Filtern
Dokumenttyp
- Dissertation (5) (entfernen)
Schlagworte
- Elektroencephalographie (5) (entfernen)
Cognitive performance is contingent upon multiple factors. Beyond the impact of en-vironmental circumstances, the bodily state may hinder or promote cognitive processing. Af-ferent transmission from the viscera, for instance, is crucial not only for the genesis of affect and emotion, but further exerts significant influences on memory and attention. In particular, afferent cardiovascular feedback from baroreceptors demonstrated subcortical and cortical inhibition. Consequences for human cognition and behavior are the impairment of simple perception and sensorimotor functioning. Four studies are presented that investigate the mod-ulatory impact of baro-afferent feedback on selective attention. The first study demonstrates that the modulation of sensory processing by baroreceptor activity applies to the processing of complex stimulus configurations. By the use of a visual masking task in which a target had to be selected against a visual mask, perceptual interference was reduced when target and mask were presented during the ventricular systole compared to the diastole. In study two, selection efficiency was systematically manipulated in a visual selection task in which a target letter was flanked by distracting stimuli. By comparing participants" performance under homogene-ous and heterogeneous stimulus conditions, selection efficiency was assessed as a function of the cardiac cycle phase in which the targets and distractors were presented. The susceptibility of selection performance to the stimulus condition at hand was less pronounced during the ventricular systole compared to the diastole. Study one and two therefore indicate that inter-ference from irrelevant sensory input, resulting from temporally overlapping processing traces or from the simultaneous presentation of distractor stimuli, is reduced during phases of in-creased baro-afferent feedback. Study three experimentally manipulated baroreceptor activity by systematically varying the participant- body position while a sequential distractor priming task was completed. In this study, negative priming and distractor-response binding effects were obtained as indices of controlled and automatic distractor processing, respectively. It was found that only controlled distractor processing was affected by tonic increases in baro-receptor activity. In line with study one and two these results indicate that controlled selection processes are more efficient during enhanced baro-afferent feedback, observable in dimin-ished aftereffects of controlled distractor processing. Due to previous findings that indicated baro-afferent transmission to affect central, rather than response-related processing stages, study four measured lateralized-readiness potentials (LRPs) and reaction times (RTs), while participants, again, had to selectively respond to target stimuli that were surrounded by dis-tractors. The impact of distractor inhibition on stimulus-related, but not on response-related LRPs suggests that in a sequential distractor priming task, the sensory representations of dis-tractors, rather than motor responses are targeted by inhibition. Together with the results from studies one through three and the finding of baroreceptor-mediated behavioral inhibition tar-geting central processing stages, study four corroborates the presumption of baro-afferent signal transmission to modulate controlled processes involved in selective attention. In sum, the work presented shows that visual selective attention benefits from in-creased baro-afferent feedback as its effects are not confined to simple perception, but may facilitate the active suppression of neural activity related to sensory input from distractors. Hence, due to noise reduction, baroreceptor-mediated inhibition may promote effective selec-tion in vision.
Stress has been considered one of the most relevant factors promoting aggressive behavior. Animal and human pharmacological studies revealed the stress hormones corticosterone in rodents and cortisol in humans to constitute a particularly important neuroendocrine determinate in facilitating aggression and beyond that, assumedly in its continuation and escalation. Moreover, cortisol-induced alterations of social information processing, as well as of cognitive control processes, have been hypothesized as possible influencing factors in the stress-aggression link. So far, the immediate impact of a preceding stressor and thereby stress-induced rise of cortisol on aggressive behavior as well as higher-order cognitive control processes and social information processing in this context have gone mostly unheeded. The present thesis aimed to extend the hitherto findings of stress and aggression in this regard. For this purpose two psychophysiological studies with healthy adults were carried out, both using the socially evaluated-cold pressor test as an acute stress induction. Additionally to behavioral data and subjective reports, event related potentials were measured and acute levels of salivary cortisol were collected on the basis of which stressed participants were divided into cortisol-responders and "nonresponders. Study 1 examined the impact of acute stress-induced cortisol increase on inhibitory control and its neural correlates. 41 male participants were randomly assigned to the stress procedure or to a non-stressful control condition. Beforehand and afterwards, participants performed a Go Nogo task with visual letters to measure response inhibition. The effect of acute stress-induced cortisol increase on covert and overt aggressive behavior and on the processing of provoking stimuli within the aggressive encounter was investigated in study 2. Moreover, this experiment examined the combined impact of stress and aggression on ensuing affective information processing. 71 male and female participants were either exposed to the stress or to the control condition. Following this, half of each group received high or low levels of provocation during the Taylor Aggression Paradigm. At the end of the experiment, a passive viewing paradigm with affective pictures depicting positive, negative, or aggressive scenes with either humans or objects was realized. The results revealed that men were not affected by a stress-induced rise in cortisol on a behavioral level, showing neither impaired response inhibition nor enhanced aggressive behavior. In contrast, women showed enhanced overt and covert aggressive behavior under a surge of endogenous cortisol, confirming previous results, albeit only in case of high provocation and only up to the level of the control group. Unlike this rather moderate impact on behavior, cortisol showed a distinct impact on neural correlates of information processing throughout inhibitory control, aggression-eliciting stimuli, and emotional pictures for both men and women. At this, stress-induced increase of cortisol resulted in enhanced N2 amplitudes to Go stimuli, whereas P2 amplitudes to both and N2 to Nogo amplitudes retained unchanged, indicating an overcorrection and caution of the response activation in favor of successful inhibitory control. The processing of aggression-eliciting stimuli during the aggressive encounter was complexly altered by stress differently for women and men. Under increased cortisol levels, the frontal or parietal P3 amplitude patterns were either diminished or reversed in the case of high provocation compared to the control group and to cortisol-nonresponders, indicating a desensitization towards aggression-eliciting stimuli in males, but a more elaborate processing of those in women. Moreover, stress-induced cortisol and provocation jointly altered subsequent affective information processing at early as well as later stages of the information processing stream. Again, increased levels of cortisol led opposite directed amplitudes in the case of high provocation relative to the control group and cortisol-nonresponders, with enhanced N2 amplitudes in men and reduced P3 and LPP amplitudes in men and women for all affective pictures, suggesting initially enhanced emotional reactivity in men, but ensuing reduced motivational attention and enhanced emotion regulation in both, men and women. As a result, these present findings confirm the relevance of HPA activity in the elicitation and persistence of human aggressive behavior. Moreover, they reveal the significance of compensatory and emotion regulatory strategies and mechanisms in response to stress and provocation, indorsing the relevance of social information and cognitive control processes. Still, more research is needed to clarify the conditions which lead to the facilitation of aggression and by which compensatory mechanisms this is prevented.
Magnet Resonance Imaging (MRI) and Electroencephalography (EEG) are tools used to investigate the functioning of the working brain in both humans and animal studies. Both methods are increasingly combined in separate or simultaneous measurements under the assumption to benefit from their individual strength while compensating their particular weaknesses. However, little attention has been paid to how statistical analyses strategies can influence the information that can be retrieved from a combined EEG fMRI study. Two independent studies in healthy student volunteers were conducted in the context of emotion research to demonstrate two approaches of combining MRI and EEG data of the same participants. The first study (N = 20) applied a visual search paradigm and found that in both measurements the assumed effects were absent by not statistically combining their results. The second study (N = 12) applied a novelty P300 paradigm and found that only the statistical combination of MRI and EEG measurements was able to disentangle the functional effects of brain areas involved in emotion processing. In conclusion, the observed results demonstrate that there are added benefits of statistically combining EEG-fMRI data acquisitions by assessing both the inferential statistical structure and the intra-individual correlations of the EEG and fMRI signal.
Ziel der Studie war es, die Wirksamkeit zweier psychotherapeutischer Mikrointerventionen zur Emotionsregulation und zur progressiven Relaxation und die damit einhergehenden Veränderungen auf psychometrischer und elektrokortikaler Ebene zu untersuchen. Die Stichprobe bestand aus 65 klinischen Versuchspersonen der Warteliste der Poliklinischen Psychotherapieambulanz der Universität Trier. In einer EEG-Erhebung vor und nach den Mikrointerventionen wurden neben dem Ruhe-EEG ereigniskorrelierte Potentiale (EKPs) aufgezeichnet. Im EKP-Paradigma wurden die Probanden instruiert negativ-valente Bilder aus dem IAPS-System entweder anzuschauen oder die gezeigte Situation kognitiv zu einer weniger negativen Interpretation der Bilder umzudeuten. Nach der EEG-Aufzeichnung wurden die Probanden randomisiert einer standardisierten 90-minütigen psychotherapeutischen Intervention zum kognitiven Reframing bzw. zur progressiven Relaxation zugewiesen. Im Anschluss wurde die EEG-Erhebung mit dem Ruhe-EEG und dem EKP mit einem parallelisierten Pool negativ valenter Bilder erneut durchgeführt. Auf psychometrischer Ebene wurde u.a. der positive und negative Affekt mit dem PANAS im Verlauf der Untersuchung zu insgesamt vier Messzeitpunkten erfasst. Neben dem Alpha-Frequenzband des Ruhe-EEGs wurde bei den EKPs die P3 und das Späte Positive Potential (LPP) untersucht. Die Ergebnisse geben Hinweise darauf, dass die psychotherapeutischen Mikrointerventionen zu differentiellen Effekten auf psychometrischer und elektrokortikaler Ebene führten. Auf der psychometrischen Ebene zeigte sich bei den Teilnehmern der Entspannungsintervention direkt nach der Intervention eine Abnahme des negativen Affekts, während sich dies bei den Teilnehmern der Reframing-Intervention erst im Verlauf der zweiten EEG-Messung mit dem Umdeuten der negativ valenten Bilder zeigte. Auf der elektrokortikalen Ebene waren die Ergebnisse weniger einheitlich. Durch die Entspannungs-Intervention konnte im Verlauf der Untersuchung eine Zunahme der P3-Amplituden festgestellt werden, während die Reframing-Teilnehmer über die Messzeitpunkte eine Abnahme der P3-Amplituden aufwiesen. Dies könnte so interpretiert werden, dass durch das Erlernen des Reframings das emotionale Arousal reduziert werden konnte. Bei dem LPP waren hingegen keine differentiellen Effekte der Mikrointerventionen nachweisbar. Bei beiden Interventionen kam es zu einer Zunahme der LPP-Amplituden. Bei der Analyse der Alpha-Aktivität des Ruhe-EEGs wurde bei den Entspannungs-Teilnehmern im Vergleich zu den Reframing-Teilnehmern nach der Mikrointervention eine größere Alpha-Aktivität gefunden. Diese Unterschiede wurden am deutlichsten in der linken Hemisphäre sowie in den zentralen und parietalen Hirnregionen. Eine höhere Alpha-Aktivität geht mit einer niedrigeren kortikalen Aktivität einher, so dass man davon ausgehen kann, dass die Entspannungs-Teilnehmer diese Hirnregionen während der Intervention weniger ausgeprägt nutzten. Zusammenfassend geben die Befunde erste Hinweise auf eine differentielle Wirkung der beiden Mikrointerventionen.
Cortisol is a stress hormone that acts on the central nervous system in order to support adaptation and time-adjusted coping processes. Whereas previous research has focused on slow emerging, genomic effects of cortisol likely mediated by protein synthesis, there is only limited knowledge about rapid, non-genomic cortisol effects on in vivo neuronal cell activity in humans. Three independent placebo-controlled studies in healthy men were conducted to test effects of 4 mg cortisol on central nervous system activity, occurring within 15 minutes after intravenous administration. Two of the studies (N = 26; N = 9) used continuous arterial spin labeling as a magnetic resonance imaging sequence, and found rapid bilateral thalamic perfusion decrements. The third study (N = 14) revealed rapid cortisol-induced changes in global signal strength and map complexity of the electroencephalogram. The observed changes in neuronal functioning suggest that cortisol may act on the thalamic relay of non-relevant background as well as on task specific sensory information in order to facilitate the adaptation to stress challenges. In conclusion, these results are the first to coherently suggest that a physiologically plausible amount of cortisol profoundly affects functioning and perfusion of the human CNS in vivo by a rapid, non-genomic mechanism.