4.7 Article

Working memory load reduces corticospinal suppression to former go and trained no-go cues

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SCIENTIFIC REPORTS
卷 11, 期 1, 页码 -

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NATURE PORTFOLIO
DOI: 10.1038/s41598-021-91040-6

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  1. Australian Research Council [DP160102871, DP190100410]
  2. Economic and Social Research Council Studentship [ES/J50015X/1]

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This study found that inhibiting motor system activity to former go cues relies on goal-directed cognitive control processes. Under low working memory load, corticospinal excitability to trained stop and go cues was suppressed. Conversely, under high working memory load, cortical suppression to go cues was reduced, indicating the need for executive control mechanisms.
Environmental cues associated with an action can prime the motor system, decreasing response times and activating motor regions of the brain. However, when task goals change, the same responses to former go-associated cues are no longer required and motor priming needs to be inhibited to avoid unwanted behavioural errors. The present study tested whether the inhibition of motor system activity to presentations of former go cues is reliant on top-down, goal-directed cognitive control processes using a working memory (WM) load manipulation. Applying transcranial magnetic stimulation over the primary motor cortex to measure motor system activity during a Go/No-go task, we found that under low WM, corticospinal excitability was suppressed to former go and trained no-go cues relative to control cues. Under high WM, the cortical suppression to former go cues was reduced, suggesting that the underlying mechanism required executive control. Unexpectedly, we found a similar result for trained no-go cues and showed in a second experiment that the corticospinal suppression and WM effects were unrelated to local inhibitory function as indexed by short-interval intracortical inhibition. Our findings reveal that the interaction between former response cues and WM is complex and we discuss possible explanations of our findings in relation to models of response inhibition.

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