Department Psychology & Neuroscience, University of Colorado Boulder, 2860 Wilderness Place, Boulder, CO, 80301, USA.
Department Psychology & Neuroscience, University of Colorado Boulder, 2860 Wilderness Place, Boulder, CO, 80301, USA.
Physiol Behav. 2023 May 1;263:114107. doi: 10.1016/j.physbeh.2023.114107. Epub 2023 Feb 4.
Early life stress (ELS) can set the stage for susceptibility to cognitive and emotional dysfunction in adulthood by disrupting typical neural development. The prefrontal cortex (PFC) continues to mature during early life, making this region particularly vulnerable to disruption for animals who experience ELS. Despite this, the effects of ELS experience on in vivo PFC function in awake and behaving adult animals are currently poorly understood. To assess this, we employed an instrumental conflict task to assess how hungry adult rats, either ELS (wet bedding) or unstressed Controls, were able to flexibly alter their motivation for food reward seeking (lever presses) in situations that were either threatening or safe. During this task, in vivo electrophysiological recordings (both single unit and local field potentials [LFPs]) were made in the rats' ventral-medial PFC (vmPFC). We found that ELS rats were less motivated to lever press for rewards than Controls in the threat situations during repeated extinction sessions. In recordings taken during this suppression task, Control vmPFC neurons displayed reliable differences between motivated actions, such as between rewarded and unrewarded presses, but ELS neurons failed to differentiate these action-outcome differences. We also found differences in task-related LFP activity between groups; in particular, prior ELS experience appears to induce abnormal changes in low-frequency oscillations during shock-associated threat stimuli prior to presses, as well as diminished higher-frequency oscillations following rewarded presses. Collectively, we demonstrate that ELS experience produces persistent impairment in motivational regulation that is associated with significant changes in in vivo PFC signals. Specifically, ELS-experienced adults fail to appropriately update motivated action strategies under threat conditions, and likewise fail to appropriately monitor and update action/outcome relationships in motivated behavior. These ELS-related changes may therefore lay the foundation for heightened susceptibility to mental-health disorders in adults such as substance abuse and post-traumatic stress disorder.
早期生活应激 (ELS) 可通过破坏典型的神经发育,为成年后认知和情绪功能障碍的易感性奠定基础。前额皮质 (PFC) 在生命早期仍在成熟,因此对于经历 ELS 的动物来说,该区域特别容易受到干扰。尽管如此,ELS 经历对清醒和行为活跃的成年动物体内 PFC 功能的影响目前仍知之甚少。为了评估这一点,我们采用了一种工具性冲突任务来评估饥饿的成年大鼠(ELS(湿垫料)或未受压力的对照)在威胁或安全的情况下,如何灵活地改变他们对食物奖励寻求(压杆)的动机。在这项任务中,我们在大鼠的腹内侧前额皮质 (vmPFC) 中进行了体内电生理记录(单细胞和局部场电位 [LFPs])。我们发现,与对照组相比,ELS 大鼠在多次消退过程中,在威胁情况下对奖励的动机较低。在抑制任务期间进行的记录中,对照组 vmPFC 神经元在激励动作之间(例如,奖励和非奖励按压之间)显示出可靠的差异,但 ELS 神经元未能区分这些动作-结果差异。我们还发现两组之间与任务相关的 LFPs 活动存在差异;特别是,之前的 ELS 经历似乎会在与按压相关的威胁刺激之前诱导与低频振荡相关的异常变化,以及在奖励按压后高频振荡减少。总的来说,我们证明 ELS 经历会导致动机调节持续受损,这与体内 PFC 信号的重大变化有关。具体来说,经历 ELS 的成年人在威胁条件下无法适当更新激励行动策略,同样无法在激励行为中适当监测和更新行动/结果关系。因此,这些与 ELS 相关的变化可能为成年人易患心理健康障碍(如药物滥用和创伤后应激障碍)奠定基础。