Literature DB >> 19167474

The herbicide linuron reduces testosterone production from the fetal rat testis during both in utero and in vitro exposures.

Vickie S Wilson1, Christy R Lambright, Johnathan R Furr, Kembra L Howdeshell, L Earl Gray.   

Abstract

In utero exposure to linuron, an urea-based herbicide, results in a pattern of malformations of androgen-dependent tissues in adult male rat offspring resembling that produced by some phthalate esters which are known to decrease fetal testosterone production. This study investigated the impact of in utero linuron treatment on fetal testis gene expression and testosterone production. Timed-pregnant Sprague Dawley rats were administered corn oil vehicle, 12.5, 25, 50 or 75mg linuron/day/kg orally from GD13 to 18. Ex vivo testosterone (T) production was significantly decreased at 50 and 75mg/kg when analyzed on a per litter basis. Unlike the phthalate esters, linuron treatment did not affect insl3, cyp17a, cyp11a or StAR mRNA expression. Control GD18 fetal testes were then incubated with increasing concentrations of linuron (1-300microM) to evaluate if linuron inhibited T production in vitro. T production was significantly reduced at 30microM and above. Progesterone production was not affected in any of the studies indicating that linuron directly inhibited testosterone production in the absence of cytotoxicity. These results indicate the malformations induced by linuron and phthalate esters in male offspring are similar because both reduce fetal T levels during the critical period of sex differentiation but suggest that the mechanisms differ.

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Year:  2009        PMID: 19167474     DOI: 10.1016/j.toxlet.2008.12.017

Source DB:  PubMed          Journal:  Toxicol Lett        ISSN: 0378-4274            Impact factor:   4.372


  14 in total

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3.  Reproductive toxicity of linuron following gestational exposure in rats and underlying mechanisms.

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Journal:  Toxicol Lett       Date:  2016-12-19       Impact factor: 4.372

4.  Maternal linuron exposure alters testicular development in male offspring rats at the whole genome level.

Authors:  Jianwei Bai; Hua Han; Feng Wang; Liyu Su; Hongwei Ding; Xiyin Hu; Binli Hu; Hong Li; Wei Zheng; Yan Li
Journal:  Toxicology       Date:  2017-07-11       Impact factor: 4.221

5.  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
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6.  Endocrine Disruption and Reproductive Pathology.

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Journal:  Toxicol Pathol       Date:  2019-12       Impact factor: 1.902

7.  Concentration addition, independent action and generalized concentration addition models for mixture effect prediction of sex hormone synthesis in vitro.

Authors:  Niels Hadrup; Camilla Taxvig; Mikael Pedersen; Christine Nellemann; Ulla Hass; Anne Marie Vinggaard
Journal:  PLoS One       Date:  2013-08-22       Impact factor: 3.240

Review 8.  Effect of endocrine disruptor pesticides: a review.

Authors:  Wissem Mnif; Aziza Ibn Hadj Hassine; Aicha Bouaziz; Aghleb Bartegi; Olivier Thomas; Benoit Roig
Journal:  Int J Environ Res Public Health       Date:  2011-06-17       Impact factor: 3.390

9.  Quantification of the Uncertainties in Extrapolating From In Vitro Androgen Receptor Antagonism to In Vivo Hershberger Assay Endpoints and Adverse Reproductive Development in Male Rats.

Authors:  Leon E Gray; Johnathan R Furr; Christy S Lambright; Nicola Evans; Phillip C Hartig; Mary C Cardon; Vickie S Wilson; Andrew K Hotchkiss; Justin M Conley
Journal:  Toxicol Sci       Date:  2020-08-01       Impact factor: 4.109

10.  Overexpression of PRL7D1 in Leydig Cells Causes Male Reproductive Dysfunction in Mice.

Authors:  Yaping Liu; Xingyu Su; Jie Hao; Maoxin Chen; Weijia Liu; Xiaogang Liao; Gang Li
Journal:  Int J Mol Sci       Date:  2016-01-13       Impact factor: 5.923

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