期刊论文详细信息
NEUROSCIENCE LETTERS 卷:693
The central extended amygdala in fear and anxiety: Closing the gap between mechanistic and neuroimaging research
Review
Fox, Andrew S.1,2,3  Shackman, Alexander J.4,5,6 
[1] Dept Psychol, Davis, CA 95616 USA
[2] Univ Calif Davis, Davis, CA 95616 USA
[3] Univ Calif Davis, Calif Natl Primate Res Ctr, Davis, CA 95616 USA
[4] Univ Maryland, Dept Psychol, College Pk, MD 20742 USA
[5] Univ Maryland, Neurosci & Cognit Sci Program, College Pk, MD 20742 USA
[6] Univ Maryland, Maryland Neuroimaging Ctr, College Pk, MD 20742 USA
关键词: Affective neuroscience;    Anxiety disorders;    BST/BNST;    Emotion;    Individual differences;    Neuroimaging;    Nonhuman primate;   
DOI  :  10.1016/j.neulet.2017.11.056
来源: Elsevier
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【 摘 要 】

Anxiety disorders impose a staggering burden on public health, underscoring the need to develop a deeper understanding of the distributed neural circuits underlying extreme fear and anxiety. Recent work highlights the importance of the central extended amygdala, including the central nucleus of the amygdala (Ce) and neighboring bed nucleus of the stria terminalis (BST). Anatomical data indicate that the Ce and BST form a tightly interconnected unit, where different kinds of threat-relevant information can be integrated to assemble states of fear and anxiety. Neuroimaging studies show that the Ce and BST are engaged by a broad spectrum of potentially threat-relevant cues. Mechanistic work demonstrates that the Ce and BST are critically involved in organizing defensive responses to a wide range of threats. Studies in rodents have begun to reveal the specific molecules, cells, and microcircuits within the central extended amygdala that underlie signs of fear and anxiety, but the relevance of these tantalizing discoveries to human experience and disease remains unclear. Using a combination of focal perturbations and whole-brain imaging, a new generation of nonhuman primate studies is beginning to close this gap. This work opens the door to discovering the mechanisms underlying neuroimaging measures linked to pathological fear and anxiety, to understanding how the Ce and BST interact with one another and with distal brain regions to govern defensive responses to threat, and to developing improved intervention strategies.

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