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Citation
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HERO ID
5019336
Reference Type
Journal Article
Title
Systematic developmental neurotoxicity assessment of a representative PAH Superfund mixture using zebrafish
Author(s)
Geier, MC; James Minick, D; Truong, L; Tilton, S; Pande, P; Anderson, KA; Teeguardan, J; Tanguay, RL
Year
2018
Is Peer Reviewed?
1
Journal
Toxicology and Applied Pharmacology
ISSN:
0041-008X
EISSN:
1096-0333
Volume
354
Page Numbers
115-125
Language
English
PMID
29630969
DOI
10.1016/j.taap.2018.03.029
Web of Science Id
WOS:000442335500012
URL
https://linkinghub.elsevier.com/retrieve/pii/S0041008X18301212
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Abstract
Superfund sites often consist of complex mixtures of polycyclic aromatic hydrocarbons (PAHs). It is widely recognized that PAHs pose risks to human and environmental health, but the risks posed by exposure to PAH mixtures are unclear. We constructed an environmentally relevant PAH mixture with the top 10 most prevalent PAHs (SM10) from a Superfund site derived from environmental passive sampling data. Using the zebrafish model, we measured body burden at 48 hours post fertilization (hpf) and evaluated the developmental and neurotoxicity of SM10 and the 10 individual constituents at 24 hours post fertilization (hpf) and 5 days post fertilization (dpf). Zebrafish embryos were exposed from 6 to 120 hpf to (1) the SM10 mixture, (2) a variety of individual PAHs: pyrene, fluoranthene, retene, benzo[a]anthracene, chrysene, naphthalene, acenaphthene, phenanthrene, fluorene, and 2-methylnaphthalene. We demonstrated that SM10 and only 3 of the individual PAHs were developmentally toxic. Subsequently, we constructed and exposed developing zebrafish to two sub-mixtures: SM3 (comprised of 3 of the developmentally toxicity PAHs) and SM7 (7 non-developmentally toxic PAHs). We found that the SM3 toxicity profile was similar to SM10, and SM7 unexpectedly elicited developmental toxicity unlike that seen with its individual components. The results demonstrated that the overall developmental toxicity in the mixtures could be explained using the general concentration addition model. To determine if exposures activated the AHR pathway, spatial expression of CYP1A was evaluated in the 10 individual PAHs and the 3 mixtures at 5 dpf. Results showed activation of AHR in the liver and vasculature for the mixtures and some individual PAHs. Embryos exposed to SM10 during development and raised in chemical-free water into adulthood exhibited decreased learning and responses to startle stimulus indicating that developmental SM10 exposures affect neurobehavior. Collectively, these results exemplify the utility of zebrafish to investigate the developmental and neurotoxicity of complex mixtures.
Keywords
Aryl hydrocarbon receptor; Behavior; Biomarker; Cytochrome P4501A; Passive sampling; Polycyclic aromatic hydrocarbons
Tags
IRIS
•
Naphthalene
Database Searches
WOS
Combined data set
Data set for title/abstract screening
Excluded - PECO criteria not met (TIAB)
Supplemental material
Mechanistic
Mechanisms of cancer
Feb 2019 Update
WOS
•
Naphthalene (2021 Evidence mapping publication)
Database Searches
WOS
Combined data set
Data set for title/abstract screening
Excluded – PECO criteria not met
Supplemental material
Mechanistic
Mechanisms of cancer
Feb 2019 Update
WOS
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