Department of Neurosciences, University of New Mexico School of Medicine, Albuquerque, NM, 87131, USA; New Mexico Alcohol Research Center, UNM Health Sciences Center, Albuquerque, NM, USA.
Department of Psychology, University of New Mexico, Albuquerque, NM, USA.
Neuropharmacology. 2023 Sep 15;236:109599. doi: 10.1016/j.neuropharm.2023.109599. Epub 2023 May 20.
Although it is well established that alcohol consumption during pregnancy can lead to lifelong difficulties in offspring, Fetal Alcohol Spectrum Disorders (FASD) remain a common neurodevelopmental syndrome. Translational behavioral tools that target similar brain circuits across species can facilitate understanding of these cognitive consequences. Touchscreen behavioral tasks for rodents enable easy integration of dura recordings of electroencephalographic (EEG) activity in awake behaving animals, with clear translational generalizability. Recently, we showed that Prenatal Alcohol Exposure (PAE) impairs cognitive control on the touchscreen 5-Choice Continuous Performance Task (5C-CPT) which requires animals to touch on target trials (hit) and withhold responding on non-target trials (correct rejection). Here, we extended these findings to determine whether dura EEG recordings would detect task-relevant differences in medial prefrontal cortex (mPFC) and posterior parietal cortex (PPC) corresponding with behavioral alterations in PAE animals. Replicating previous findings, PAE mice made more false alarm responses versus controls and had a significantly lower sensitivity index. All mice, regardless of sex or treatment, demonstrated increased frontal theta-band power during correct trials that followed an error (similar to post-error monitoring commonly seen in human participants). All mice showed a significant decrease in parietal beta-band power when performing a correct rejection versus a hit. PAE mice of both sexes showed a significantly larger decrease in parietal beta-band power when successfully rejecting non-target stimuli. These findings suggest that moderate exposure to alcohol during development can have long lasting effects on cognitive control, and task-relevant neural signals may provide a biomarker of impaired function across species.
虽然众所周知,怀孕期间饮酒会导致后代终生出现困难,但胎儿酒精谱系障碍(FASD)仍然是一种常见的神经发育综合征。针对跨物种相似大脑回路的转化行为工具可以促进对这些认知后果的理解。用于啮齿动物的触摸屏行为任务使在清醒行为动物中进行 dura 脑电图(EEG)活动记录变得容易,具有明确的转化通用性。最近,我们发现产前酒精暴露(PAE)会损害在触摸屏 5 选择连续绩效任务(5C-CPT)上的认知控制,该任务要求动物在目标试验上触摸(命中)并在非目标试验上抑制反应(正确拒绝)。在这里,我们扩展了这些发现,以确定 dura EEG 记录是否会检测到与 medial prefrontal cortex(mPFC)和 posterior parietal cortex(PPC)相关的任务相关差异,这些差异与 PAE 动物的行为改变相对应。重复先前的发现,PAE 小鼠与对照组相比做出更多的假警报反应,且敏感性指数显著降低。无论性别或治疗如何,所有小鼠在跟随错误的正确试验中均表现出额叶θ波段功率增加(类似于人类参与者中常见的后错误监测)。所有小鼠在执行正确拒绝与命中时,顶叶β波段功率均显着降低。雄性和雌性的 PAE 小鼠在成功拒绝非目标刺激时,顶叶β波段功率的降低幅度明显更大。这些发现表明,在发育过程中适度暴露于酒精会对认知控制产生持久影响,并且与任务相关的神经信号可能为跨物种的功能障碍提供生物标志物。