Human Neurophysiology and Neuromodulation Laboratory, Department of Communication Sciences and Disorders, Louisiana State University, Baton Rouge, Louisiana, USA.
Human Brain Research Laboratory, Department of Neurosurgery, University of Iowa Hospitals and Clinics, Iowa City, Iowa, USA.
Psychophysiology. 2023 Aug;60(8):e14289. doi: 10.1111/psyp.14289. Epub 2023 Mar 8.
Evidence suggests that planning and execution of speech and limb movement are subserved by common neural substrates. However, less is known about whether they are supported by a common inhibitory mechanism. P3 event-related potentials (ERPs) is a neural signature of motor inhibition, which are found to be generated by several brain regions including the right dorsolateral prefrontal cortex (rDLPFC). However, the relative contribution of rDLPFC to the P3 response associated with speech versus limb inhibition remains elusive. We investigated the contribution of rDLPFC to the P3 underlying speech versus limb movement inhibition. Twenty-one neurotypical adults received both cathodal and sham high-definition transcranial direct current stimulation (HD-tDCS) over rDLPFC. ERPs were subsequently recorded while subjects were performing speech and limb Go/No-Go tasks. Cathodal HD-tDCS decreased accuracy for speech versus limb No-Go. Both speech and limb No-Go elicited a similar topographical distribution of P3, with significantly larger amplitudes for speech versus limb at a frontocentral location following cathodal HD-tDCS. Moreover, results showed stronger activation in cingulate cortex and rDLPFC for speech versus limb No-Go following cathodal HD-tDCS. These results indicate (1) P3 is an ERP marker of amodal inhibitory mechanisms that support both speech and limb inhibition, (2) larger P3 for speech versus limb No-Go following cathodal HD-tDCS may reflect the recruitment of additional neural resources-particularly within rDLPFC and cingulate cortex-as compensatory mechanisms to counteract the temporary stimulation-induced decline in speech inhibitory process. These findings have translational implications for neurological conditions that concurrently affect speech and limb movement.
有证据表明,言语和肢体运动的计划和执行由共同的神经基质来完成。然而,对于它们是否由共同的抑制机制支持,人们知之甚少。P3 事件相关电位(ERP)是运动抑制的神经特征,它是由包括右侧背外侧前额叶皮层(rDLPFC)在内的几个脑区产生的。然而,rDLPFC 对与言语抑制相关的 P3 反应的相对贡献仍然难以捉摸。我们研究了 rDLPFC 对言语与肢体运动抑制相关的 P3 的贡献。21 名神经典型成年人接受 rDLPFC 双侧阴极和假阴极高强度经颅直流电刺激(HD-tDCS)。随后,在受试者执行言语和肢体 Go/No-Go 任务时记录 ERP。阴极 HD-tDCS 降低了言语与肢体 No-Go 的准确性。言语和肢体 No-Go 都引起了类似的 P3 地形图分布,在阴极 HD-tDCS 后额中央位置,言语的 P3 振幅明显大于肢体。此外,结果表明,在阴极 HD-tDCS 后,言语与肢体 No-Go 时,扣带回皮层和 rDLPFC 的激活更强。这些结果表明:(1)P3 是一种 ERP 标记,表明支持言语和肢体抑制的模态无关抑制机制;(2)阴极 HD-tDCS 后,言语与肢体 No-Go 的 P3 更大,可能反映了额外神经资源的募集——特别是在 rDLPFC 和扣带回皮层——作为补偿机制,以抵消暂时刺激诱导的言语抑制过程下降。这些发现对同时影响言语和肢体运动的神经疾病具有转化意义。