Asymmetry of automatic change detection shown by the visual mismatch negativity: An additional feature is identified faster than missing features

In two experiments, we demonstrated that an asymmetric effect of the brain electric activity that is elicited by nonattended visual stimuli is similar to the one found in responses observed in the performance of visual search tasks. The automatic detection of violated sequential regularities was investigated by measuring the visual mismatch negativity (vMMN) component of event-related brain potentials (ERPs). In Experiment 1, within a sequence of stimulus displays with O characters, infrequently presented Q characters elicited an earlier vMMN than did infrequent O characters within a sequence of Q characters. In Experiment 2, similar asymmetric results emerged if only 16 % of the characters were different within an infrequent display. In both experiments, these stimuli were irrelevant; during the stimulus sequences, participants performed a demanding videogame. We suggest that the underlying match/mismatch and decision processes are similar in the vMMN and in the attention-related visual search paradigm, at least in the case of the stimuli in the present experiments

The visual mismatch negativity is sensitive to symmetry as perceptual category

We investigated the sensitivity of visual mismatch negativity (vMMN) to an abstract and non-semantic category, the vertical mirror symmetry. Event-related potentials were recorded to random and symmetric square patterns, delivered in passive oddball paradigm (participants played a video game). In one of the conditions, symmetric patterns were frequent (standard) stimuli and the random patterns were infrequent (deviant) stimuli, in the other condition the probabilities were reversed. We compared the ERPs to symmetric stimuli as deviants and as standards, and similarly, the ERPs to the random deviants and random standards. As the difference between the ERPs to random deviant and random standard stimuli a posterior negativity emerged in two latency ranges (112–120-ms and 284–292-ms). These negativities were considered as visual mismatch negativity (vMMN) components. We suggest the two vMMN components are organized in cascade error signals. However, there was no significant difference between the ERPs to the symmetric deviants and symmetric standards. Emergence of vMMN to the deviant random stimuli is considered as a deviation of a perceptual category (in the symmetric standard’s sequence presented). Accordingly, random stimuli acquired no perceptual category, for this reason the symmetric deviant (in the random standard’s sequence presented) elicited no vMMN. The results show that the memory system underlying visual mismatch negativity is capable of coding perceptual categories such as bilateral symmetry, even if the stimulus patterns are unrelated to the ongoing behavior

Age and sex effects on paired-pulse suppression and prepulse inhibition of auditory evoked potentials

Responses to a sensory stimulus are inhibited by a preceding stimulus; if the two stimuli are identical, paired-pulse suppression (PPS) occurs; if the preceding stimulus is too weak to reliably elicit the target response, prepulse inhibition (PPI) occurs. PPS and PPI represent excitability changes in neural circuits induced by the first stimulus, but involve different mechanisms and are impaired in different diseases, e.g., impaired PPS in schizophrenia and Alzheimer’s disease and impaired PPI in schizophrenia and movement disorders. Therefore, these measures provide information on several inhibitory mechanisms that may have roles in clinical conditions. In the present study, PPS and PPI of the auditory change-related cortical response were examined to establish normative data on healthy subjects (35 females and 32 males, aged 19–70 years). We also investigated the effects of age and sex on PPS and PPI to clarify whether these variables need to be considered as biases. The test response was elicited by an abrupt increase in sound pressure in a continuous sound and was recorded by electroencephalography. In the PPS experiment, the two change stimuli to elicit the cortical response were a 15-dB increase from the background of 65 dB separated by 600 ms. In the PPI experiment, the prepulse and test stimuli were 2- and 10-dB increases, respectively, with an interval of 50 ms. The results obtained showed that sex exerted similar effects on the two measures, with females having stronger test responses and weaker inhibition. On the other hand, age exerted different effects: aging correlated with stronger test responses and weaker inhibition in the PPS experiment, but had no effects in the PPI experiment. The present results suggest age and sex biases in addition to normative data on PPS and PPI of auditory change-related potentials. PPS and PPI, as well as other similar paradigms, such as P50 gating, may have different and common mechanisms. Collectively, they may provide insights into the pathophysiologies of diseases with impaired inhibitory function

An exploration of pre-attentive visual discrimination using event-related potentials

The Mismatch Negativity (MMN) has been characterised as a ‘pre-attentive’ component of an Event-Related Potential (ERP) that is related to discriminatory processes. Although well established in the auditory domain, characteristics of the MMN are less well characterised in the visual domain. The five main studies presented in this thesis examine visual cortical processing using event-related potentials. Novel methodologies have been used to elicit visual detection and discrimination components in the absence of a behavioural task. Developing paradigms in which a behavioural task is not required may have important clinical applications for populations, such as young children, who cannot comply with the demands of an active task. The ‘pre-attentive’ nature of visual MMN has been investigated by modulating attention. Generators and hemispheric lateralisation of visual MMN have been investigated by using pertinent clinical groups. A three stimulus visual oddball paradigm was used to explore the elicitation of visual discrimination components to a change in the orientation of stimuli in the absence of a behavioural task. Monochrome stimuli based on pacman figures were employed that differed from each other only in terms of the orientation of their elements. One such stimulus formed an illusory figure in order to capture the participant’s attention, either in place of, or alongside, a behavioural task. The elicitation of a P3a to the illusory figure but not to the standard or deviant stimuli provided evidence that the illusory figure captured attention. A visual MMN response was recorded in a paradigm with no task demands. When a behavioural task was incorporated into the paradigm, a P3b component was elicited consistent with the allocation of attentional resources to the task. However, visual discrimination components were attenuated revealing that the illusory figure was unable to command all attentional resources from the standard deviant transition. The results are the first to suggest that the visual MMN is modulated by attention. Using the same three stimulus oddball paradigm, generators of visual MMN were investigated by recording potentials directly from the cortex of an adolescent undergoing pre-surgical evaluation for resection of a right anterior parietal lesion. To date no other study has explicitly recorded activity related to the visual MMN intracranially using an oddball paradigm in the absence of a behavioural task. Results indicated that visual N1 and visual MMN could be temporally and spatially separated, with visual MMN being recorded more anteriorly than N1. The characteristic abnormality in retinal projections in albinism afforded the opportunity to investigate each hemisphere in relative isolation and was used, for the first time, as a model to investigate lateralisation of visual MMN and illusory contour processing. Using the three stimulus oddball paradigm, no visual MMN was elicited in this group, and so no conclusions regarding the lateralisation of visual MMN could be made. Results suggested that both hemispheres were equally capable of processing an illusory figure. As a method of presenting visual test stimuli without conscious perception, a continuous visual stream paradigm was developed that used a briefly presented checkerboard stimulus combined with masking for exploring stimulus detection below and above subjective levels of perception. A correlate of very early cortical processing at a latency of 60-80 ms (CI) was elicited whether stimuli were reported as seen or unseen. Differences in visual processing were only evident at a latency of 90 ms (CII) implying that this component may represent a correlate of visual consciousness/awareness. Finally, an oddball sequence was introduced into the visual stream masking paradigm to investigate whether visual MMN responses could be recorded without conscious perception. The stimuli comprised of black and white checkerboard elements differing only in terms of their orientation to form an x or a +. Visual MMN was not recorded when participants were unable to report seeing the stimulus. Results therefore suggest that behavioural identification of the stimuli was required for the elicitation of visual MMN and that visual MMN may require some attentional resources. On the basis of these studies it is concluded that visual MMN is not entirely independent of attention. Further, the combination of clinical and non-clinical investigations provides a unique opportunity to study the characterisation and localisation of putative mechanisms related to conscious and non-conscious visual processing