P300 Event-related Brain Potential Research Articles

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.

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.

Acute caffeine effect on repeatedly measured P300

The acute effect of a single-dose of caffeine on the P300 event-related brain potential (ERP) was assessed in a study using a repeatedly presented auditory oddball button-press task. A dose (5mg/kg body-weight) of either caffeine or placebo lactose, dissolved in a cup of decaffeinated coffee, was administered double-blindly to coffee drinkers who had abstained from coffee for 24hrs, with the presentation order of the sessions counterbalanced and separated by 2-4 weeks. The caffeine-treatment condition demonstrated a smaller P300 amplitude and a shorter latency overall than the placebo treatment condition. The mean P300 amplitude value difference (caffeine minus placebo) increased with the successive trial blocks. Caffeine ingestion appears to yield a lower resource-consumption and a net increase in allocating attention resources for task performance across repeated measurements.

Multiple time-frequency components account for the complex functional reactivity of P300.

Consecutive and overlapping time-frequency (TF) components of auditory event-related brain potentials (ERPs) were analyzed to examine whether multiple co-existing components may account for the complex functional reactivity of P300. Auditory ERPs of 14 adult subjects were decomposed by means of the wavelet transform (WT), and TF components within P300 were tested in a systematic manner for the effects of major P300 determinants: stimulus probability, active discrimination, and mental count task. The results demonstrated that several partly or fully simultaneous delta, theta, and alpha TF components significantly depend on the factors eliciting P300, and also manifest distinct patterns of task reactivity and scalp distribution. Thus, specific functional processes that underlie the P300 ERP can be distinguished that help to account for its responsiveness to task variables.

P300 subcomponent abnormalities in schizophrenia: III. Deficits in unaffected siblings of schizophrenic probands

Background: Reduced P300 amplitude is a robust finding in patients with schizophrenia. In previous investigations, we reported reductions of specific subcomponents of the auditory oddball P300 that were independent of acute symptomatology and persistent over time, consistent with a trait abnormality. To clarify whether these stable deficits represented genetic markers of vulnerability to schizophrenia, event-related brain potentials (ERPs) from patients were compared to those from their own healthy siblings and unrelated control subjects. Methods: Auditory P300 ERPs were acquired from 11 schizophrenic patients, 12 healthy siblings and 23 matched control subjects. Five P300 subcomponents were identified using current source density measures: frontal, bilateral parietal, and bilateral temporal. Results: Consistent with previous reports, patients had reduced parietal and frontal P300 amplitudes. The healthy siblings of the schizophrenic probands had an isolated reduction of the frontal P300. Conclusions: Frontal P300 amplitude is a potential endophenotypic marker of genetic vulnerability to schizophrenia in individuals who otherwise show no evidence of clinical symptomatology. Given the functional interpretation of the frontal P300 as a physiological correlate of cognitive orienting, this supports the hypothesis that impairments of the neural substrate underlying attentional mechanisms are selective indicators of genetic susceptibility to schizophrenia in high-risk individuals.

P300 and blink instructions

Objectives: The effects of instructions to refrain from blinking on the P300 event-related brain potential (ERP) from auditory and visual stimuli were assessed.Methods: An oddball paradigm was employed in which young adult subjects (n=20) silently counted the infrequent target stimuli and were given either no instructions or told “do not blink” in different conditions, with auditory and visual stimulus tasks employed for all subjects. ERPs were recorded from the midline electrodes, with amplitude and latency of the P300 and other components obtained.Results: P300 amplitude for both modalities and target/standard stimulus conditions was smaller and visual peak latency longer in the “do not blink” condition. Blink instructions did not directly affect the other components.Conclusions: Instructions to refrain from blinking can decrease P300 amplitude and can increase peak latency.

Comparison of P300 from passive and active tasks for auditory and visual stimuli

The P300 event-related brain potential (ERP) was elicited with a stimulus-sequence paradigm for auditory and visual stimuli in separate active and passive task response conditions. Auditory stimuli in the passive task yielded P300 waveforms similar to those obtained from the active task condition. Visual stimuli in the passive task yielded much smaller P300 waveforms that were not morphologically consistent with those from the active task. The results suggest that auditory stimuli produce more robust P300 components than visual stimuli in passive task situations.

On P300 measurement stability: habituation, intra-trial block variation, and ultradian rhythms

P300 event-related brain potentials (ERPs) were elicited using a simple discrimination task in which participants discriminated two different equiprobable visual stimuli with button-press responses ( n=20). A total of ten trial blocks were presented at 10-min intervals. P300 amplitude declined significantly, but peak latency did not change reliably across trial blocks. P300 amplitude demonstrated a reliable cyclical fluctuation across trial blocks, although P300 latency did not. Intra-trial block ERP variability was assessed by computing the correlation coefficients between the target and standard stimuli for amplitude and latency measures across participants within each trial block. P300 amplitude correlations were weakest at the Fz electrode, more strongly associated at Cz, and were most strongly correlated at Pz across trial blocks. P300 latency correlations were somewhat weaker and similar in strength across electrodes sites. The correlational patterns for both P300 amplitude and latency demonstrated reliable cyclical variation. The N100 component produced strong and consistent correlations for both amplitude and latency, whereas the P200 and N200 component measures evinced cyclical correlational patterns similar to the P300 across trial blocks. These results suggest that the stability of P300 and other component measures can vary appreciably within and across trial blocks in a manner that reflects ultradian variation in arousal level.

Auditory P300 development from an active, passive and single-tone paradigms

The P300 (P3) event-related brain potential (ERP) was elicited with auditory stimuli in order to compare three different tasks and to assess the effect of ageing from childhood to adolescence. Seventy-two subjects, ranging in age from 6 to 14 divided into three age groups, were selected for this study. In the active task, the subject was required to discriminate between standard and target tones (oddball); in the passive task condition, the subject did not respond to either the standard or target stimulus; in the single task, a target but not a standard tone stimulus was presented and the subject was required to react to the target tone. Our results show that the passive sequence and the single-tone paradigm yielded similar P300 waveform to those obtained from the active task. Separate age/ERP component latency and amplitude linear regression were computed. A significant negative correlation between age and P3 latency was found. The event-related potential P3 wave shows consistent and significant age-related changes in human cerebral function, regardless of the methodology used. These findings suggest that the passive and single-tone paradigms can be a useful way to elicit the P3 ERP component.

Subtypes of Family History and Conduct Disorder: Effects on P300 During the Stroop Test

The goal of the present study was to identify neurophysiological differences associated with a family history of substance dependence, and its subtypes (paternal alcohol, cocaine, or opiate dependence), and with conduct disorder, and its subtypes (aggression, deceitfulness/theft, and rules violations). P300 event-related brain potentials were recorded from 210 males and females, aged 15–20 years while they performed the Stroop color-word compatibility test. Analyses revealed no significant effects of familial substance dependence on P300. However, an elevated number of conduct disorder problems was associated with a statistically significant reduction in P300 amplitude. The P300 amplitude reduction was related to the severity of the “rules violation” subtype, but was unrelated to aggression or deceitfulness and theft. It is concluded that conduct disorder can explain many of the P300 findings previously attributed to a family history of alcohol dependence. Furthermore, it appears that conduct disorder may be a heterogenous classification comprised of neurophysiologically different subtypes.

P300 event-related potential and serotonin-1A activity in depression

The identification of the brain structures and neurotransmitters responsible for the generation and/or modulation of P300 could lead to important clinical implications. Since serotonin disturbances seem to play a critical role in depression, the aim of the study was to assess the possible relationships between the P300 event-related brain potential and serotonergic activity in depression. The study was conducted among 45 major depressive inpatients, and serotonergic activity was assessed by prolactin (PRL) response to flesinoxan (a 5-HT1A agonist). Results showed a significant negative correlation between P300 amplitude and PRL response to flesinoxan ( r = –0.40, P = 0.007 at Cz; r = –0.47, P = 0.001 at Pz). In contrast, both P300 latency and reaction time were not related to endocrine response. This study supports a role for serotonin-1A in the neurobiological modulation of P300 amplitude.

Auditory and visual P300 topography from a 3 stimulus paradigm

Objective: The P300 event-related brain potential (ERP) was elicited with auditory and visual stimuli in a separate session of a 3 stimulus oddball paradigm, and the scalp topography was assessed with 15 electrode locations.Methods: Target (0.10), standard (0.80), and infrequent non-target (0.10) stimuli in the auditory task were 2000, 1000 and 500 Hz tone, and in the visual task, ‘X’, ‘O’, and ‘H’, respectively. The stimuli were presented in a random series, once every 2 s, and participants responded only to the target (N=12).Results: Target stimuli elicited larger P300 components than non-target did in both stimulus modalities. For both target and non-target stimuli, P300 amplitude was larger and latency longer for the visual compared with the auditory stimulus. Analysis of normalized P300 amplitude data indicated that the target and non-target P300s from both modalities had identical topography.Conclusion: The findings suggest that both target and non-target stimuli in 3 stimulus oddball paradigm elicited the same type of P300 (P3b) for both stimulus modalities.

P300, Alcoholism Heritability, and Stimulus Modality

The P300 event-related brain potential (ERP) was elicited with auditory and visual stimuli from members of 13 families who were at high risk (HR) for alcoholism (father diagnosed as alcoholic) and 13 families at low risk (LR) for alcoholism. Each family consisted of a father, mother, and at least two biological children. The intrafamily member correlations (father vs. child, mother vs. child, child vs. child) for P300 amplitude were obtained for 15 electrode sites. P300 amplitude from auditory stimuli was not correlated among HR family members, but was positively correlated among LR family members. P300 amplitude from visual stimuli was positively correlated among both HR and LR family members. When taken in conjunction with previous findings, the present results suggest that P300 amplitude from auditory stimuli may not be as reliable as ERPs from visual stimuli for the assessment of alcoholism heritability.

Neuropsychological Performance and Cognitive Olfactory Event-Related Brain Potentials in Young and Elderly Adults

The P3 event-related brain potential (ERP) reflects neuroelectric activity related to the speed of cognitive processing and allocation of attentional resources. The objective of the present study was to assess the relationship between the P3 and Slow Wave components of the olfactory event-related potential (OERP) with neuropsychological performance in young (n = 16) and elderly (n = 16) adults. OERPs were recorded monopolarly from midline electrode sites while subjects estimated the odor magnitude of each stimulus, eliciting highly reproducible P3s. Results showed that the late cognitive components (P3 amplitude, P3 latency and Slow Wave area) decline with age and that this decreased neuronal efficiency is associated with reductions in the neuropsychological performance indexed by the Trail Making Test and the California Verbal Learning Test.

Habituation of P300 from visual stimuli

The P300 event-related brain potential (ERP) was elicited with visual stimuli using an oddball task in which the subjects made button press responses to discriminate target and standard stimuli. Each stimulus occurred randomly with a 0.50 probability, and 10 trial blocks were presented at 10-min inter-block-intervals (IBIs). P300 amplitude declined reliably across trial blocks, and an interaction between trial block number and electrode site was observed. No habituation effects were found for P300 latency or for N100, P200, or N200 amplitude. The results suggest that P300 amplitude from visual stimuli habituates when short IBIs and a sufficient number of trial blocks are employed. Theoretical implications are discussed with respect to attentional resource allocation and context updating.

Serotonergic modulation of the P300 event related brain potential

Serotonergic modulation of the P300 event related brain potential

Serotonergic modulation of the P300 event related brain potential

While dopaminergic, noradrenergic, cholinergic and gabaergic effects on the P300 component of the human event-related brain potential have been largely described, little is known about serotonergic influence. Therefore, we investigated the relationship between P300 and serotonergic activity as reflected by prolactin (PRL) response to flesinoxan, a 5-HT1A full agonist, among 28 normal subjects. Results showed a significant negative correlation between P300 amplitude and PRL response to flesinoxan (r=−0·47, p=0·01 at Cz; r=−0·45, p=0·01 at Pz). In contrast, both P300 latency and reaction time were not related to endocrine response. This study supports a role for serotonin in the neurobiological modulation of P300 amplitude. Clinical implications of these results are considered. © 1998 John Wiley & Sons, Ltd.

Quantitative trait loci analysis of human event-related brain potentials: P3 voltage

The P3 event-related brain potential (ERP) is a positive-going voltage change of scalp-recorded electroencephalographic activity that occurs between 300–500 ms after stimulus onset. It is elicited when a stimulus is perceived, memory operations are engaged, and attentional resources are allocated toward its processing. Because this ERP component reflects fundamental cognitive processing, it has found wide utility as an assessment of human mental function in basic and clinical studies. In particular, P3 attributes are heritable and have demonstrated considerable promise as a means to identify individuals at genetic risk for alcoholism. We have conducted a quantitative linkage analysis on a large sample from families with a high density of affected individuals. The analyses suggest that several regions of the human genome contain genetic loci related to the generation of the P3 component of the ERP, which are possible candidate loci underlying the functional organization of human neuroelectric activity.

P300 clinical utility and control of variability.

The P300 event-related brain potential (ERP) has been used to study normal aging as well as patient populations with a variety of neurologic and psychiatric disorders. The P300 has demonstrated reasonable success as a means to assess disturbances in cognitive function, and its clinical utility has been enhanced by the identification of factors that contribute to the variability of ERP measurements. In this article, the neuropsychological theory of P300 is reviewed, ways in which this brain potential can be used as a measure of cognitive efficiency are defined, and methodologic issues that must be considered for successful clinical ERP applications are outlined. This approach is then extended to specific recommendations concerning the technical and practical aspects of P300 recording, so that a well-defined normative database can be developed for evaluating individual patients. When appropriate procedures are used, the P300 can provide a highly useful means to quantify human cognitive capability.

P300 subcomponent abnormalities in schizophrenia: I. Physiological evidence for gender and subtype specific differences in regional pathology

P300 event-related brain potential (ERP) amplitude is reduced in patients with schizophrenia. Little attention has been paid to gender differences underlying this abnormality, despite clinical differences between male and female schizophrenics. Studies have also largely ignored the fact that the P300 represents the activity of multiple neural generators and have not assessed the separate activity of different subcomponents. Auditory P300 ERPs were recorded from 65 patients (42 male, 23 female) and 48 controls (30 male, 18 female). Positive and negative symptoms were assessed with standardized rating scales, and patients were subtyped as deficit or nondeficit. Five P300 subcomponents were identified using current source density measures: frontal (P3f), bilateral parietal (P3pL, P3pR), and bilateral temporal (P3tL, P3tR). Three subcomponents (P3tL, P3f, P3pR) were reduced in patients. The left temporal (P3tL) deficit was common across patient groups, but the overall profile of P300 abnormalities varied by gender and deficit/nondeficit status. Women had greater P3tL and P3f decrements; P3pR was abnormal in men. Deficit and nondeficit patients resembled men and women, respectively, independent of gender. P3f and P3tL amplitudes were correlated and unrelated to symptomatology. P3pR was related to Brief Psychiatric Rating Scale score. A left temporal abnormality exists in schizophrenia, along with two different profiles of regional pathology, which segregate by gender and deficit/nondeficit status. This supports the hypothesis of two distinct illness subtypes and suggests a physiological basis for phenotypic gender and deficit/nondeficit differences. P300 subcomponent abnormalities may serve as subtype markers. Correlated left temporal and frontal dysfunction is consistent with a frontotemporal neural network disturbance in some schizophrenics. Further investigation of the longitudinal stability and familial inheritance of these subcomponent abnormalities is warranted.