1. Progressive uterine artery occlusion in the Guinea pig leads to defects in placental structure that relate to fetal growth
- Author
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Emilio A. Herrera, Jorge Lopez-Tello, Amanda N. Sferruzzi-Perri, Maria Angeles Jimenez-Martinez, Bernardo J. Krause, Sferruzzi-Perri, Amanda [0000-0002-4931-4233], and Apollo - University of Cambridge Repository
- Subjects
0301 basic medicine ,Offspring ,Placenta ,Guinea Pigs ,Intrauterine growth restriction ,Arterial Occlusive Diseases ,Placental insufficiency ,Fetal Development ,Andrology ,03 medical and health sciences ,0302 clinical medicine ,Pregnancy ,IUGR ,medicine.artery ,Diffusing capacity ,Occlusion ,Animals ,Medicine ,Uterine artery ,reproductive and urinary physiology ,Fetus ,Fetal Growth Retardation ,030219 obstetrics & reproductive medicine ,business.industry ,Obstetrics and Gynecology ,Trophoblast ,Guinea pig ,Placental morphology ,medicine.disease ,Constriction ,Disease Models, Animal ,Uterine Artery ,030104 developmental biology ,medicine.anatomical_structure ,Fetal Weight ,Reproductive Medicine ,embryonic structures ,Ameroid constrictor ,Female ,business ,Developmental Biology - Abstract
Intrauterine growth restriction (IUGR) is a common obstetric complication with immediate and life-long consequences for offspring health. Yet the mechanisms underlying its aetiology require elucidation. Recent work in the guinea pig shows that progressive uterine artery occlusion induced IUGR and vascular dysfunction in pups. Here we explore the extent to which uterine artery occlusion influences fetal outcomes via impacts on placental morphology. Our study demonstrates that uterine artery occlusion severely compromised both the labyrinth exchange zone (increased fibrosis and reduced vascularisation, trophoblast volume, surface area and diffusing capacity) and interlobium zone (increased apoptosis), which likely contributed to the IUGR observed., JL-T and ANS-P are supported by a Newton International and Dorothy Hodgkin Research Fellowships from the Royal Society, respectively. EAH is supported by FONDECYT 1151119 and, BJK is supported by FONDECYT 1181341 and VRI-Puente P1714/2017.
- Published
- 2018
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