Because eye muscles never cocontract and do not deal with external loads, one can write an equation that relates motoneuron firing rate to eye position and velocity - a very uncommon situation in the CNS. The semicircular canals transduce head velocity in a linear manner by using a high background discharge rate, imparting linearity to the premotor circuits that generate eye movements. This has allowed deducing some of the signal processing involved, including a neural network that integrates. These ideas are often summarized by block diagrams. Unfortunately, they are of little value in describing the behavior of single neurons - a fmding supported by neural network models.

Because eye muscles never cocontract and do not deal with external loads, one can write an equation that relates motoneuron firing rate to eye position and velocity - a very uncommon situation in the CNS. The semicircular canals transduce head velocity in a linear manner by using a high background discharge rate, imparting linearity to the premotor circuits that generate eye movements. This has allowed deducing some of the signal processing involved, including a neural network that integrates. These ideas are often summarized by block diagrams. Unfortunately, they are of little value in describing the behavior of single neurons - a fmding supported by neural network models.

Because eye muscles never cocontract and do not deal with external loads, one can write an equation that relates motoneuron firing rate to eye position and velocity - a very uncommon situation in the CNS. The semicircular canals transduce head velocity in a linear manner by using a high background discharge rate, imparting linearity to the premotor circuits that generate eye movements. This has allowed deducing some of the signal processing involved, including a neural network that integrates. These ideas are often summarized by block diagrams. Unfortunately, they are of little value in describing the behavior of single neurons - a fmding supported by neural network models.

The vestibulo-ocular reflex (VOR) is the primary mechanism that controls the compensatory eye movements that stabilize retinal images duringrapid head motion. The primary pathways of this system are feed-forward, with inputs from the semicircular canals and outputs to the oculomotor system. Since visual feedback is not used directly in the VOR computation, the system must exploit motor learning to perform correctly. Lisberger(1988) has proposed a model for adapting the VOR gain using image-slip information from the retina. We have designed and tested analog very largescale integrated(VLSI) circuitry that implements a simplified version of Lisberger's adaptive VOR model.

The vestibulo-ocular reflex (VOR) is the primary mechanism that controls the compensatory eye movements that stabilize retinal images during rapid head motion. The primary pathways of this system are feed-forward, with inputs from the semicircular canals and outputs to the oculomotor system. Since visual feedback is not used directly in the VOR computation, the system must exploit motor learning to perform correctly. Lisberger(1988) has proposed a model for adapting the VOR gain using image-slip information from the retina. We have designed and tested analog very largescale integrated (VLSI) circuitry that implements a simplified version of Lisberger's adaptive VOR model.

The vestibulo-ocular reflex (VOR) is the primary mechanism that controls the compensatory eye movements that stabilize retinal images during rapid head motion. The primary pathways of this system are feed-forward, with inputs from the semicircular canals and outputs to the oculomotor system. Since visual feedback is not used directly in the VOR computation, the system must exploit motor learning to perform correctly. Lisberger(1988) has proposed a model for adapting the VOR gain using image-slip information from the retina. We have designed and tested analog very largescale integrated (VLSI) circuitry that implements a simplified version of Lisberger's adaptive VOR model.