Pontine and Collicular Inputs to Forel�s Field Neurons Generating Vertical Saccades in the Alert Cat

2015 ◽  
pp. 183-196
Author(s):  
Shozo Nakao ◽  
Yoshimitsu Shiraishi ◽  
Wen-Bin Li
Keyword(s):  
Alert Cat ◽  
Vertical Saccades

Synaptic responses of red nucleus neurons in the alert cat to cortical and cerebellar inputs

1987 ◽  
Vol 73 (1) ◽  
pp. 38-42 ◽  
Author(s):  
V.V. Fanardjian ◽  
J.S. Sarkissian ◽  
I.A. Manvelian
Keyword(s):  
Red Nucleus ◽  
Alert Cat ◽  
Synaptic Responses

scholarly journals Multisensory Integration in the Superior Colliculus of the Alert Cat

1998 ◽  
Vol 80 (2) ◽  
pp. 1006-1010 ◽  
Author(s):  
Mark T. Wallace ◽  
M. Alex Meredith ◽  
Barry E. Stein
Keyword(s):  
Superior Colliculus ◽  
Multisensory Integration ◽  
Sensory Response ◽  
Functional Link ◽  
Sensory Stimuli ◽  
Response Properties ◽  
Alert Cat

Wallace, Mark T., M. Alex Meredith, and Barry E. Stein. Multisensory integration in the superior colliculus of the alert cat. J. Neurophysiol. 80: 1006–1010, 1998. The modality convergence patterns, sensory response properties, and principles governing multisensory integration in the superior colliculus (SC) of the alert cat were found to have fundamental similarities to those in anesthetized animals. Of particular interest was the observation that, in a manner indistinguishable from the anesthetized animal, combinations of two different sensory stimuli significantly enhanced the responses of SC neurons above those evoked by either unimodal stimulus. These observations are consistent with the speculation that there is a functional link among multisensory integration in individual SC neurons and cross-modality attentive and orientation behaviors.

scholarly journals Bilateral control of interceptive saccades: evidence from the ipsipulsion of vertical saccades after caudal fastigial inactivation

2021 ◽  
Author(s):  
Clara Bourrelly ◽  
Julie Quinet ◽  
Laurent Goffart
Keyword(s):  
Purkinje Cells ◽  
Visual Target ◽  
Strongly Correlated ◽  
Bilateral Control ◽  
Target Speed ◽  
Burst Neurons ◽  
Oculomotor Vermis ◽  
Vertical Saccades ◽  
Saccade Size ◽  
Saccade Velocity

The caudal fastigial nuclei (cFN) are the output nuclei by which the medio-posterior cerebellum influences the production of saccades toward a visual target. On the basis of the organization of their efferences to the premotor burst neurons and the bilateral control of saccades, the hypothesis was proposed that the same unbalanced activity accounts for the dysmetria of all saccades during cFN unilateral inactivation, regardless of whether the saccade is horizontal, oblique, or vertical. We further tested this hypothesis by studying, in two head-restrained macaques, the effects of unilaterally inactivating the caudal fastigial nucleus on saccades toward a target moving vertically with a constant, increasing or decreasing speed. After local muscimol injection, vertical saccades were deviated horizontally toward the injected side with a magnitude that increased with saccade size. The ipsipulsion indeed depended upon the tested target speed, but not its instantaneous value because it did not increase (decrease) when the target accelerated (decelerated). By subtracting the effect on contralesional horizontal saccades from the effect on ipsilesional ones, we found that the net bilateral effect on horizontal saccades was strongly correlated with the effect on vertical saccades. We explain how this correlation corroborates the bilateral hypothesis and provide arguments against the suggestion that instantaneous saccade velocity would somehow be "encoded" by the discharge of Purkinje cells in the oculomotor vermis.

Activity of Mesencephalic Vertical Burst Neurons During Saccades and Smooth Pursuit

2000 ◽  
Vol 83 (4) ◽  
pp. 2080-2092 ◽  
Author(s):  
M. Missal ◽  
S. de Brouwer ◽  
P. Lefèvre ◽  
E. Olivier
Keyword(s):  
Vertical Velocity ◽  
Smooth Pursuit ◽  
Medial Longitudinal Fasciculus ◽  
Eye Position ◽  
Interstitial Nucleus Of Cajal ◽  
Burst Neurons ◽  
Preferred Direction ◽  
Saccade Onset ◽  
Vertical Saccades ◽  
Eye Velocity

The activity of vertical burst neurons (BNs) was recorded in the rostral interstitial nucleus of the medial longitudinal fasciculus (riMLF-BNs) and in the interstitial nucleus of Cajal (NIC-BNs) in head-restrained cats while performing saccades or smooth pursuit. BNs emitted a high-frequency burst of action potentials before and during vertical saccades. On average, these bursts led saccade onset by 14 ± 4 ms (mean ± SD, n = 23), and this value was in the range of latencies (∼5–15 ms) of medium-lead burst neurons (MLBNs). All NIC-BNs ( n = 15) had a downward preferred direction, whereas riMLF-BNs showed either a downward ( n = 3) or an upward ( n = 5) preferred direction. We found significant correlations between saccade and burst parameters in all BNs: vertical amplitude was correlated with the number of spikes, maximum vertical velocity with maximum of the spike density, and saccade duration with burst duration. A correlation was also found between instantaneous vertical velocity and neuronal activity during saccades. During fixation, all riMLF-BNs and ∼50% of NIC-BNs (7/15) were silent. Among NIC-BNs active during fixation (8/15), only two cells had an activity correlated with the eye position in the orbit. During smooth pursuit, most riMLF-BNs were silent (7/8), but all NIC-BNs showed an activity that was significantly correlated with the eye velocity. This activity was unaltered during temporary disappearance of the visual target, demonstrating that it was not visual in origin. For a given neuron, its on-direction during smooth pursuit and saccades remained identical. The activity of NIC-BNs during both saccades and smooth pursuit can be described by a nonlinear exponential function using the velocity of the eye as independent variable. We suggest that riMLF-BNs, which were not active during smooth pursuit, are vertical MLBNs responsible for the generation of vertical saccades. Because NIC-BNs discharged during both saccades and pursuit, they cannot be regarded as MLBNs as usually defined. NIC-BNs could, however, be the site of convergence of both the saccadic and smooth pursuit signals at the premotoneuronal level. Alternatively, NIC-BNs could participate in the integration of eye velocity to eye position signals and represent input neurons to a common integrator.

Acute Superior Oblique Palsy in Monkeys: II. Changes in Dynamic Properties during Vertical Saccades

2007 ◽  
Vol 48 (6) ◽  
pp. 2612 ◽  
Author(s):  
Xiaoyan Shan ◽  
Howard S. Ying ◽  
Jing Tian ◽  
Christian Quaia ◽  
Mark F. Walker ◽  
...  
Keyword(s):  
Dynamic Properties ◽  
Superior Oblique Palsy ◽  
Vertical Saccades ◽  
Superior Oblique

Brain Stem Omnipause Neurons and the Control of CombinedEye-Head Gaze Saccades in the Alert Cat

1998 ◽  
Vol 79 (6) ◽  
pp. 3060-3076 ◽  
Author(s):  
Martin Paré ◽  
Daniel Guitton
Keyword(s):  
Gaze Control ◽  
Error Signal ◽  
Gaze Shifts ◽  
Gaze Shift ◽  
The Gaze ◽  
Alert Cat ◽  
Motor Error ◽  
Omnipause Neurons ◽  
Gaze Saccades ◽  
Stimulation Of

Paré, Martin and Daniel Guitton. Brain stem omnipause neurons and the control of combined eye-head gaze saccades in the alert cat. J. Neurophysiol. 79: 3060–3076, 1998. When the head is unrestrained, rapid displacements of the visual axis—gaze shifts (eye-re-space)—are made by coordinated movements of the eyes (eye-re-head) and head (head-re-space). To address the problem of the neural control of gaze shifts, we studied and contrasted the discharges of omnipause neurons (OPNs) during a variety of combined eye-head gaze shifts and head-fixed eye saccades executed by alert cats. OPNs discharged tonically during intersaccadic intervals and at a reduced level during slow perisaccadic gaze movements sometimes accompanying saccades. Their activity ceased for the duration of the saccadic gaze shifts the animal executed, either by head-fixed eye saccades alone or by combined eye-head movements. This was true for all types of gaze shifts studied: active movements to visual targets; passive movements induced by whole-body rotation or by head rotation about stationary body; and electrically evoked movements by stimulation of the caudal part of the superior colliculus (SC), a central structure for gaze control. For combined eye-head gaze shifts, the OPN pause was therefore not correlated to the eye-in-head trajectory. For instance, in active gaze movements, the end of the pause was better correlated with the gaze end than with either the eye saccade end or the time of eye counterrotation. The hypothesis that cat OPNs participate in controlling gaze shifts is supported by these results, and also by the observation that the movements of both the eyes and the head were transiently interrupted by stimulation of OPNs during gaze shifts. However, we found that the OPN pause could be dissociated from the gaze-motor-error signal producing the gaze shift. First, OPNs resumed discharging when perturbation of head motion briefly interrupted a gaze shift before its intended amplitude was attained. Second, stimulation of caudal SC sites in head-free cat elicited large head-free gaze shifts consistent with the creation of a large gaze-motor-error signal. However, stimulation of the same sites in head-fixed cat produced small “goal-directed” eye saccades, and OPNs paused only for the duration of the latter; neither a pause nor an eye movement occurred when the same stimulation was applied with the eyes at the goal location. We conclude that OPNs can be controlled by neither a simple eye control system nor an absolute gaze control system. Our data cannot be accounted for by existing models describing the control of combined eye-head gaze shifts and therefore put new constraints on future models, which will have to incorporate all the various signals that act synergistically to control gaze shifts.

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