Huster René J, Messel Mari S, Thunberg Christina, Raud Liisa
Multimodal Imaging and Cognitive Control Lab, Department of Psychology, University of Oslo, Oslo, Norway; Cognitive and Translational Neuroscience Cluster, Department of Psychology, University of Oslo, Oslo, Norway.
Multimodal Imaging and Cognitive Control Lab, Department of Psychology, University of Oslo, Oslo, Norway; Cognitive and Translational Neuroscience Cluster, Department of Psychology, University of Oslo, Oslo, Norway; Sunnaas Rehabilitation Hospital, Nesodden, Norway.
Cortex. 2020 Nov;132:334-348. doi: 10.1016/j.cortex.2020.05.021. Epub 2020 Aug 5.
Inhibitory control, i.e., the ability to stop or suppress actions, thoughts, or memories, represents a prevalent and popular concept in basic and clinical neuroscience as well as psychology. At the same time, it is notoriously difficult to study as successful inhibition is characterized by the absence of a continuously quantifiable direct behavioral marker. It has been suggested that the P3 latency, and here especially its onset latency, may serve as neurophysiological marker of inhibitory control as it correlates with the stop signal reaction time (SSRT). The SSRT estimates the average stopping latency, which itself is unobservable since no overt response is elicited in successful stop trials, based on differences in the distribution of go reaction times and the delay of the stop-relative to the go-signal in stop trials. In a meta-analysis and an independent electroencephalography (EEG) experiment, we found that correlations between the P3 latency and the SSRT are indeed replicable, but also unspecific. Not only does the SSRT also correlate with the N2 latency, but both P3 and N2 latency measures show similar or even higher correlations with other behavioral parameters such as the go reaction time or stopping accuracy. The missing specificity of P3-SSRT correlations, together with the general pattern of associations, suggests that these manifest effects are driven by underlying latent processes other than inhibition, such as behavioral adaptations in context of performance monitoring operations.
抑制控制,即停止或抑制行为、思想或记忆的能力,在基础和临床神经科学以及心理学中是一个普遍且流行的概念。与此同时,由于成功的抑制以缺乏可连续量化的直接行为标记为特征,因此研究起来非常困难。有人提出,P3潜伏期,尤其是其起始潜伏期,可能作为抑制控制的神经生理标记,因为它与停止信号反应时间(SSRT)相关。SSRT估计平均停止潜伏期,由于在成功的停止试验中没有引发明显反应,所以它本身是不可观察的,它是基于在进行试验中的反应时间分布差异以及相对于进行信号的停止延迟来估计的。在一项荟萃分析和一项独立的脑电图(EEG)实验中,我们发现P3潜伏期与SSRT之间的相关性确实是可重复的,但也是非特异性的。不仅SSRT也与N2潜伏期相关,而且P3和N2潜伏期测量与其他行为参数,如进行反应时间或停止准确性,显示出相似甚至更高的相关性。P3 - SSRT相关性缺乏特异性,以及关联的总体模式,表明这些明显的效应是由抑制以外的潜在过程驱动的,例如在绩效监测操作背景下的行为适应。