Article ID Journal Published Year Pages File Type
5860517 Toxicology Letters 2013 7 Pages PDF
Abstract

•A chemically induced animal model of the human MRKH syndrome.•A phthalate syndrome in female rats: uterine and vaginal agenesis.•A phthalate mixture disrupts male and female rat sexual differentiation.•Differences in critical periods for disrupted sex differentiation and mortality.

Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is characterized by uterine and vaginal canal aplasia in normal karyotype human females and is a syndrome with poorly defined etiology. Reproductive toxicity of phthalate esters (PEs) occurs in rat offspring exposed in utero, a phenomenon that is better studied in male offspring than females. The current study reports female reproductive tract malformations in the Sprague-Dawley rat similar to those characteristic of MRKH syndrome, following in utero exposure to a mixture of 5 PEs. We determined that females are ∼2-fold less sensitive to the effects of the 5-PE mixture than males for reproductive tract malformations. We were not fully successful in defining the critical exposure period for females; however, incidence of malformations was 88% following dosing from GD8 to 19 versus 22% and 0% for GD8-13 and GD14-19, respectively. Overall, this study provides valuable information regarding female vulnerability to in utero phthalate exposure and further characterizes a potential model for the human MRKH syndrome.

Related Topics
Life Sciences Environmental Science Health, Toxicology and Mutagenesis
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