Literature DB >> 20484383

Determination of the di-(2-ethylhexyl) phthalate NOAEL for reproductive development in the rat: importance of the retention of extra animals to adulthood.

Chad R Blystone1, Grace E Kissling, Jack B Bishop, Robert E Chapin, Gary W Wolfe, Paul M D Foster.   

Abstract

Deriving No Observed Adverse Effect Level (NOAEL) or benchmark dose is important for risk assessment and can be influenced by study design considerations. In order to define the di-(2-ethylhexyl) phthalate (DEHP) dose-response curve for reproductive malformations, we retained more offspring to adulthood to improve detection of these malformations in the reproductive assessment by continuous breeding study design. Sprague-Dawley rats were given a dietary administration of 1.5 (control), 10, 30, 100, 300, 1000, 7500, and 10,000 ppm DEHP. Male pups were evaluated for gross reproductive tract malformations (RTMs) associated with the "phthalate syndrome." DEHP treatment had minimal effects on P0 males. There was a statistically significant increase in F1 and F2 total RTMs (testis, epididymides, seminal vesicle, and prostate) in the 7500-ppm dose group and F1 10,000-ppm dose group. The 10,000-ppm exposed F1 males did not produce an F2 generation. The NOAEL for F1 and F2 RTM combined data, because in utero exposures were similar, were 100 ppm (4.8 mg/kg/day), which was close to the 5% response benchmark dose lower confidence limit of 142 ppm. The utility of evaluating more pups per litter was examined by generating power curves from a Monte Carlo simulation. These curves indicate a substantial increase in detection rate when three males are evaluated per litter rather than one. A 10% effect across male pups would be detected 5% of the time if one pup per litter was evaluated, but these effects would be detected 66% of the time if three pups per litter were evaluated. Taken together, this study provides a well-defined dose response of DEHP-induced RTMs and demonstrates that retention of more adult F1 and F2 males per litter, animals that were already produced, increases the ability to detect RTMs and presumably other low-incidence phenomena.

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Year:  2010        PMID: 20484383      PMCID: PMC2905405          DOI: 10.1093/toxsci/kfq147

Source DB:  PubMed          Journal:  Toxicol Sci        ISSN: 1096-0929            Impact factor:   4.849


  11 in total

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2.  The plasticizer diethylhexyl phthalate induces malformations by decreasing fetal testosterone synthesis during sexual differentiation in the male rat.

Authors:  L G Parks; J S Ostby; C R Lambright; B D Abbott; G R Klinefelter; N J Barlow; L E Gray
Journal:  Toxicol Sci       Date:  2000-12       Impact factor: 4.849

3.  A note on Shirley's nonparametric test for comparing several dose levels with a zero-dose control.

Authors:  D A Williams
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4.  Effects of in utero exposure to linuron on androgen-dependent reproductive development in the male Crl:CD(SD)BR rat.

Authors:  B S McIntyre; N J Barlow; D G Wallace; S C Maness; K W Gaido; P M Foster
Journal:  Toxicol Appl Pharmacol       Date:  2000-09-01       Impact factor: 4.219

Review 5.  Endocrine-disrupting chemicals: prepubertal exposures and effects on sexual maturation and thyroid function in the male rat. A focus on the EDSTAC recommendations. Endocrine Disrupter Screening and Testing Advisory Committee.

Authors:  T E Stoker; L G Parks; L E Gray; R L Cooper
Journal:  Crit Rev Toxicol       Date:  2000-03       Impact factor: 5.635

6.  Endocrine active agents: implications of adverse and non-adverse changes.

Authors:  Paul M D Foster; Barry S McIntyre
Journal:  Toxicol Pathol       Date:  2002 Jan-Feb       Impact factor: 1.902

7.  Reproductive assessment by continuous breeding: evolving study design and summaries of ninety studies.

Authors:  R E Chapin; R A Sloane
Journal:  Environ Health Perspect       Date:  1997-02       Impact factor: 9.031

8.  Benchmark Dose Workshop: criteria for use of a benchmark dose to estimate a reference dose.

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Review 9.  Fifteen years after "Wingspread"--environmental endocrine disrupters and human and wildlife health: where we are today and where we need to go.

Authors:  Andrew K Hotchkiss; Cynthia V Rider; Chad R Blystone; Vickie S Wilson; Phillip C Hartig; Gerald T Ankley; Paul M Foster; Clark L Gray; L Earl Gray
Journal:  Toxicol Sci       Date:  2008-02-16       Impact factor: 4.849

10.  Transgenerational effects of Di (2-ethylhexyl) phthalate in the male CRL:CD(SD) rat: added value of assessing multiple offspring per litter.

Authors:  Leon Earl Gray; Norman J Barlow; Kembra L Howdeshell; Joseph S Ostby; Johnathan R Furr; Clark L Gray
Journal:  Toxicol Sci       Date:  2009-05-29       Impact factor: 4.849

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  19 in total

1.  Regulatory Forum opinion piece: New testing paradigms for reproductive and developmental toxicity--the NTP modified one generation study and OECD 443.

Authors:  Paul M D Foster
Journal:  Toxicol Pathol       Date:  2014-05-26       Impact factor: 1.902

2.  Influence of Study Design on Developmental and Reproductive Toxicology Study Outcomes.

Authors:  Paul M D Foster
Journal:  Toxicol Pathol       Date:  2016-10-05       Impact factor: 1.902

3.  Twenty-five years after "Wingspread"- Environmental endocrine disruptors (EDCs) and human health.

Authors:  Leon Earl Gray
Journal:  Curr Opin Toxicol       Date:  2017-04

4.  Dose Addition Models Based on Biologically Relevant Reductions in Fetal Testosterone Accurately Predict Postnatal Reproductive Tract Alterations by a Phthalate Mixture in Rats.

Authors:  Kembra L Howdeshell; Cynthia V Rider; Vickie S Wilson; Johnathan R Furr; Christy R Lambright; L Earl Gray
Journal:  Toxicol Sci       Date:  2015-09-08       Impact factor: 4.849

5.  Prenatal Exposure to DEHP Induces Neuronal Degeneration and Neurobehavioral Abnormalities in Adult Male Mice.

Authors:  Radwa Barakat; Po-Ching Lin; Chan Jin Park; Catherine Best-Popescu; Hatem H Bakry; Mohamed E Abosalem; Nabila M Abdelaleem; Jodi A Flaws; CheMyong Ko
Journal:  Toxicol Sci       Date:  2018-08-01       Impact factor: 4.849

6.  A short-term in vivo screen using fetal testosterone production, a key event in the phthalate adverse outcome pathway, to predict disruption of sexual differentiation.

Authors:  Johnathan R Furr; Christy S Lambright; Vickie S Wilson; Paul M Foster; Leon E Gray
Journal:  Toxicol Sci       Date:  2014-05-05       Impact factor: 4.849

7.  Non-monotonic dose effects of in utero exposure to di(2-ethylhexyl) phthalate (DEHP) on testicular and serum testosterone and anogenital distance in male mouse fetuses.

Authors:  Rylee Phuong Do; Richard W Stahlhut; Davide Ponzi; Frederick S Vom Saal; Julia A Taylor
Journal:  Reprod Toxicol       Date:  2012-10-03       Impact factor: 3.143

8.  Simvastatin and dipentyl phthalate lower ex vivo testicular testosterone production and exhibit additive effects on testicular testosterone and gene expression via distinct mechanistic pathways in the fetal rat.

Authors:  Brandiese E J Beverly; Christy S Lambright; Johnathan R Furr; Hunter Sampson; Vickie S Wilson; Barry S McIntyre; Paul M D Foster; Gregory Travlos; L Earl Gray
Journal:  Toxicol Sci       Date:  2014-07-23       Impact factor: 4.849

9.  Transgenerational effects of Di (2-ethylhexyl) phthalate in the male CRL:CD(SD) rat: added value of assessing multiple offspring per litter.

Authors:  Leon Earl Gray; Norman J Barlow; Kembra L Howdeshell; Joseph S Ostby; Johnathan R Furr; Clark L Gray
Journal:  Toxicol Sci       Date:  2009-05-29       Impact factor: 4.849

10.  Ordinal dose-response modeling approach for the phthalate syndrome.

Authors:  Todd D Blessinger; Susan Y Euling; Lily Wang; Karen A Hogan; Christine Cai; Gary Klinefelter; Anne-Marie Saillenfait
Journal:  Environ Int       Date:  2019-11-26       Impact factor: 9.621

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