Differential responses of “simple” and “complex” cells of cat's striate cortex during saccadic eye movements

1980 ◽  
Vol 20 (6) ◽  
pp. 553-556 ◽  
Author(s):  
M. Kimura ◽  
Y. Komatsu ◽  
K. Toyama
1988 ◽  
Vol 1 (1) ◽  
pp. 135-143 ◽  
Author(s):  
James T. McIlwain

AbstractEye movements were recorded with the scleral search coil method while striate cortex (area 17) was stimulated in alert cats with their heads fixed. Regardless of where stimulation was applied in the retinotopic map, eye position at the onset of stimulation strongly affected the amplitudes of evoked saccades, but had much less influence on their directions. Application of long stimulus trains evoked repeated saccades at all sites tested. Highly convergent or goal-directed saccades were not observed. Cortically evoked saccades appeared to habituate with repeated stimulation and had higher thresholds and longer latencies that those reported for saccades evoked from the superior colliculus. The directions of cortically evoked saccades generally agreed with those predicted from the retinotopic coordinates of the stimulus sites, but saccade amplitudes were usually lower than expected. It is suggested that these findings are consistent with certain characteristics of eye-head coordination in the cat's normal visual orienting behavior. The results are difficult to reconcile with the hypothesis that goal-directed saccades are a normal response to targets outside the cat's oculomotor range.


1998 ◽  
Vol 18 (19) ◽  
pp. 8086-8094 ◽  
Author(s):  
Judith A. Hirsch ◽  
Christine A. Gallagher ◽  
José-Manuel Alonso ◽  
Luis M. Martinez

2005 ◽  
Vol 93 (1) ◽  
pp. 1-19 ◽  
Author(s):  
E. J. Tehovnik ◽  
W. M. Slocum ◽  
C. E. Carvey ◽  
P. H. Schiller

The purpose of this review is to critically examine phosphene induction and saccadic eye movement generation by electrical microstimulation of striate cortex (area V1) in humans and monkeys. The following issues are addressed: 1) Properties of electrical stimulation as they pertain to the activation of V1 elements; 2) the induction of phosphenes in sighted and blind human subjects elicited by electrical stimulation using various stimulation parameters and electrode types; 3) the induction of phosphenes with electrical microstimulation of V1 in monkeys; 4) the generation of saccadic eye movements with electrical microstimulation of V1 in monkeys; and 5) the tasks involved for the development of a cortical visual prosthesis for the blind. In this review it is concluded that electrical microstimulation of area V1 in trained monkeys can be used to accelerate the development of an effective prosthetic device for the blind.


1984 ◽  
Vol 1 (4) ◽  
pp. 207-222 ◽  
Author(s):  
Keisuke Toyama ◽  
Minoru Kimura ◽  
Yukio Komatsu

2000 ◽  
Vol 12 (5) ◽  
pp. 1057-1066 ◽  
Author(s):  
Brian Blais ◽  
Leon N. Cooper ◽  
Harel Shouval

Most simple and complex cells in the cat striate cortex are both orientation and direction selective. In this article we use single-cell learning rules to develop both orientation and direction selectivity in a natural scene environment. We show that a simple principal component analysis rule is inadequate for developing direction selectivity, but that the BCM rule as well as similar higher-order rules can. We also demonstrate that the convergence of lagged and nonlagged cells depends on the velocity of motion in the environment, and that strobe rearing disrupts this convergence, resulting in a loss of direction selectivity.


1995 ◽  
Vol 12 (5) ◽  
pp. 805-817 ◽  
Author(s):  
N.v. Swindale

AbstractThis paper examines how the responses of cells in area 17 of the cat vary as a function of the vernier offset between a bright and a dark bar. The study was prompted by the finding that human vernier acuity is reduced for bars or edges of opposite contrast sign (Mather & Morgan, 1986; O'Shea & Mitchell, 1990). Both simple and complex cells showed V-shaped tuning curves for reverse contrast stimuli: i.e. response was minimum at alignment, and increased with increasing vernier offset. For vernier bars with the same contrast sign, γ-shaped tuning curves were found, as reported earlier (Swindale & Cynader, 1986). Sensitivity to offset was inversely correlated in the two paradigms. However, complex cells with high sensitivity to offsets in a normal vernier stimulus were significantly less sensitive to offsets in reverse contrast stimuli. A cell's response to a vernier stimulus in which both bars are bright can be predicted by the shape of its orientation tuning curve, if the vernier stimulus is approximated by a single bar with an orientation equal to that of a line joining the midpoints of the two component bars (Swindale & Cynader, 1986). This approximation did not hold for the reverse contrast condition: orientation tuning curves for compound barswere broad and shallow, rather than bimodal, with peaks up to 40 deg from the preferred orientation. Results from simple cells were compared with predictions made by a linear model of the receptive field. The model predicted the V-shaped tuning curves found for reverse contrast stimuli. It also predicted that absolute values of tuning slopes for vernier offsets in reverse contrast stimuli might sometimes be higher than with normal stimuli. This was observed in some simple cells. The model was unable to explain the shape of orientation tuning curves for compound bars, nor could it explain the breakdown of the equivalent orientation approximation.


1977 ◽  
Vol 40 (1) ◽  
pp. 74-94 ◽  
Author(s):  
C. W. Mohler ◽  
R. H. Wurtz

1. We studied the effect of lesions placed in striate cortex or superior colliculus on the detection of visual stimuli and the accuracy of saccadic eye movements. The monkeys (Macaca mulatta) first learned to respond to a 0.25 degrees spot of light flashed for 150-200 ms in one part of the visual field while they were fixating in order to determine if they could detect the light. The monkeys also learned in a different task to make a saccade to the spot of light when the fixation point went out, and the accuracy of the saccades was measured. 2. Following a unilateral partial ablation of the striate cortex in two monkeys they could not detect the spot of light in the resulting scotoma or saccade to it. The deficit was only relative; if we increased the brightness of the stimulus from the usual 11 cd/m2 to 1,700 cd/m2 against a background of 1 cd/m2 the monkeys were able to detect and to make a saccade to the spot of light. 3. Following about 1 mo of practice on the detection and saccade tasks, the monkeys recovered the ability to detect the spots of light and to make saccades to them without gross errors (saccades made beyond an area of +/-3 average standard deviations). Lowering the stimulus intensity reinstated both the detection and saccadic errors...


2003 ◽  
Vol 17 (4) ◽  
pp. 870-878 ◽  
Author(s):  
Edward J. Tehovnik ◽  
Warren M. Slocum ◽  
Peter H. Schiller

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