Abelson James L, Khan Samir, Liberzon Israel, Young Elizabeth A
Department of Psychiatry and Molecular and Behavioral Neuroscience Institute, Trauma, Stress and Anxiety Research Group, University of Michigan, Ann Arbor, Michigan 48109-0118, USA.
Depress Anxiety. 2007;24(1):66-76. doi: 10.1002/da.20220.
Dysregulation of the hypothalamic-pituitary-adrenal (HPA) axis may play a role in panic disorder. HPA studies in patients with panic disorder, however, have produced inconsistent results. Seeking to understand the inconsistencies, we reexamined endocrine data from four studies of patients with panic disorder, in light of animal data highlighting the salience of novelty, control, and social support to HPA axis activity. Patients with panic disorder were studied (1) at rest over a full circadian cycle, (2) before and after activation by a panicogenic respiratory stimulant (doxapram) that does not directly stimulate the HPA axis, and (3) before and after a cholecystokinin B (CCK-B) agonist that is panicogenic and does directly stimulate the HPA axis. Patients with panic disorder had elevated overnight cortisol levels, which correlated with sleep disruption. ACTH and cortisol levels were higher in a challenge paradigm (doxapram) than in a resting state study, and paradigm-related ACTH secretion was exaggerated in patients with panic disorder. Panic itself could be elicited without HPA axis activation. Patients with panic disorder showed an exaggerated ACTH response to pentagastrin stimulation, but this response was normalized by prior exposure to the experimental context or psychological preparation to reduce novelty and enhance sense of control. Novelty is one of a number of contextual cues known from animal work to activate the HPA axis. The HPA axis abnormalities seen in patients with panic disorder in the four experiments reviewed here might all be due to exaggerated HPA axis reactivity to novelty cues. Most of the published panic/HPA literature is consistent with the hypothesis that HPA axis dysregulation in panic is due to hypersensitivity to contextual cues. This hypothesis requires experimental testing.
下丘脑 - 垂体 - 肾上腺(HPA)轴功能失调可能在惊恐障碍中起作用。然而,针对惊恐障碍患者的HPA研究结果并不一致。为了理解这些不一致之处,我们根据动物实验数据重新审视了四项惊恐障碍患者研究中的内分泌数据,这些动物实验数据突出了新奇性、控制感和社会支持对HPA轴活动的重要性。对惊恐障碍患者进行了如下研究:(1)在一个完整的昼夜周期内进行静息状态研究;(2)在由不直接刺激HPA轴的致惊恐呼吸兴奋剂(多沙普仑)激活前后进行研究;(3)在由致惊恐且直接刺激HPA轴的胆囊收缩素B(CCK - B)激动剂作用前后进行研究。惊恐障碍患者夜间皮质醇水平升高,且与睡眠中断相关。在激发试验范式(多沙普仑)中促肾上腺皮质激素(ACTH)和皮质醇水平高于静息状态研究,且惊恐障碍患者中与范式相关的ACTH分泌更为夸张。无需激活HPA轴即可引发惊恐发作本身。惊恐障碍患者对五肽胃泌素刺激的ACTH反应更为夸张,但通过事先接触实验环境或进行心理准备以减少新奇感并增强控制感后,这种反应可恢复正常。新奇性是已知能激活HPA轴的多种环境线索之一。在本文回顾的四项实验中,惊恐障碍患者出现的HPA轴异常可能均归因于HPA轴对新奇线索的反应过度。大多数已发表的关于惊恐障碍/HPA轴的文献与以下假设一致:惊恐障碍中HPA轴功能失调是由于对环境线索过敏。这一假设需要进行实验验证。