Literature DB >> 17536998

Role of the placenta in fetal programming: underlying mechanisms and potential interventional approaches.

Thomas Jansson1, Theresa L Powell.   

Abstract

Adverse influences during fetal life alter the structure and function of distinct cells, organ systems or homoeostatic pathways, thereby 'programming' the individual for an increased risk of developing cardiovascular disease and diabetes in adult life. Fetal programming can be caused by a number of different perturbations in the maternal compartment, such as altered maternal nutrition and reduced utero-placental blood flow; however, the underlying mechanisms remain to be fully established. Perturbations in the maternal environment must be transmitted across the placenta in order to affect the fetus. Here, we review recent insights into how the placenta responds to changes in the maternal environment and discuss possible mechanisms by which the placenta mediates fetal programming. In IUGR (intrauterine growth restriction) pregnancies, the increased placental vascular resistance subjects the fetal heart to increased work load, representing a possible direct link between altered placental structure and fetal programming of cardiovascular disease. A decreased activity of placental 11beta-HSD-2 (type 2 isoform of 11beta-hydroxysteroid dehydrogenase) activity can increase fetal exposure to maternal cortisol, which programmes the fetus for later hypertension and metabolic disease. The placenta appears to function as a nutrient sensor regulating nutrient transport according to the ability of the maternal supply line to deliver nutrients. By directly regulating fetal nutrient supply and fetal growth, the placenta plays a central role in fetal programming. Furthermore, perturbations in the maternal compartment may affect the methylation status of placental genes and increase placental oxidative/nitrative stress, resulting in changes in placental function. Intervention strategies targeting the placenta in order to prevent or alleviate altered fetal growth and/or fetal programming include altering placental growth and nutrient transport by maternally administered IGFs (insulin-like growth factors) and altering maternal levels of methyl donors.

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Year:  2007        PMID: 17536998     DOI: 10.1042/CS20060339

Source DB:  PubMed          Journal:  Clin Sci (Lond)        ISSN: 0143-5221            Impact factor:   6.124


  151 in total

1.  The GLP-1 analog, liraglutide prevents the increase of proinflammatory mediators in the hippocampus of male rat pups submitted to maternal perinatal food restriction.

Authors:  Y Diz-Chaves; L Toba; J Fandiño; L C González-Matías; L M Garcia-Segura; F Mallo
Journal:  J Neuroinflammation       Date:  2018-12-05       Impact factor: 8.322

Review 2.  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 3.  Adipose tissue and fetal programming.

Authors:  M E Symonds; M Pope; D Sharkey; H Budge
Journal:  Diabetologia       Date:  2012-03-09       Impact factor: 10.122

Review 4.  Development and function of the human fetal adrenal cortex: a key component in the feto-placental unit.

Authors:  Hitoshi Ishimoto; Robert B Jaffe
Journal:  Endocr Rev       Date:  2010-11-04       Impact factor: 19.871

5.  The placenta is the center of the chronic disease universe.

Authors:  Kent L Thornburg; Nicole Marshall
Journal:  Am J Obstet Gynecol       Date:  2015-10       Impact factor: 8.661

Review 6.  The Placenta as a Mediator of Stress Effects on Neurodevelopmental Reprogramming.

Authors:  Stefanie L Bronson; Tracy L Bale
Journal:  Neuropsychopharmacology       Date:  2015-08-07       Impact factor: 7.853

7.  Placental Proteomics Reveal Insights into Fetal Alcohol Spectrum Disorders.

Authors:  Katie L Davis-Anderson; Sebastian Berger; Emilie R Lunde-Young; Vishal D Naik; Heewon Seo; Greg A Johnson; Hanno Steen; Jayanth Ramadoss
Journal:  Alcohol Clin Exp Res       Date:  2017-08-09       Impact factor: 3.455

8.  Prenatal and postnatal stress and asthma in children: Temporal- and sex-specific associations.

Authors:  Alison Lee; Yueh-Hsiu Mathilda Chiu; Maria José Rosa; Calvin Jara; Robert O Wright; Brent A Coull; Rosalind J Wright
Journal:  J Allergy Clin Immunol       Date:  2016-03-04       Impact factor: 10.793

9.  Convergent ERK1/2, p38 and JNK mitogen activated protein kinases (MAPKs) signalling mediate catecholoestradiol-induced proliferation of ovine uterine artery endothelial cells.

Authors:  Rosalina Villalon Landeros; Sheikh O Jobe; Gabrielle Aranda-Pino; Gladys E Lopez; Jing Zheng; Ronald R Magness
Journal:  J Physiol       Date:  2017-06-05       Impact factor: 5.182

10.  Expression of the placental transcriptome in maternal nutrient reduction in baboons is dependent on fetal sex.

Authors:  Laura A Cox; Cun Li; Jeremy P Glenn; Kenneth Lange; Kimberly D Spradling; Peter W Nathanielsz; Thomas Jansson
Journal:  J Nutr       Date:  2013-09-18       Impact factor: 4.798

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