The Placenta as a Mediator of Stress Effects on Neurodevelopmental Reprogramming

被引:162
作者
Bronson, Stefanie L. [1 ]
Bale, Tracy L. [1 ]
机构
[1] Univ Penn, Sch Vet Med, Dept Biomed Sci, Philadelphia, PA 19104 USA
关键词
CORTICOTROPIN-RELEASING HORMONE; PRENATAL MATERNAL STRESS; INSULIN-RECEPTOR SUBSTRATE-1; UTERINE ARTERY RESISTANCE; GENE-EXPRESSION; IN-UTERO; DNA METHYLATION; TROPHOBLAST INCLUSIONS; SERINE PHOSPHORYLATION; NUTRIENT TRANSPORT;
D O I
10.1038/npp.2015.231
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Adversity experienced during gestation is a predictor of lifetime neuropsychiatric disease susceptibility. Specifically, maternal stress during pregnancy predisposes offspring to sex-biased neurodevelopmental disorders, including schizophrenia, attention deficit/hyperactivity disorder, and autism spectrum disorders. Animal models have demonstrated disease-relevant endophenotypes in prenatally stressed offspring and have provided unique insight into potential programmatic mechanisms. The placenta has a critical role in the deleterious and sex-specific effects of maternal stress and other fetal exposures on the developing brain. Stress-induced perturbations of the maternal milieu are conveyed to the embryo via the placenta, the maternal-fetal intermediary responsible for maintaining intrauterine homeostasis. Disruption of vital placental functions can have a significant impact on fetal development, including the brain, outcomes that are largely sex-specific. Here we review the novel involvement of the placenta in the transmission of the maternal adverse environment and effects on the developing brain.
引用
收藏
页码:207 / 218
页数:12
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