Department of Psychiatry, University of California San Diego, San Diego, CA, USA.
Neuroscience, Roche Innovation Center Basel, F. Hoffmann-La Roche Ltd., Basel, Switzerland.
Psychiatry Res. 2015 Sep 30;233(3):394-401. doi: 10.1016/j.pscychresns.2015.06.016. Epub 2015 Jun 30.
This study investigated the temporal pattern of brain response to emotional stimuli during 28 days of alprazolam treatment among patients with generalized anxiety disorder (GAD) randomized 2:1 to drug or placebo in a double-blind design. Functional magnetic resonance imaging scans obtained during an emotion face matching task (EFMT) and an affective stimulus expectancy task (STIMEX) were performed at baseline, one hour after initial drug administration and 28 days later. Alprazolam significantly reduced scores on the Hamilton Anxiety Scale and the Penn State Worry Questionnaire after one week and 28 days of treatment. Brain activation in the amygdala during the EFMT and in the insula during the STIMEX was reduced one hour after alprazolam administration but returned to baseline levels at Day 28. Exploratory analyses revealed significant treatment differences in brain activity during the STIMEX on Day 28 in frontal lobe, caudate nucleus, middle temporal gyrus, secondary visual cortex, and supramarginal gyrus. These results are consistent with the notion that the neural mechanisms supporting sustained treatment effects of benzodiazepines in GAD differ from those underlying their acute effects.
这项研究调查了在双盲设计中,28 天的阿普唑仑治疗期间,广泛性焦虑症(GAD)患者的大脑对情绪刺激的反应的时间模式,这些患者随机分为 2:1 的药物组或安慰剂组。在基线、首次药物治疗后一小时和 28 天后进行了情绪面孔匹配任务(EFMT)和情感刺激预期任务(STIMEX)的功能磁共振成像扫描。阿普唑仑在一周和 28 天的治疗后显著降低了汉密尔顿焦虑量表和宾夕法尼亚州担忧问卷的评分。在 EFMT 期间杏仁核和 STIMEX 期间脑岛的大脑激活在阿普唑仑给药后一小时减少,但在第 28 天恢复到基线水平。探索性分析显示,在第 28 天 STIMEX 期间额叶、尾状核、中颞叶、次级视觉皮层和缘上回的大脑活动存在显著的治疗差异。这些结果与以下观点一致,即支持苯二氮䓬类药物在 GAD 中持续治疗效果的神经机制与它们的急性作用的神经机制不同。