Central influences on spinal afferent conduction.

Control of thalamic transmission by corticofugal and ascending reticular pathways in the visual system.

Inhibition of central vestibular neurons from the contralateral labyrinth and its mediating pathway.

The mammalian red nucleus.

A new bipolar electrode for electromyography

Functional connections of tonic and kinetic vestibular neurons with primary vestibular afferents.

Chemicals as tools in the study of excitable membranes.

NEURAL ACTIVITY IN MECHANORECEPTIVE CUTANEOUS AFFERENTS: STIMULUS-RESPONSE RELATIONS, WEBER FUNCTIONS, AND INFORMATION TRANSMISSION.

Ce rapport analyse l'organisation anatomique du systeme limbique, ses principales connexions avec les autres compartiments du cerveau et sa physiologie en rapport avec le comportement de l'animal

DEPOLARIZATION OF PRESYNAPTIC FIBERS IN THE CUNEATE NUCLEUS.

IDENTIFICATION OF RELAY CELLS AND INTERNEURONS IN THE CUNEATE NUCLEUS.

1. Monkeys were trained to look to brief visual targets presented in a completely darkened room. On some trials, after the visual target disappeared but before a saccade to the target could be initiated, the eyes were driven to another position in the orbit by electrical stimulation of the superior colliculus. Retinocentric models of the saccadic system predict that a saccade with a predetermined distance and direction based entirely on retinal error will occur. If this were the case, gaze would miss the target location by a distance and direction equal to the vector of the stimulation-induced movement. Spatial models assume that the retinal error signal will be combined with information about the change in eye position produced by stimulation and predict that the animal will look to the position of the target in space. 2. Results confirm the predictions of spatial models. Animals compensated for the stimulation-induced perturbation by looking to the position of the target in space. The result predicted by retinocentric models-a saccade with a direction and amplitude based on retinal error alone-was never observed. 3. The eye movement that compensated for the change in eye position produced by stimulation was a saccade, not a passive, lowvelocity movement to an orbital position of mechanical equilibrium established by a tonic pattern of motoneuron activation specified by the visual target. This indicates that a new saccade command, based on stored information about the location of the retinal image and information about the new position of the eyes, had been issued. Computation of the vector of the compensatory saccade does not necessarily increase the latency of target acquisition. The interval between the end of a stimulation-induced saccade and the beginning of the compensatory saccade was frequently 20 ms or less, permitting the animal to acquire the target with a normal latency.

Sensory and motor responses of precentral cortex cells during comparable passive and active joint movements.

Tetrodotoxin-resistant sodium and calcium components of action potentials in dorsal root ganglion cells of the adult mouse.

Discharge of cerebellar neurons related to two maintained postures and two prompt movements. I. Nuclear cell output.

Nucleus locus ceruleus: new evidence of anatomical and physiological specificity.