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Continuous-processing related ERPS in schizophrenic and normal children.

The continuous performance task (CPT) has proven to be sensitive to schizophrenic impairments. Multichannel event-related potential (ERP) data were recorded from schizophrenic and normal children during performance of easy and hard versions of the CPT. Schizophrenics produced fewer hits, more false alarms, and prolonged reaction times. Poor performance in schizophrenics was associated with four ERP abnormalities: (1) Schizophrenics did not exhibit the normal increase in amplitude of an early-onset, processing-related negativity from nontarget to target stimuli, suggesting a failure to appropriately allocate attentional resources to discriminative processing. (2) Although P3 amplitude to targets was not significantly smaller in schizophrenic children, the distribution of P3 amplitude between target and nontarget responses in the easy and hard versions of the CPT was abnormal, suggesting that schizophrenics differed in the strategic allocation of resources in later stages of CPT processing. (3) In all task conditions schizophrenics showed a parietal negative component with a latency of 400 msec seen in younger, but not older normal children, suggestive of maturational lag. (4) ERP data demonstrated absence of right-lateralized P1/N1 amplitude in schizophrenic children. Taken together these data indicate that at several stages of information processing, schizophrenics are deficient in the control and strategic allocation of processing resources.

Attention↗

Inhibitory mechanism in zebrafish optic tectum: visual response properties of tectal cells altered by picrotoxin and bicuculline.

In previous work we described 4 types of visual response among tectal cells of the zebrafish. Cells of one class, type I, have no spontaneous activity, but respond phasically at ON and OFF. Their responses to moving edges, to stimuli that grow in size, and to stimuli equal in size and shape to the whole receptive field (RF) suggest that these cells may receive inhibitory input from near neighbor cells of the same type in the tectum, as well as excitatory input from retinal fibers. In order to further investigate this hypothesis we have studied the effects of drugs on physiological properties of type I cells recorded in the stratum periventriculare layer of the zebrafish tectum. Small (10-50 nl) injections of drugs were made in the tectum while recording 100-500 microns away with extracellular microelectrodes. Both picrotoxin and bicuculline produce the following effects: (1) onset of spontaneous bursting multiunit activity. This noise can be recorded at all depths within the tectum; (2) abolition of the second postsynaptic wave of the optic nerve shock field potential and the current source responsible for it, which occurs in the upper tectal layers at 8 ms latency. This probably represents the secondary activation of inhibitory synapses in those layers; (3) alteration of visual response properties of individual type I tectal cells. The duration of response to small flashing spots and to stimuli that grow in size both increase significantly. Responses to moving edges, which normally occur mostly as the significantly. Responses to moving edges, which normally occur mostly as the edge is crossing the RF border, become extended to encompass the entire RF. Finally, the cells show reduced negative spatial summation following drug injection. All of these effects are fully reversible with time after injection as the drugs wash out. Control injections (of teleost Ringer's solution, 100 mM HCl, 165 mM NaCl, and strychnine 2 mM or 5 mM) do not elicit any of these effects. The results reported here are consistent with the hypothesis that tectal type I cells receive a delayed inhibitory input, probably via GABA synapses, which determines major properties of the visual response.

Animals↗

Changes in neuronal activity related to the repetition and relative familiarity of visual stimuli in rhinal and adjacent cortex of the anaesthetised rat.

Employing the same techniques as have been used with conscious rats, this study describes neuronal responses signalling information concerning the prior occurrence of visual stimuli in unconscious rats. Recordings of the activity of 387 neurons were made while anaesthetised rats were shown objects. Changes in neuronal responses related to stimulus repetition and the relative familiarity of visual stimuli were sought. The areas sampled were lateral occipital cortex, area TE of temporal cortex, perirhinal cortex and the hippocampal formation. The response to the first presentations of unfamiliar objects was significantly different from that to their second presentations for 30 (35%) of 86 visually responsive neurones; for 23 of the neurones the response was smaller when the stimulus was repeated, whereas for 7 it was larger. For all of these neurones the response change was maintained across intervening trials on which other stimuli were shown. For 4 (25%) of 16 neurones so tested, the response decrement persisted across at least 10 intervening trials. The activity of 63 neurones was recorded while rats were shown highly familiar as well as unfamiliar objects. The response to unfamiliar objects was significantly different from that to highly familiar objects for 3 (23%) of 13 visually responsive neurones. The types of neuronal response and their incidence expressed as a proportion of the number of visually responsive neurones were similar to those found in unanaesthetised rats (though the proportion of visually responsive neurones encountered in the anaesthetised rat was lower). The results indicate that information concerning the prior occurrence of stimuli is processed even under anaesthesia.

Analysis of Variance↗

Apparent motion confounds early vernier visual evoked potentials.

Human scalp potentials evoked by vernier stimuli have been recorded for offsets less than the diameter of a foveal cone, but always for abruptly moving stimuli. Those evoked potentials were related to the magnitude of vernier offset. Here we report results for stimuli containing no apparent motion confound, using multichannel recordings and multivariate analysis methods which stress the concept of a sampling of the scalp field. We found evidence of cortical activity dependent on the direction of vernier offset, at much shorter latencies (ca. 75 ms) than previously reported, but no evidence of early cortical activity related to the magnitude of offset. Repeating the experiments and analysis using a stimulus containing apparent motion, we found evidence of cortical activity dependent on the magnitude of offset at both 75 and 200 ms, but none related to direction of offset. These findings suggest that previous studies which contained the apparent motion confound might not have obtained visual evoked potentials entirely due to vernier offset.

Electroencephalography↗

Dependence of visual evoked potentials on change of stimulated retinal area associated with different pattern displacements.

An attempt was made to distinguish between the effects of the moving edges and the change in the area of stimulated retina on pattern shift visual potentials, elicited by checkerboard pattern displacements varying through 0.25, 0.50, 0.75 and full pattern reversal. Twelve healthy subjects were stimulated binocularly with a horizontally orientated pattern (whole field 17 degrees, check size 28' of visual angle). Four of them were additionally presented with a diagonally orientated pattern. Two sets of 32 averages were taken for each stimulus condition and peak-to-peak amplitudes P50-N70 and P100-N140 were measured. The change of the stimulated retinal area is a quadratic function of the diagonally orientated pattern. The change in amplitude of P50-N70 fits well with the curve of the area change, but that in the amplitude of P100-N140 does not. Each of the amplitudes also seems to have a different orientation of hypothetical dipole vectors.

Adult↗

Stimulus repetition and an amplitude increase of the occipital late positive component in the human visual evoked potential.

VEPs to number and checkerboard stimuli were measured from F3, F4, P3, P4, Cz, O1 and O2 electrode loci. A trial was composed of 8 successive stimuli: a warning stimulus (WS) and 7 task stimuli. The task stimuli were a hexad composed of 6 identical stimuli (intratrial stimulus positions 1-6) and a single stimulus (position 7). A subject's task was either naming the numbers or pattern matching the checkerboards in the hexad and in position 7. Centrofrontal N140s and parietal N180s to the number and checkerboard stimuli did not change in amplitude across stimulus positions 1-7. Parietal and centrofrontal P350s were large in amplitude at positions 1 and 7 and decreased at positions 2-6. Parietal P270s and centrofrontal P200s to the number and checkerboard stimuli behaved in the same way as the P350s with respect to the stimulus positions. Occipital N180s to the number and checkerboard stimuli were maximum in amplitude at position 1, decreased with stimulus repetition (positions 2-6) and increased at position 7. Occipital P270s to the number and checkerboard stimuli were almost the same in amplitude at position 1. The P270 to the number stimulus increased in amplitude with stimulus repetition (positions 2-6) and decreased at position 7. The P270 to the checkerboard stimulus was the same in amplitude at positions 1-3 increased at positions 4-6 and slightly decreased at position 7. These P270 amplitude changes were interpreted as due to the amplitude changes of the overlapping occipital N250 which reflected task-specific perceptual activities.

Adolescent↗

Brain stem auditory, pattern-reversal visual, and short-latency somatosensory evoked potentials: latencies in relation to age, sex, and brain and body size.

To determine standards of normality for auditory, somatosensory and visual evoked potentials commonly used in the assessment of neurological disease, 8 AEP, 1 VEP and 12 SEP components were recorded to stimulation of left and right ears, eyes, and median nerves in 286 normal subjects ranging in age from 4 to 95 years. Peak and interpeak latencies, and left-right differences in latency, were analyzed as a function of age, sex, and estimates of brain and body size. Major features of the results were: (1) Peak latencies of all components showed statistically significant increases in latency with age except that VEP P100 latency decreased significantly between 4 and 19 years and did not change between 20 and 59 years. (2) In adults the peak latencies of all components were significantly later in males than in females. For AEPs and VEPs these differences were explained by sex differences in brain size, and for adult SEPs were explained by sex differences in arm and shoulder dimensions. No significant sex differences in VEP and SEP latencies were seen in children. (3) Most interpeak latencies showed significant differences in relation to age or sex. (4) Age and sex are useful predictors of latency for nearly all peak and interpeak latencies; in addition, height is a useful predictor of SEP peak latencies. (5) Left-right latency differences showed little age-related, and no sex-related, change. The interlaboratory use of these or other normative data was discussed. It was concluded that these AEP and SEP norms can probably be used in other laboratories if stimulating and recording conditions are similar. However, VEP results are difficult to transfer due to the poorly understood effects of variation in stimulus conditions. Some issues regarding the optimal characterization of norms were also discussed.

Adolescent↗

Presenile dementia--the use of the flash and pattern VEP in diagnosis.

Flash, pattern reversal and pattern onset-offset VEPs were recorded in 17 patients with a clinical diagnosis of presenile dementia. The results were compared with those from two control groups--17 normal volunteers of equivalent ages and 17 patients from the same psychiatric hospital with affective disorders but no clinical evidence of dementia. The flash P2 component was found to be significantly delayed in the group of patients with dementia, but the latency of the P1 component and pattern VEP components were all within normal limits. This unusual finding presents a useful index for the diagnosis of presenile dementia.

Aged↗

Monocular pattern-shift visual evoked potentials in hemispheric strokes.

Monocular pattern-shift visual evoked potentials were obtained in (i) 33 patients with unilateral non-hemorrhagic hemispheric infarction (age 50-79 years; 23 males, 10 females), (ii) 21 age- and sex-matched patient controls (control group or CGI) with no remote or recent stroke, normal neurological examination and similar incidence of diabetes mellitus, hypertension and heart disease, and (iii) 21 age- and sex-matched healthy elderly community volunteers (CGII). Subjects with history of glaucoma, cataracts, other media opacities or symptomatic retinal lesions were not considered or included in any of the 3 study groups. In addition, all subjects in each of the 3 groups had a normal ocular and fundoscopic examination. The mean interocular P100 latency difference in the stroke group was significantly greater than that in CGI or II (P less than 0.01). The mean interocular P100 amplitude ratio (small P100/large P100) in the stroke subjects was significantly different from that of CGI or II (P less than 0.02). The mean P100 latency on ocular stimulation ipsilateral to the side of infarction was significantly longer than that of either left or right ocular stimulation in CGI or II (P less than 0.01). The mean P100 latency on ocular stimulation contralateral to the side of infarction was similarly but less significantly longer than that on left or right ocular stimulation in CGI or II (P less than 0.05). Evidence of anterior visual pathway dysfunction was thus elicited in the stroke population using the technique.

Aged↗

Subdurally recorded pattern and luminance EPs in the alert rhesus monkey.

Two rhesus monkeys (Macaca mulatta) were trained to fixate a TV screen on which checkerboard and bar patterns could be presented. Stainless steel skull electrodes and electrode bundles under the dura, each containing 7 leads permitting 7 recording sites at 5 mm intervals, were placed over the temporal-occipital cortex and used to obtain visually evoked potentials (VEPs). The following conclusions were reached: VEPs recorded with skull electrodes resemble scalp recorded VEPs. Subdural electrodes may yield larger VEP amplitudes than skull or scalp electrodes. Subdural VEPs vary more in shape with recording site than scalp or skull recorded VEPs. Apart from differences in shape there are topographical differences between luminance and pattern EPs; the luminance EP is localized near the occiput and the pattern EP is most pronounced at the temporal site overlying the foveal projection area. For a given recording site it can be seen that: (a) the amplitude of the pattern reversal EP is smaller than that of the pattern onset EP; (b) the shape of the reversal EP resembles the pattern offset EP; and (c) the shape of the pattern onset EP is rather invariant to check size and bar width. On the basis of the pattern EP the striate and prestriate cortical areas can be distinguished as follows: (a) the prestriate cortex yields a positive-negative-positive (PNP) response complex to pattern onset and the striate cortex a PN response complex; and (b) the striate cortex responds to finer patterns than the prestriate cortex.

Animals↗

Aberrant wave forms to pattern reversal stimulation: clinical significance and electrographic 'solutions'.

Aberrant wave forms (AWFs) which are pattern visual evoked potentials (PVEPs) with ambiguous P2 peaks, were found in 13.7% of our patient population and not in our control group. The distribution of AWFs among the clinical entities of chronic myelopathy, questionable early MS, MS without visual lesions, MS with visual lesions and other neurological disorders, were similar to that of normally formed PVEPs with delayed P2 peaks. AWFs therefore appear to have a similar clinical significance to that of delayed, normally formed PVEPs, whether or not their latencies are within the normal range. Electrographic fields of non-aberrant PVEPs with well defined P2 peaks were studied to define the following obligate P2 characteristics: P2 always attained highest amplitude at the midline occipital position (Ox), hemifield stimulation using Fz as a reference always evoked a larger NPN complex over the hemisphere ipsilateral to stimulation than over the contralateral hemisphere. Multiple-channel analysis of both fullfield and hemifield stimulation and bipolar transverse montages reconstructed from referential recordings were employed to identify the P2 peak in AWFs. Bipolar reconstruction identified the P2 peak in 61% of all instances in which it was employed while hemifield stimulation did so in 84% of instances. In the 82 instances in which both were employed, hemifield stimulation identified the P2 in 84% as compared to only 33% for bipolar reconstruction. Therefore, although bipolar reconstruction may often identify the P2, hemifield stimulation is more effective for particularly complex situations.

Adolescent↗

Effect of spatial frequency on transient and steady-state VEPs: stimulation with checkerboard, square-wave grating and sinusoidal grating patterns.

We recorded VEPs to the alteration of checkerboard, square-wave grating and sinusoidal grating patterns to evaluate the contribution of the fundamental spatial frequency and higher harmonic components in 12 normal subjects. Their fundamental spatial frequencies were equated and ranged from 0.5 to 8.0 c/deg. Both the transient VEP (T-VEP) and steady-state VEP (S-VEP) were obtained. The latency and amplitude of P100 of T-VEPs were measured. S-VEPs were Fourier analyzed, and phase and amplitude of the second harmonic response were measured. The mean P100 latency and the mean phase had a U-shaped function with a peak at a fundamental spatial frequency of 2.0 c/deg irrespective of the stimulus patterns, while the mean P100 amplitude and the mean amplitude of S-VEPs did not show such spatial selectivity. At low and medium spatial frequencies, differences in P100 latency, phase and amplitude between pattern types were more pronounced. However, this difference became insignificant at high spatial frequencies. These results indicate that VEP responses are predominantly determined by the fundamental spatial frequency, and that the contribution of higher harmonics to VEP responses is not negligible. Our results are consistent with the concept that the human visual system may use spatial frequency-domain information.

Adult↗

Visual discrimination and P300 are affected in parallel by cholinergic agents in the behaving monkey.

We studied the acute effect of cholinergic agents, scopolamine alone and scopolamine pretreatment and acetyl-L-carnitine (ALC) on visual event-related potentials (ERPs) in a monkey performing in a go/no-go visual oddball discrimination task. The same monkey was studied repeatedly for a period extending over 1.5 years. Scopolamine is known to cause cognitive impairment in primates. In the concentrations used, primary evoked potentials did not change significantly whereas P300 latency increased maximally 20-40 min following scopolamine administration. Acetyl-L-carnitine on its own increased P300 amplitude and decreased its latency. When ALC administration was preceded by scopolamine, both P300 latency and amplitude maximally increased in 25-45 min. Apparently ALC's effect on the latency and amplitude of visual P300 of the monkey is largely via muscarinic mechanisms. Our results suggest that scopolamine may provide a valuable tool to separate cognitive from primary visual processes.

Acetylcarnitine↗

P300 habituation from visual stimuli?

The P3(00) event-related brain potential (ERP) was elicited with visual stimuli using an oddball task in which the subject indicated with a finger tap response the occurrence of a target stimulus that occurred randomly on 20% of the trials and refrained from responding to a standard stimulus. A total of six trial blocks were collected, with an equal number of artifact-free epochs averaged for both stimulus types. P3 amplitude from the target stimuli did not decrease across trial blocks; P3 amplitude from the standard stimuli did decrease across trial blocks. P3 latency from both the target and standard stimuli increased across trial blocks. No changes in amplitude or latency independent of the P3 effects were obtained for the other ERP components with trial block. The results suggest that P3 components elicited by visual stimuli do not readily habituate for actively discriminated target stimuli. The theoretical implications are discussed in the context of previous findings.

Adult↗

Changes in the human visually evoked cortical potential in response to chromatic modulation of a sinusoidal grating.

Human visually evoked cortical potentials (VECPs) were recorded from 4 subjects in response to the counterphase alternation of an equal brightness chromatic grating pattern. The pattern was constructed from 2 monochromatic sinusoidal gratings registered 180 deg out of phase. Eleven wavelengths from 450 to 650 nm (at 20 nm intervals) were used. Each wavelength was paired in the grating stimulus with every other to produce a total of 55 different chromatic gratings. The chromatic modulation depth (contrast) of each grating was varied and resulting VECPs were recorded. VECP amplitude was found to vary linearly with log chromatic modulation depth. VECP threshold values were inferred by extrapolation of linear regression lines to zero VECP amplitude. Chromatic modulation sensitivity functions were derived and a multidimensional scaling analysis of the data for each subject was performed. The data were adequately described by a two-dimensional geometric configuration of the 11 wavelengths used. The configurations were similar in shape to those obtained psychophysically by Butler and Riggs (1978) Vision Res. 18, 1407-1416, who used a similar stimulus pattern. Their shapes are consistent with an opponent-color model of color vision.

Adult↗

Spatial frequency mechanisms in human vision investigated by evoked potential recording.

Two visually evoked brain responses were elicited simultaneously by stimulating the eye with two superimposed sinewave grating patterns that were temporally modulated at slightly different rates. The VEP to one grating was comparatively little affected by the presence of the other grating when the two spatial frequencies were very different, but mutual attenuation grew stronger and stronger as the spatial frequencies of the two gratings were progressively brought together. The attenuation rose to a sharp maximum when the two spatial frequencies were equal. This held at each of the five spatial frequencies tested. This finding can be explained if the spatially-selective mechanisms responsible for grating VEPs contain multiple subunits of narrower spatial frequency bandwidth. The two-grating technique was also used to search for evidence of multiple subunits that are most sensitive at the same spatial frequency, but are tuned to different temporal frequencies. Findings were quite different for temporal and for spatial tuning. Attenuation of one grating VEP was greatest when the temporal frequency of the other grating fell within a broad frequency range of about 3-30 reversals sec-1: maximum attenuation could occur when the gratings had quite different temporal frequencies. This finding denies that for every given temporal frequency there is a subunit maximally sensitive to that frequency.

Adolescent↗