Department of Psychiatry, Massachusetts General Hospital, Charlestown, Massachusetts; Department of Psychological and Brain Sciences, University of Massachusetts, Amherst, Massachusetts.
Department of Psychiatry, Massachusetts General Hospital, Charlestown, Massachusetts; Department of Psychiatry, Harvard Medical School, Charlestown, Massachusetts; Athinoula A. Martinos Center for Biomedical Imaging, Charlestown, Massachusetts.
Biol Psychiatry Cogn Neurosci Neuroimaging. 2021 Mar;6(3):299-309. doi: 10.1016/j.bpsc.2020.09.013. Epub 2020 Sep 24.
We assessed the impact of total and partial sleep loss on neural correlates of fear conditioning, extinction learning, and extinction recall in healthy young adults.
Participants (56.3% female, age 24.8 ± 3.4 years) were randomized to a night of normal sleep (NS) (n = 48), sleep restriction (SR) (n = 53), or sleep deprivation (SD) (n = 53). All completed fear conditioning and extinction learning phases the following morning. Extinction recall was tested in the evening of the same day. Task-based contrasts were modeled at the beginning of, at the end of, and across the fear conditioning and extinction learning phases, and at the beginning of extinction recall. These contrasts were compared among the 3 groups by means of analysis of variance. Nonparametric permutation corrected analyses using a cluster-determining threshold of p < .005 and a familywise error of p < .05.
At the end of fear conditioning, NS activated medial prefrontal regions, SR activated motor areas, and participants in the SD group showed no significant activations. Across extinction learning, only NS activated both salience (fear) and extinction (regulatory) areas. For extinction recall, SD activated similar regions as NS across extinction learning, while SR activated salience and motor areas. During early fear conditioning, compared with NS, SD activated more medial prefrontal and SR activated more salience network areas. For extinction recall, NS activated more prefrontal areas and SD activated more of both salience- and extinction-related areas than SR.
Relative to NS, SR may enhance fear-related and diminish extinction-related activity, whereas SD may delay engagement of extinction learning. Findings may have clinical implications for populations and occupations in which sleep loss is common.
我们评估了完全和部分睡眠剥夺对健康年轻成年人恐惧条件反射、消退学习和消退记忆的神经相关因素的影响。
参与者(女性占 56.3%,年龄 24.8±3.4 岁)随机分为正常睡眠(NS)组(n=48)、睡眠限制(SR)组(n=53)或睡眠剥夺(SD)组(n=53)。所有参与者均在次日早晨完成恐惧条件反射和消退学习阶段。同日傍晚进行消退记忆测试。在恐惧条件反射和消退学习阶段的开始、结束和整个阶段,以及消退记忆测试的开始,都对基于任务的对比进行了建模。通过方差分析比较了 3 组之间的差异。使用非参数置换校正分析,采用聚类确定阈值 p<0.005 和组间错误率 p<0.05。
在恐惧条件反射的结束阶段,NS 激活了内侧前额叶区域,SR 激活了运动区域,而 SD 组的参与者没有显示出显著的激活。在整个消退学习过程中,只有 NS 激活了突显(恐惧)和消退(调节)区域。对于消退记忆测试,SD 在整个消退学习过程中与 NS 激活了相似的区域,而 SR 激活了突显和运动区域。在早期恐惧条件反射阶段,与 NS 相比,SD 激活了更多的内侧前额叶区域,而 SR 激活了更多的突显网络区域。对于消退记忆测试,NS 激活了更多的前额叶区域,而 SD 激活了更多的突显和与消退相关的区域,比 SR 多。
与 NS 相比,SR 可能增强了与恐惧相关的活动,减少了与消退相关的活动,而 SD 可能延迟了消退学习的参与。这些发现可能对睡眠不足常见的人群和职业具有临床意义。