Placebo analgesia induced by verbal suggestion in the context of experimentally induced fear and anxiety.

The role of state anxiety and state fear in placebo effects is still to be determined. We aimed to investigate the effect of fear of movement-related pain (FMRP) and contextual pain related anxiety (CPRA) on the magnitude of placebo analgesia induced by verbal suggestion. Fifty-six female participants completed a modified voluntary joystick movement paradigm (VJMP) where half participated in a predictable pain condition (PC), in which one of the joystick movements is always followed by pain and the other movement is never followed by pain, and half in an unpredictable pain condition (UC), in which pain was delivered unpredictably. By varying the level of pain predictability, FMRP and CPRA were induced in PC and UC respectively. Colour stimuli were presented at the beginning of each trail. Half of the participants were verbally informed that the green or red colour indicated less painful stimuli (experimental groups), the other half did not receive any suggestion (control groups). We measured self-reported pain intensity, expectancy of pain intensity (PC only), pain related fear and anxiety (eyeblink startle response and self-ratings) and avoidance behaviour (movement-onset latency and duration). The results indicate that the placebo effect was successfully induced in both experimental conditions. In the PC, the placebo effect was predicted by expectancy. Despite the fact that FMRP and CPRA were successfully induced, no difference was found in the magnitude of the placebo effect between PC and UC. Concluding, we did not find a divergent effect of fear and anxiety on placebo analgesia.

On the locus of the effect of alerting on response conflict: An event-related EEG study with a speed-accuracy tradeoff manipulation.

The present study investigated the locus of the effect of alerting on response conflict, and examined whether this effect may be interpreted as an alerting-triggered imbalance of speed-accuracy tradeoff (SAT). Participants performed the flanker task with an alerting tone in half of the trials and SAT manipulation. Behavioral results showed the usual increase of the conflict effect (incongruent-congruent flankers) in the alerting trials. This interaction was not affected by SAT manipulation in response times, although accuracy emphasis abolished alerting effects in error rates. Event-related potential (ERP) results showed that alerting increased the conflict by facilitating the selection and activation of stimulus-response links, reflected in modulations of the P3b component, and by enhancing the activation of incorrect response evoked by incongruent flankers, reflected in an increased initial incorrect activation in the lateralized readiness potential (LRP). Time-frequency analysis showed that the alerting-triggered increase of conflict entailed stronger response of executive mechanisms, reflected in a larger conflict-related midfrontal theta-band power. These EEG effects were not affected by SAT manipulation. In conclusion, alerting affects both the emergence of conflict and conflict control, and this alerting-conflict interaction could not be explained in terms of SAT.

Religious Fundamentalism Modulates Neural Responses to Error-Related Words: The Role of Motivation Toward Closure.

Examining the relationship between brain activity and religious fundamentalism, this study explores whether fundamentalist religious beliefs increase responses to error-related words among participants intolerant to uncertainty (i.e., high in the need for closure) in comparison to those who have a high degree of toleration for uncertainty (i.e., those who are low in the need for closure). We examine a negative-going event-related brain potentials occurring 400 ms after stimulus onset (the N400) due to its well-understood association with the reactions to emotional conflict. Religious fundamentalism and tolerance of uncertainty were measured on self-report measures, and electroencephalographic neural reactivity was recorded as participants were performing an emotional Stroop task. In this task, participants read neutral words and words related to uncertainty, errors, and pondering, while being asked to name the color of the ink with which the word is written. The results confirm that among people who are intolerant of uncertainty (i.e., those high in the need for closure), religious fundamentalism is associated with an increased N400 on error-related words compared with people who tolerate uncertainty well (i.e., those low in the need for closure).

Influence of transient spatial attention on the P3 component and perception of painful and non-painful electric stimuli in crossed and uncrossed hands positions.

Recent reports show that focusing attention on the location where pain is expected can enhance its perception. Moreover, crossing the hands over the body's midline is known to impair the ability to localise stimuli and decrease tactile and pain sensations in healthy participants. The present study investigated the role of transient spatial attention on the perception of painful and non-painful electrical stimuli in conditions in which a match or a mismatch was induced between skin-based and external frames of reference (uncrossed and crossed hands positions, respectively). We measured the subjective experience (Numerical Rating Scale scores) and the electrophysiological response elicited by brief electric stimuli by analysing the P3 component of Event-Related Potentials (ERPs). Twenty-two participants underwent eight painful and eight non-painful stimulus blocks. The electrical stimuli were applied to either the left or the right hand, held in either a crossed or uncrossed position. Each stimulus was preceded by a direction cue (leftward or rightward arrow). In 80% of the trials, the arrow correctly pointed to the spatial regions where the stimulus would appear (congruent cueing). Our results indicated that congruent cues resulted in increased pain NRS scores compared to incongruent ones. For non-painful stimuli such an effect was observed only in the uncrossed hands position. For both non-painful and painful stimuli the P3 peak amplitudes were higher and occurred later for incongruently cued stimuli compared to congruent ones. However, we found that crossing the hands substantially reduced the cueing effect of the P3 peak amplitudes elicited by painful stimuli. Taken together, our results showed a strong influence of transient attention manipulations on the NRS ratings and on the brain activity. Our results also suggest that hand position may modulate the strength of the cueing effect, although differences between painful and non-painful stimuli exist.

Post-Decision Wagering Affects Metacognitive Awareness of Emotional Stimuli: An Event Related Potential Study.

The present research investigated metacognitive awareness of emotional stimuli and its psychophysiological correlates. We used a backward masking task presenting participants with fearful or neutral faces. We asked participants for face discrimination and then probed their metacognitive awareness with confidence rating (CR) and post-decision wagering (PDW) scales. We also analysed psychophysiological correlates of awareness with event-related potential (ERP) components: P1, N170, early posterior negativity (EPN), and P3. We have not observed any differences between PDW and CR conditions in the emotion identification task. However, the "aware" ratings were associated with increased accuracy performance. This effect was more pronounced in PDW, especially for fearful faces, suggesting that emotional stimuli awareness may be enhanced by monetary incentives. EEG analysis showed larger N170, EPN and P3 amplitudes in aware compared to unaware trials. It also appeared that both EPN and P3 ERP components were more pronounced in the PDW condition, especially when emotional faces were presented. Taken together, our ERP findings suggest that metacognitive awareness of emotional stimuli depends on the effectiveness of both early and late visual information processing. Our study also indicates that awareness of emotional stimuli can be enhanced by the motivation induced by wagering.

Electrocortical indices of attention correlate with the need for closure.

Need for closure (NFC), defined as a desire for a quick and unambiguous answer to a question and an aversion to uncertainty, usually leads to a more structured, persistent, and rigid cognitive style. We suggested that this cognitive characteristic could be related to differences in a simple sensory gating control mechanism as reflected in event-related potentials (N1 component). We expected that the higher an individual's NFC, the more attention he/she would allocate to the selected stimuli or the feature of the stimuli, which is manifested in an increased N1 component. We tested this assumption in two experiments where NFC was measured by a scale and event-related potentials were recorded during the Stroop task and the Visual Distractor task. In line with the hypotheses, we found that NFC was associated with amplified processing of stimuli at an early sensory stage, which was evidenced in an increased N1 component. We suggested that this early sensory gating mechanism protects high NFC individuals against anxiety-producing uncertainty.

Individual differences in epistemic motivation and brain conflict monitoring activity.

It is well documented that motivation toward closure (NFC), defined as a desire for a quick and unambiguous answer to a question and an aversion to uncertainty, is linked to more structured, rigid, and persistent cognitive styles. However, the neurocognitive correlates of NFC have never been tested. Thus, using event-related potentials, we examined the hypothesis that NFC is associated with the neurocognitive process for detecting discrepancies between response tendencies and higher level intentions. We found that greater NFC is associated with lower conflict-related anterior cingulate activity, suggesting lower sensitivity to cues for altering a habitual response pattern and lower sensitivity to committing errors. This study provides evidence that high NFC acts as a bulwark against anxiety-producing uncertainty and minimizes the experience of error.

Psychometric intelligence and P3 of the event-related potentials studied with a 3-stimulus auditory oddball task.

Relationship between psychometric intelligence measured with Raven's Advanced Progressive Matrices (RAPM) and event-related potentials (ERP) was examined using 3-stimulus oddball task. Subjects who had scored higher on RAPM exhibited larger amplitude of P3a component. Additional analysis using the Standardized Low Resolution Electromagnetic Tomography (sLORETA) revealed that this effect corresponds with stronger activity within the frontal cortex and the cingulate gyrus. High intelligence can also be linked with greater P3b response and stronger activity within the parietal cortex and the posterior cingulate gyrus. It may be concluded that the processes related to the initial stage of attention engagement as indexed by P3a, as well as the later stimulus evaluation and classification reflected in P3b, are more intense in subjects scoring higher on RAPM. The quality of mental abilities can therefore be related to differences of the activity in frontal and parietal brain regions.

Neural generators of the auditory evoked potential components P3a and P3b.

The aim of the present study was to define the scalp topography of the two subcomponents of the P3 component of the auditory evoked potential elicited in a three-stimulus oddball paradigm and to identify their cortical generators using the standardized low resolution electromagnetic tomography (sLORETA). Subjects were presented with a random sequence of auditory stimuli and instructed to respond to an infrequently occurring target stimulus inserted into a sequence of frequent standard and rare non-target stimuli. Results show that the magnitude of the frontal P3a is determined by the relative physical difference among stimuli, as it was larger for the stimulus more deviant from the standard. Major neural generators of the P3a were localized within frontal cortex and anterior cingulate gyrus. In contrast to this, the P3b, showing maximal amplitude at parietal locations, was larger for stimuli demanding a response than for the rare non-target. Major sources of the P3b included the superior parietal lobule and the posterior part of the cingulate gyrus. Our findings are in line with the hypothesis that P3a is related to alerting activity during the initial allocation of attention, while P3b is related to activation of a posterior network when the neuronal model of perceived stimulation is compared with the attentional trace.

Trait anxiety and involuntary processing of facial emotions.

There is suggestion that trait anxiety influences the processing of threat-related information. To test this hypothesis we recorded ERPs in response to subliminally presented and backward masked fearful and neutral faces, and non-face objects, in the preselected low- and high-anxious individuals. The amplitude of N170 was found to be larger when elicited by faces in comparison to non-faces, however it was not found to be emotion-sensitive or modulated by anxiety level. Differences between low- and high-anxious individuals appeared in a time window of the P1 component. At later stages, within the EPN component, stronger negativity specific for fearful faces was recorded exclusively in the low-anxious participants. Our findings indicate that anxiety level modulates early stages of information processing, as reflected in the P1 component. This leads to anxiety-related differences in involuntary emotional expression detection at later stages (EPN component).

Attention modulates emotional expression processing.

To investigate the time course of emotional expression processing, we recorded ERPs to facial stimuli. The first task was to discriminate emotional expressions. Enhanced negativity of the face-specific N170 was elicited by emotional as opposed to neutral faces, followed by the occipital negativity (240-340 ms poststimulus). The second task was to classify face gender. Here, N170 was unaffected by the emotional expression. However, emotional expression effect was expressed in the anterior positivity (160-250 ms poststimulus) and subsequent occipital negativity (240-340 ms poststimulus). Results support the thesis that structural encoding relevant to gender recognition and simultaneous expression analysis are independent processes. Attention modulates facial emotion processing 140-185 ms poststimulus. Involuntary differentiation of facial expression was observed later (160-340 ms poststimulus), suggesting unintentional attention capture.

The auditory P3 from passive and active three-stimulus oddball paradigm.

The aim of this study was the comparison of basic characteristics of the P3 subcomponents elicited in passive and active versions of the auditory oddball paradigm. A 3-stimulus oddball paradigm was employed in which subjects were presented with random sequence of tones while they performed a discrimination task in visual modality with no response to the tone (passive task) or responded to an infrequently occurring target stimulus inserted into sequence of frequent standard and rare non-target stimuli (active task). Results show that the magnitude of the frontal P3 response is determined by the relative perceptual distinctiveness among stimuli. The amplitude of frontal component is larger for the stimuli more deviated from the standard in both passive and active tasks. In all cases however, a maximum over central or fronto-central scalp regions was demonstrated. Moreover, amplitude of this component was influenced by the strength of attentional focus--a significantly larger response was obtained in the active session than in its passive counterpart. The apparent parietal P3 responses were obtained only in the active condition. The amplitude of this component is larger for the target than the non-target across all electrode sites, but both demonstrated a parietal maxima. This findings suggest that generation of early frontal P3 could be related to alerting activity of frontal cortex irrespective of stimulus context, while generation of later parietal P3 is related to temporo-parietal network activated when neuronal model of perceived stimulation and attentional trace are comparing.

The P3 produced by auditory stimuli presented in a passive and active condition: modulation by visual stimuli.

The aim of this study was to investigate how the processing of auditory stimuli is affected by the simultaneous presentation of visual stimuli. This was approached in an active and passive condition, during which a P3 was elicited in the human EEG by single auditory stimuli. Subjects were presented tones, either alone or accompanied by the simultaneous exposition of pictures. There were two different sessions. In the first, the presented tones demanded no further cognitive activity from the subjects (passive or 'ignore' session), while in the second session subjects were instructed to count the tones (active or 'count' session). The central question was whether inter-modal influences of visual stimulation in the active condition would modulate the auditory P3 in the same way as in the passive condition. Brain responses in the ignore session revealed only a small P3-like component over the parietal and frontal cortex, however, when the auditory stimuli co-occurred with the visual stimuli, an increased frontal activity in the window of 300-500 ms was observed. This could be interpreted as the reflection of a more intensive involuntary attention shift, provoked by the preceding visual stimulation. Moreover, it was found that cognitive load caused by the count instruction, resulted in an evident P3, with maximal amplitude over parietal locations. This effect was smaller when auditory stimuli were presented on the visual background. These findings might support the thesis that available resources were assigned to the analysis of visual stimulus, and thus were not available to analyze the subsequent auditory stimuli. This reduction in allocation of resources for attention was restricted to the active condition only, when the matching of a template with incoming information results in a distinct P3 component. It is discussed whether the putative source of this effect is a change in the activity of the frontal cortex.