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ToxSci Advance Access originally published online on December 20, 2007
Toxicological Sciences 2008 105(1):5-23; doi:10.1093/toxsci/kfm303
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© The Author 2007. Published by Oxford University Press on behalf of the Society of Toxicology. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

Nonadditive effects of PAHs on Early Vertebrate Development: mechanisms and implications for risk assessment

Sonya M. Billiard{dagger},§,1, Joel N. Meyer{dagger}, Deena M. Wassenberg{ddagger}, Peter V. Hodson§ and Richard T. Di Giulio*,{dagger}

* Health Canada, Health Products and Food Branch, Bureau of Chemical Safety, Ottawa, Ontario K1A 0L2, Canada {dagger} Integrated Toxicology Program, Nicholas School of the Environment, Duke University, Durham, North Carolina 27708-0328 {ddagger} College of Biological Sciences, University of Minnesota, St Paul, Minnesota 55108 § School of Environmental Studies, Queen's University, Kingston, Ontario K7L 3N6, Canada

1 To whom correspondence should be addressed at Health Canada, Health Products and Food Branch, Bureau of Chemical Safety, 251 Sir Frederick Banting Driveway, Postal Locator 2204C, Ottawa, Ontario K1A OL2, Canada. E-mail: sonya_billiard{at}hc-sc.gc.ca.

Received September 4, 2007; accepted December 11, 2007


   Abstract

Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous environmental contaminants. Traditionally, much of the research has focused on the carcinogenic potential of specific PAHs, such as benzo(a)pyrene, but recent studies using sensitive fish models have shown that exposure to PAHs alters normal fish development. Some PAHs can induce a teratogenic phenotype similar to that caused by planar halogenated aromatic hydrocarbons, such as dioxin. Consequently, mechanism of action is often equated between the two classes of compounds. Unlike dioxins, however, the developmental toxicity of PAH mixtures is not necessarily additive. This is likely related to their multiple mechanisms of toxicity and their rapid biotransformation by CYP1 enzymes to metabolites with a wide array of structures and potential toxicities. This has important implications for risk assessment and management as the current approach for complex mixtures of PAHs usually assumes concentration addition. In this review we discuss our current knowledge of teratogenicity caused by single PAH compounds and by mixtures and the importance of these latest findings for adequately assessing risk of PAHs to humans and wildlife. Throughout, we place particular emphasis on research on the early life stages of fish, which has proven to be a sensitive and rapid developmental model to elucidate effects of hydrocarbon mixtures.

Key Words: PAHs; DLCs; developmental toxicity; synergism; AHR; CYP1A; risk assessment.


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