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.     

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.     

Unit responses from commissural fibers of optic lobes of fish

The paired optic lobes of teleost fish are connected by two commissures. One of these, the tectal commissure, was studied with metal microelectrodes. Fibers are rhythmically active for prolonged periods in the dark and respond to light by a decrease in the rate of discharge. There is a rebound acceleration when the light is turned of. Each fiber is influenced by light in one eye only, and there is no response when light is projected into the opposite eye. This behavior resembles the "off" response recorded from the optic lobes and the optic nerve of fish. Unlike most units from the visual pathways of lower animals, single commissural fibers do not seem to give any recognizable response to patterned input such as small light or dark objects or small light sources stationary or moving anywhere in the visual field, nor do they respond to a vertical black bar moved over a white background.     

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.     

Optics of arthropod compound eye

The extent to which light can escape from one ommatidium into its neighbors in the compound eye has been examined by recording from single receptors during stimulation of single facets. In the "apposition" eye of the drone honeybee and locust, optical interaction is extremely small. In the "superposition" eye of the crayfish, more than half the light captured by the average cell gets in through neighboring facets, even when screening pigments are in the fully lightadapted position.     

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.     

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.     

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.     

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.     

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.     

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.     

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.     

Scanpaths in eye movements during pattern perception

Subjects learned and recognized patterns which were marginally visible, requiring them to fixate directly each feature to which they wished to attend. Fixed "scanpaths," specific to subject and pattern, appeared in their saccadic eye movements, both intermittently during learning and in initial eye movements during recognition. A proposed theory of pattern perception explains these results.     

Discharge of frontal eye field neurons during eye movements in unanesthetized monkeys

Single unit activity was recorded from the frontal eye fields (area 8) in unanesthetized monkeys seated in a primate chair with the head restrained. The frontal eye field units were identified by antidromic response to stimulation of the cerebral peduncle. The findings indicate that most of the neurons discharge only after initiation of eye movements. These cells showed steady discharge when the eyes were immobile and oriented in a specific direction.     

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.     

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.     

Dreaming sleep in man: changes in urine volume and osmolality

Epochs of dreaming sleep, as measured by rapid eye movements, consistently correlated with biphasic change in urine volume and osmolality in catheterized human subjects. Marked decrease in volumne and increase in oslnolality were followed by a hypotonic diuresis.     

土壤的老化对PCB138的可提取性和生物可利用性的影响

为探讨老化行为对多氯联苯(Polychlorinated biphenyls,PCBs)在土壤中的可提取性和生物可利用性的影响,选取2,2′,3,4,4′,5-六氯联苯(PCB138)作为目标污染物,进行90 d的老化试验,比较了超纯水提取、正丁醇溶液提取、超声提取(正己烷/丙酮)和索氏抽提(正己烷/二氯甲烷)等4种方法对土壤中不同老化时间PCB138的提取率;以赤子爱胜蚓(Eisenia fetida)为土壤模式参照生物,在不同的老化时间里测定蚯蚓体内PCB138的含量与脂肪含量。结果表明,4种方法提取PCB138的能力依次为索氏抽提(正己烷/二氯甲烷)≈超声提取(正己烷/丙酮)正丁醇提取超纯水溶液提取;索氏抽提、超声提取和正丁醇溶液提取的提取率从最初的87%~93%、85%~90%、50%~60%分别下降到70%~76%、65%~73%、25%~45%,在30~45 d时总提取量保持稳定,而超纯水提取PCB138的量有限,显示出最低的提取能力且为非重复性结果。PCB138在蚯蚓体内富集量随接触时间增加而增加,在老化30 d左右其体内PCB138富集量最大;在老化30~60 d时,蚯蚓体内的PCB138的含量逐渐下降,健康状况良好的蚯蚓脂肪含量有所下降但不明显。正丁醇溶液提取、超声提取和索氏抽提对PCB138的提取率,以及老化土壤中蚯蚓对PCB138的富集量,均说明PCB138在土壤中的生物有效性随着老化时间的延长而降低。     

The latency of pathways containing the site of motor learning in the monkey vestibulo-ocular reflex

The vestibulo-ocular reflex helps to stabilize retinal images by generating smooth eye movements that are equal to and opposite each rotatory head movement. It is well known that the reflex undergoes adaptive plasticity or "motor learning" whenever there is persistent image motion during head turns: the resulting changes in the reflex occur gradually and help to restore image stability. A new approach makes it possible to identify the pathways containing the site of motor learning according to their total latency in response to natural vestibular stimuli. The fastest pathways required 14 milliseconds to initiate a vestibulo-ocular reflex, but the site of motor learning was in pathways having latencies of at least 19 milliseconds.