Visual receptive fields sensitive to absolute and relative motion during tracking

Some neurons in the visual cortex of awake monkeys visually tracking a moving target showed receptive fields that were excited only by stimulus motion relative to a background, while other neurons responded to any kind of stimulus motion. This result was found with two methods, one in which tracking eye movements were identical in both relative-motion and absolute-motion conditions, and another in which stimulus motions on the retina were identical in both conditions. This response pattern can differentiate translation of the retinal image during eye movement from motion of objects in the world.     

Periodic respiratory pattern occurring in conjunction with eye movements during sleep

With each flurry of rapid eye movements during the sleep of human subjects there is a decreased amplitude of respiration and a slight increase in rate. Occasionally the rhythmic breathing pattern may even resemble Cheyne-Stokes respiration. The consistency of this breathing pattern suggests that respiration in this stage of sleep is not a direct function of dream content.     

A structural basis for Hering's law: projections to extraocular motoneurons

Conjugate eye movements are executed through the concurrent activation of several muscles in both eyes. The neural mechanisms that underlie such synergistic muscle activations have been a matter of considerable experimentation and debate. In order to investigate this issue, the projections of a class of primate premotoneuronal cells were studied, namely, the vertical medium-lead burst neurons (VMLBs), which drive vertical rapid eye movements. Axons of upward VMLBs ramify bilaterally within motoneuron pools that supply the superior rectus and inferior oblique muscles of both eyes. Axons of downward VMLBs ramify ipsilaterally in the inferior rectus portion of the oculomotor nucleus and in the trochlear nucleus. Thus, VMLBs can drive vertical motoneuron pools of both eyes during conjugate vertical rapid eye movements; these data support Hering's law.     

Excitability changes in cat lateral geniculate cells during saccadic eye movements

The excitability of lateral geniculate cells to orthodromic volleys decreased during saccadic eye movements. This decrease was caused by retinal impulses generated by a quick displacement of the image of the visual field associated with eye movements. This may be a mechanism for saccadic suppression.     

Sleep: suppression of rapid eye movement phase in the cat after electroconvulsive shock

Electroconvulsive shock, administered for 5 to 7 days, reduced the daily rapid eye movement sleep time of seven cats to as little as 28 percent of base line levels. After day 4, eye movements during periods of cortical activation without tonic electromyographic activity were greatlyreduced. Although partially deprived of rapid eye movements for as long as 7 days, the cats showed no compensatory rise in rapid eye movement time during the recovery period, but controls equally deprived gave significant rebounds. Rapid eye movement time of anesthetized cats was not affected by current that usually produces con vulsions; it was lowered in animals convulsed with metrazol, but the same dosage of this drug, administered so as to avoid convulsions, had little eflect.It appears that some aspect of the convulsion is responsible for lowering the rapid eye movement time.     

Neuronal correlates of eye movements in the visual cortex of the cat

About 10 percent of the cells in the visual cortex of awake cats do not respond to stationary parallel stripes in any orientation or to stripes moving across the visual field in any direction at a moderate speed (up to 132 degrees per second), but these cells are either excited or inhibited during saccadic eye movements when the animal faces a patterned visual environment. Of nineteen such cells tested in total darkness, seven discharged in association with eye movements. For saccade-related discharges, the latency during retinal stimulation is typically shorter than the latencey in total darkness.     

Spontaneous middle ear muscle activity in man: a rapid eye movement sleep phenomenon

Changes in compliance of the tympanic membrane have been detected in normal human sleep, presumably due to spontaneous contraction of the stapedius and tensor tympani muscles of the middle ear. In the waking state, these muscles generally respond to loud sound (middle ear reflex). Middle ear muscle activity typically erupts before or at the onset of rapid eye movement (REM) sleep and persists throughout the REM period in a discontinuous pattern resembling that exhibited by rapid eye movements. Approximately 80 percent of all nocturnal middle ear muscle activity is contained in REM sleep. Half of the remaining 20 percent occurs in the 10-minute intervals just prior to the onset of REM sleep. Middle ear muscle activity is often associated with other phasic events such as momentary enhancement of electromyogram inhibition, apnea, and K complexes. Rapid eye movements and middle ear muscle activity, though significantly correlated in REM sleep, are not always simultaneous.     

Eye and head movements in peripheral vision: nature of compensatory eye movements

Simultaneous recordings of both eye and head movements in response to a peripheral signal indicated that the backward compensatory eye movement was initiated during the constant velocity of the head rotation. This compensatory movement began before the eyes had actually reached the peripheral signal.     

Superior colliculus cell responses related to eye movements in awake monkeys

Single cell responses were recorded from the superior colliculus of awake monkeys trained to move their eyes. A class of cells that discharged before eye movements was found in the intermediate and deep layers of the colliculus. The response of the cells was most vigorous before saccadic eye movements within a particular range of directions. These cells had no visual receptive fields, and visually guided eye movements were not necessary for their discharge, since they responded in total darkness before spontaneous eye movements and vestibular nystagmus.     

Shaping the vertebrate body plan by polarized embryonic cell movements

Polarized cell movements shape the major features of the vertebrate body plan during development. The head-to-tail body axis of vertebrates is elongated in embryonic stages by "convergent extension" tissue movements. During these movements cells intercalate between one another transverse to the elongating body axis to form a narrower, longer array. Recent discoveries show that these polarized cell movements are controlled by homologs of genes that control the polarity of epithelial cells in the developing wing and eye of the fruit fly, Drosophila.     

Photoelectric technique for measuring eye movements

By the system described, the movement of a stimulus and the correlated tracking movements of the eye are recorded simultaneously. The technique for measuring the eye movements consists of detecting and amplifying by photomultiplication the total amount of light passing through a small slit upon which is imaged a small portion of the light-dark field represented by the iris and sclera of the eye. This total amount of light varies directly with the angular position of the eye.     

Generation of torsional and vertical eye position signals by the interstitial nucleus of Cajal

The neural integrator, which converts eye velocity signals into position signals, is central to oculomotor theory. Similar integrators are probably necessary in any neural system that changes and maintains muscular tension. The integrator for horizontal eye position is in the pons, but the locations of the vertical and torsional integrators have not been clearly defined. Recording three-dimensional eye movements in alert monkeys during microstimulation and pharmacological inactivation of midbrain sites showed that the interstitial nucleus of Cajal generates both the torsional and vertical eye position signals. Up and down signals are linked with clockwise signals in the right brain and counterclockwise signals in the left brain. This three-dimensional coordinate system achieves orthogonality and bilateral symmetry without redundancy and optimizes energy efficiency for horizontal visual scanning.     

Spatial orientation in weightlessness and readaptation to earth's gravity

Unusual vestibular responses to head movements in weightlessness may produce spatial orientation illusions and symptoms of space motion sickness. An integrated set of experiments was performed during Spacelab 1, as well as before and after the flight, to evaluate responses mediated by the otolith organs and semicircular canals. A variety of measurements were used, including eye movements, postural control, perception of orientation, and susceptibility to space sickness.     

Two- rather than three-dimensional representation of saccades in monkey superior colliculus

Saccades are controlled by neurons in the brainstem reticular formation that receive input from the superior colliculus and cortex. Recently two quantitative models have been proposed for the role of the colliculus in the generation of three-dimensional eye movements. In order to test these models, three-dimensional eye movements were measured in the alert monkey to investigate whether the saccadic motor map of the superior colliculus is two-dimensional, representing retinal target vectors, or three-dimensional, representing three-dimensional motor error for the rotation of the eye. Electrical stimulation of the superior colliculus produced two-dimensional, not three-dimensional, eye movements. It is therefore concluded that the collicular motor map is two-dimensional.     

Changes of simple and complex spike activity of cerebellar purkinje cells with sleep and waking

Action potentials of cerebellar Purkinje cells were observed in intact monkeys during sleep and waking. Purkinje cells exhibit two sorts of action potentials, called simple and complex spikes, and these two sorts of spikes were differently affected by sleep. Simple-spike activity (generated by the parallel fiber inputs to the Purkinje cell) was highest during sleep with rapid eye movements as compared with both waking and sleep with electroencephalographic slow waves. In contrast, complex-spike activity (generated by the climbing fiber inputs to the Purkinje cell) was lowest during sleep with rapid eye movements. The complex action potential of the Purkinje cell consists of an initial large spike followed by one or more smaller secondary spikes, and the number of these secondary spikes was found to be independent of the background discharge frequency of the simple spike. This independence suggests a possible role of presynaptic factors rather than the excitability level of the Purkinje cell itself in determining the number of secondary discharges occurring in the complex spike.     

A pathway in primate brain for internal monitoring of movements

It is essential to keep track of the movements we make, and one way to do that is to monitor correlates, or corollary discharges, of neuronal movement commands. We hypothesized that a previously identified pathway from brainstem to frontal cortex might carry corollary discharge signals. We found that neuronal activity in this pathway encodes upcoming eye movements and that inactivating the pathway impairs sequential eye movements consistent with loss of corollary discharge without affecting single eye movements. These results identify a pathway in the brain of the primate Macaca mulatta that conveys corollary discharge signals.     

Metacontrast and saccadic suppression

A vertical slit of light illuminated during horizontal saccadic eye movements appeared as a horizontally extended smear when stimulation was terminated before the saccade ended. However, on trials for which duration of illumination of the slit was extended into the period after the saccade, the smear appeared shorter and dimmer, and a clear image of the slit was seen. With further increases in duration, no smears were seen at the highest luminance of the slit employed, although smears were more than 2 log units above threshold when flashes were brief. This saccadic suppression is discussed in terms of metacontrast, with the accumulated luminance in the period after the saccade primarily responsible for masking the effects of the stimulation received during the movement of the eye.     

Paradoxical sleep in two species of avian predator (Falconiformes)

Periods of disconjugate. and conjugate eye movements occur during the sleep cycle in Buteo jamaicensis arborealis and Herpetotheres cachinnans chapmanni. Electromyograms are essentially isoelectric throughout sleep. Slow waves appear only in short bursts of low amplitude in contrast to the long trains of high-amplitude waves reported for chickens and pigeons.     

Relating a component of physiological nystagmus to visual display

A transactional position suggests the hypothesis that there should be changes in the fine eye movements of a fixating subject if the fixated visual display is altered. It is shown that the mean saccadic eye movements are unequivocally different with different positions of the stimulus within the visual field.