The effect of eccentricity and colour on negativity in pattern onset visual evoked potentials

The effects of stimulus size, eccentricity and colour on the amplitudes of N100 and N130 were investigated in pattern onset VEPs. For black-and-white pattern stimulation, the first set of stimuli was derived from a full dartboard pattern. Central stimulation of various extents was produced by patterns with reduced number of outer rings and for eccentric stimuli a number of central rings were removed from the full pattern. It was found that amplitude of N100 was maximal in VEPs to central stimuli and that it was greatly reduced when eccentric stimulation was applied. The amplitude of N130 showed no significant change in relation to the type of stimulus. When checkerboard stimuli of identical configuration were used for black-and-white pattern stimulation instead of dartboards, systematic changes in peak latencies of N100 were observed in relation to check size. In VEPs to centrally presented small checks the emergence of an early negative peak preceding N100 was recorded at 75 msec. In VEPs to coarse checkerboards presented centrally N100 was often observed with a delayed peak latency of 110 msec. Changes in N130 were not regular when checkerboards with different check sizes were presented centrally. For eccentric checkerboard stimulation, both negative peaks N100 and N130 were revealed. Their peak latencies were similar to those observed in the case of dartboard paracentral stimulation. In VEPs to patterns projected through red or blue filters, regular changes were observed in both negative peaks. Introduction of the red filter led to enhancement of the N100 amplitude in VEPs to dartboard and to checkerboards with fine checks, but it caused no effect on N100 in the VEPs to coarse checkerboards. Introduction of the blue filter led to a decrease in the N100 amplitude in VEPs to dartboard and fine checkerboards and to a slight increase of N100 in VEPs to coarse checkerboards. Changes in N130 were observed only when the blue filter was introduced and they corresponded to those which take place when the level of illumination changes from photopic to mesopic.     

The influence of pattern size on amplitude, latency and wave form of retinal and cortical potentials elicited by checkerboard pattern reversal and stimulus onset-offset.

Transient pattern electroretinograms (PERGs) and visual evoked potentials (VEPs) were recorded with checkerboard pattern reversal and equiluminance stimulus onset-offset, elicited by a high quality moving mirror stimulator. Different sized checkerboard patterns (0.35-4.2 c/deg) were used as stimulus patterns. The wave forms of the equiluminance stimulus onset responses were similar to ERGs evoked with luminance decrease and the stimulus offset PERGs were like ERGs elicited by luminance increase. The PERG c wave and the VEP showed spatial frequency tuning with pattern reversal and stimulus offset. Spatial frequency tuning was not detectable with PERG a and b waves. Pattern reversal and stimulus onset evoked PERGs had no major spectral components above 40 Hz; stimulus offset evoked PERGs contained components up to 55.3 Hz. Retino-cortical time--measured as a latency difference of the PERG b wave to VEP P100--was identical with pattern reversal and stimulus onset and about 12 msec longer with stimulus offset. Our results suggest that the 3 stimulation modes, reversal, onset and offset induce different types of processing at the retinal and cortical levels. PERG a and b waves to our high luminance/contrast stimuli contain no pattern specific information and the c waves are the sum of luminance and pattern specific responses.     

The effect of adaptation to the stimulating pattern on the latency and wave form of visual evoked potentials

Visual evoked potentials (VEPs) elicited with a checkerboard stimulus after adaptation to an unpatterned grey field were compared to those obtained after adaptation to the stimulating pattern for an equal interval of time. When 3--4 sec elapsed between the adapting interval and recording of the VEP, the latency of the principal positive peak increased by 4 msec with pattern-reversal, but not with pattern-onset stimulation, while the amplitude was unchanged. However, when the pattern-onset VEP was recorded immediately after adaptation, the principal negative peak of the response was lost and the latency of its principal positive peak increased by 14 msec, causing it to mimic the conventional pattern-reversal VEP in both wave form and latency, and suggesting that adaptation may cause the wave form differences in the VEPs obtained by these two methods.     

Equiluminant red-green and blue-yellow VEPs in multiple sclerosis.

The primate visual system is composed by two color-opponent pathways--red-green (R-G) and blue-yellow (B-Y)--subserved by the so-called parvo- and koniocellular streams respectively. The authors' aim was to compare the relative involvement of chromatic visual subsystems in multiple sclerosis (MS). In 30 MS patients with different forms of MS they recorded visual evoked potentials (VEPs) to onset (300 msec) and offset (700 msec) of equiluminant R-G and B-Y sinusoidal gratings of different contrast (90% and 25%). Equiluminance was established psychophysically by establishing the R-G and the B-Y color ratio at which chromatic gratings alternating at 15 and 10 Hz respectively had minimum visibility. The negative wave at stimulus onset with a peak latency of 120 to 160 msec was evaluated. Ordinary VEPs to luminance (LUM) contrast (black-white reversing checkerboards of 15' check size and 50% contrast) were also recorded for comparison. Latencies of R-G VEPs were abnormal in 53.3% and 58.3% of patients at 90% and 25% contrast respectively, whereas abnormal B-Y VEPs were 56.6% and 48.3%. Latencies of LUM VEPs were abnormal in 45% of patients. Interocular latency asymmetries were abnormal in 59.2% and 33.3% of patients for R-G, and 51.8% and 62.9% for B-Y. Latency asymmetries for LUM VEP were abnormal in 46.4% of patients. The higher rate of VEP abnormalities found with equiluminant chromatic stimuli compared with achromatic stimuli confirms the general vulnerability of color-opponent visual pathways in MS, even if the number of patients with abnormal findings was not significantly different when both test conditions were compared. VEPs to R-G and B-Y equiluminant stimuli appear to be involved approximately to the same extent.     

The early wave of the visual evoked potential to sinusoidal gratings: responses to quadrant stimulation as a function of spatial frequency

VEPs were elicited by sinusoidal grating patterns of differing spatial frequencies presented in each of the 4 quadrants of the visual field. Analysis of the early wave of the VEP indicated a pattern of polarity inversions when wave forms were compared across the horizontal meridian of the visual field. With the exception of low spatial frequencies, clear polarity inversions also occurred across the vertical meridian of the visual field in the case of laterally placed electrodes. Comparison of the clearly identifiable early peak with records for the same subject using central field stimulation showed the complexity of the latter records and the inherent difficulty of isolating and interpreting specific component waves of the VEP without adequate topographical data from quadrant stimulation.     

Visual evoked potential interhemispheric transfer time in different frequency bands.

OBJECTIVE: Visual evoked potentials (VEP) have been used to estimate interhemispheric transfer time (IHTT). However, the complex wave of VEP is most probably formed by different generators of neural populations that act through different frequency channels. If the main peaks of VEP are established by different types of generators, which can also be connected to each other by a different type of callosal fibres, we would be able to estimate a wide range of various IHTT by measuring the latency between time-locked peaks of narrow band-pass filtered VEP. This research aimed to test this hypothesis. METHODS: Nine right-handed men were presented with a reversal of a checkerboard pattern as stimuli at RVF or LVF, and EEG was recorded at O1, O2, P3, P4. The grand-averaged VEPs were transformed to the frequency domain by means of the fast Fourier transform to obtain the amplitude frequency characteristics. Band-pass filters were chosen adequately, according to tuning frequencies indicated by clear peaks in the amplitude frequency characteristics. The chosen band pass filters (4-8 Hz, 8-15 Hz, 15-20 Hz, 20-32 Hz) were applied to the VEP of the subjects, and 4 different components of VEPs for each VEP were obtained. The latency of P100 and N160 of unfiltered VEP was measured. In the band-pass digital filter applied VEPs, positive and negative peaks, which are consistent with P100 and N160, were measured for each subject. Latency differences between hemispheres for digitally unfiltered and filtered VEPs were computed to estimate IHTT. RESULTS: In the different frequency bands, different IHTTs were estimated, ranging from 3 ms to 30 ms. Approximately 16 ms for theta band, 11 ms for alpha band, 6 ms for 15-20 Hz and 3 ms for 20-32 Hz bands were found. CONCLUSIONS: Our findings support the hypothesis which states that unfiltered VEPs provide us with only a rough estimation of IHTT. Also, they are consistent with anatomical findings that describe callosal fibres of varying dimensions, predicting various velocities between hemispheres.     

Spatial distribution of potentials evoked by half-field pattern-reversal and pattern-onset stimuli.

Spatial distributions of visual potentials (VEPs) evoked by half-field checkerboard pattern-reversal and pattern-onset stimuli were studied in 13 subjects, using an 11 lead unipolar array. The main aim was to confirm findings, obtained by previous workers with bipolar recordings, that half-field pattern-reversal VEP's are confined to the contralateral hemisphere and that half-field pattern-onset VEPs are asymmetrical, with greater right hemisphere involvement. Pattern-reversal VEP's contained four consistent peaks, designated here by polarity and peak latency as: (a) P95, positivity contra-lateral and negativity ipsilateral to the field stimulated; (b) P125, predominantly ipsilateral positivity; (c) N165, predominantly ipsilateral negativity; (d) P225; predominantly midline positivity. Pattern-onset VEPs contained three consistent peaks: (a) P125, mainly contraleteral positivity; (B) N175, mainly contralateral negativity; (c) P225, midline positivity. Distributions of pattern-reversal and pattern-onset peaks resembled one another only for P225, suggesting different cortical representation for the other events of the two kinds of VEP. Bipolar pattern-reversal VEPs were largely contralateral, but unipolar recordings showed that this was due to steeper contralateral potential gradients, as ipislateral activity was widespread. Pattern-onset peaks did not differ in amplitude with respect to the half-field stimulated. Previously reported asymmetries were not confirmed. The P125 and N175 pattern-onset peaks were almost entirely restricted to the contralateral hemisphere, but the distributions by half-field were mirror-images of one another. Half-field pattern-onset stimuli could be used to investigate the responsiveness of each hemisphere, although differential hemispheric involvement was not shown. Several differences in amplitude and distribution resulted from varying the width of the vertical central dark strip.     

The pattern reversal VEP in short-gestation infants

Visual evoked potentials (VEPs) to pattern reversal stimulation have been obtained in 10 premature babies. The babies were born between 32 and 35 weeks gestational age and had pattern reversal VEPs recorded on at least 2 separate occasions. The responses were obtained from 33 weeks gestational age, and all babies had their initial recording at or before 37 weeks gestational age. The pattern reversal stimulation was produced on a small hand-held television monitor. The black and white checks subtended a visual angle of 2 degrees. Flash VEPs were also recorded on each occasion for comparison. The pattern reversal response consisted of a major positive (P1) component around 280 msec. The latency of the P1 component correlated negatively with gestational age. Although the flash VEP in the same babies was often dominated by the initial negative component no similar negative components were seen in the pattern reversal response.     

Mapped distribution of pattern reversal VEPs to central field and lateral half-field stimuli of different spatial frequencies.

Visual evoked potentials (VEPs) to pattern reversal vertical bar stimuli of 3 different sizes (1, 2, 4 c/deg) were recorded from 19 scalp derivations in 50 controls. The stimuli were presented on a full-field (FF) screen of 24 degrees visual angle, and on left and right half-fields (HF) of 12 degrees radius. In 15 controls partial HF stimuli were presented on the central 3 and 6 degrees and as hemiannular stimuli of 12 degrees with occlusion of the central 3 and 6 degrees. An antero-posterior polarity reversal of the N1-P1-N2 sequence was observed for FF VEPs. A tangential polarity reversal was observed for HF VEPs. Also with central or hemiannular stimuli polarity reversals of all VEP components were observed within the scalp. Variants of VEP distribution, absence or prominence of some of the ipsi- or contralateral VEP components were observed in 8-40% of controls. The FF and HF VEP distribution, and the variant VEP asymmetries were partly dependent on the pattern spatial frequency.     

Transient visually evoked potentials to sinusoidal gratings in optic neuritis.

Transient visually evoked potentials (VEPs) to sinusoidal gratings over a range of spatial frequencies have been recorded in cases of optic neuritis. The use of the response to pattern onset in addition to the response to pattern reversal extended the range to higher spatial frequencies by up to two octaves. There was an increase in VEP delay and a greater degree of discrimination from a control group at higher spatial frequencies. This finding is discussed in the light of previous reports of luminance and checkerboard VEPs in demyelinating optic nerve disease. An attempt is made to relate amplitude changes in various VEP components to contrast sensitivity measurements in this group of patients.     

Cortical and subcortical components of the pattern VEP

Studies in the past have shown that wavelength related VEPs can be recorded from both cortical and noncortical sites. Elements of pattern-specific VEPs for both transient and pattern-reversal stimuli are also obtained from these sites. From the noncortical montage consistent responses are obtained with a major component at about 100 msec, which has been found for both the wavelength related and pattern related VEP. In contrast, the cortical VEP to both types of stimuli include two major components, at around 100 and 200 msec. In pattern reversal these components react quite differently to changes in spatial frequency. The component around 100 msec reacts strongly to a wide range of spatial frequencies when recorded from either cortical or noncortical sites. In contrast, the component around 200 msec, obtained with cortical recording, reacts very strongly to high spatial frequencies and very weakly to low spatial frequencies. This finding corresponds to recent results of single-cell studies in the macaque LGN and striate cortex.     

Visual evoked potential abnormalities in a girl with brain stem encephalitis (Bickerstaff)

A 16-month-old girl was admitted because of bilateral ophthalmoplegia, left blepharoptosis, and disturbance of consciousness. Her symptoms resolved spontaneously within a week after admission, but mild left abducens palsy remained. The cranial computed tomography showed a mild non-specific brain atrophy. The auditory brain stem response was normal. Visual evoked potentials (VEPs) to flash stimuli were repeated serially after the onset. No significative patterns of VEP were evoked during the acute stage. However, three months after the onset, an asymmetrical pattern, namely left-sided abnormalities (not-identified P 100 wave, etc.), was observed. The asymmetrical pattern of VEP diminished six months after. And a bilaterally normal VEP pattern was found twelve months after.     

Intracortical generators of the flash VEP in monkeys

Flash visual evoked potentials (VEPs) in unanesthetized monkeys were recorded from the cortical surface and from closely spaced intracortical sites together with associated multiple unit activity (MUA). The VEP depth profiles were subjected to current source density (CSD) analysis to delineate the laminar pattern of transmembrane current flows manifested by extracellular source and sinks. The initial surface recorded components (P15 and P18) were generated subcortically within the thalamocortical radiations. The distribution of current sources and sinks associated with two subsequent surface negative components. N24 and N40. demonstrates their generation within laminae IVA and IVCb respectively, both parvocellular thalamorecipient layers. Oscillatory potentials resembling those seen in human VEPs are observed riding on N40; analysis of MUA in conjunction with sources and sinks coincident with these wavelets provides evidence that they derive from both thalamocortical and cortical activity. MUA in the 20-60 msec range shows phasic increases throughout lamina IV, which are maximum in amplitude within lamina IVA. This increased firing is concurrent with the sinks observed within the parvocellular thalamorecipient sublaminae IVCb and IVA. A subsequent component, P65, coincident with a decrease in MUA to below the spontaneous level co-located with a lamina IVCb current source, probably arises from intracortically generated inhibitory activity within IVCb. The next VEP component, a surface negative potential at 95 msec, is coincident with current sources and sinks in lamina III, and is consistent with stellate cell input to supragranular elements. VEP components after N95 are not associated with either MUA or CSD activity and are probably generated in extrastriate cortex. Human counterparts of the simian VEP are proposed.     

Mapping study of somatosensory evoked potentials during selective spatial attention.

We have investigated the effects of selective spatial attention on early and middle-latency SEPs. Baseline control responses to electrical stimulation of 2 digits of the hand were recorded first in conditions of mental relaxation, in the absence of any cognitive task, to obtain truly 'neutral' responses uncontaminated by cognitive components. Then, during a 'task condition,' identical stimuli were applied to the same two fingers, but the subject's attention was driven towards the stimulated territory by the bias of mechanical taps delivered to the same digits. The earliest effect of directing attention towards the territory stimulated was a positive shift on contralateral somatosensory responses, with onset at 27.4 +/- 4 msec post stimulus. This SEP modification: (a) did not entail any change in the scalp distribution of components, as assessed by topographic mapping, and (b) was not present when attention was directed towards the hand contralateral to that receiving electrical stimuli. A second effect was represented by a parieto-central negativity in the 60-80 msec latency range; this feature could also be observed during contralaterally driven attention and was associated with topographical changes in SEP scalp distribution. Finally, a late centro-frontal negativity beginning at 90-100 msec (N140) appeared during ipsilateral attention, while P100 was not enhanced. Subcortical P14 and primary cortical N20 were not significantly affected by the tasks. We conclude that the 'early positive shift' is linked to the spatial aspects of selective attention and represents in part modulation of obligatory components (P25 through P45) existing in control SEPs; it probably corresponds with the deflections with similar polarity and time-course that have been described by others in response to somatosensory target stimuli. Conversely, 60-80 msec negative enhancement is less spatially selective and may represent non-specific arousal effects. The late negative component (N140) shares several features with the 'processing negativity' described in auditory paradigms and could represent the equivalent of this effect in the somatosensory system.     

Binocularity in the little owl, Athene noctua. II. Properties of visually evoked potentials from the Wulst in response to monocular and binocular stimulation with sine wave gratings

Visually evoked potentials (VEPs) have been recorded from the Wulst surface of the little owl, Athene noctua, in response to counterphase-reversal of sinusoidal gratings with different contrast, spatial frequency and mean luminance, presented either monocularly or binocularly. Monocular full-field stimuli presented to either eye evoked VEPs of similar amplitude, waveform and latency. Under binocular viewing, VEPs approximately doubled in amplitude without waveform changes. VEPs with similar characteristics could be obtained in response to stimulation of the contralateral, but not ipsilateral, hemifield. These results suggest that a 50% recrossing occurs in thalamic efferents and that different ipsilateral and contralateral regions converge onto the same Wulst sites. The VEP amplitude progressively decreased with increase of the spatial frequency beyond 2 cycles/degree, and the high spatial frequency cut-off (VEP acuity) was under binocular viewing (8 cycles/degree) higher than under monocular (5 cycles/degree) viewing (200 cd/m2, 45% contrast). The VEP acuity increased with increase in the contrast and decreased with reduction of the mean luminance. The binocular gain in both VEP amplitude and VEP acuity was largest at the lowest luminance levels. Binocular VEP summation occurred in the medium-high contrast range. With decreased contrast, both monocular and binocular VEPs progressively decreased in amplitude and tended to the same contrast threshold. The VEP contrast threshold depended on the spatial frequency (0.6-1.8% in the range 0.12-2 cycles/degree). Binocular VEPs often showed facilitatory interaction (binocular/monocular amplitude ratio greater than 2), but the binocular VEP amplitude did not change either by changing the stimulus orientation (horizontal vs. vertical gratings) or by inducing different retinal disparities.(ABSTRACT TRUNCATED AT 250 WORDS)     

Sequential spatial maps of visual potentials evoked by checkerboard-pattern reversal: effect of the retinal field stimulated on response topography

Sequential color maps of visual potentials evoked by the reversal of various checkerboard patterns were recorded in 10 young adults using a 16 channel montage. It was found that each of the components of the N75-P100-N145 occipital complex had a specific spatial distribution on the scalp and was selectively influenced by the size, the spatial frequency, the luminance and possibly the wave length of the stimulus. Component N75 was found to be elicited by the more peripheral area of the TV stimulus (12 degrees X 16 degrees). Component P100 was associated with a frontal negativity of similar latency favoring the hypothesis of a dipolar occipital generator. With half-field stimulations the dipole orientation was modified, leading to a 'paradoxical' lateralization of P100 in most cases. However the reverse situation (P100 contralateral to the stimulated half-field) was observed in 4 and 3 subjects out of 10 with left and right half-field stimulations respectively. Thus VEP to full-field TV pattern reversal cannot be recommended to investigate hemianopic patients. Component N145 was of maximal amplitude when elicited by the reversal of small foveal patterns (2.18 degrees), especially red light emitting diodes.     

Effects of single-pulse transcranial magnetic stimulation (TMS) on functional brain activity: a combined event-related TMS and evoked potential study.

OBJECTIVE: To further evaluate the potential of slew-rate limiting amplifiers to record electrophysiological signals in spite of concurrent transcranial magnetic stimulation (TMS), and to explore the effects of single-pulse TMS on electroencephalographic (EEG) correlates of functional brain activity. METHODS: Visual-evoked potentials (VEPs) to checkerboards were recorded in 7 right-handed subjects, while single-pulse TMS was applied to the occipital pole either at visual stimulus onset, during the build-up or at the expected peak of the early VEP component P1 (VIS&TMS). Timing of TMS was individually adjusted based on each subject's VEP-latency. A condition of TMS without concurrent visual stimulation (TMS(alone)) served for subtraction purposes (VIS&TMS minus TMS(alone)) to partial out TMS-related contaminations of the EEG signal. RESULTS: When TMS was applied at visual stimulus onset, VEPs (as calculated by subtraction) perfectly matched control VEPs to visual stimulation alone. TMS at around P1, in contrast, modified the targeted (P1) and the subsequent VEP component (N1), independently of whether TMS was given at build-up or peak. CONCLUSIONS: The retrieval of regular VEPs with concomitant TMS at visual stimulus onset suggests that the employed EEG system and subtraction procedure are suited for combined EEG-TMS studies. The VEP changes following TMS at around P1 provide direct clues on the temporal dynamics of TMS pulse effects on functional activity in the human brain. Our data suggest effects of relatively long duration (approximately 100 ms) when TMS is applied while functional neuronal activity evolves.     

Pattern-reversal visual evoked potentials and retinal eccentricity

The effect of stimulation of discrete areas of the retina on visual evoked potentials (VEP) was studied in 16 normal volunteers. The stimulus consisted of a constant luminance 2 degrees 18' field containing checks of 34'30' reversing at a frequency of 500 msec. The amplitude of the VEP was highest at the fixation point and inside the 2 degrees isopter. Rapid amplitude decrement was noted with stimuli located within the 2-4 degrees isopters. No identifiable response was obtained outside the 4 degrees or 6 degrees isopter with a 2 degrees 18' stimulus. VEP could, however, be elicited by increasing the size of the stimulus. The smallest size of a field required to evoke a detectable response also varied in relations to retinal eccentricity. Stimulation at 0 degree, 8 degrees and 14 degrees horizontal eccentricities with fields of a size estimated to activate an equivalent amount visual cortex produced VEPs of similar amplitude.     

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.     

Maturation of visual evoked potentials across adolescence

Adolescence represents the period of transition from childhood to adulthood and is characterized by significant changes in brain structure and function. We studied changes in the functional visual processing in the brain across adolescence. Visual evoked potentials (VEPs) to three types of pattern reversal checkerboard stimuli were measured in 90 adolescents (10-18 years) and 10 adults. Across adolescence, the N75 and P100 VEP peaks decreased in size while the N135 peak increased slightly in size. The latency of VEP peaks showed no reliable change across adolescence. The results suggest that even very basic visual sensory function continues to develop throughout adolescence. The results indicate significant changes in visual parvocellular and magnocellular pathways across adolescence.