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Biomedical subjects

B W van Dijk

Publications and source records attributed to B W van Dijk.

At least 19 recordsLinked to original sources

Coherency and connectivity in oscillating neural networks: linear partialization analysis.

This paper studies the relation between the functional synaptic connections between two artificial neural networks and the correlation of their spiking activities. The model neurons had realistic non-oscillatory dynamic properties and the networks showed oscillatory behavior as a result of their internal synaptic connectivity. We found that both excitation and inhibition cause phase locking of the oscillating activities. When the two networks excite each other the oscillations synchronize with zero phase lag, whereas mutual inhibition between the networks resulted in an anti-phase (half period phase difference) synchronization. Correlations between the activities of the two networks can also be caused by correlated external inputs driving the systems (common input). Our analysis shows that when the networks exhibit oscillatory behavior and the rate of the common input is smaller than a characteristic network oscillator frequency, the cross-correlation functions between the activities of two systems still carry information about the mutual synaptic connectivity. This information can be retrieved with linear partialization, removing the influence of the common input. We further explored the network responses to periodic external input. We found that when the input is of a frequency smaller than a certain threshold, the network responds with bursts at the same frequency as the input. Above the threshold, the network responds with a fraction of the input frequency. This frequency threshold, characterizing the oscillatory properties of the network, is also found to determine the limit to which linear partialization works.

Computer Simulation

Non-linear dynamics of columns of cat visual cortex revealed by simulation and experiment.

Correlation images were derived from simultaneous recordings of 12 signals representing the synaptic activity at different layers of a column in cat visual cortex (area 18) and 12 signals representing the local average spiking activity at the same locations. Because the ongoing activity and the activity evoked by stroboscopic flashes yielded the same correlation image, ongoing activity is caused by an input to a column similar to flash-evoked activity and is thus not endogenous. Moving bar stimuli evoked bursts of oscillations (25-75 Hz band) in the correlation image. The rhythm of these oscillations was not related to any frequency component in the stimulus. In all correlation images we observed that synaptic activity in one layer resulted in simultaneous spiking activity in all layers with latency differences smaller than 2 ms (the sample interval used). Similar behaviour was observed in a simulation experiment where we 'realistically' modelled one column of visual cortex with 1000 three-compartmental neurons in 11 functional layers. When such a model column was tuned to yield a stable and excitable system with low ongoing activity, activation of any of the layers caused simultaneous activity in all 11 layers. Both the simulation and the experimental results suggest that a column can be regarded as a basic processing element sending the same information over all its outputs to other columns within the same cortical region, other visual areas and subcortical structures.

Animals

Contour from motion processing occurs in primary visual cortex.

Relative motion is one of the most salient cues for segmentation of a visual scene into separate objects. This is illustrated by the vivid contours that are perceived when random dot patterns move in different directions. Once motion is halted in such displays the segmentation contours disappear. This makes random dot patterns ideal for the study of contour from motion processing in isolation. Contour from motion processing obviously relies on direction-selective neurons, which are found in many visual cortical areas. It is, however, largely unknown at what level of processing their signals interact to serve the global process of motion-based image segmentation. To answer this question, we recorded visually evoked potentials, both in man and in awake monkey, to a stimulus specifically designed to signal the presence of neuronal activity related to contour from motion processing. We report here that response components specific to contour from motion were elicited only when the stimulus yielded a contour percept. In awake monkey, the sources of these components were located within the supra- and infra-granular layers of primary visual cortex. We conclude that V1 is involved in image segmentation processing.

Animals

Motion-onset visual-evoked potentials as a function of retinal eccentricity in man.

Visual-evoked potentials were elicited by the motion-onset of a black-and-white square-wave grating of 2.4 cycles/deg that drifted from right to left at a velocity of 3 deg/s. The center of the 2 x 2 deg stimulus field was binocularly viewed either foveally or at eccentricities of 6, 12, or 20 deg in the lower visual field along the vertical meridian. Peak-to-peak amplitudes P1-N2 and N2-P2 were found to decrease non-linearly as a function of eccentricity. The VEP-amplitudes were standardized by setting each foveal value to 100%, and a relative measure was derived for peripheral values given by the ratio of the peripheral to the foveal values. The decrease of the relative VEP-values with eccentricity was significantly smaller than that of the relative cortical magnification factor of striate cortex in man, whereas it agreed fairly well with that of the relative point-image size of the area MT in Macaque monkey. In this respect, the motion-onset VEP is distinct from the pattern-reversal VEP, the amplitude of which decreases much more rapidly with retinal eccentricity; hence, it may involve different generating structures of the brain.

Adolescent

Topography of occipital EEG-reduction upon visual stimulation.

Visual stimuli were designed to drive a high proportion of the neurons in restricted parts of the human visual cortex. These stimuli were used to examine changes in the ongoing EEG during visual stimulation. The topographic organization of these changes was studied. It was found that the EEG from those parts of the cortex that are exposed to the stimulus is strongly reduced in amplitude. This stimulus dependency is indicative that cortical processing results itself in a reduction of the ongoing EEG, presumably due to desynchronization of neurons. The method shows that ongoing EEG can be used for functional mapping of cortical areas and is therefore valuable in situations where stimulus locked activity can not be measured.

Brain Mapping

Confidence limits for the parameter estimation in the dipole localization method on the basis of spatial correlation of background EEG.

A new residual function in the inverse problem of equivalent dipole localization methods is proposed which is based on the spatial correlation of the background EEG. This residual has the advantage that it allows the calculation of confidence limits for dipole model parameters. The method was applied to VEP data, and it was studied how the localization precision depends on the recording time of the EEG. It was found that the tangential position of an equivalent dipole can be located at 99% confidence in a region of the order 7 x 7mm for a head radius of 10cm, while the 99% confidence interval of the depth estimate is approximately 1cm, with a recording time of 20 minutes. It was also observed that an EEG recording time of more than 10-15 minutes is needed to obtain stable localization precision estimates.

Brain

Visual stimulation reduces EEG activity in man.

Data are presented which show that background electric activity of the human brain is reduced by visual stimulation. Occipital EEG amplitude decreases 5-15% for all frequencies analyzed (0.2-40 Hz) upon pattern stimulation. The reduction is stimulus-specific, i.e. is the strongest for stimuli that activate a large number of visual cortical neurons.

Electroencephalography

Color opponency in cone-driven horizontal cells in carp retina. Aspecific pathways between cones and horizontal cells.

The spectral and dynamic properties of cone-driven horizontal cells in carp retina were evaluated with silent substitution stimuli and/or saturating background illumination. The aim of this study was to describe the wiring underlying the spectral sensitivity of these cells. We will present electrophysiological data that indicate that all cone-driven horizontal cell types receive input from all spectral cone types, and we will present evidence that all cone-driven horizontal cell types feedback to all spectral cone types. These two findings are the basis for a model for the spectral and dynamic behavior of all cone-driven horizontal cells in carp retina. The model can account for the spectral as well as the dynamic behavior of the horizontal cells. It will be shown that the strength of the feedforward and feedback pathways between a horizontal cell and a particular spectral cone type are roughly proportional. This model is in sharp contrast to the Stell model, where the spectral behavior of the three horizontal cell types is explained by a cascade of feedforward and feedback pathways between cones and horizontal cells. The Stell model accounts for the spectral but not for the dynamic behavior of the horizontal cells.

Animals

Lateral feedback from monophasic horizontal cells to cones in carp retina. I. Experiments.

The spatial and color coding of the monophasic horizontal cells were studied in light- and dark-adapted retinae. Slit displacement experiments revealed differences in integration area for the different cone inputs of the monophasic horizontal cells. The integration area measured with a 670-nm stimulus was larger than that measured with a 570-nm stimulus. Experiments in which the diameter of the test spot was varied, however, revealed at high stimulus intensities a larger summation area for 520-nm stimuli than for 670-nm stimuli. The reverse was found for low stimulus intensities. To investigate whether these differences were due to interaction between the various cone inputs to the monophasic horizontal cell, adaptation experiments were performed. It was found that the various cone inputs were not independent. Finally, some mechanisms for the spatial and color coding will be discussed.

Animals

Lateral feedback from monophasic horizontal cells to cones in carp retina. II. A quantitative model.

About half of the monophasic horizontal cells in carp retina receive input from both red- and green-sensitive cones. Since the horizontal cells feed back to cones, the color and feedback pathways result in wavelength- and intensity-dependent changes of the dynamics and of the receptive field amplitude profile of the horizontal cell responses. In this paper we present a quantitative model that describes adequately the color and spatial coding and the dynamics of the responses from monophasic horizontal cells in carp. Lateral feedback plays a distinct role in this model.

Animals

Spatial patterns of visual cortical fast EEG during conditioned reflex in a rhesus monkey.

A preliminary assay was made of the existence of time-space coherence patterns of fast EEG activity in the visual cortex of a Rhesus monkey. The primary intent of the present study was to evaluate the similarities and differences in relation to the olfactory bulb, where such coherences have been described and have been demonstrated to be associated with behaviour. Segments 1.5 s in duration were recorded simultaneously without averaging from 16 to 35 subdural electrodes fixed over the left occipital lobe in an array 3.6 cm X 2.8 cm. Each segment was taken during the delivery of a visual conditioned stimulus (CS) and the performance of a conditioned response (CR) by a well-trained Rhesus monkey. The EEGs appeared chaotic with irregular bursts lasting 75-200 ms, resembling those in the olfactory EEG but with lower peak frequencies. Fourier spectra showed broad distributions of power resembling '1/f noise' with multiple peaks in the range of 20-40 Hz. Time intervals were selected where coherent activity seemed to be present at a number of electrodes. A dominant component waveform that was common to all channels was extracted by principal components analysis (PCA) of each segment. The distribution of the power of this component across the electrodes (the factor loadings) was used to describe the spatial pattern of the coherent cortical activity. Statistical analyses suggested that different patterns could be associated to the CS and the CR, as has been found in the olfactory system. These patterns remained stable over a 6 week recording interval. The patterns can be better discriminated, when the factor loadings of each channel are normalized to zero mean and unit variance, to discard a basic pattern of power distribution, which may reflect anatomical and electrode positioning factors that are related to behavioral information processing by the cortex. The wide spatial distribution of the common patterns found suggests that EEG patterns that manifest differing states of the visual cortex may also be accessible with scalp electrodes.

Animals

The variation in the light responses of carp retinal ganglion cells is independent of response amplitude.

The variation of the response rate of carp retinal ganglion cells to photopic light stimulation was studied. It was found that the standard deviation was independent of the mean of the response rate, even when responses showed compression. This finding is in agreement with a late origin of retinal noise. Implications of the existence of intrinsic constant amplitude retinal noise and of the presence of a mean maintained activity are discussed.

Action Potentials

Principal components analysis for source localization of VEPs in man.

This study defines and compares the topologies of the visual evoked potentials to various stimuli such as pattern onset/offset, pattern reversal, pattern motion and high frequency luminance flicker. The responses recorded from 24 occipital derivations were examined using a three sphere conductance model to represent the head, with the assumption that activity from an underlying cortical source is equivalent to a single dipole. Principal components analysis was used to find the dimensionality of the data space. From this analysis could be concluded that all stimuli evoked responses in the primary visual cortex. Only pattern onset, and to a lesser degree pattern offset and pattern reversal, yielded activity in higher visual areas. In particular it has been shown that the CI, CII interval of the pattern onset response has its origins in two different cortical regions. A fast positive (CI)-negative (part of the CII) component arises from area 18 (or 19), a slower negative (initial part of CII) component comes from area 17.

Evoked Potentials, Visual

Linear color opponency in carp retinal ganglion cells.

Double opponent (i.e. red/green cone opponent in center and surround of the receptive field) ganglion cells in photopic carp retina were studied. It was found that a subclass of these cells (about 30%) was linearly opponent. For these cells the response to stimulation of the receptive field center could be constructed by summation of the responses due to stimulation of the red and green cone components separately. These linear opponent cells had smaller receptive field sizes than the nonlinear double opponent ganglion cells. Both strong (i.e. showing a marked sign inversion when wavelength is varied) and weak color opponency (i.e. showing no such inversion) can be found in the same linear double opponent ganglion cells. It is shown that such different behaviour can be understood from the change in amplitude, when intensity is varied, of the red and green cone components of the center responses of the cells. For small spots and low intensities, the red cone component dominates, which results in weak opponency; for large spots or high intensities strong opponency is observed.

Action Potentials

Color fundamentals deduced from carp ganglion cell responses.

Retinal ganglion cell responses were used to derive the action spectra (fundamentals) of the photopic color mechanisms in carp. Both silencing and chromatic adaptation techniques were used. The former proved to be more successful than the latter, because weak (even subthreshold) dynamic signals in one mechanism (mostly the red) caused strong effects on the other mechanisms. With chromatic adaptation these interacting signals were unavoidable, whereas with the silencing technique the modulation of the silenced mechanism was eliminated. The resultant pure action spectra agree well with the electrophysiological data of cone pedicles and horizontal cells. They differ, however, from the log-absorption specta found by microspectrophotometry. Apart from the differences in the slope of the long wavelength tails, the spectra also differ in the short wavelength region. The latter may indicate that in A-2 pigments, the beta-band absorption has a lower efficiency than the main-band absorption.

Action Potentials