Treating the Developing versus Developed Brain: Translating Preclinical Mouse and Human Studies

被引:79
作者
Casey, B. J. [1 ]
Glatt, Charles E. [1 ]
Lee, Francis S. [1 ]
机构
[1] Cornell Univ, Sackler Inst Dev Psychobiol, Dept Psychiat, Weill Cornell Med Coll, New York, NY 10065 USA
关键词
COGNITIVE-BEHAVIORAL THERAPY; LATERAL AMYGDALA NEURONS; MEDIAL PREFRONTAL CORTEX; ACID AMIDE HYDROLASE; C-FOS EXPRESSION; FEAR EXTINCTION; DEVELOPMENTAL EMERGENCE; INTERCALATED NEURONS; VENTRAL HIPPOCAMPUS; PRELIMBIC CORTEX;
D O I
10.1016/j.neuron.2015.05.020
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Behaviors and underlying brain circuits show characteristic changes across the lifespan that produce sensitive windows of vulnerability and resilience to psychopathology. Understanding the developmental course of these changes may inform which treatments are best at what ages. Focusing on behavioral domains and neurobiological substrates conserved from mouse to human supports reciprocal hypothesis generation and testing that leverages the strengths of each system in understanding their development. Introducing human genetic variants into mice can further define effects of individual variation on normative development, how they contribute to risk and resilience for mental illness, and inform personalized treatment opportunities. This article emphasizes the period of adolescence, when there is a peak in the emergence of mental illness, anxiety disorders in particular. We present cross-species studies relating fear learning to anxiety across development and discuss how clinical treatments can be optimized for individuals and targeted to the biological states of the developing brain.
引用
收藏
页码:1358 / 1368
页数:11
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