Literature DB >> 17564903

Transplacental transfer of monomethyl phthalate and mono(2-ethylhexyl) phthalate in a human placenta perfusion system.

Tina Mose1, Lisbeth E Knudsen, Morten Hedegaard, Gerda K Mortensen.   

Abstract

The transplacental passage of monomethylphtalate (mMP) and mono (2-ethylhexyl) phthalate (mEHP) was studied using an ex vivo placental perfusion model with simultaneous perfusion of fetal and maternal circulation in a single cotyledon. Umbilical cord blood and placental tissue collected both before and after perfusion were also analyzed. Placentas were obtained immediately after elective cesarean section and dually perfused in a recirculation system. mMP or mEHP was added to maternal perfusion medium to obtain concentrations at 10 and 25 microg/L, respectively. The placental transfer was followed analyzing samples from fetal and maternal perfusion media by liquid chromatography-mass spectrometry-mass spectrometry (LC-MS-MS). Four perfusions with mMP indicated a slow transplacental transfer, with a feto-maternal ratio (FM ratio) of 0.30 +/- 0.03 after 150 min of perfusion. Four perfusions with mEHP indicated a very slow or nonexisting placental transfer. mEHP was only detected in fetal perfusion media from two perfusions, giving rise to FM ratios of 0.088 and 0.20 after 150 min of perfusion. Detectable levels of mMP, mEHP, monoethylphthalate (mEP), and monobutylphthalate were found in tissue. Higher tissue levels of mMP after perfusions with mMP compared to perfusions with mEHP suggest an accumulation of mMP during perfusion. No tendency for accumulation of mEHP was observed during perfusions with mEHP compared to perfusions with mMP. Detectable levels of mEHP and mEP were found in umbilical cord plasma samples. mMP and possibly other short-chained phthalate monoesters in maternal blood can cross the placenta by slow transfer, whereas the results indicate no placental transfer of mEHP. Further studies are recommended.

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Year:  2007        PMID: 17564903     DOI: 10.1080/10915810701352721

Source DB:  PubMed          Journal:  Int J Toxicol        ISSN: 1091-5818            Impact factor:   2.032


  25 in total

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Review 2.  Effects of prenatal exposure to endocrine disruptors and toxic metals on the fetal epigenome.

Authors:  Paige A Bommarito; Elizabeth Martin; Rebecca C Fry
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4.  Fetal phthalates and bisphenols and childhood lipid and glucose metabolism. A population-based prospective cohort study.

Authors:  Chalana M Sol; Susana Santos; Liesbeth Duijts; Alexandros G Asimakopoulos; Maria-Pilar Martinez-Moral; Kurunthachalam Kannan; Vincent W V Jaddoe; Leonardo Trasande
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5.  Behavioral effects in adult rats exposed to low doses of a phthalate mixture during the perinatal or adolescent period.

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6.  Identifying periods of susceptibility to the impact of phthalates on children's cognitive abilities.

Authors:  Nan Li; George D Papandonatos; Antonia M Calafat; Kimberly Yolton; Bruce P Lanphear; Aimin Chen; Joseph M Braun
Journal:  Environ Res       Date:  2019-03-05       Impact factor: 6.498

7.  Effects of in utero di-butyl phthalate and butyl benzyl phthalate exposure on offspring development and male reproduction of rat.

Authors:  Rahish Ahmad; A K Gautam; Y Verma; S Sedha; Sunil Kumar
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8.  Prenatal di(2-ethylhexyl)phthalate exposure and length of gestation among an inner-city cohort.

Authors:  Robin M Whyatt; Jennifer J Adibi; Antonia M Calafat; David E Camann; Virgina Rauh; Hari K Bhat; Frederica P Perera; Howard Andrews; Allan C Just; Lori Hoepner; Deliang Tang; Russ Hauser
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Review 9.  Epigenetics in the placenta.

Authors:  Matthew A Maccani; Carmen J Marsit
Journal:  Am J Reprod Immunol       Date:  2009-08       Impact factor: 3.886

10.  Perinatal Exposure to an Environmentally Relevant Mixture of Phthalates Results in a Lower Number of Neurons and Synapses in the Medial Prefrontal Cortex and Decreased Cognitive Flexibility in Adult Male and Female Rats.

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