Smooth eye movement response to complex motion sequences.

Author(s):  
Julie Mapes Lindholm ◽  
Paul A. Wetzel ◽  
Timothy M. Askins
2021 ◽  
Vol 54 (13) ◽  
pp. 311-316
Author(s):  
Vladislav Prud ◽  
Arthur Mukhamedov ◽  
Ernest Sleptsov ◽  
Olga Andrianova ◽  
Viktor Chertopolokhov ◽  
...  

2011 ◽  
Vol 43 (3) ◽  
pp. 879-887 ◽  
Author(s):  
Cameron B. Jeter ◽  
Saumil S. Patel ◽  
Anne B. Sereno

1992 ◽  
Vol 31 (6) ◽  
pp. 626-629 ◽  
Author(s):  
E. Gordon ◽  
S. Coyle ◽  
J. Anderson ◽  
P. Healey ◽  
J. Cordaro ◽  
...  

2021 ◽  
Vol 11 (4) ◽  
pp. 557-566
Author(s):  
Ian S. Curthoys

I list a summary of the major clinical observations of SVIN in patients with total unilateral vestibular loss (TUVL) and show how basic results from neurophysiology can explain these clinical observations. The account integrates results from single neuron recordings of identified semicircular canal and otolith afferent neurons in guinea pigs in response to low frequency skull vibration with evidence of the eye movement response in cats to selective semicircular canal stimulation (both individual and combined) and a simple model of nystagmus generation to show how these results explain most of the major characteristics of SVIN.


1996 ◽  
Vol 76 (5) ◽  
pp. 3136-3148 ◽  
Author(s):  
K. M. McConville ◽  
R. D. Tomlinson ◽  
E. Q. NA

1. Secondary position-vestibular-pause (PVP) neurons in the vestibuloocular reflex (VOR) pathway of adult rhesus monkeys were studied during combined semicircular canal and otolith stimulation. The head was rotated at 0.5 Hz with the axis of rotation centered between the otolith organs (on-axis, ON) and with the axis of rotation 23 cm in front of the otoliths (off-axis, OFF). Both conditions were tested with two different vergence angles by the use of 14-cm (near target, NT) and 100-cm (far target, FT) targets. 2. The tangential translational stimulus to the otoliths in the OFF trials should result in a compensatory eye movement that is opposite in direction to that resulting from the angular stimulus to the canals. The otolith stimulus should be great enough to reverse the eye movement response in the NT OFF trials according to geometric calculations. This reversal in eye movement direction occurred as expected although the latency of the reversal (70 ms) was somewhat greater than expected and the magnitude of the reversal was less than predicted solely on the basis of geometric considerations. 3. The responses of the PVP neurons were corrected for eye position sensitivity to investigate the head movement response components. The amplitude of the response in 22 of 24 PVP cells was reduced in the NT OFF condition compared with the FT OFF condition. This difference was not sufficient in itself to explain the observed reversal in eye movement response. 4. The average sensitivities of the neurons to rotation during the FT and NT ON trials were 1.38 and 1.41 spikes.s-1.deg-1.s-1, respectively. This is too small an increase to account for the increase in the angular VOR gain with near targets (approximately 25%); therefore cells other than PVP neurons must be responsible. 5. The average sensitivities of the PVP neurons to translational accelerations obtained from the FT and NT OFF trials were 305 and 484 spikes.s-1.g-1, respectively, which is higher than most otolith afferent sensitivities reported for 0.5-Hz stimuli in the literature. The otolith component is modified by ocular convergence (59% increase in sensitivity), but this increase is too small to account for the change in the translational VOR gain between the two conditions. 6. Although recordings were only obtained from seven eye-head-velocity cells, the results indicate that these neurons may provide the additional signals not present in the PVP cells. These neurons exhibited large differences between ON and OFF rotations and were found to substantially increase their modulation during the NT conditions compared with that observed during the FT conditions.


1999 ◽  
Author(s):  
David S. Wooding ◽  
Geraint M. Roberts ◽  
Jane Phillips-Hughes

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