Abstract

Switching between tasks requires individuals to inhibit mental representations of the previous task demands and to activate representations of the new task demands. The inhibition of the executed task remains active for a while so that when the inhibited task set must be re-activated shortly after, the need to overcome residual task set inhibition leads to behavioral costs. In a sham-controlled balanced-order within-subjects experimental design we investigated whether applying right anodal/left cathodal transcranial direct current stimulation (tDCS) over the dorsolateral prefrontal or parietal cortex modulated the ability to overcome persistent task inhibition during task switching. Results showed that right anodal/left cathodal tDCS over the parietal cortex improves performance selectively when switching back to a recently inhibited task that requires previous inhibition to be overcome. Right Anodal/left cathodal tDCS over the prefrontal cortex improves performance during task switching in general, either when re-engaging in a inhibited task or when engaging in a non-inhibited task. Results suggest a different contribution of prefrontal and parietal regions to task switching, with parietal cortex being selectively involved in overcoming persistent task inhibition and prefrontal cortex being more generally involved in the control of task set during task switching.

Highlights

  • The ability to flexibly adjust behavior to a changing environment by promoting the processing of current goal-relevant information at the expense of the no longer relevant one is a key factor for efficient adaptation and survival, when irrelevant information interferes with current intention, eliciting conflicting responses

  • Response adaptation to changing task demands has been often studied in laboratory by means of the task switching procedure, wherein participants typically alternate between performing each of two or more possible tasks afforded by the same stimulus

  • The need to reconfigure the internal control settings required to perform a new task is considered a source of the so-called switch cost [4,5,6], that is the reaction time (RT) difference that typically results from the slower performance on trials where the participant has to switch to a different task compared to trials where the participant has to repeat a task

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Summary

Introduction

The ability to flexibly adjust behavior to a changing environment by promoting the processing of current goal-relevant information at the expense of the no longer relevant one is a key factor for efficient adaptation and survival, when irrelevant information interferes with current intention, eliciting conflicting responses. Response adaptation to changing task demands has been often studied in laboratory by means of the task switching procedure, wherein participants typically alternate between performing each of two or more possible tasks afforded by the same stimulus (see [2,3] for reviews). In this procedure, the control settings appropriate for one task become no longer relevant when a new task is required, so that cognitive control is necessary for the instantiation of the appropriate task set (e.g., defining the new relevant information at perceptual and motor levels). The need to overcome this suppressed state leads to a behavioral cost, named n-2 task repetition cost, which has been demonstrated by showing that switching back to a task that has been executed very recently (e.g., A-B-A task sequences) is harder than switching back to task that has been executed a less recently (e.g., C-B-A task sequence; e.g., [13,14])

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