Prenatal cocaine exposure alters functional activation in the ventral prefrontal cortex and its structural connectivity with the amygdala.
Prenatal cocaine exposure alters functional activation in the ventral prefrontal cortex and its structural connectivity with the amygdala.
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DOI：
10.1016/j.pscychresns.2012.12.005
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发表时间：
2013-07-30
影响因子：
11.3
通讯作者：
Hu X
中科院分区：
文献类型：
--
作者：
Li Z;Santhanam P;Coles CD;Ellen Lynch M;Hamann S;Peltier S;Hu X
Prenatal cocaine exposure (PCE) is associated with arousal dysregulation, and alterations of amygdala activity in response to emotional arousal were previously reported. However, voluntary regulation of emotional affect, enabling appropriate neural response to different streams of stimuli, must also engage prefrontal regions, yet PCE impact on these prefrontal mechanisms has not been investigated. Recent neuroimaging studies have shown the involvement of ventral prefrontal cortex (vPFC) in the modulation of amygdala reactivity and the mediation of effective emotion regulation. Based on these findings, using functional magnetic resonance imaging (fMRI) and diffusion tensor imaging (DTI), the present study compared functional activations of vPFC as well as its structural connectivity with amygdala between groups of PCE and control adolescents. In a working memory task with emotional distracters, the PCE adolescents exhibited less capability of increasing their vPFC activation in response to increased memory load, which corresponded with their less suppressed amygdala activation. Reduced structural connectivity between vPFC and amygdala were also observed from DTI measurement in the PCE group. In addition, correlations between amygdala activation and (i) vPFC activation, as well as (ii) amygdala-vPFC structural connectivity, were observed in the control but not in the PCE group. These data complemented previous findings of PCE impact on amygdala activity and extended our understanding of the neurobiological mechanisms of PCE effect on arousal dysregulation reported in human and animal studies.
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影响因子：
2.9
作者：
Coles, CD;Bard, KA;Lynch, ME
通讯作者：
Lynch, ME
影响因子：
5.7
作者：
Cohen, MS
通讯作者：
Cohen, MS
影响因子：
2.3
作者：
Bracht, Tobias;Tuescher, Oliver;Saur, Dorothee
通讯作者：
Saur, Dorothee
影响因子：
4
作者：
Bendersky, M;Lewis, M
通讯作者：
Lewis, M
影响因子：
2.9
作者：
COLES, CD;PLATZMAN, KA;FALEK, A
通讯作者：
FALEK, A