Morgan Barak E
MRC/UCT Medical Imaging Research Unit, Division of Biomedical Engineering, Department of Human Biology, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.
Curr Psychiatry Rep. 2006 Aug;8(4):270-8. doi: 10.1007/s11920-006-0062-7.
Behavioral inhibition (BI) during early childhood has been associated with subsequent development of anxiety disorders. However, understanding of the neuroanatomical substrates of BI in humans generally has not kept pace with that of anxiety disorders. Recent interpretations and implementations of Gray's and Kagan's concepts of BI are examined from the perspective of current neurobiological models. Particular attention is given to evidence pointing to conceptual and operational limitations of self-report scales purported to measure trait BI in adults, and especially to inconsistent correlations between such behavioral inhibition system (BIS) scores and amygdala and autonomic responses to fear- or startle-inducing stimuli. Evidence showing a dissociation of both BI and trait anxiety from the amygdala is considered. Possible reasons for the poor association between BIS and trait anxiety self-report scale scores and predicted physiological outputs of the BIS are identified. Reasons to distinguish between the neural bases of BI as against trait anxiety also are discussed. The need to critically examine the role of the amygdala in BI and trait anxiety, as well as to consider other brain areas that appear to be involved in subserving these emotional traits, is emphasized.
儿童早期的行为抑制(BI)与随后焦虑症的发展有关。然而,对人类BI神经解剖学基础的理解总体上未能跟上焦虑症的研究步伐。从当前神经生物学模型的角度审视了对格雷和卡根的BI概念的最新解释与应用。特别关注了那些表明旨在测量成人特质BI的自我报告量表在概念和操作上存在局限性的证据,尤其是此类行为抑制系统(BIS)得分与杏仁核以及对恐惧或惊吓诱导刺激的自主反应之间不一致的相关性。考虑了显示BI和特质焦虑均与杏仁核分离的证据。确定了BIS与特质焦虑自我报告量表得分之间关联不佳以及BIS预测生理输出的可能原因。还讨论了区分BI与特质焦虑神经基础的原因。强调了批判性审视杏仁核在BI和特质焦虑中的作用以及考虑其他似乎参与维持这些情绪特质的脑区的必要性。