Fetal Programming of Brain Development: Intrauterine Stress and Susceptibility to Psychopathology

被引:96
作者
Buss, Claudia [1 ,5 ]
Entringer, Sonja [1 ,5 ]
Wadhwa, Pathik D. [1 ,2 ,3 ,4 ,5 ]
机构
[1] Univ Calif Irvine, Dept Pediat, Sch Med, Irvine, CA 92697 USA
[2] Univ Calif Irvine, Dept Psychiat & Human Behav, Sch Med, Irvine, CA 92697 USA
[3] Univ Calif Irvine, Dept Obstet & Gynecol, Sch Med, Irvine, CA 92697 USA
[4] Univ Calif Irvine, Dept Epidemiol, Sch Med, Irvine, CA 92697 USA
[5] Univ Calif Irvine, Sch Med, Dev Hlth & Dis Res Program, Irvine, CA 92697 USA
关键词
CORTICOTROPIN-RELEASING HORMONE; 11-BETA-HYDROXYSTEROID DEHYDROGENASE TYPE-2; PRENATAL IMMUNE ACTIVATION; NEURAL STEM-CELLS; HIPPOCAMPAL VOLUME; MATERNAL CORTISOL; GENE-EXPRESSION; THYROID-HORMONE; FEMALE RATS; NEUROPSYCHIATRIC DISORDERS;
D O I
10.1126/scisignal.2003406
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The fetal brain is highly plastic and is not only receptive to but requires cues from its environment to develop properly. Based on an understanding of evolutionary biology, developmental plasticity, and life history theory, one can predict that stressors are an important environmental condition that may influence brain development. In fact, the available empirical evidence appears to support the notion that exposure to excess stress in intrauterine life has the potential to adversely affect short- and long-term neurodevelopmental outcomes with implications for altered susceptibility for mental health disorders in childhood and adult life. In this presentation, we provide a rationale for proposing that endocrine and inflammatory stress mediators are key candidate pathways for programming brain development. These mediators are responsive to a diverse set of intrauterine perturbations and alter key signaling pathways critical for brain development, including but not limited to mammalian target of rapamycin, Wnt (wingless), Sonic hedgehog, and reelin signaling. We suggest that recent advances in neuroimaging and other methods now afford us an unprecedented opportunity to advance our understanding of this important topic. Additionally, we provide empirical evidence from two recently published papers for fetal programming of human brain development. We conclude by suggesting some future directions for expanding this field of research.
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页数:7
相关论文
共 90 条
[1]   Insulin-like growth factor-I increases astrocyte intercellular gap junctional communication and connexin43 expression in vitro [J].
Åberg, ND ;
Blomstrand, F ;
Åberg, MAL ;
Björklund, U ;
Carlsson, B ;
Carlsson-Skwirut, C ;
Bang, P ;
Eriksson, PS .
JOURNAL OF NEUROSCIENCE RESEARCH, 2003, 74 (01) :12-22
[2]  
Achenbach T.M, 2001, Multicultural supplement to the manual for the ASEBA preschool forms profiles: Child Behavior Checklist for ages 1 1/2-5
[3]   Trajectories of brain development: point of vulnerability or window of opportunity? [J].
Andersen, SL .
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS, 2003, 27 (1-2) :3-18
[4]   Plasticity of Gray Matter Volume: The Cellular and Synaptic Plasticity That Underlies Volumetric Change [J].
Anderson, Brenda J. .
DEVELOPMENTAL PSYCHOBIOLOGY, 2011, 53 (05) :456-465
[5]  
[Anonymous], 1983, STOCHASTIC MODELLING
[6]   Sex differences in prenatal epigenetic programing of stress pathways [J].
Bale, Tracy L. .
STRESS-THE INTERNATIONAL JOURNAL ON THE BIOLOGY OF STRESS, 2011, 14 (04) :348-356
[7]   Evidence of female-specific glial deficits in the hippocampus in a mouse model of prenatal stress [J].
Behan, Aine T. ;
Van den Hove, Daniel L. A. ;
Mueller, Lynn ;
Jetten, Marlon J. A. ;
Steinbusch, Harry W. M. ;
Cotter, David R. ;
Prickaerts, Jos .
EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2011, 21 (01) :71-79
[8]   METABOLIC CLEARANCE RATE, BLOOD PRODUCTION, INTERCONVERSION AND TRANSPLACENTAL PASSAGE OF CORTISOL AND CORTISONE IN PREGNANCY NEAR TERM [J].
BEITINS, IZ ;
BAYARD, F ;
ANCES, IG ;
KOWARSKI, A ;
MIGEON, CJ .
PEDIATRIC RESEARCH, 1973, 7 (05) :509-519
[9]   Brain anatomy of major depression II. Focus on amygdala [J].
Bellani, M. ;
Baiano, M. ;
Brambilla, P. .
EPIDEMIOLOGY AND PSYCHIATRIC SCIENCES, 2011, 20 (01) :33-36
[10]   Placental 11 beta-hydroxysteroid dehydrogenase: A key regulator of fetal glucocorticoid exposure [J].
Benediktsson, R ;
Calder, AA ;
Edwards, CRW ;
Seckl, JR .
CLINICAL ENDOCRINOLOGY, 1997, 46 (02) :161-166