Literature DB >> 20728228

Developing tools for risk assessment in protected species: Relative potencies inferred from competitive binding of halogenated aromatic hydrocarbons to aryl hydrocarbon receptors from beluga (Delphinapterus leucas) and mouse.

Brenda A Jensen1, Christopher M Reddy, Robert K Nelson, Mark E Hahn.   

Abstract

Persistent organic pollutants such as halogenated aromatic hydrocarbons (HAHs) biomagnify in food webs and accumulate to high concentrations in top predators like odontocete cetaceans (toothed whales). The most toxic HAHs are the 2,3,7,8-substituted halogenated dibenzo-p-dioxins and furans, and non-ortho-substituted polychlorinated biphenyls (PCBs), which exert their effects via the aryl hydrocarbon receptor (AHR). Understanding the impact of HAHs in wildlife is limited by the lack of taxon-specific information about the relative potencies of toxicologically important congeners. To assess whether Toxic Equivalency Factors (TEFs) determined in rodents are predictive of HAH relative potencies in a cetacean, we used beluga and mouse AHRs expressed in vitro from cloned cDNAs to measure the relative AHR-binding affinities of ten HAHs from five different structural classes. The rank order of mean IC(50)s for competitive binding to beluga AHR was: TCDD<TCDF<PCB-126<PCB-169<PCB-77<PCB-81⋘PCB-156∼PCB-128<PCB-105<PCB-118. The rank order of mean IC(50)s for binding to the mouse AHR was TCDD<TCDF<PCB-126<PCB-169<PCB-81<PCB-77<PCB-156≪PCB-128∼PCB-105∼PCB-118. K(i) values for binding of HAHs to beluga and mouse AHRs were highly correlated (r(2)=0.96). Comparison of K(i) values suggested that the beluga AHR had a higher affinity than the mouse AHR for most of the HAHs tested, consistent with the ∼2-fold higher [(3)H]TCDD binding affinity determined previously. These results are consistent with the World Health Organization mammalian TEFs for non- and mono-ortho PCB congeners. The comparatively high HAH binding affinities of the beluga AHR relative to those of an AHR from a dioxin-responsive mouse suggests that beluga, and perhaps cetaceans in general, may be particularly sensitive to the toxic effects of AHR agonists. Further study is warranted in order to more fully address this important question affecting protected and endangered species.
Copyright © 2010 Elsevier B.V. All rights reserved.

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Year:  2010        PMID: 20728228      PMCID: PMC3175004          DOI: 10.1016/j.aquatox.2010.07.021

Source DB:  PubMed          Journal:  Aquat Toxicol        ISSN: 0166-445X            Impact factor:   4.964


  41 in total

1.  Cloning and expression of a human Ah receptor cDNA.

Authors:  K M Dolwick; J V Schmidt; L A Carver; H I Swanson; C A Bradfield
Journal:  Mol Pharmacol       Date:  1993-11       Impact factor: 4.436

2.  Analysis of the four alleles of the murine aryl hydrocarbon receptor.

Authors:  A Poland; D Palen; E Glover
Journal:  Mol Pharmacol       Date:  1994-11       Impact factor: 4.436

3.  The examination and quantitation of tissue cytosolic receptors for 2,3,7,8-tetrachlorodibenzo-p-dioxin using hydroxylapatite.

Authors:  T A Gasiewicz; R A Neal
Journal:  Anal Biochem       Date:  1982-07-15       Impact factor: 3.365

4.  Relationship between the inhibition constant (K1) and the concentration of inhibitor which causes 50 per cent inhibition (I50) of an enzymatic reaction.

Authors:  Y Cheng; W H Prusoff
Journal:  Biochem Pharmacol       Date:  1973-12-01       Impact factor: 5.858

Review 5.  Polychlorinated biphenyls (PCBs), dibenzo-p-dioxins (PCDDs), dibenzofurans (PCDFs), and related compounds: environmental and mechanistic considerations which support the development of toxic equivalency factors (TEFs).

Authors:  S Safe
Journal:  Crit Rev Toxicol       Date:  1990       Impact factor: 5.635

6.  Dioxin binding activities of polymorphic forms of mouse and human arylhydrocarbon receptors.

Authors:  M Ema; N Ohe; M Suzuki; J Mimura; K Sogawa; S Ikawa; Y Fujii-Kuriyama
Journal:  J Biol Chem       Date:  1994-11-04       Impact factor: 5.157

7.  Catalytic and immunochemical characterization of hepatic microsomal cytochromes P450 in beluga whale (Delphinapterus leucas).

Authors:  R D White; M E Hahn; W L Lockhart; J J Stegeman
Journal:  Toxicol Appl Pharmacol       Date:  1994-05       Impact factor: 4.219

8.  Chlorobenzenes, chlorinated pesticides, coplanar chlorobiphenyls and other organochlorine compounds in Greenland biota.

Authors:  Katrin Vorkamp; Frank Riget; Marianne Glasius; Maria Pécseli; Michel Lebeuf; Derek Muir
Journal:  Sci Total Environ       Date:  2004-09-20       Impact factor: 7.963

9.  Cloning of the Ah-receptor cDNA reveals a distinctive ligand-activated transcription factor.

Authors:  K M Burbach; A Poland; C A Bradfield
Journal:  Proc Natl Acad Sci U S A       Date:  1992-09-01       Impact factor: 11.205

10.  Binding of polychlorinated biphenyls classified as either phenobarbitone-, 3-methylcholanthrene- or mixed-type inducers to cytosolic Ah receptor.

Authors:  S Bandiera; S Safe; A B Okey
Journal:  Chem Biol Interact       Date:  1982-04       Impact factor: 5.192

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  2 in total

Review 1.  Aryl hydrocarbon receptor ligands in cancer: friend and foe.

Authors:  Iain A Murray; Andrew D Patterson; Gary H Perdew
Journal:  Nat Rev Cancer       Date:  2014-12       Impact factor: 60.716

2.  PCB 126 and other dioxin-like PCBs specifically suppress hepatic PEPCK expression via the aryl hydrocarbon receptor.

Authors:  Wenshuo Zhang; Robert M Sargis; Paul A Volden; Christopher M Carmean; Xiao J Sun; Matthew J Brady
Journal:  PLoS One       Date:  2012-05-16       Impact factor: 3.240

  2 in total

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