Literature DB >> 12852418

The human first trimester gestational sac limits rather than facilitates oxygen transfer to the foetus--a review.

E Jauniaux1, B Gulbis, G J Burton.   

Abstract

Oxygen (O2) free radicals are a potential teratologic threat to the foetal tissues and are known to be involved in the pathophysiology of common human pregnancy disorders such as miscarriage and pre-eclampsia. During the first two months of human gestation, the placenta surrounds the whole gestational sac, the villi contain only a few capillaries located mainly within the centre of the mesenchymal core, the trophoblastic layer is twice the thickness it will be in the second trimester, the foetal red cells are nucleated and the exocoelomic cavity (ECC) occupies most of the space inside the gestational sac. The ECC contains no oxygen transport system, but anti-oxidant molecules that may provide additional protection to the embryo from oxidative damage are present. Ultrasound and anatomical studies have also demonstrated that the intervillous circulation starts in the periphery of the placenta at around 9 weeks of gestation, and that it becomes continuous and diffuse in the entire placenta only after 12 weeks. Overall, these anatomical features provide indirect evidence that the architecture of the human first trimester gestational sac limits foetal exposure to O2 to what is strictly necessary for its development. These results are in agreement with the concept that the placenta and foetus develop in a physiologically low O2 environment and that its metabolism must be essentially anaerobic. Because of these anatomical arrangements, different nutritional pathways to those operating during most of pregnancy must serve the first-trimester foetus. Up to 9 weeks of gestation, foetal nutrition appears to depend on uterine glandular secretions that are delivered into the intervillous space, supplemented by maternal plasma proteins and other molecules that may percolate through the trophoblastic shell. These molecules diffuse through, or are transported by, the trophoblast of the villi and the chorionic plate into the ECC. From here they are absorbed by the secondary yolk sac (SYS), in which the extraembryonic circulation is probably first established. At the end of the first trimester, the SYS and two-thirds of the placental mass degenerate, and the ECC is progressively obliterated by the enlarging amniotic cavity. The trophoblastic plugs occluding the utero-placental arteries are gradually dislocated, allowing maternal blood to flow into the intervillous space, and the uterine glands involute. These major anatomical transformations modify considerably the spatial relationships between the maternal tissues and the developing embryo, and, consequently, the materno-embryonic exchange pathways. Overall the comparison of morphological features with physiological findings reveals that the architecture of the human first trimester gestational sac is designed to limit foetal exposure to oxygen to that which is strictly necessary for its development, and that during early pregnancy alternative nutritional pathways are in use.

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Year:  2003        PMID: 12852418     DOI: 10.1053/plac.2002.0932

Source DB:  PubMed          Journal:  Placenta        ISSN: 0143-4004            Impact factor:   3.481


  38 in total

1.  An imbalance between angiogenic and anti-angiogenic factors precedes fetal death in a subset of patients: results of a longitudinal study.

Authors:  Roberto Romero; Tinnakorn Chaiworapongsa; Offer Erez; Adi L Tarca; Maria Teresa Gervasi; Juan Pedro Kusanovic; Pooja Mittal; Giovanna Ogge; Edi Vaisbuch; Shali Mazaki-Tovi; Zhong Dong; Sun Kwon Kim; Lami Yeo; Sonia S Hassan
Journal:  J Matern Fetal Neonatal Med       Date:  2010-05-12

Review 2.  Trophoblast differentiation during embryo implantation and formation of the maternal-fetal interface.

Authors:  Kristy Red-Horse; Yan Zhou; Olga Genbacev; Akraporn Prakobphol; Russell Foulk; Michael McMaster; Susan J Fisher
Journal:  J Clin Invest       Date:  2004-09       Impact factor: 14.808

Review 3.  In utero oxidative stress epigenetically programs antioxidant defense capacity and adulthood diseases.

Authors:  Rita S Strakovsky; Yuan-Xiang Pan
Journal:  Antioxid Redox Signal       Date:  2012-01-11       Impact factor: 8.401

Review 4.  The role of the placenta in fetal exposure to heavy metals.

Authors:  Claudia Gundacker; Markus Hengstschläger
Journal:  Wien Med Wochenschr       Date:  2012-05

Review 5.  Placental-related diseases of pregnancy: Involvement of oxidative stress and implications in human evolution.

Authors:  Eric Jauniaux; Lucilla Poston; Graham J Burton
Journal:  Hum Reprod Update       Date:  2006-05-08       Impact factor: 15.610

6.  Establishment of human trophoblast progenitor cell lines from the chorion.

Authors:  Olga Genbacev; Matthew Donne; Mirhan Kapidzic; Matthew Gormley; Julie Lamb; Jacqueline Gilmore; Nicholas Larocque; Gabriel Goldfien; Tamara Zdravkovic; Michael T McMaster; Susan J Fisher
Journal:  Stem Cells       Date:  2011-09       Impact factor: 6.277

Review 7.  Biological roles of uterine glands in pregnancy.

Authors:  Thomas E Spencer
Journal:  Semin Reprod Med       Date:  2014-06-24       Impact factor: 1.303

Review 8.  Human trophoblast progenitors: where do they reside?

Authors:  Olga Genbacev; Julie D Lamb; Akraporn Prakobphol; Matt Donne; Michael T McMaster; Susan J Fisher
Journal:  Semin Reprod Med       Date:  2013-01-17       Impact factor: 1.303

9.  Placental Alpha Hemoglobin Stabilizing Protein (AHSP) and recurrent miscarriage.

Authors:  Monica Emanuelli; Monia Cecati; Davide Sartini; Piergiorgio Stortoni; Alessandra Corradetti; Stefano R Giannubilo; Angelo Turi; Andrea L Tranquilli
Journal:  Cell Stress Chaperones       Date:  2008-08-15       Impact factor: 3.667

Review 10.  Oxygen, the Janus gas; its effects on human placental development and function.

Authors:  Graham J Burton
Journal:  J Anat       Date:  2008-10-13       Impact factor: 2.610

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