Institute for Biomagnetism and Biosignalanalysis, University of Münster, Germany.
Hum Brain Mapp. 2010 Aug;31(8):1260-71. doi: 10.1002/hbm.20933.
Both the N200 and P300, which are, for example, evoked by Go/Nogo or Stop-Signal tasks, have long been interpreted as indicators for inhibition processes. Such interpretations have recently been challenged, and interest in the exact neural generators of these brain responses is continuously growing. Using recent methodological advancements, source estimations for the N200 and P300 as evoked by a tactile response inhibition task were computed. Current density reconstructions were also calculated accounting for interindividual differences in head geometry by incorporating information from T1-weighted magnetic resonance images. To ease comparability with relevant paradigms, the task was designed to mimic important characteristics of both Go/Nogo and Stop-Signal tasks as prototypes for a larger set of paradigms probing response inhibition. A network of neural generators was revealed, which has previously been shown to act in concert with executive control processes and thus is in full agreement with observations from other modalities. Importantly, a spatial segregation of midcingulate sources was observed. Our experimental data indicate that a left anterior region of the midcingulate cortex (MCC) is a major neural generator of the N200, whereas the midcingulate generator of the P300 is located in the right posterior MCC. Analyses of the P300 also revealed several areas, which have previously been associated with motor functions, for example, the precentral region. Our data clearly suggest a neuroanatomical and therefore also functional dissociation of the N200 and P300, a finding that cannot easily be provided by other imaging techniques.
N200 和 P300 都可以通过 Go/Nogo 或停止信号任务诱发,长期以来一直被解释为抑制过程的指标。最近,这些解释受到了挑战,人们对这些脑反应的确切神经发生源的兴趣不断增加。利用最近的方法学进展,计算了由触觉反应抑制任务诱发的 N200 和 P300 的源估计值。还通过将 T1 加权磁共振图像的信息纳入其中,计算了考虑头几何个体差异的电流密度重建。为了便于与相关范式进行比较,该任务旨在模拟 Go/Nogo 和停止信号任务的重要特征,作为探测反应抑制的更大范式集的原型。揭示了一个神经网络发生器,该发生器以前曾与执行控制过程协同作用,因此与来自其他模态的观察结果完全一致。重要的是,观察到中扣带回的空间分离。我们的实验数据表明,中扣带回皮质(MCC)的左前区域是 N200 的主要神经发生器,而 P300 的中扣带回发生器位于右后 MCC。对 P300 的分析还揭示了几个以前与运动功能相关的区域,例如中央前区。我们的数据清楚地表明 N200 和 P300 的神经解剖学和功能分离,这一发现不容易被其他成像技术提供。