Cargando…

Toxicity assessment of hexafluoropropylene oxide-dimer acid on morphology, heart physiology, and gene expression during zebrafish (Danio rerio) development

Hexafluoropropylene oxide-dimer acid (HFPO-DA) is one of the emerging replacements for the “forever” carcinogenic and toxic long-chain PFAS. HFPO-DA is a polymerization aid used for manufacturing fluoropolymers, whose global distribution and undetermined toxic properties are a concern regarding huma...

Descripción completa

Detalles Bibliográficos
Autores principales: Gong, Sylvia, McLamb, Flannery, Shea, Damian, Vu, Jeanne P., Vasquez, Miguel F., Feng, Zuying, Bozinovic, Kesten, Hirata, Ken K., Gersberg, Richard M., Bozinovic, Goran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10017623/
https://www.ncbi.nlm.nih.gov/pubmed/36462083
http://dx.doi.org/10.1007/s11356-022-24542-z
_version_ 1784907630500642816
author Gong, Sylvia
McLamb, Flannery
Shea, Damian
Vu, Jeanne P.
Vasquez, Miguel F.
Feng, Zuying
Bozinovic, Kesten
Hirata, Ken K.
Gersberg, Richard M.
Bozinovic, Goran
author_facet Gong, Sylvia
McLamb, Flannery
Shea, Damian
Vu, Jeanne P.
Vasquez, Miguel F.
Feng, Zuying
Bozinovic, Kesten
Hirata, Ken K.
Gersberg, Richard M.
Bozinovic, Goran
author_sort Gong, Sylvia
collection PubMed
description Hexafluoropropylene oxide-dimer acid (HFPO-DA) is one of the emerging replacements for the “forever” carcinogenic and toxic long-chain PFAS. HFPO-DA is a polymerization aid used for manufacturing fluoropolymers, whose global distribution and undetermined toxic properties are a concern regarding human and ecological health. To assess embryotoxic potential, zebrafish embryos were exposed to HFPO-DA at concentrations of 0.5–20,000 mg/L at 24-, 48-, and 72-h post-fertilization (hpf). Heart rate increased significantly in embryos exposed to 2 mg/L and 10 mg/L HFPO-DA across all time points. Spinal deformities and edema phenotypes were evident among embryos exposed to 1000–16,000 mg/L HFPO-DA at 72 hpf. A median lethal concentration (LC(50)) was derived as 7651 mg/L at 72 hpf. Shallow RNA sequencing analysis of 9465 transcripts identified 38 consistently differentially expressed genes at 0.5 mg/L, 1 mg/L, 2 mg/L, and 10 mg/L HFPO-DA exposures. Notably, seven downregulated genes were associated with visual response, and seven upregulated genes were expressed in or regulated the cardiovascular system. This study identifies biological targets and molecular pathways affected during animal development by an emerging, potentially problematic, and ubiquitous industrial chemical. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11356-022-24542-z.
format Online
Article
Text
id pubmed-10017623
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Springer Berlin Heidelberg
record_format MEDLINE/PubMed
spelling pubmed-100176232023-03-17 Toxicity assessment of hexafluoropropylene oxide-dimer acid on morphology, heart physiology, and gene expression during zebrafish (Danio rerio) development Gong, Sylvia McLamb, Flannery Shea, Damian Vu, Jeanne P. Vasquez, Miguel F. Feng, Zuying Bozinovic, Kesten Hirata, Ken K. Gersberg, Richard M. Bozinovic, Goran Environ Sci Pollut Res Int Research Article Hexafluoropropylene oxide-dimer acid (HFPO-DA) is one of the emerging replacements for the “forever” carcinogenic and toxic long-chain PFAS. HFPO-DA is a polymerization aid used for manufacturing fluoropolymers, whose global distribution and undetermined toxic properties are a concern regarding human and ecological health. To assess embryotoxic potential, zebrafish embryos were exposed to HFPO-DA at concentrations of 0.5–20,000 mg/L at 24-, 48-, and 72-h post-fertilization (hpf). Heart rate increased significantly in embryos exposed to 2 mg/L and 10 mg/L HFPO-DA across all time points. Spinal deformities and edema phenotypes were evident among embryos exposed to 1000–16,000 mg/L HFPO-DA at 72 hpf. A median lethal concentration (LC(50)) was derived as 7651 mg/L at 72 hpf. Shallow RNA sequencing analysis of 9465 transcripts identified 38 consistently differentially expressed genes at 0.5 mg/L, 1 mg/L, 2 mg/L, and 10 mg/L HFPO-DA exposures. Notably, seven downregulated genes were associated with visual response, and seven upregulated genes were expressed in or regulated the cardiovascular system. This study identifies biological targets and molecular pathways affected during animal development by an emerging, potentially problematic, and ubiquitous industrial chemical. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11356-022-24542-z. Springer Berlin Heidelberg 2022-12-03 2023 /pmc/articles/PMC10017623/ /pubmed/36462083 http://dx.doi.org/10.1007/s11356-022-24542-z 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 Research Article
Gong, Sylvia
McLamb, Flannery
Shea, Damian
Vu, Jeanne P.
Vasquez, Miguel F.
Feng, Zuying
Bozinovic, Kesten
Hirata, Ken K.
Gersberg, Richard M.
Bozinovic, Goran
Toxicity assessment of hexafluoropropylene oxide-dimer acid on morphology, heart physiology, and gene expression during zebrafish (Danio rerio) development
title Toxicity assessment of hexafluoropropylene oxide-dimer acid on morphology, heart physiology, and gene expression during zebrafish (Danio rerio) development
title_full Toxicity assessment of hexafluoropropylene oxide-dimer acid on morphology, heart physiology, and gene expression during zebrafish (Danio rerio) development
title_fullStr Toxicity assessment of hexafluoropropylene oxide-dimer acid on morphology, heart physiology, and gene expression during zebrafish (Danio rerio) development
title_full_unstemmed Toxicity assessment of hexafluoropropylene oxide-dimer acid on morphology, heart physiology, and gene expression during zebrafish (Danio rerio) development
title_short Toxicity assessment of hexafluoropropylene oxide-dimer acid on morphology, heart physiology, and gene expression during zebrafish (Danio rerio) development
title_sort toxicity assessment of hexafluoropropylene oxide-dimer acid on morphology, heart physiology, and gene expression during zebrafish (danio rerio) development
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10017623/
https://www.ncbi.nlm.nih.gov/pubmed/36462083
http://dx.doi.org/10.1007/s11356-022-24542-z
work_keys_str_mv AT gongsylvia toxicityassessmentofhexafluoropropyleneoxidedimeracidonmorphologyheartphysiologyandgeneexpressionduringzebrafishdanioreriodevelopment
AT mclambflannery toxicityassessmentofhexafluoropropyleneoxidedimeracidonmorphologyheartphysiologyandgeneexpressionduringzebrafishdanioreriodevelopment
AT sheadamian toxicityassessmentofhexafluoropropyleneoxidedimeracidonmorphologyheartphysiologyandgeneexpressionduringzebrafishdanioreriodevelopment
AT vujeannep toxicityassessmentofhexafluoropropyleneoxidedimeracidonmorphologyheartphysiologyandgeneexpressionduringzebrafishdanioreriodevelopment
AT vasquezmiguelf toxicityassessmentofhexafluoropropyleneoxidedimeracidonmorphologyheartphysiologyandgeneexpressionduringzebrafishdanioreriodevelopment
AT fengzuying toxicityassessmentofhexafluoropropyleneoxidedimeracidonmorphologyheartphysiologyandgeneexpressionduringzebrafishdanioreriodevelopment
AT bozinovickesten toxicityassessmentofhexafluoropropyleneoxidedimeracidonmorphologyheartphysiologyandgeneexpressionduringzebrafishdanioreriodevelopment
AT hiratakenk toxicityassessmentofhexafluoropropyleneoxidedimeracidonmorphologyheartphysiologyandgeneexpressionduringzebrafishdanioreriodevelopment
AT gersbergrichardm toxicityassessmentofhexafluoropropyleneoxidedimeracidonmorphologyheartphysiologyandgeneexpressionduringzebrafishdanioreriodevelopment
AT bozinovicgoran toxicityassessmentofhexafluoropropyleneoxidedimeracidonmorphologyheartphysiologyandgeneexpressionduringzebrafishdanioreriodevelopment