Literature DB >> 23720389

Evaluation of critical body residue data for acute narcosis in aquatic organisms.

L S McCarty1, J A Arnot, D Mackay.   

Abstract

The Environmental Residue Effects Database was evaluated to identify critical body residues of organic chemicals causing acute baseline neutral narcosis in aquatic organisms. Over 15 000 records for >400 chemicals were evaluated. Mean molar critical body residues in the final data set of 161 records for 29 chemicals were within published ranges but varied within and among chemicals and species (~3 orders of magnitude), and lipid normalization did not consistently decrease variability. All 29 chemicals can act as baseline neutral narcotics, but chemicals and/or their metabolites may also act by nonnarcotic modes of action. Specifically, nonnarcotic toxicity of polycyclic aromatic hydrocarbons and/or their biotransformation derivatives may be a significant source of variability. Complete testing of the narcosis-critical body residue hypothesis was confounded by data gaps for key toxicity modifying factors such as metabolite formation/toxicity, lipid content/composition, other modes of toxic action, and lack of steady-state status. Such problems impede determination of the precise, accurate toxicity estimates necessary for sound toxicological comparisons. Thus, neither the data nor the chemicals in the final data set should be considered definitive. Changes to testing designs and methods are necessary to improve data collection and critical body residue interpretation for hazard and risk assessment. Each of the toxicity metrics discussed-wet weight and lipid weight critical body residues, volume fraction in organism lipid, and chemical activity-has advantages, but all are subject to the same toxicity modifying factors.
© 2013 SETAC.

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Year:  2013        PMID: 23720389     DOI: 10.1002/etc.2289

Source DB:  PubMed          Journal:  Environ Toxicol Chem        ISSN: 0730-7268            Impact factor:   3.742


  4 in total

1.  Measurement of kinetic parameters for biotransformation of polycyclic aromatic hydrocarbons by trout liver S9 fractions: Implications for bioaccumulation assessment.

Authors:  John W Nichols; Melanie A Ladd; Patrick N Fitzsimmons
Journal:  Appl In Vitro Toxicol       Date:  2018

2.  The chemical exposure toxicity space (CETS) model: Displaying exposure time, aqueous and organic concentration, activity, and onset of toxicity.

Authors:  Donald Mackay; Alena K D Celsie; J Mark Parnis; Lynn S McCarty; Jon A Arnot; David E Powell
Journal:  Environ Toxicol Chem       Date:  2016-12-30       Impact factor: 3.742

3.  Comparative toxicity of hydrocarbons for evaluation of Lysmata boggessi as an experimental proxy for deep-water column micronekton.

Authors:  D Abigail Renegar; Nicholas R Turner; Gopal Bera; Eileen G Whitemiller; Bernhard M Riegl; José L Sericano; Anthony Knap
Journal:  Toxicol Rep       Date:  2022-03-26

4.  Evaluation of the Inherent Toxicity Concept in Environmental Toxicology and Risk Assessment.

Authors:  L S McCarty; C J Borgert; L D Burgoon
Journal:  Environ Toxicol Chem       Date:  2020-11-10       Impact factor: 3.742

  4 in total

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