Early adverse experience as a developmental risk factor for later psychopathology:: Evidence from rodent and primate models

被引:748
作者
Sánchez, MM [1 ]
Ladd, CO [1 ]
Plotsky, PM [1 ]
机构
[1] Emory Univ, Sch Med, Dept Psychiat & Behav Sci, Atlanta, GA 30303 USA
关键词
D O I
10.1017/S0954579401003029
中图分类号
B844 [发展心理学(人类心理学)];
学科分类号
040202 ;
摘要
Increasing evidence supports the view that the interaction of perinatal exposure to adversity with individual genetic liabilities may increase an individual's vulnerability to the expression of psycho- and physiopathology throughout lifer The early environment appears to program some aspects of neurobiological development and. in turn. behavioral, emotional, cognitive, and physiological development. Several rodent and primate models of early adverse experience have been analyzed in this review, including those that "model" maternal separation or loss, abuse or neglect, and social deprivation. Accumulating evidence shows that these early traumatic experiences are associated with long-term alterations in coping style, emotional and behavioral regulation. neuroendocrine responsiveness to stress, social "fitness," cognitive function. brain morphology. neurochemistry, and expression levels of central nervous system genes that have been related to anxiety and mood disorders. Studies are underway to identify important aspects of adverse early experience. such as (a) the existence of "sensitive periods" during development associated with alterations in particular output systems, (b) the presence of "windows of opportunity" during which targeted interventions (e.g., nurturant parenting or supportive-enriching environment) may prevent or reverse dysfunction. (c) the identity of gene polymorphisms contributing to the individual's variability in vulnerability, and (d) a means to translate the timing of these developmental "sensitive periods" across species.
引用
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页码:419 / 449
页数:31
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共 237 条
[91]  
HUBEL DH, 1975, COLD SPRING HARB SYM, V40, P581
[92]  
HUOT RL, 2001, IN PRESS PSYCHOPHARM
[93]  
INSEL TR, 1988, J NEUROSCI, V8, P4151
[94]   THE ROLE OF THE HIPPOCAMPUS IN FEEDBACK-REGULATION OF THE HYPOTHALAMIC-PITUITARY-ADRENOCORTICAL AXIS [J].
JACOBSON, L ;
SAPOLSKY, R .
ENDOCRINE REVIEWS, 1991, 12 (02) :118-134
[95]   THE MATURATION OF THE PITUITARY-ADRENAL AXIS IN THE NEWBORN RAT [J].
JAILER, JW .
ENDOCRINOLOGY, 1950, 46 (05) :420-425
[96]   NEST TEMPERATURE - EFFECTS ON MATERNAL-BEHAVIOR, PUP DEVELOPMENT, AND INTERACTIONS WITH HANDLING [J].
JANS, JE ;
WOODSIDE, BC .
DEVELOPMENTAL PSYCHOBIOLOGY, 1990, 23 (06) :519-534
[97]   Central corticotropin-releasing hormone receptors modulate hypothalamic-pituitary-adrenocortical and sympathoadrenal activity during stress [J].
Jezova, D ;
Ochedalski, T ;
Glickman, M ;
Kiss, A ;
Aguilera, G .
NEUROSCIENCE, 1999, 94 (03) :797-802
[98]   ANALYSIS OF ENVIRONMENTAL DEPRIVATION - COGNITIVE AND SOCIAL-DEVELOPMENT IN ROMANIAN ORPHANS [J].
KALER, SR ;
FREEMAN, BJ .
JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY AND ALLIED DISCIPLINES, 1994, 35 (04) :769-781
[99]   Asymmetric frontal brain activity, cortisol, and behavior associated with fearful temperament in rhesus monkeys [J].
Kalin, NH ;
Larson, C ;
Shelton, SE ;
Davidson, RJ .
BEHAVIORAL NEUROSCIENCE, 1998, 112 (02) :286-292
[100]   DEPRESSION IN INFANT MONKEYS SEPARATED FROM THEIR MOTHERS [J].
KAUFMAN, IC ;
ROSENBLU.LA .
SCIENCE, 1967, 155 (3765) :1030-&