The electroretinogram, visual evoked potentials and spike discharges in the visual cortex of the albino rat

1969 ◽  
Vol 27 (7) ◽  
pp. 657
2020 ◽  
Vol 1 (1) ◽  
Author(s):  
Sae Kaneko ◽  
Ichiro Kuriki ◽  
Søren K Andersen

Abstract Colors are represented in the cone-opponent signals, L-M versus S cones, at least up to the level of inputs to the primary visual cortex. We explored the hue selective responses in early cortical visual areas through recordings of steady-state visual evoked potentials (SSVEPs), elicited by a flickering checkerboard whose color smoothly swept around the hue circle defined in a cone-opponent color space. If cone opponency dominates hue representation in the source of SSVEP signals, SSVEP amplitudes as a function of hue should form a profile that is line-symmetric along the cardinal axes of the cone-opponent color space. Observed SSVEP responses were clearly chromatic ones with increased SSVEP amplitudes and reduced response latencies for higher contrast conditions. The overall elliptic amplitude profile was significantly tilted away from the cardinal axes to have the highest amplitudes in the “lime-magenta” direction, indicating that the hue representation in question is not dominated by cone-opponency. The observed SSVEP amplitude hue profile was better described as a summation of a perceptual response and cone-opponent responses with a larger weight to the former. These results indicate that hue representations in the early visual cortex, measured by the SSVEP technique, are possibly related to perceptual color contrast.


2008 ◽  
Vol 21 (2) ◽  
pp. 86-92 ◽  
Author(s):  
Whittingstall Kevin ◽  
Wilson Doug ◽  
Schmidt Matthias ◽  
Stroink Gerhard

Sensors ◽  
2019 ◽  
Vol 19 (22) ◽  
pp. 4890
Author(s):  
Torsten Straßer ◽  
Susanne Kramer ◽  
Melanie Kempf ◽  
Tobias Peters ◽  
Anne Kurtenbach ◽  
...  

The aim of this study was to investigate the use of inexpensive and easy-to-use hydrogel “marble” electrodes for the recording of electrical potentials of the human visual cortex using visual evoked potentials (VEPs) as example. Top hat-shaped holders for the marble electrodes were developed with an electrode cap to acquire the signals. In 12 healthy volunteers, we compared the VEPs obtained with conventional gold-cup electrodes to those obtained with marble electrodes. Checkerboards of two check sizes—0.8° and 0.25°—were presented. Despite the higher impedance of the marble electrodes, the line noise could be completely removed by averaging 64 single traces, and VEPs could be recorded. Linear mixed-effect models using electrode type, stimulus, and recording duration revealed a statistically significant effect of the electrode type on only VEP N75 peak latency (mean ± SEM: 1.0 ± 1.2 ms) and amplitude (mean ± SEM: 0.8 ± 0.9 µV) The mean amplitudes of the delta, theta, alpha, beta, and gamma frequency bands of marble electrodes were statistically significantly different and, on average, 25% higher than those of gold-cup electrodes. However, the mean amplitudes showed a statistically significant strong correlation (Pearson’s r = 0.8). We therefore demonstrate the potential of the inexpensive and efficient hydrogel electrode to replace conventional gold-cup electrodes for the recording of VEPs and possibly other recordings from the human cortex.


i-Perception ◽  
2018 ◽  
Vol 9 (1) ◽  
pp. 204166951775271 ◽  
Author(s):  
Valerie Nunez ◽  
Robert M. Shapley ◽  
James Gordon

In the early visual cortex V1, there are currently only two known neural substrates for color perception: single-opponent and double-opponent cells. Our aim was to explore the relative contributions of these neurons to color perception. We measured the perceptual scaling of color saturation for equiluminant color checkerboard patterns (designed to stimulate double-opponent neurons preferentially) and uniformly colored squares (designed to stimulate only single-opponent neurons) at several cone contrasts. The spatially integrative responses of single-opponent neurons would produce the same response magnitude for checkerboards as for uniform squares of the same space-averaged cone contrast. However, perceived saturation of color checkerboards was higher than for the corresponding squares. The perceptual results therefore imply that double-opponent cells are involved in color perception of patterns. We also measured the chromatic visual evoked potential (cVEP) produced by the same stimuli; checkerboard cVEPs were much larger than those for corresponding squares, implying that double-opponent cells also contribute to the cVEP response. The total Fourier power of the cVEP grew sublinearly with cone contrast. However, the 6-Hz Fourier component’s power grew linearly with contrast-like saturation perception. This may also indicate that cortical coding of color depends on response dynamics.


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