Abstract Title:

Gestational bisphenol S impairs placental endocrine function and the fusogenic trophoblast signaling pathway.

Abstract Source:

Arch Toxicol. 2018 Mar 17. Epub 2018 Mar 17. PMID: 29550860

Abstract Author(s):

Jeremy Gingrich, Yong Pu, Jennifer Roberts, Rajendiran Karthikraj, Kurunthachalam Kannan, Richard Ehrhardt, Almudena Veiga-Lopez

Article Affiliation:

Jeremy Gingrich


Exposure to bisphenolic chemicals during pregnancy occurs in> 90% of pregnancies. Bisphenolic compounds can cross the placental barrier reaching fetal circulation. However, the effects of emerging bisphenolic compounds, such as bisphenol S (BPS), on placental function remain untested. The aim was to determine if bisphenol A (BPA) or BPS, at an environmentally relevant dose, impairs placental function. Pregnant sheep were randomly distributed into three treatment groups (n = 7-8/group): control, BPA, and BPS. All animals received daily injections of corn oil (control), BPA, or BPS (0.5 mg/kg; s.c.; internal fetal doses were ~ 2.6 ng/mL unconjugated BPA and ~ 7.7 ng/mL of BPS) from gestational day 30-100. After a 20-day washout period, placentas were weighed and placentomes collected. Placental endocrine function was assessed on biweekly maternal blood samples. Gestational exposure to BPS, but not BPA, reduced maternal circulating pregnancy-associated glycoproteins without change in placental weight or placental stereology. BPS-exposed placentas had 50% lower e-cadherin protein expression, ~ 20% fewer binucleate cells, and ~ threefold higher glial cell missing-1 protein expression. BPA placentas were not affected highlightingthe intrinsic differences among bisphenolic chemicals. This is the first study to demonstrate that gestational BPS can result in placental endocrine dysfunction and points to a dysregulation in the fusogenic trophoblast signaling pathway.

Study Type : Animal Study
Additional Links
Problem Substances : Bisphenol S : CK(514) : AC(172)

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