Periconceptional alcohol exposure causes female-specific perturbations to trophoblast differentiation and placental formation in the rat

Author:

Kalisch-Smith Jacinta I.1ORCID,Steane Sarah E.1ORCID,Simmons David G.1ORCID,Pantaleon Marie1ORCID,Anderson Stephen T.1,Akison Lisa K.12ORCID,Wlodek Mary E.3ORCID,Moritz Karen M.12ORCID

Affiliation:

1. School of Biomedical Sciences, Faculty of Medicine, The University of Queensland, St Lucia, QLD 4072, Australia

2. Child Health Research Centre, The University of Queensland, South Brisbane, QLD 4101, Australia

3. Department of Physiology, School of Biomedical Sciences, Faculty of Medicine, Dentistry and Health Sciences, The University of Melbourne, Parkville, Victoria 3010, Australia

Abstract

ABSTRACT The development of pathologies during pregnancy, including pre-eclampsia, hypertension and fetal growth restriction (FGR), often originates from poor functioning of the placenta. In vivo models of maternal stressors, such as nutrient deficiency, and placental insufficiency often focus on inadequate growth of the fetus and placenta in late gestation. These studies rarely investigate the origins of poor placental formation in early gestation, including those affecting the pre-implantation embryo and/or the uterine environment. The current study characterises the impact on blastocyst, uterine and placental outcomes in a rat model of periconceptional alcohol exposure, in which 12.5% ethanol is administered in a liquid diet from 4 days before until 4 days after conception. We show female-specific effects on trophoblast differentiation, embryo-uterine communication, and formation of the placental vasculature, resulting in markedly reduced placental volume at embryonic day 15. Both sexes exhibited reduced trophectoderm pluripotency and global hypermethylation, suggestive of inappropriate epigenetic reprogramming. Furthermore, evidence of reduced placental nutrient exchange and reduced pre-implantation maternal plasma choline levels offers significant mechanistic insight into the origins of FGR in this model.

Funder

National Health and Medical Research Council

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

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