A neural model of the saccade generator in the reticular formation

A neural model is developed of the neural circuitry in the reticular formation that is used to generate saccadic eye movements. The model simulates the behavior of identified cell types-such as long-lead burst neurons, short-lead excitatory and inhibitory burst neurons, omnipause neurons, and tonic neurons-under many experimental conditions. Simulated phenomena include: saccade staircases, duration and amplitude of cell discharges for saccades of variable amplitude, component stretching to achieve straight oblique saccades, saturation of saccade velocity after saturation of saccade amplitude in response to high stimulation frequencies, trade-offs between saccade velocity and duration to generate constant saccade amplitude, conservation of saccade amplitude in response to sufficiently brief stimulation of omnipause neurons, and high velocity smooth eye movements evoked by high levels of electrical stimulation of the superior colliculus. Previous saccade generator models have not explained this range of data. These models have also invoked mechanisms for which no neurophysiological evidence has been forthcoming, such as resetable integrators, perfect integrators, or target position movement commands. The present model utilizes only known reticular formation neurons. It suggests that a key part of the feedback loop within the saccade generator is realized by inhibitory feedback from short-lead to long-lead burst neurons, in response to excitatory feedforward signals from long-lead to short-lead burst neurons. When this property is combined with opponent interactions between agonist and antagonist muscle-controlling neurons, and motor error, or vector, inputs from the superior colliculus and other saccade-controlling brain regions, all of the above data can be explained. Taken together, these components generate a saccade reset cycle whereby activation of long-lead burst neurons inhibits omnipause neurons and thereby disinhibits short-lead excitatory burst neurons. The excitatory short-lead burst neurons can then respond to excitatory inputs from the long-lead burst neurons. Outputs from the excitatory short-lead burst neurons are integrated by the tonic cells while they also inhibit the long-lead burst neurons via inhibitory burst interneurons. When this inhibition is complete, the omnipause neurons are disinhibited. The omnipause neurons can then, once again, inhibit the short-lead burst neurons, whose inhibition of the long-lead burst neurons is thereby removed. The saccadic cycle can then begin again. In response to sustained electrical input, this cycle generates a staircase of identical saccades whose properties match the data much better than the staircases proposed by alternative models. A comparative analysis of the hypotheses and predictive capabilities of other saccade generator models is provided.

[1]  David L. Sparks,et al.  Movement fields of saccade-related burst neurons in the monkey superior colliculus , 1980, Brain Research.

[2]  M. J. Nichols,et al.  Nonstationary properties of the saccadic system: new constraints on models of saccadic control. , 1995, Journal of neurophysiology.

[3]  S. Grossberg,et al.  A neural model of saccadic eye movement control explains task-specific adaptation , 1999, Vision Research.

[4]  C. Scudder A new local feedback model of the saccadic burst generator. , 1988, Journal of neurophysiology.

[5]  M. J. Nichols,et al.  Component stretching during oblique stimulation-evoked saccades: the role of the superior colliculus. , 1996, Journal of neurophysiology.

[6]  D. Munoz,et al.  Comparison of the discharge characteristics of brain stem omnipause neurons and superior colliculus fixation neurons in monkey: implications for control of fixation and saccade behavior. , 1998, Journal of neurophysiology.

[7]  D. Signorini,et al.  Neural networks , 1995, The Lancet.

[8]  A. Fuchs,et al.  Characteristics and functional identification of saccadic inhibitory burst neurons in the alert monkey. , 1988, Journal of neurophysiology.

[9]  E. Keller,et al.  Colliculoreticular organization in primate oculomotor system. , 1977, Journal of neurophysiology.

[10]  J. Cronly-Dillon,et al.  Vision and visual dysfunction. , 1994, Journal of cognitive neuroscience.

[11]  E. Keller,et al.  Use of interrupted saccade paradigm to study spatial and temporal dynamics of saccadic burst cells in superior colliculus in monkey. , 1994, Journal of neurophysiology.

[12]  Stephen Grossberg,et al.  Studies of mind and brain , 1982 .

[13]  R. Wurtz,et al.  Fixation cells in monkey superior colliculus. II. Reversible activation and deactivation. , 1993, Journal of neurophysiology.

[14]  S. Gielen,et al.  A quantitative analysis of generation of saccadic eye movements by burst neurons. , 1981, Journal of neurophysiology.

[15]  R. Wurtz,et al.  Fixation cells in monkey superior colliculus. I. Characteristics of cell discharge. , 1993, Journal of neurophysiology.

[16]  S. Grossberg,et al.  A Neural Model of Multimodal Adaptive Saccadic Eye Movement Control by Superior Colliculus , 1997, The Journal of Neuroscience.

[17]  A. Hodgkin The conduction of the nervous impulse , 1964 .

[18]  S. Grossberg Contour Enhancement , Short Term Memory , and Constancies in Reverberating Neural Networks , 1973 .

[19]  Peter H. Schiller,et al.  The effect of superior colliculus ablation on saccades elicted by cortical stimulation , 1977, Brain Research.

[20]  L M Optican,et al.  Model with distributed vectorial premotor bursters accounts for the component stretching of oblique saccades. , 1997, Journal of neurophysiology.

[21]  P. Bach-y-Rita,et al.  Basic Mechanisms of Ocular Motility and Their Clinical Implications , 1976 .

[22]  Stephen Grossberg,et al.  Neural dynamics of adaptive sensory-motor control : ballistic eye movements , 1986 .

[23]  A. Fuchs,et al.  Activity of brain stem neurons during eye movements of alert monkeys. , 1972, Journal of neurophysiology.

[24]  R. Wurtz,et al.  Saccade-related activity in monkey superior colliculus. II. Spread of activity during saccades. , 1995, Journal of neurophysiology.

[25]  R. Wurtz,et al.  Saccade-related activity in monkey superior colliculus. I. Characteristics of burst and buildup cells. , 1995, Journal of neurophysiology.

[26]  J. Gnadt,et al.  Analysis of the step response of the saccadic feedback: computational models , 1997, Experimental Brain Research.

[27]  H Shimazu,et al.  Monosynaptic activation of medium-lead burst neurons from the superior colliculus in the alert cat. , 1996, Journal of neurophysiology.

[28]  E. Keller Participation of medial pontine reticular formation in eye movement generation in monkey. , 1974, Journal of neurophysiology.

[29]  Peter Ford Dominey,et al.  A cortico-subcortical model for generation of spatially accurate sequential saccades. , 1992, Cerebral cortex.

[30]  N. J. Gandhi,et al.  Spatial distribution and discharge characteristics of superior colliculus neurons antidromically activated from the omnipause region in monkey. , 1997, Journal of neurophysiology.

[31]  P. Schiller,et al.  Single-unit recording and stimulation in superior colliculus of the alert rhesus monkey. , 1972, Journal of neurophysiology.

[32]  D. Sparks,et al.  Site and parameters of microstimulation: evidence for independent effects on the properties of saccades evoked from the primate superior colliculus. , 1996, Journal of neurophysiology.