Department of Psychological and Brain Sciences and Institute for Neuroscience, Texas A&M University, College Station, TX, USA.
Nat Neurosci. 2021 May;24(5):677-684. doi: 10.1038/s41593-021-00825-5. Epub 2021 Apr 1.
Reconsolidation may be a viable therapeutic target to inhibit pathological fear memories. In the clinic, incidental or imaginal reminders are used for safe retrieval of traumatic memories of experiences that occurred elsewhere. However, it is unknown whether indirectly retrieved traumatic memories are sensitive to disruption. Here we used a backward (BW) conditioning procedure to indirectly retrieve and manipulate a hippocampus (HPC)-dependent contextual fear engram in male rats. We show that conditioned freezing to a BW conditioned stimulus (CS) is mediated by fear to the conditioning context, activates HPC ensembles that can be covertly captured and chemogenetically activated to drive fear, and is impaired by post-retrieval protein synthesis inhibition. These results reveal that indirectly retrieved contextual fear memories reactivate HPC ensembles and undergo protein synthesis-dependent reconsolidation. Clinical interventions that rely on indirect retrieval of traumatic memories, such as imaginal exposure, may open a window for editing or erasure of neural representations that drive pathological fear.
再巩固可能是抑制病理性恐惧记忆的一个可行的治疗靶点。在临床上,偶然或想象的提示被用于安全地提取发生在其他地方的创伤性记忆。然而,目前尚不清楚间接提取的创伤性记忆是否容易受到干扰。在这里,我们使用反向(BW)条件作用程序来间接检索和操纵雄性大鼠中海马(HPC)依赖性情境恐惧记忆痕迹。我们表明,对 BW 条件刺激(CS)的条件性冻结是由对条件化情境的恐惧介导的,激活了可以被隐蔽捕获并通过化学遗传激活来驱动恐惧的 HPC 集合,并且受到检索后蛋白质合成抑制的损害。这些结果表明,间接检索到的情境恐惧记忆会重新激活 HPC 集合,并经历依赖于蛋白质合成的再巩固。依赖于创伤性记忆的间接检索的临床干预,如想象暴露,可能为编辑或擦除驱动病理性恐惧的神经表征打开一个窗口。