external HTS in vitro results to identify specific molecular targets and neurosignalling pathways. We found that, as an integrative measure of normal development, significant alterations in movement highlighted active chemicals representing several modes of action. These early behavioral responses were predictive for 17 specific developmental abnormalities and mortality measured at 5 dpf, often at lower (i.e., more potent) concentrations than those at which morphological effects were observed. Therefore, this system can provide rapid characterization of chemical-elicited behavioral responses at an early developmental stage that are predictive of observable adverse effects later in life. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00204-015-1554-1) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2015-07-01 2016 /pmc/articles/PMC4701642/ /pubmed/26126630 http://dx.doi.org/10.1007/s00204-015-1554-1 Text en © The Author(s) 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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.
spellingShingle Reproductive Toxicology
Reif, David M.
Truong, Lisa
Mandrell, David
Marvel, Skylar
Zhang, Guozhu
Tanguay, Robert L.
High-throughput characterization of chemical-associated embryonic behavioral changes predicts teratogenic outcomes
title High-throughput characterization of chemical-associated embryonic behavioral changes predicts teratogenic outcomes
title_full High-throughput characterization of chemical-associated embryonic behavioral changes predicts teratogenic outcomes
title_fullStr High-throughput characterization of chemical-associated embryonic behavioral changes predicts teratogenic outcomes
title_full_unstemmed High-throughput characterization of chemical-associated embryonic behavioral changes predicts teratogenic outcomes
title_short High-throughput characterization of chemical-associated embryonic behavioral changes predicts teratogenic outcomes
title_sort high-throughput characterization of chemical-associated embryonic behavioral changes predicts teratogenic outcomes
topic Reproductive Toxicology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4701642/
https://www.ncbi.nlm.nih.gov/pubmed/26126630
http://dx.doi.org/10.1007/s00204-015-1554-1
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