High‐definition transcranial direct current stimulation over right dorsolateral prefrontal cortex differentially modulates inhibitory mechanisms for speech vs. limb movement

Author:

Johari Karim1ORCID,Berger Joel I.2

Affiliation:

1. Human Neurophysiology and Neuromodulation Laboratory, Department of Communication Sciences and Disorders Louisiana State University Baton Rouge Louisiana USA

2. Human Brain Research Laboratory, Department of Neurosurgery University of Iowa Hospitals and Clinics Iowa City Iowa USA

Abstract

AbstractEvidence 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.

Funder

College of Humanities and Social Sciences, Louisiana State University

Louisiana Board of Regents

Medical Research Council Canada

Publisher

Wiley

Subject

Experimental and Cognitive Psychology,Neuropsychology and Physiological Psychology,Biological Psychiatry,Cognitive Neuroscience,Developmental Neuroscience,Endocrine and Autonomic Systems,Neurology,Experimental and Cognitive Psychology,Neuropsychology and Physiological Psychology,General Neuroscience

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