Amplitude-time characteristics of the long-latency components (<Emphasis Type="Italic">N</Emphasis>1, <Emphasis Type="Italic">N</Emphasis>2, and <Emphasis Type="Italic">P</Emphasis>300) of acoustic evoked potential in healthy subjects

The aim of the study was to trace the cumulative changes in the amplitude-time parameters of the AEP (acoustic evoked potential) components N1, N2, and P300 in the experimental situations of different complexities (counting and listening to sounds) and to compare the differences between young and mature subjects. The AEP was recorded in 12 healthy subjects aged 18 to 22 years and in 12 subjects aged 32 to 59 years. It was revealed that the components N1, N2, and P300 recorded in the situation of listening without any preliminary instruction did not differ in young and mature individuals. In the younger subjects, a higher N1 amplitude was revealed when they counted sounds, compared to listening, whereas the latency values of this component did not differ, irrespective of the complexity of the task. The component N2 was shown to demonstrate latency stability in relation to the age and the experimental situation. The N2 amplitude was higher in the situation of counting sounds in both age groups. The amplitude-time parameters of P300 did not differ in subjects of different ages in the listening task. The features of the components N1, N2, and P300 revealed in young and mature subjects in the experimental situations differing in complexity lead us to suggest that, with age, humans develop adaptive mechanisms contributing to successful task performance.     

Auditory event-related potentials dissociate early and late memory processes

Event-related potentials (ERPs) to environmental sounds were recorded from 15 young control subjects in an auditory recognition memory task. Subjects listened to a continuous string of binaurally presented sounds, 20% of which were presented once and 80% were repeated. Of the repeated sounds, some repeated immediately after the initial presentation (2 sec; short delay repetition) while others repeated after 2–6 intervening sounds (4–12 sec; long delay repetition). Subjects were instructed to indicate whether they had heard the sounds before by pressing a “yes” or “no” button.The initial stimulus presentation and long delay repetition stimuli generated both an N4 component and a prolonged latency P3 component while the short delay repetition stimuli elicited no N4 component and an earlier latency P3 component. Subjects' responses were faster and more accurate for short delay repetition. All stimuli generated a sustained frontal negative component (SFN). These data indicate that auditory recognition memory for environmental sounds may involve two processes. The P3 generated by both short and long delay repetition stimuli may index activation of a neocortical template matching system. The N4 generated by initial stimulus presentations and long delay repetition is proposed to measure additional activation of limbic memory systems at long retention intervals.     

P300 and the menstrual cycle

Event-related potentials (ERPs) were elicited with an auditory discrimination paradigm in 20 adult female subjects on the first day of their menstrual cycles and approximately 14 days later. The amplitude and latency of the N1, P2, N2 and P3 (P300) components were measured for the two assessment times. No differences in either amplitude or latency for any of the components were observed as a function of menstrual cycle. Half the subjects who took oral contraceptives were compared to the other half who did not. No differences or interactions between these subgroups were obtained for any component amplitude or latency. It was concluded that menstrual cycle and use of oral contraceptives do not affect the P3 or other ERP components.     

Developmental changes in P1 and N1 central auditory responses elicited by consonant-vowel syllables

Normal maturation and functioning of the central auditory system affects the development of speech perception and oral language capabilities. This study examined maturation of central auditory pathways as reflected by age-related changes in the P1/N1 components of the auditory evoked potential (AEP). A synthesized consonant-vowel syllable (ba) was used to elicit cortical AEPs in 86 normal children ranging in age from 6 to 15 years and ten normal adults. Distinct age-related changes were observed in the morphology of the AEP waveform. The adult response consists of a prominent negativity (N1) at about 100 ms, preceded by a smaller P1 component at about 50 ms. In contrast, the child response is characterized by a large P1 response at about 100 ms. This wave decreases significantly in latency and amplitude up to about 20 years of age. In children, P1 is followed by a broad negativity at about 200 ms which we term N1b. Many subjects (especially older children) also show an earlier negativity (N1a). Both N1a and N1b latencies decrease significantly with age. Amplitudes of N1a and N1b do not show significant age-related changes. All children have the N1b; however, the frequency of occurrence of N1a increases with age. Data indicate that the child P1 develops systematically into the adult response; however, the relationship of N1a and N1b to the adult N1 is unclear. These results indicate that maturational changes in the central auditory system are complex and extend well into the second decade of life.     

The features of auditory passive perception while listening to sounds in healthy persons of young or advanced age (event-related potentials and psychology test analysis)

The study analyzed auditory event-related potentials (ERPs) in 37 healthy right-handed subjects without any neurological or psychiatric disorders. Young age group consisted of 18 persons aged from 10 to 27; advanced age group included 19 persons aged from 32 to 59 years. ERPs were recorded from 32 scalp electrodes according to 10–20 System. Two-tones oddball paradigm including standard and target tones was used for ERP-recording. The sound sequence was given to examinees without any preliminary instruction. Complex psychology testing included Stroop Color and Word Test and Wisconsin Card Sorting Test. Significantly larger amplitude of N200 was detected in young subjects compared to advanced age ones. Wavelet-analysis revealed stronger wavelet-connections in the frontal–central area on the time range of P300 in in advanced age examinees vs. young ones. The correlation of the data of psychological tests examining the executive functions was detected with latency of P300 in young examinees and with amplitude of P300 in advanced age ones. Obtained data suggest that switching from one activity to another is prevalent in young persons and focusing on a current activity in advances age persons.     

SEPs to median nerve stimulation: normative data for paediatrics

Somatosensory evoked potentials (SEPs) provide neurologists with an assessment of the neuraxis from peripheral nerve to sensory cortex. Their value is particularly relevant in paediatric neurology as sensory clinical examination can be difficult in young infants and children. The clinical utility of SEPs, however, requires knowledge of the alterations in wave form which occur with growth and development. This study presents normative SEP data from 4 months-35 years. Different non-linear maturational patterns were seen in spinal and central segments of the nervous system. The cervical components (N12, N13) changed little in latency until 2–3 years, the N20 decreased in latency until 2–3 years and P22 decreased in latency until 6–8 years, after which latencies increased until adulthood. The greatest latency changes occurred in N12 and N13, the least in N20. Wave from morphology and interpeak latencies also changed with age. Adult morphology was achieved early (from 1 year), but central conduction time (N13–N20) reached adult values only at 6–8 years. This study provides normative values of SEPs during maturation and a functional assessment of pathways known to myelinate and mature at varying rates.     

Event-related potentials recorded from the scalp and nasopharynx. II. N2, P3 and slow wave

Scalp and nasopharyngeal recordings of the N2, P3 and slow wave components were compared in a target-detection task. The effects of probability, interstimulus interval, intensity, discrimination difficulty, attention, stimulus omission and modality were evaluated. Waves of opposite polarity to the scalp N2 and P3 components were recorded in the nasopharynx. The scalp and nasopharyngeal N2 components showed different patterns of variation across experimental conditions. These findings indicate that there are two different cerebral processes occurring at the latency of the scalp N2. The scalp and nasopharyngeal P3 components consistently covaried across conditions, suggesting a single underlying process. The slow wave was observed only in the scalp recordings.     

Characteristics of the spatio-temporal organization of the P300 component of AEP during the "active" and "passive" stimulus perception in healthy subjects

The concern of the work was in detection and analysis of P300 component of the acoustic evoked potential in healthy subjects in different experimental situations. During counting the rare sounds, P300 was most pronounced in the frontocentral and parietooccipital areas mainly of the left-hemisphere. The response shape was correlated with characteristics of the basic rhythm of the background EEG. Responses of simple and complex shapes were distinguished. The simplest responses were recorded in subjects with hypersynchronous alpha-rhythm. Analysis of three-dimensional dipole source localization showed that structures of the brainstem, limbic system, and frontal lobes participate in generation of the wave. In all the subjects, the decisive role in response generation was played by the brainstem structures. In persons with hypersynchronous alpha-rhythm, the contribution of the frontal lobes was less pronounced. During "passive" listening of sounds, P300 parameters significantly differed from those observed during counting only in 46% of cases (in persons having no hypersynchronous alpha-rhythm). A simplification of the response shape during "passive" listening was observed in these cases, the area of the maximal response expression was shifted to symmetrical areas of the right-hemisphere, the number of dipole sources reduced due to a decrease in the contribution of the frontal and limbic structures into the response generation.     

Effects of aging on event-related brain potentials (ERPs) in a visual detection task

Event-related brain potentials (ERPs) were recorded from 74 subjects (45 men) between 18 and 82 years of age in a simple visual detection task. On each trial the subject reported the location of a triangular flash of light presented briefly 20° laterally to the left or right visual field or to both fields simultaneously. ERPs to targets exhibited a similar morphology including P1, N1, P2, N2, and P3 components across all age groups. The principal effects of advancing age were (1) a marked reduction in amplitude of the posterior P1 component (75–150 latency) together with an amplitude increase of an anterior positivity at the same latency; (2) an increase in amplitude of the P3 component that was most prominent over frontal scalp areas; and (3) a linear increase in P3 peak latency. These results extend the findings of age-related changes in P3 peak latency and distribution to a non-oddball task in the visual modality and raise the possibility that short-latency ERPs may index changes in visual attention in the elderly.     

Electrophysiologic study of the reactions of the brain to regular and skipped acoustic stimuli in man

Human electrical cerebral reactions to acoustic stimuli and to their omission at fixed moments of a restricted rhythmic sequence repeatedly presented in conditions of distraction and attraction of attention to stimuli, were recorded on the vertex. By special methods of bioelectrical signals processing on a computer, the potentials are singled out in response to stimulus omission (SO) with each set ordinal number, which, as well as the potentials, evoked by the actual stimulus (AS), possessed a main negative-positive complex N1P2. In conditions of attention distraction, the negative component of this complex had a latency of 144 ms and the positive one--about 207 ms. In the situation of the attraction of attention to stimuli a decrease of N1 latency up to 125 ms, took place, as well as complication of SO configuration due to the appearance of a later positive oscillation with a latency of about 560 ms, and parametres stabilization of SO as a whole. The analogous dynamics of N1 latency was characteristic of AS in both situations. The mechanisms of SO formation are discussed in connection with trace processes in the central nervous system.     

Long latency auditory evoked potentials: intensity, inter-stimulus interval, and habituation

Experiment 1 elicited the P1, N1, P2, and N2 components of the long latency auditory evoked potential (AEP) using a 1000 Hz tone presented at 30, 50, or 70 dB SPL and 1-, 3-, or 5-second inter-stimulus intervals to assess the relative effects of the combination of these variables on component amplitude and latency. Four blocks of 16 tone presentations each were recorded from each subject to determine if changes in the AEP would occur because of short-term habituation. Both stimulus factors interacted significantly in a systematic fashion for the amplitude measures, with increases in latency also associated with increases in intensity and inter-stimulus interval. Only minor changes across the four trial blocks for either the amplitude or latency measures were observed over the various stimulus presentation conditions. Experiment 2 employed the same tone stimulus presented at 50 dB SPL and a 3-second inter-stimulus interval. Eight blocks of 64 trials were recorded from each subject on each day for four days to investigate long-term habituation effects. No substantial changes in any of the component amplitudes or latencies were obtained across the 32 trial blocks. It was concluded that intensity and inter-stimulus interval interact to determine AEP amplitude as well as latency values and that the constituent components do not change appreciably with repeated stimulus presentations, even after several days.     

Identification of pain,intensity and P300 components in the pain evoked potential

This study examined the relationships among 3 components of the somatosensory evoked potential (SEP) to painful stimuli. Painful stimuli were produced using intracutaneous electrical stimulation of a fingertip and two levels of non-painful stimuli were produced by superficial electrical stimulation of a neighboring fingertip. SEPs were recorded from Cz-A1 and Pz-A1, and difference waves were computed for 3 components: (1) a pain component (the difference between SEPs to painful vs. strong but non-painful stimuli); (2) an intensity component that is not related to pain (the difference between SEPs to strong non-painful vs. mild non-painful stimuli); and (3) a P300 component (the difference between SEPs to the same stimuli under Target instructions vs. Standard instructions).The positive peaks in the 3 types of difference waves differed in both latency and topography, although with latency and topography overlap. The intensity component had an earlier positive peak than the pain component, and the pain component had an earlier positive peak than the P300 component. The pain and intensity components were larger at Cz than Pz, whereas the P300 component was larger at Pz than Cz. Under certain conditions, the pain evoked SEP consists of a weighted combination of the 3 components, complicating interpretation of the positive peaks in the recorded wave forms.     

The P300 event-related potentials in dementia of the Alzheimer type. Correlations between P300 and monoamine metabolites

We studied auditory event-related potentials (ERPs) in 40 patients with dementia of the Alzheimer type (DAT). Peak latencies and amplitudes of N100, P200 and P300 components were measured. To study the possible relationships between the ERPs and monoaminergic neurotransmitter functions, CSF neurotransmitter metabolites were also analyzed. In patients with DAT, the P300 amplitude was significantly reduced and the P300 latency was prolonged. CSF concentrations of 5-hydroxyindoleacetic acid (5-HIAA) and homovanillic acid (HVA) were decreased. The P300 amplitude was significantly correlated with the 5-HIAA concentration. There were no correlations between the P300 components and the HVA concentration. These findings suggest that the serotonergic system modulates the P300 component of ERPs in patients with DAT.     

The relationship between median nerve somatosensory evoked potential latencies and age and growth parameters in young children

Median nerve somatosensory evoked potentials (SEPs) were recorded in a group of 35 normal children aged 6–36 months and related to body length, body weight and head circumference. Recordings were made while the child was awake using the following derivations: ipsilateral clavicle - Fpz; seventh cervical vertebra (CV7) - Fpz; contralateral C′ - Fpz. the clavicular-Fpz response was bilobed in 77% of the recordings, the initial being designated CL1 and the following negativity, CL2. Early negativities, coincident in latency with CL1 and CL2, were often present inin CV7-Fpz recordings, however, a negativity longer in latency than CL2 was always present, was designated CVN, and preceded a prominent positivity. A scalp-recorded early negativity (N1) and a following positivity (P1) were well defined in all recordings.The latency of CL1, CL2 and CVN increased with an increase in age and stature. In contrast, significant negative correlations were found between the latency of N1, P1, age and statur. The CL1-CVN interpeak latency did not correlate significantly with age, while the central conduction time (CVN-N1) declined with an increase in age and stature. These findings confirmed the complexity of SEP absolute and interpeak latency changes with an increase in age and stature in young children.     

Age-dependent changes of short-latency somatosensory evoked potentials in healthy adults

Age-dependent changes of short-latency somatosensory evoked potentials following median nerve stimulation in humans were investigated in two groups of healthy adults aged 20-30 and 50-60 years. Normative values for both age groups are given. Compared to the younger group, in the older one P27 latency and N20-P27 interpeak latency were about 2 ms longer, and P27-N35 and P27-P45 interpeak latencies were significantly decreased. These findings suggest that N20 and P27 are generated by different structures and that the subsequent components do not depend on P27.     

Age-related changes in event-related potentials in visual discrimination tasks

Visual event-related potentials and reaction times in physical and semantic discrimination tasks were studied in 29 normal subjects between the ages of 21 and 74 years. The NA, N2 and P3 components of the evoked potential, and simple and GO/NOGO reaction times were observed in both kinds of discrimination. Significant age-related slowing of the GO/NOGO reaction time was observed only in the semantic discrimination task. The N2 and P3 latencies elicited by both the physical and semantic stimuli were significantly and positively correlated with age, although there was no significant correlation between the NA latency and age. The interpeak latency between N2 and P3 showed no age-related changes. The decline of cognitive information processing with advancing age was evident from the classification of a perceived event as reflected by the N2 component.     

Evoked cortical activity to sounds of differing signal meaning in young and elderly subjects

In elderly people, in comparison with the young ones, the latency of wave P300 is increased in response to all applied acoustic signals, the amplitude of P300 is lower only in response to significant stimuli. No age changes of the wave N150 parameters are noticed. P300 (or N150) wave amplitude depends on signal significance of the sound; it is the lowest in response to significant stimuli and the highest to the ignored ones. Possible reasons of this paradoxical phenomenon are discussed. Preferential participation of different stages of cortical information processing is determined by the difficulty of perceptive task solution. Cortical electrical reaction to separate stimuli is significantly determined by the context of the information perceived in the given period, creating psychological state of the personality.     

P300, stimulus intensity,and modality

Auditory and visual stimulus intensity levels were manipulated systematically in separate conditions to assess the influence of these variables on the P300 event-related brain potential (ERP). Increases in stimulus intensity produced increases in P300 amplitude and decreases in peak latency for both modalities, although the latency effects were stronger for visual stimulation. Similar, somewhat weaker stimulus intensity effects also were observed for the N100, P200, and N200 components. The findings suggest that stimulus intensity contributes to both P300 amplitude and latency measures in important ways and are discussed in relation to the use of ERPs in applied contexts.     

Diurnal variation in the P300 component of human cognitive event-related potential

Diurnal variation in the P300 component of the human cognitive event-related potential (ERP) was examined. The P300 component is considered to be a measure of neuroelectric activity related to cognitive functions such as attention allocation and information processing. Nine diurnally active healthy male subjects whose sleep-wake rhythms were synchronized prior to the experiment were studied. The P300 components oral temperature, heart rate, left- and right-hand grip strength, reaction time, subjectively rated sleepiness, attention level, and fatigue were measured at 08:00, 11:00, 14:00, 17:00, and 20:00. Significant diurnal variations in P300 latency, P300 amplitude, oral temperature, heart rate, left- and right-hand grip strength, subjectively rated sleepiness, and attention level were observed. The P300 latency at 08:00 was significantly longer than at 11:00, 17:00, and 20:00, while the P300 amplitude at 08:00 was significantly greater than at 17:00 and 20:00. The P300 latency was correlated positively with subjectively rated sleepiness and negatively correlated with subjectively rated attention level. These results suggest the existence of diurnal variation in human cognitive functions.     

Age-related changes of reaction time and p300 for low-contrast color stimuli: Effects of yellowing of the aging human lens

We measured reaction time (RT), P300, and subjective evaluation for color Landolt-Cs with a gray color background presented on a CRT display. Seven young and 7 elderly subjects (mean ages: 21.6 and 68.4 years, respectively) participated, and the young subjects wore glasses with filters simulating spectral transmittance of an aging human lens as a test condition. The results for young subjects not wearing the filters showed that RT and P300 latency are constant among different test colors. In contrast, the results for elderly subjects showed that RT and P300 varied substantially depending upon the test colors and RT and P300 latency became longer than those of young subjects, particularly for gray and blue stimuli. In addition, the results for the young subjects with filters showed tendencies similar to those in elderly subjects. These results indicate that the yellowing of the human lens strongly influences reaction time and cognition time for color targets, suggesting that wearing the filters enables the young to simulate RT qualitatively as well as visibility of the elderly because both the simulated filter and the aging human lens modify the effective luminance, effective luminance contrast and effective color difference between the color target and the background on the retina. We also found that the reciprocal of RT and P300 latency could be expressed in a multiple regression model consisting of effective luminance, effective luminance contrast, effective color difference and age. Absolute values of RT and P300 latency in young subjects with filters, however, did not quantitatively coincide with those of the elderly subjects. There were differences of RT and P300 latency between the young with filters and the elderly, indicating that higher order age-related delay could be involved.