The Human BNST: Functional Role in Anxiety and Addiction

被引:226
作者
Avery, S. N. [1 ,2 ]
Clauss, J. A. [1 ,2 ,3 ]
Blackford, J. U. [1 ,4 ]
机构
[1] Vanderbilt Univ, Sch Med, Dept Psychiat, Nashville, TN 37212 USA
[2] Vanderbilt Univ, Vanderbilt Brain Inst, Neurosci Grad Program, Nashville, TN 37212 USA
[3] Vanderbilt Univ Sch Med, Nashville, TN USA
[4] Vanderbilt Univ, Dept Psychol, Nashville, TN 37212 USA
关键词
CORTICOTROPIN-RELEASING-FACTOR; FEAR-POTENTIATED STARTLE; CEREBRAL HEMISPHERE INTEGRATION; SUBSTANCE USE DISORDERS; DSM-IV DISORDERS; BED NUCLEUS; STRIA TERMINALIS; INDUCED REINSTATEMENT; EXTENDED AMYGDALA; CONDITIONED FEAR;
D O I
10.1038/npp.2015.185
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The consequences of chronic stress on brain structure and function are far reaching. Whereas stress can produce short-term adaptive changes in the brain, chronic stress leads to long-term maladaptive changes that increase vulnerability to psychiatric disorders, such as anxiety and addiction. These two disorders are the most prevalent psychiatric disorders in the United States, and are typically chronic, disabling, and highly comorbid. Emerging evidence implicates a tiny brain region-the bed nucleus of the stria terminalis (BNST)-in the body's stress response and in anxiety and addiction. Rodent studies provide compelling evidence that the BNST plays a central role in sustained threat monitoring, a form of adaptive anxiety, and in the withdrawal and relapse stages of addiction; however, little is known about the role of BNST in humans. Here, we review current evidence for BNST function in humans, including evidence for a role in the production of both adaptive and maladaptive anxiety. We also review preliminary evidence of the role of BNST in addiction in humans. Together, these studies provide a foundation of knowledge about the role of BNST in adaptive anxiety and stress-related disorders. Although the field is in its infancy, future investigations of human BNST function have tremendous potential to illuminate mechanisms underlying stress-related disorders and identify novel neural targets for treatment.
引用
收藏
页码:126 / 141
页数:16
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