Literature DB >> 7835546

Accumulation of polychlorinated dibenzo-p-dioxins and dibenzofurans in liver of control laboratory rats.

J P Vanden Heuvel1, G C Clark, A m Tritscher, G W Lucier.   

Abstract

Polychlorinated dibenzo-p-dioxins (PCDDs), dibenzofurans (PCDFs), and biphenyls belong to a class of compounds, the polyhalogenated aromatic hydrocarbons (PHAHs), which are ubiquitous environmental contaminants. Due to the existence of a common mechanism of action, i.e., binding to the Ah receptor, the activity of members of this class of compounds is generally expressed relative to the prototypical 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) as toxic equivalency factors (TEFs). In the present studies we examined the presence of liver of untreated PCDFs in standard laboratory feed and in the liver of untreated rats at three different ages (60, 140, and 200 days) in terms of concentration and in toxic equivalents (TEQs, TEF x concentration). Feed was shown to contain trace amounts of PCDDs and PCDFs and control rat liver was shown to contain several PCDD and PCDF congeners in terms of concentration of congener and concentration of TEQs contributed by that congener. The total concentration of TEQs increased with increasing age in rat liver, going from 20 ppt TEQ at 60 days to 78 ppt TEQ at 200 days of age. This accumulation in dioxin-like activity was due primarily to PCDFs. In particular the congener 2,3,4,7,8-pentachlorodibenzofuran accrued in untreated rat liver accounting for approximately 80% of the total TEQ at 200 days of age. These studies affirm the pervasive presence of PHAHs and suggest prudence in evaluating chronic rat studies in which interference from background levels of PCDDs and PCDFs may be a factor.

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Year:  1994        PMID: 7835546     DOI: 10.1006/faat.1994.1128

Source DB:  PubMed          Journal:  Fundam Appl Toxicol        ISSN: 0272-0590


  6 in total

1.  Immunotoxic effects of exposure of rats to xenobiotics via maternal lactation. Part I 2,3,7,8-tetrachlorodibenzo-p-dioxin.

Authors:  J S Badesha; G Maliji; B Flaks
Journal:  Int J Exp Pathol       Date:  1995-12       Impact factor: 1.925

2.  Accumulation of M1dG DNA adducts after chronic exposure to PCBs, but not from acute exposure to polychlorinated aromatic hydrocarbons.

Authors:  Yo-Chan Jeong; Nigel J Walker; Deborah E Burgin; Grace Kissling; Mayetri Gupta; Lawrence Kupper; Linda S Birnbaum; James A Swenberg
Journal:  Free Radic Biol Med       Date:  2008-05-15       Impact factor: 7.376

3.  Toxicity evaluation of bisphenol A administered by gavage to Sprague Dawley rats from gestation day 6 through postnatal day 90.

Authors:  K Barry Delclos; Luísa Camacho; Sherry M Lewis; Michelle M Vanlandingham; John R Latendresse; Greg R Olson; Kelly J Davis; Ralph E Patton; Gonçalo Gamboa da Costa; Kellie A Woodling; Matthew S Bryant; Mani Chidambaram; Raul Trbojevich; Beth E Juliar; Robert P Felton; Brett T Thorn
Journal:  Toxicol Sci       Date:  2014-02-04       Impact factor: 4.849

4.  Pyrimido[1,2-a]-purin-10(3H)-one, M1G, is less prone to artifact than base oxidation.

Authors:  Yo-Chan Jeong; Jun Nakamura; Patricia B Upton; James A Swenberg
Journal:  Nucleic Acids Res       Date:  2005-11-10       Impact factor: 16.971

Review 5.  Animal models of human response to dioxins.

Authors:  J A Grassman; S A Masten; N J Walker; G W Lucier
Journal:  Environ Health Perspect       Date:  1998-04       Impact factor: 9.031

Review 6.  Comparisons of estimated human body burdens of dioxinlike chemicals and TCDD body burdens in experimentally exposed animals.

Authors:  M J DeVito; L S Birnbaum; W H Farland; T A Gasiewicz
Journal:  Environ Health Perspect       Date:  1995-09       Impact factor: 9.031

  6 in total

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