National Institute of Mental Health.
J Cogn Neurosci. 2019 Jul;31(7):1054-1064. doi: 10.1162/jocn_a_01387. Epub 2019 Mar 18.
The mismatch negativity (MMN) is an ERP component seen in response to unexpected "novel" stimuli, such as in an auditory oddball task. The MMN is of wide interest and application, but the neural responses that generate it are poorly understood. This is in part due to differences in design and focus between animal and human oddball paradigms. For example, one of the main explanatory models, the "predictive error hypothesis", posits differences in timing and selectivity between signals carried in auditory and prefrontal cortex (PFC). However, these predictions have not been fully tested because (1) noninvasive techniques used in humans lack the combined spatial and temporal precision necessary for these comparisons and (2) single-neuron studies in animal models, which combine necessary spatial and temporal precision, have not focused on higher order contributions to novelty signals. In addition, accounts of the MMN traditionally do not address contributions from subcortical areas known to be involved in novelty detection, such as the amygdala. To better constrain hypotheses and to address methodological gaps between human and animal studies, we recorded single neuron activity from the auditory cortex, dorsolateral PFC, and basolateral amygdala of two macaque monkeys during an auditory oddball paradigm modeled after that used in humans. Consistent with predictions of the predictive error hypothesis, novelty signals in PFC were generally later than in auditory cortex and were abstracted from stimulus-specific effects seen in auditory cortex. However, we found signals in amygdala that were comparable in magnitude and timing to those in PFC, and both prefrontal and amygdala signals were generally much weaker than those in auditory cortex. These observations place useful quantitative constraints on putative generators of the auditory oddball-based MMN and additionally indicate that there are subcortical areas, such as the amygdala, that may be involved in novelty detection in an auditory oddball paradigm.
失匹配负波(MMN)是一种在对意想不到的“新奇”刺激(如听觉Oddball 任务)做出反应时出现的 ERP 成分。MMN 具有广泛的兴趣和应用,但产生它的神经反应却知之甚少。这部分是由于动物和人类 Oddball 范式在设计和重点上存在差异。例如,主要的解释模型之一,“预测误差假说”,假设在听觉和前额叶皮层(PFC)中携带的信号之间存在时间和选择性上的差异。然而,这些预测尚未得到充分验证,原因有二:(1)人类使用的非侵入性技术缺乏进行这些比较所需的空间和时间精度;(2)在动物模型中进行的单细胞研究虽然结合了必要的空间和时间精度,但没有关注新颖性信号的高级别贡献。此外,MMN 的传统解释通常不涉及到参与新颖性检测的皮质下区域的贡献,如杏仁核。为了更好地限制假设,并解决人类和动物研究之间的方法学差距,我们在模仿人类使用的听觉 Oddball 范式的情况下,从两只猕猴的听觉皮层、背外侧 PFC 和基底外侧杏仁核记录了单个神经元的活动。与预测误差假说的预测一致,PFC 中的新颖性信号通常比听觉皮层中的信号晚,并且是从听觉皮层中看到的刺激特异性效应中抽象出来的。然而,我们发现杏仁核中的信号在幅度和时间上与 PFC 中的信号相当,并且 PFC 和杏仁核中的信号通常比听觉皮层中的信号弱得多。这些观察结果对基于听觉 Oddball 的 MMN 的潜在发生器进行了有用的定量限制,并进一步表明,在听觉 Oddball 范式中,可能有皮质下区域(如杏仁核)参与新颖性检测。