1,721,131 research outputs found
Pulse waveform and current direction alter network-level TMS-induced functional connectivity: Evidence from TMS-EEG
Dataset and analyses for the study 'Pulse waveform and current direction alter network-level TMS-induced functional connectivity: Evidence from TMS-EEG' by Delia Lucarelli, Giacomo Guidali, Roberto Guidotti, Giulia Pieramico, Nadia Bolognini, Gian Luca Romani, Vittorio Pizzella & Laura Marzett
Pulse waveform and current direction alter network-level TMS-induced functional connectivity: Evidence from TMS-EEG
Dataset and analyses for the study 'Pulse waveform and current direction alter network-level TMS-induced functional connectivity: Evidence from TMS-EEG' by Delia Lucarelli, Giacomo Guidali, Roberto Guidotti, Giulia Pieramico, Nadia Bolognini, Gian Luca Romani, Vittorio Pizzella & Laura Marzett
Empathic neural reactivity to noxious stimuli delivered to body parts and non-corporeal objects
Neuroimaging studies report that the experience of observing or imagining the pain of others is mapped on a set of neural structures that largely overlap those called into play during the personal experience of pain (the so-called pain matrix). Empathy for pain is a multifaceted process that may be triggered by higher-order variables (such as imagination of others' suffering) or by the direct vision of painful situations. Most functional magnetic resonance imaging studies indicate that the empathic mapping of others' pain may rely on the affective and not on the sensorimotor division of the pain matrix. However, as empathy for pain is a complex, multifarious process, it is possible that different brain regions, even beyond the classic pain matrix, may be called into action in different circumstances. By using functional magnetic resonance imaging we explored the neural activity induced by needles deeply penetrating a hand or a non-corporeal object. We found that observation of pain in others brought about activation in the middle cingulate, left premotor and left and right supramarginal regions. This pattern of neural activity indicates that the direct vision of strong painful stimuli delivered to others activates neural regions in the onlooker's brain specifically concerned with the resonant, interindividual sharing of basic sensorimotor reactivity to pain. We also found that bilateral posterior parietal and temporo-occipital regions were activated during observation of painful stimuli delivered to the body of others as well as to non-body stimuli. Therefore, our study expands current knowledge on the neural reactivity to potentially dangerous stimuli delivered in the peripersonal space
Electrophysiological Correlates of Stimulus-driven Reorienting Deficits after Interference with Right Parietal Cortex during a Spatial Attention Task: A TMS-EEG Study
TMS interference over right intraparietal sulcus (IPS) causally disrupts behaviorally and EEG rhythmic correlates of endogenous spatial orienting before visual target presentation [Capotosto, P., Babiloni, C., Romani, G. L., & Corbetta, M. Differential contribution of right and left parietal cortex to the control of spatial attention: A simultaneous EEG-rTMS study. Cerebral Cortex, 22, 446-454, 2012; Capotosto, P., Babiloni, C., Romani, G. L., & Corbetta, M. Fronto-parietal cortex controls spatial attention through modulation of anticipatory alpha rhythms. Journal of Neuroscience, 29, 5863-5872, 2009]. Here we combine data from our previous studies to examine whether right parietal TMS during spatial orienting also impairs stimulus-driven reorienting or the ability to efficiently process unattended stimuli, that is, stimuli outside the current focus of attention. Healthy volunteers (n = 24) performed a Posner spatial cueing task while their EEG activity was being monitored. Repetitive TMS (rTMS) was applied for 150 msec simultaneously to the presentation of a central arrow directing spatial attention to the location of an upcoming visual target. Right IPS-rTMS impaired target detection, especially for stimuli presented at unattended locations; it also caused a modulation of the amplitude of parieto-occipital positive ERPs peaking at about 480 msec (P3) post-target. The P3 significantly decreased for unattended targets and significantly increased for attended targets after right IPS-rTMS as compared with sham stimulation. Similar effects were obtained for left IPS stimulation albeit in a smaller group of volunteers. We conclude that disruption of anticipatory processes in right IPS has prolonged effects that persist during target processing. The P3 decrement may reflect interference with postdecision processes that are part of stimulus-driven reorienting. Right IPS is a node of functional interaction between endogenous spatial orienting and stimulus-driven reorienting processes in human vision
Resting-state Modulation of Alpha Rhythms by Interference with Angular Gyrus Activity
The default mode network is active during restful wakefulness and suppressed during goal-driven behavior. We hypothesize that inhibitory interference with spontaneous ongoing, that is, not task-driven, activity in the angular gyrus (AG), one of the core regions of the default mode network, will enhance the dominant idling EEG alpha rhythms observed in the resting state. Fifteen right-handed healthy adult volunteers underwent to this study. Compared with sham stimulation, magnetic stimulation (1 Hz for 1 min) over both left and right AG, but not over FEF or intraparietal sulcus, core regions of the dorsal attention network, enhanced the dominant alpha power density (8-10 Hz) in occipitoparietal cortex. Furthermore, right AG-rTMS enhanced intrahemispheric alpha coherence (8-10 Hz). These results suggest that AG plays a causal role in the modulation of dominant low-frequency alpha rhythms in the resting-state condition
Effects of viewing affective pictures on sEMG activity of masticatory and postural muscles
Recently there has been an upsurge of interest in the question to what extent the human motor control system is influenced by the emotional state of the actor. The aim of this study was to evaluate whether emotional inputs modify the activity of masticatory and postural muscles. Twenty healthy young adults viewed affective pictures, while surface electromyography (sEMG) of masticatory and postural muscles was recorded to investigate the coupling between emotional reactions and body muscular activity. One hundred and twenty pictures, chosen from the International Affective Picture System (IAPS), divided in two blocks of six sets, were presented to the subjects. sEMG data were statistically analyzed (RM ANOVA on Ranks). Root Mean Square (RMS) amplitudes, comparing the subsequent sets (Neutral, Unpleasant, Neutral, Pleasant) with the first and the last Baseline set, changed significantly only randomly. The results show that emotional inputs seems not influence the activity of masticatory and postural muscles, recorded by sEMG. (c) 2013 Elsevier Ireland Ltd. All rights reserved
Sensory-motor mechanisms in human parietal cortex underlie arbitrary visual decisions
The neural mechanism underlying simple perceptual decision-making in monkeys has been recently conceptualized as an integrative process in which sensory evidence supporting different response options accumulates gradually over time. For example, intraparietal neurons accumulate motion information in favor of a specific oculomotor choice over time. It is unclear, however, whether this mechanism generalizes to more complex decisions that are based on arbitrary stimulus-response associations. In a task requiring arbitrary association of visual stimuli (faces or places) with different actions (eye or hand-pointing movements), we found that activity of effector-specific regions in human posterior parietal cortex reflected the 'strength' of the sensory evidence in favor of the preferred response. These regions did not respond to sensory stimuli per se but integrated sensory evidence toward the decision outcome. We conclude that even arbitrary decisions can be mediated by sensory-motor mechanisms that are completely triggered by contextual stimulus-response associations
Haptic perception and body representation in lateral and medial occipito-temporal cortices
Although vision is the primary sensory modality that humans and other primates use to identify objects in the environment, we can recognize crucial object features (e.g., shape, size) using the somatic modality. Previous studies have shown that the occipito-temporal areas dedicated to the visual processing of object forms, faces and bodies also show category-selective responses when the preferred stimuli are haptically explored out of view. Visual processing of human bodies engages specific areas in lateral (extrastriate body area, EBA) and medial (fusiform body area, FBA) occipito-temporal cortex. This study aimed at exploring the relative involvement of EBA and FBA in the haptic exploration of body parts. During fMRI scanning, participants were asked to haptically explore either real-size fake body parts or objects. We found a selective activation of right and left EBA, but not of right FBA, while participants haptically explored body parts as compared to real objects. This suggests that EBA may integrate visual body representations with somatosensory information regarding body parts and form a multimodal representation of the body. Furthermore, both left and right EBA showed a comparable level of body selectivity during haptic perception and visual imagery. However, right but not left EBA was more activated during haptic exploration than visual imagery of body parts, ruling out that the response to haptic body exploration was entirely due to the use of visual imagery. Overall, the results point to the existence of different multimodal body representations in the occipito-temporal cortex which are activated during perception and imagery of human body parts. (C) 2011 Elsevier Ltd. All rights reserved
Brain structures activated by overt and covert emotional visual stimuli
Research data suggest that the amygdala and some related brain structures modulate the processing of emotional visual stimuli even when they are not consciously perceived. In this study, we examined neural responses to investigate whether and how other brain areas anatomically connected to the amygdala might become activated during both overt and covert presentation of conditioned emotional visual stimuli. In the covert presentation, a conditioned angry face was shown for 15 ms followed by a neutral masking face (CSmask). In the overt condition, an angry face associated with a painful stimulus (CS+), a happy (H) and a neutral face (N) were presented for 75 ms. Based on results of functional magnetic resonance imaging (fMRI) in 10 healthy volunteers, we show evidence that a network of brain structures anatomically connected to the amygdala (including the anterior insula, the fusiform gyrus and the superior temporal sulcus) are involved in the subliminal processing of visual emotional stimuli. Of particular interest was the dissociation between the anterior and posterior insula: the anterior insula responded to both overt and covert presentation of the conditioned stimulus, whereas the posterior insula responded only to the overt presentation of the face associated with a painful electrical stimulation. This response pattern suggests that the anterior insula, the fusiform gyrus and the temporal sulcus cooperate with the amygdala in the unconscious processing of pain-conditioned stimuli
Bilateral neuromagnetic activation of human primary sensorimotor cortex in preparation and execution of unilateral voluntary finger movements
Extracranial magnetoencephalographic activity was separately recorded (25 channels) from bilateral primary sensorimotor cortex (M1-S1) of normal right-handers during unilateral finger movements. Standard dipole analysis indicated only a contralateral M1-S1 source for first movement-evoked field (MEF1) peaking at about 115 ms after electromyographic onset. However, the subtraction of the magnetic field generated by this source from the recorded magnetic field disclosed a low-amplitude ipsilateral central-parietal MEF1 that was explained by an ipsilateral M1-S1 source. (C) 1999 Published by Elsevier Science B.V. All rights reserved
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