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The neurophysiological mechanisms underlying the integration of perception and action are an important topic in cognitive neuroscience. Yet, connections between neurophysiology and cognitive theoretical frameworks have rarely been established. The theory of event coding (TEC) details how perceptions and actions are associated (bound) in a common representational domain (the "event file"), but the neurophysiological mechanisms underlying these processes are hardly understood. We used complementary neurophysiological methods to examine the neurophysiology of event file processing (i.e., event-related potentials [ERPs], temporal EEG signal decomposition, EEG source localization, time-frequency decomposition, EEG network analysis). We show that the P3 ERP component and activity modulations in inferior parietal regions (BA40) reflect event file binding processes. The relevance of this parietal region is corroborated by source localization of temporally decomposed EEG data. We also show that temporal EEG signal decomposition reveals a pattern of results suggesting that event file processes can be dissociated from pure stimulus and response-related processes in the EEG signal. Importantly, it is also documented that event file binding processes are reflected by modulations in the network architecture of theta frequency band activity. That is, when stimulus-response bindings in event files hamper response selection this was associated with a less efficient theta network organization. A more efficient organization was evident when stimulus-response binding in event files facilitated response selection. Small-world network measures seem to reflect event file processing. The results show how cognitive-theoretical assumptions of TEC can directly be mapped to the neurophysiology of response selection., (© 2020 The Authors. Human Brain Mapping published by Wiley Periodicals, Inc.)

Inhibitory control deficits are a hallmark in ADHD. Yet, inhibitory control includes a multitude of entities (e.g. 'inhibition of interferences' and 'action inhibition'). Examining the interplay between these kinds of inhibitory control provides insights into the architecture of inhibitory control in ADHD. Combining a Simon task and a Go/Nogo task, we assessed the interplay of 'inhibition of interferences' and 'action inhibition'. This was combined with EEG recordings, EEG data decomposition and source localization. Simon interference effects in Go trials were larger in ADHD. At the neurophysiological level, this insufficient inhibition of interferences in ADHD related to the superior parietal cortex. Simon interference effects were absent in action inhibition (Nogo) trials in ADHD, compared to controls. This was supported by bayesian statistics. The power of effects was higher than 95%. The differential effects between the groups were associated with modulations of neurophysiological response selection processes in the superior frontal gyrus. ADHD is not only associated with deficits in inhibitory control. Rather, the organization and architecture of the inhibitory control system is different in ADHD. Distinguishable inhibitory control processes operate on a hierarchical 'first come, first serve' basis and are not integrated in ADHD. This is a new facet of ADHD., (Copyright © 2019 The Authors. Published by Elsevier Ltd.. All rights reserved.)

Task switching processes reflect a faculty of cognitive flexibility. The underlying neural mechanisms and functional cortical networks have frequently been investigated using neurophysiological (EEG) or functional imaging methods. However, task switching processes are subject to strong intra-individual variability, especially when tested under varying levels of working memory demands. This intra-individual variability compromises the reliable estimation of neurophysiological processes and related functional neuroanatomical networks. In this study, we combine residue iteration decomposition (RIDE) of event-related potentials (ERPs) and source localization methods to circumvent this problem. Due to strong intra-individual variability, behavioral effects between memory-based and cue-based task switching were not reflected by classical ERPs, but were so after applying RIDE. Using RIDE, modulations paralleling the behavioral data were specifically reflected by processes related to the updating of internal representations for response selection (reflected by the C-cluster in the P3-component time range) rather than by stimulus and motor-related processes (reflected by the S-cluster and R-cluster). The C-cluster-processes were associated with activation differences in the inferior parietal cortex, including the temporo-parietal junction (TPJ, BA40) and likely reflect mechanisms related to the updating of internal representations and task sets for response selection. The results underline the necessity to use temporal decomposition methods to control the problem of intra-individual signal variability to decipher the neurophysiology and functional neuroanatomy of cognitive processes.

Cognitive flexibility is a major requirement for successful behavior. nNeural oscillations in the alpha frequency band were repeatedly associated with cognitive flexibility in task-switching paradigms. Alpha frequencies are modulated by working memory load and are used to process information during task switching, however we do not know how this oscillatory network communication is modulated. In order to understand the mechanisms that drive cognitive flexibility, ERPs, oscillatory power and how the communication within these networks is organized are of importance. The EEG data show that during phases reflecting preparatory processes to pre-activate task sets, alpha oscillatory power but not the small world properties of the alpha network architecture was modulated. During the switching only the N2 ERP component showed clear modulations. After the response, alpha oscillatory power reinstates and therefore seems to be important to deactivate or maintain the previous task set. For these reactive control processes the network architecture in terms of small-world properties is modulated. Effects of memory load on small-world aspects were seen in repetition trials, where small-world properties were higher when memory processes were relevant. These results suggest that the alpha oscillatory network becomes more small-world-like when reactive control processes during task switching are less complex.

Background: A major facet of obsessive–compulsive disorder (OCD) is cognitive inflexibility. However, sometimes, cognitive flexibility can be needed to reuse recently abandoned mental sets. Therefore, cognitive flexibility can in certain cases be useful to reinstate some form of rigid, repetitive behavior characterizing OCD. We test the counterintuitive hypothesis that under such circumstances, cognitive flexibility is better in OCD patients than controls. Methods: We examined N = 20 adolescent OCD patients and N = 22 controls in a backward inhibition (BI) paradigm. This was combined with event‐related potential (ERP) recordings and source localization. The BI effect describes the cost of overcoming the inhibition of a recently abandoned mental set that is relevant again. Therefore, a strong BI effect is disadvantageous for cognitive flexibility. Results: Compared to controls, OCD patients revealed a smaller backward inhibition effect. The EEG data revealed larger P1 amplitudes in backward inhibition trials in the OCD group, which was due to activation differences in the inferior frontal gyrus (BA47). The severity of clinical symptoms predicted these neurophysiological modulations. The power of the observed effects was about 95%. Conclusions: The study shows that cognitive flexibility can be better in OCD than controls. This may be the case in situations where superior abilities in the reactivation of repeating mental sets and difficulties to process new ones coincide. This may be accomplished by intensified inhibitory control mechanisms. The results challenge the view on OCD, since OCD is not generally associated with cognitive inflexibility. [ABSTRACT FROM AUTHOR]

Cognitive flexibility is a major requirement for successful goal-directed behavior and their neurobiological underpinnings are becoming better understood. However, the role of the norepinephrine system during task switching is largely enigmatic, despite neurobiological considerations make it likely that the norepinephrine system likely plays an important role. Theoretical considerations also suggest that the norepinephrine system mainly modulates task-switching processes when these rely upon working memory mechanisms. This topic was examined in the current system neurophysiological study integrating event-related potential (ERP) with pupil diameter data as a proximate the norepinephrine system activity. Combined with source localization methods, human brain structure, brain function, and phasic modulations by an important neurobiological system were integrated. The results show that cognitive-neurophysiological subprocesses during the actual switching processes, reflected by the N2 and P3 ERP components, are not modulated by the norepinephrine system. Rather, this system modulates preparatory processes in the fore period of stimuli signaling possible switches of response sets. The source localization results show that this is achieved by modulating neural processes in the temporo-parietal junction (BA40). Importantly, these phasic modulatory effects of the norepinephrine system were only evident when working memory processes had to be used to guide the selection of the appropriate responses for task switching. [ABSTRACT FROM AUTHOR]

The effects of high-dose ethanol intoxication on cognitive flexibility processes are not well understood, and processes related to hangover after intoxication have remained even more elusive. Similarly, it is unknown in how far the complexity of cognitive flexibility processes is affected by intoxication and hangover effects. We performed a neurophysiological study applying high density electroencephalography (EEG) recording to analyze event-related potentials (ERPs) and perform source localization in a task switching paradigm which varied the complexity of task switching by means of memory demands. The results show that high-dose ethanol intoxication only affects task switching (i.e. cognitive flexibility processes) when memory processes are required to control task switching mechanisms, suggesting that even high doses of ethanol compromise cognitive processes when they are highly demanding. The EEG and source localization data show that these effects unfold by modulating response selection processes in the anterior cingulate cortex. Perceptual and attentional selection processes as well as working memory processes were only unspecifically modulated. In all subprocesses examined, there were no differences between the sober and hangover states, thus suggesting a fast recovery of cognitive flexibility after high-dose ethanol intoxication. We assume that the gamma-aminobutyric acid (GABAergic) system accounts for the observed effects, while they can hardly be explained by the dopaminergic system. [ABSTRACT FROM AUTHOR]