Institute for Systems Neuroscience, University Medical Center Hamburg-Eppendorf (UKE), Martinistrasse 52, 20246, Hamburg, Germany,
Psychopharmacology (Berl). 2014 May;231(9):1949-62. doi: 10.1007/s00213-013-3338-8. Epub 2013 Nov 6.
One promising approach in the current ambition to maximise treatment benefit for anxiety disorders is the pharmacological enhancement of cognitive-behavioural treatment efficacy, which can be experimentally modelled by pharmacological enhancement of extinction learning/consolidation. Noradrenaline (NA) is involved in memory consolidation, and NAergic innervations are found in brain areas implicated in fear conditioning and extinction.
Thus, to enhance extinction memory consolidation through boosted NAergic signalling, we administered 4 mg reboxetine (RBX) immediately after extinction learning (day 2, 24 h after conditioning on day 1) in a randomised, placebo (PLC)-controlled design. At a delayed memory test (day 8), we probed cued and contextual fear and extinction memories before and after a reinstatement manipulation.
After reinstatement, we find significantly enhanced amygdala and posterior hippocampus activation in the RBX group, areas implicated in fear memory expression, while the PLC group exhibited enhanced activation in areas associated with extinction memory expression (vmPFC, anterior hippocampus). No group differences were found in skin conductance responses.
Thus, our data do not support our hypothesis that enhancement of NA signalling may facilitate extinction memory consolidation and provide preliminary evidence that this might rather enhance fear memories on a neural but not physiological (skin conductance responses) level.
在目前最大限度提高焦虑障碍治疗效果的目标中,一种很有前景的方法是通过药理学增强认知行为治疗的疗效,这可以通过药理学增强消退学习/巩固来进行实验模拟。去甲肾上腺素(NA)参与记忆巩固,并且在与恐惧条件反射和消退有关的大脑区域中发现了 NA 能神经支配。
因此,为了通过增强 NA 能信号来增强消退记忆的巩固,我们在消退学习后(第 1 天的条件反射后 24 小时,即第 2 天)立即给予 4mg 瑞波西汀(RBX),采用随机、安慰剂(PLC)对照设计。在延迟记忆测试(第 8 天)中,我们在重新引发操作之前和之后探测了线索和上下文恐惧以及消退记忆。
在重新引发后,我们发现 RBX 组的杏仁核和后海马区的激活明显增强,这些区域与恐惧记忆表达有关,而 PLC 组则表现出与消退记忆表达相关的区域(vmPFC、前海马区)的激活增强。在皮肤电导反应中未发现组间差异。
因此,我们的数据不支持增强 NA 信号可能促进消退记忆巩固的假设,并提供了初步证据表明,这可能在神经水平上而不是在生理水平(皮肤电导反应)上增强恐惧记忆。