2013
DOI: 10.1007/s00204-013-1186-2
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Comparison of intake and systemic relative effect potencies of dioxin-like compounds in female rats after a single oral dose

Abstract: Risk assessment for mixtures of dioxin-like compounds uses the toxic equivalency factor (TEF) approach. Although current WHO-TEFs are mostly based on oral administration, they are commonly used to determine toxicity equivalencies (TEQs) in human blood or tissues. However, the use of "intake" TEFs to calculate systemic TEQs in for example human blood, has never been validated. In this study, intake and systemic relative effect potencies (REPs) for 1,2,3,7,8-pentachlorodibenzo-p-dioxin (PeCDD), 2,3,4,7,8-pentach… Show more

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Cited by 11 publications
(15 citation statements)
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“…In the present subjects, the most contributed congeners to TEQ-PCDDs/Fs in breast milk were 1,2,3,7,8-PentaCDD (34%), 2,3,4,7,8-PentaCDF (18%), and 1,2,3,6,7,8-HexaCDF (14%), while the contribution rate of TCDD was 12% of TEQ-PCDDs/Fs. These congeners, particularly 2,3,4,7,8-PentaCDF, have different toxic effects compared with TCDD in human tissue or cells [ 17 , 18 ]. Thus, the effects of TEQ-PCDDs/Fs on motor coordination might be caused by other PCDDs/Fs congeners than TCDD.…”
Section: Discussionmentioning
confidence: 99%
“…In the present subjects, the most contributed congeners to TEQ-PCDDs/Fs in breast milk were 1,2,3,7,8-PentaCDD (34%), 2,3,4,7,8-PentaCDF (18%), and 1,2,3,6,7,8-HexaCDF (14%), while the contribution rate of TCDD was 12% of TEQ-PCDDs/Fs. These congeners, particularly 2,3,4,7,8-PentaCDF, have different toxic effects compared with TCDD in human tissue or cells [ 17 , 18 ]. Thus, the effects of TEQ-PCDDs/Fs on motor coordination might be caused by other PCDDs/Fs congeners than TCDD.…”
Section: Discussionmentioning
confidence: 99%
“…As a consequence, systemic REPs for these congeners based on a skin or plasma concentration are found to be higher when compared to the intake REPs (Fig. 1 b–e) (DeVito et al 1997 ; Van Ede et al 2013 , 2014a ). For these congeners, it is clear that the systemic REPs are closer to the in vitro REPs than to the intake REPs.…”
Section: In Vitro-derived Reps As Predictors For In Vivo Systemic Repmentioning
confidence: 91%
“…In this respect, studies using primary cultures and cell lines of rodent but in particular human cells may provide relevant information that can be used for human risk assessment if based on systemic concentrations. To assess whether indeed in vitro-derived REPs are more comparable to systemic REPs, we combined intake REPs and in vitro REPs from the 2004 REP database (Haws et al 2006 ) with the very few in vivo studies in which intake REPs as well as systemic REPs were determined (Haws et al 2006 ; DeVito et al 2000 ; Van Ede et al 2013 , 2014a ). These data are presented in Fig.…”
Section: In Vitro-derived Reps As Predictors For In Vivo Systemic Repmentioning
confidence: 99%
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