P300 and slow wave from oddball and single-stimulus visual tasks: inter-stimulus interval effects.

The effects of inter-stimulus intervals on P300 from an oddball task (target and standard stimuli) and a single-stimulus task (targets only) employing simple visual stimuli were assessed in order to determine how a relatively long ISI affects event-related brain potentials (ERPs). Young adult subjects (n=16) responded by pressing a button to a visual target stimulus of each task condition. ISI was either 2.5 or 30 s and paradigm type was either the oddball or single-stimulus task. ERPs were recorded from the midline electrodes, with amplitude, mean area, and latency of the P300 and other components assessed. The results showed that P300 morphology was dramatically affected by task and ISI such that under the 2.5 s condition, the oddball paradigm produced typical ERP components, whereas the single-stimulus condition demonstrated minimal P300 amplitude. When ISI was 30 s, both the oddball and single-stimulus tasks produced robust P300 components but also evinced strong slow wave (SW) potentials, which contributed to the ERP measurement outcomes. It is concluded that P300 from visual stimuli can be elicited with both oddball and single-stimulus tasks when ISI is relatively long. ERPs from both paradigms produced appreciable SW activity, which needs to be considered when long ISI procedures are employed.     

Typical dipole locations can be estimated using averaged somatosensory-evoked potentials and a standard brain model

It is reasonable to hypothesize that dipoles estimated from grand averaged event-related potentials based on summed-up data obtained from multiple subjects and standard head models could correspond to typical brain regions associated to a particular event. Six healthy subjects were enrolled in a study to test this hypothesis. We estimated dipoles from somatosensory-evoked potentials (SEP) elicited by electrical stimulation to the left median nerve. We also created individual three-layered (scalp, skull, and brain) head models from each subject’s magnetic resonance imaging scan, and dipoles were estimated from the individual averaged SEP with each individual head model. We then estimated dipoles using grand averaged SEP across all subjects on the standard head model created from the Montreal Neurological Institute (MNI) standard coordinate system brain template to compare the estimated dipoles located on our own head model and those on the MNI. The dipoles in the post-central gyrus were estimated from negative potentials at 20 ms from the grand averaged data incorporated with the MNI head model, corresponding to a typical location related to SEP stimulation. The results suggest the validity of estimating the dipole location from the grand averaged potential of all subjects with the MNI model if we focus on typical regions related to the task.     

Visual event-related potentials during movement imagery and the dipole analysis

Visual event-related potentials during an oddball paradigm with movement imagery tasks were recorded in 10 right-handed subjects from 32 scalp electrodes. Rare targets and non-targets elicited early (P3e) and late (P3l) P300 components. In the P3e there was no difference between the rare target and non-target. In the right-imagery task the rare target P3l amplitude was larger than the rare non-target one, whereas the rare non-target P3l amplitude was larger than the rare target one in the left-imagery task. Some of the 4 equivalent current dipole (ECD) sources were located at the subcortical regions, the cerebellum and the cingulate cortex, common to the P3e and the P3l. Moreover, another P3e dipole was localized to the parietal regions, while that of the P3l dipoles to the contralateral premotor cortex. This difference between the P3e and P3l dipoles might reflect two different neural networks related with the transformation of coordinates from visual to motor space.     

P300 topography and modality effects from a single-stimulus paradigm

The P300 event-related brain potential (ERP) was elicited with auditory and visual stimuli in two different tasks. The oddball paradigm presented both target and standard stimuli; the single-stimulus paradigm presented a target but no standard stimulus, with the intertarget interval the same as that for the oddball condition. Target probability was .20 for the oddball task, with target stimuli occurring at the same temporal frequency in the single-stimulus paradigm. Scalp topography was assessed with 15 electrode locations. P300 amplitude was larger and latency was longer for the oddball than for single-stimulus procedure. P300 from auditory stimuli was smaller and shorter in latency than that from the visual stimuli, and both modalities showed similar but not identical scalp topographies. The findings suggest that the single-stimulus paradigm may be useful in experimental and applied contexts that require very simple ERP task conditions.     

P300 habituation from auditory single-stimulus and oddball paradigms.

The habituation of auditory P300 event-related brain potential (ERP) from single-stimulus paradigm was evaluated and compared to that from oddball paradigm. Three task conditions were: oddball with a button press (oddball/press) response, single-stimulus with a button-press (single-stimulus/press) response and a silent count (single-stimulus/count) response. The oddball/press condition demonstrated larger P300 amplitude and longer latency overall than either single-stimulus condition, but P300 amplitude decreased and peak latency increased similarly over successive trial blocks for all three tasks. Thus, the oddball and single-stimulus ERP tasks produce analogous changes under repeated measurements and indicate that the single-stimulus task can serve as an alternative method for eliciting the P300 in applied and clinical settings.     

Olfactory, auditory, and visual ERPs from single trials: no evidence for habituation.

Event-related potentials (ERPs) using olfactory, auditory, and visual stimuli were recorded from young adults to assess possible component habituation across single trials among modalities. A single-stimulus ERP paradigm was used that employed a 10-min inter-stimulus interval (ISI) to minimize possible sensory adaptation and three stimulus trials for each modality to assess initial habituation effects. The present findings were: (1) P3 amplitude does not habituate appreciably over the initial three trials but may increase from the first to second trial. (2) ERPs from a single-stimulus paradigm with a very long ISI produce significantly correlated component amplitudes for the olfactory, auditory, and visual modalities. (3) P3 amplitude from olfactory stimuli demonstrated scalp topography similar to that for auditory and visual ERPs. These findings suggest that the single-stimulus task using a long ISI produces highly comparable and stable P3 components from olfactory, auditory, and visual stimuli. Application of single-stimulus paradigm to olfactory ERP methods is supported.     

Event-related brain potentials to attended and ignored olfactory and trigeminal stimuli.

Event-related brain potentials (ERPs) were recorded from 26 young adults, with equal numbers of male and female subjects, using attended and ignored, olfactory and trigeminal stimuli. The amplitudes and latencies of the N1, P2, and P3 components were recorded using a single-stimulus paradigm, with an inter-stimulus interval of 60 s, employing amyl acetate as the olfactory stimulus and ammonia as the trigeminal stimulus. Subjects estimated stimulus intensity in the attend condition or continued with a visual tracking task in the ignore condition. Results indicate that olfactory information is processed 30-70 ms faster than trigeminal information for the N1 and P2 potential and 100 ms faster for the P3 ERP component. N1/P2 interpeak amplitude was greater for the trigeminal than the olfactory stimuli, and greater in the attended than ignored condition. P3 amplitude was greater in the attend than ignore condition for olfactory information processing and equivalent for trigeminal information processing. These findings suggest that neuronal resource allocation is greatest for attended stimuli and that a painful stimulus demands neuronal resources even when ignored.     

Identification of the visual motion area (area V5) in the human brain by dipole source analysis

The retinal periphery of nine healthy subjects was stimulated with computer-generated random-dot kinematograms. These stimuli provided almost isolated visual motion information and minimal position cues. Pattern-reversal stimuli at the same location in the visual field were used for control. Stimulus-related electrical brain activity was recorded from 29 scalp electrodes. Total mean and individual data were analyzed with a spatiotemporal multiple dipole model. The scalp potentials showed a different spatial distribution for motion and pattern stimulation in the time range of 160–200 ms. In this epoch, the predominant motion-related source activity was localized in the region of the contralateral occipital-temporal-parietal border. A significant ipsilateral source activity was not found. The predominant source activity related to the pattern stimulus occurred in the same epoch. The corresponding equivalent dipole was localized more medially and deeper in the brain. The orientation of these major dipole activities was markedly different. These dipoles appeared to represent activity of distinct extrastriate areas, in contrast to earlier activity which was modelled by more posterior dipoles in the occipital lobe. The latter dipoles were at comparable contralateral locations and had similar peak activities around 100 ms, suggesting an origin in the striate cortex.     

Trajectories of shifting dipole sources of visual evoked potentials across the human brain

Visual evoked potentials in response to images of a set of horizontal and vertical lines or crosses were recorded from the brains of 18 human subjects in 34 leads. Inverse EEG analyses were used for the dynamic location of the dipole current sources of the N1, P1, and N2 waves using a two-dipole spherical model with a 1-msec step. The occipital lobes of all subjects showed significant displacement of the dipoles of evoked potential waves along predominantly arc-shaped trajectories (75.8% of cases). Trajectory durations (average about 25 msec) were characterized by insignificant interindividual variability and were independent of the type of stimulus and the phase of the evoked potential. A characteristic (occurring in 85% of cases) “jump” in the coordinates of the dipole, which constituted a rapid, sharp, and significant medial displacement, was seen between the first and second trajectories of the equivalent current dipoles (at 110–120 msec after stimulus onset). The possible significance of these data for understanding the dynamics and kinetics of processing of local image features in the human visual cortex is discussed. __________ Translated from Zhurnal Vysshei Nervnoi Deyatel'nosti imeni I. P. Pavlova, Vol. 57, No. 6, pp. 673–683, November–December, 2007.     

The Effects of Temporal and Event Uncertainty in Determining the Waveforms of the Auditory Event Related Potential (ERP)

In each of two experimental conditions, subjects were presented with a series of tones; one of two tones (1500 Hz or 1000 Hz) was presented on each trial with a probability respectively of .10 or .90. The subjects counted the rare (p=.10) tones; such counted rare tones are normally associated with a large P300 component. The two conditions differed in that in one the tunes were triggered by the subject's button press; in the other the tones were triggered by computer. Schafer and Marcus (1973) reported that all the components of event-related potentials (ERPs) elicited by self-triggered tones were substantially smaller than those elicited by machine-triggered stimuli. Our paradigm allowed a detailed assessment of the effects of self-stimulation on specific ERP components as well as the interaction of temporal with event uncertainty. Data were analyzed using a Principal Components technique. Both temporal and event uncertainty appeared to augment a negative component of the ERP with approximately 140 msec latency. Such effects, however, were confounded by the presence of slow negative potentials preceding the button press in the self-stimulation conditions. As expected, the P300 component was largest for the ERPs elicited by the rare tones. Temporal uncertainty diminished the amplitude of P300 at central electrode sites. A large slow wave was present following P300 ; its anterior-posterior distribution was altered by mode of stimulus presentation. It appears that temporal and event uncertainty have distinct effects upon the morphology and distribution of KRP components.     

Concurrent visual task effects on evoked and emitted auditory p300 in adolescents

Using an oddball stimulus presentation paradigm, the effects of divided attention on auditory P300s were studied. Auditory attention was either divided or focused, depending on the demands placed on subjects during the performance of a concomitantly presented visual task. Two types of auditory tasks were performed under each of the two auditory attention conditions. In one, subjects responded to infrequently presented high pitched tones (oddball stimuli). In the other they responded to the occasional omission of a stimulus in an otherwise rhythmically presented chain of stimuli. P300s and reaction times were recorded to both the rare tones and the omissions. The Sternberg visual memory task was used to manipulate the subject's auditory attention state. Subjects actively performed the Sternberg task during the divided auditory attention condition, whereas during the focused attention condition they were not required to respond to the visual stimuli. During focused auditory attention, evoked auditory P300s were both larger and faster than their emitted counterparts. During divided attention, auditory P300s were reduced in amplitude but latency was unaffected. Evoked auditory P300s showed evidence of containing P300a as well as P300b components, particularly when attention was shared with the visual task.     

Synchronized network activity as the origin of a P300 component in a facial attractiveness judgment task

Many studies have used the P300 as an index for cognitive processing and neurological/psychiatric disorders. Here, we combined the source separation and source localization methods to investigate the cortical origins of the P300 elicited in a facial attractiveness judgment task. For each participant, we applied second‐order blind identification (SOBI) to continuous EEG data to decompose the mixture of brain signals and noise. We then used the equivalent current dipole (ECD) models to estimate the centrality of the SOBI‐recovered P300. We found that the ECD models, consisting of dipoles in the frontal and posterior association cortices, account for 96.5 ± 0.5% of variance in the scalp projection of the component. Given that the recovered dipole activities in different brain regions share the same time course with different weights, we conclude that the P300 originates from synchronized activity between anterior and posterior parts of the brain.     

Differential activation in the medial temporal lobe during a sound-sequence discrimination task across age in human subjects

To elucidate the brain mechanisms to encode sequential events, event-related potentials (ERPs) were recorded during a sound-sequence discrimination task using young and middle-aged adult subjects. In the task, a series of six or 12 kinds of natural sounds were sequentially presented; 70-80% of the stimuli were presented in a fixed order (Non-target), but the remaining stimuli, in a random order (Target). The subjects were instructed to detect the Targets and press a button at the end of each Target. In a control task, the same sounds were randomly presented (Control), and they were instructed to press the button at the end of each sound. Behavioral results indicated that the young subjects learned the task faster than did the middle-aged subjects. Positive ERP waves were evoked by Targets and Non-targets in the parieto-occipital area around 300-700 ms after stimulus onset. The mean amplitudes during this period in the young subjects were larger in Target than Control conditions, and those in Target condition were larger in the young than middle-aged subjects. Furthermore, the mean amplitudes in the Target condition were significantly correlated with behavioral performance. Equivalent dipoles for the ERPs evoked by Targets were estimated in the medial temporal lobe including the hippocampal formation and parahippocampal gyrus. The results suggest that the ERPs around 300-700 ms latency are involved in sound-sequence information processing. Furthermore, decrease in amplitudes of this positivity in the middle-aged subjects suggests that age-related memory decline is associated with deficits in encoding and retrieval of unfamiliar sequence.     

With long intervals, inter-stimulus interval is the critical determinant of the human P300 amplitude

Previous research, using short inter-stimulus intervals (1-4 s), suggests that the P300 of the human event-related potential during oddball and single-stimulus tasks is mainly affected by target-to-target interval (TTI). The present study tested the validity of this claim at longer intervals in a learning task. Participants were assigned to either an oddball task with an inter-stimulus interval (ISI) of 9-20 s or a single-stimulus task with an ISI of 9-20 or 40-90 s and had to learn when to respond to the stimuli. In the oddball task, the target elicited larger amplitudes than did the standard. When comparing the stimuli from the short- and long-ISI conditions with the target from the oddball condition, it was found that the P300 was more positive at long-ISI stimuli than at short-ISI stimuli or oddball targets, and short-ISI stimuli and oddball targets elicited equally large P300 amplitudes. These results suggest that, in oddball tasks with long intervals, besides cognitive factors, ISI rather than TTI affects the P300 amplitude.     

P3 and Stimulus Incentive Value

Event-related potentials were recorded to two equiprobable, task-relevant visual stimuli (0.00 and 1.00) under three different conditions. In the baseline condition subjects attended to both stimuli and pressed the appropriate button to each stimulus. In the Accuracy/Incentive condition subjects earned one dollar each time the 1.00 stimulus was presented by accurately pressing the appropriate button after each stimulus. Incorrect presses to either stimulus resulted in the loss of a dollar. In the Speed-Accuracy/Incentive run, subjects could only earn one dollar to the 1.00 stimulus if they accurately pressed the correct button within 350 msec. Reaction times greater than 350 msec to either stimulus resulted in the loss of a dollar. The results indicate that the amplitude of the P3 component is significantly different to equiprobable task-relevant stimuli with differential incentive values. P3 may reflect the subjective motivational properties of stimuli.     

Dynamic Brain Topography of Somatosensory Evoked Potentials and Equivalent Dipoles in Response to Graded Painful Skin and Muscle Stimulation

The differential effects of painful stimulation of skin vs. muscle on the cerebral electrophysiology have been poorly described. This study examined the somatosensory evoked potentials (SEPs) and the associated dipole models of non-painful and graded painful electrical stimulation applied to the skin and muscle in 20 healthy subjects. With the psychophysical stimulus-response functions determined, the skin stimulation showed a steeper slope than muscle stimulation. For both types of stimulation, the SEPs indicated a similar temporo-spatial activation sequence: F4/N90-P4/P95, Fc2/N135, Cz/P250, Cz/P300, and Cz/N460. The SEP amplitudes increased significantly with the stimulus intensities in these components. The peak SEP latencies of skin stimulation were in general shorter than that of muscle stimulation. The SEP amplitudes to skin stimulation were significantly larger than those caused by muscle stimulation at every stimulus intensity level, except the early mid-latency component. In this case, muscle stimulation caused higher amplitudes over the contralateral parietal-frontal sites. For both types of stimulation, the topographic maps were quite similar. Equivalent dipole modeling revealed identical site parameters (<1.0 cm) between skin and muscle stimulation. However, the electrical skin stimulation did not correlate with the pain intensity. Pain intensity, in contrast, was uniquely associated with the Cz/P250 amplitudes for the muscle stimulation. It is concluded that non-nociceptive and nociceptive electrical stimuli applied to skin and muscle are processed in the common cerebral areas, but exhibit differential SEP effects.     

Attenuation of dipoles modelled from SEP due to a lacunar infarct or altered stimulus rate

Summary In normal subjects and patients with sensory, sensorimotor or motor deficit, due to a unilateral infarct affecting the thalamocortical radiation, SEPs to median nerve stimulation were analyzed by a spatiotemporal dipole model which describes an evoked potential by a limited number of stationary dipoles with time varying amplitudes. In the normal subjects the SEPs were explained by one dipole in the brainstem and two dipoles in the cortical hand area contralateral to stimulation, all with different time courses. Increasing the stimulus rate to 6.2 Hz yielded a reduction of the moment of both cortical dipoles but hardly affected brainstem dipole moment. In the five patients with sensory or sensorimotor deficit the strength of one or both cortical dipoles was reduced on the side of the lesion. In the patients with pure motor deficit cortical dipole activity was normal. The brainstem dipole was preserved in all patients.     

Multiple Dipole Analysis of Visual Event-Related Potentials During Oddball Paradigm with Silent Counting

In order to cope with the non-uniqueness of multiple equivalent current dipole source (ECD) solutions, a priori knowledge about P300 generators of visual event-related potentials (ERPs) during an oddball paradigm with silent counting task was incorporated into the multiple ECD localization method. Four-ECD solutions for the target P300 were selected which had the left frontal ECD. The rest of the ECDs were localized to the inferior parietal lobule, the hippocampal formation and subcortical region. By comparing the present results with those on the visual ERPs with button-pressing task, the P300 dipoles common to both the tasks were located at the frontal cortices, the hippocampal formation and the thalamus, suggesting that these structures are the main P300 generators.     

P3a from visual stimuli: typicality,task, and topography

A visual three-stimulus (target, nontarget, standard) paradigm was employed in which subjects responded only to the target. Nontarget stimulus properties were varied systematically to evaluate how stimulus typicality (non-novel vs. novel) across task discrimination (easy vs. difficult) conditions affects P3a scalp topography. Nontarget stimuli consisted of letters, small squares, large squares, and novel patterns; discrimination difficulty between the target and standard was varied across conditions. When the discrimination was easy, P300 amplitude was larger for the target than the nontarget with parietal maximums for both. In contrast, when the discrimination was difficult, nontarget amplitude (P3a) was larger and earlier than the target P300 over the frontal/central electrode sites, whereas target amplitude (P3b) was larger parietally and occurred later. P3a was largest when elicited by either the large square or novel pattern stimuli. The findings suggest that stimulus context as defined by the target/standard discrimination difficulty rather than stimulus novelty determines P3a generation.