correct saccade
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2014 ◽  
Vol 2014 ◽  
pp. 1-11 ◽  
Author(s):  
Wendy E. Huddleston ◽  
Brad E. Ernest ◽  
Kevin G. Keenan

Objective. Visual information is often used to guide purposeful movement. However, older adults have impaired responses to visual information, leading to increased risk for injuries and potential loss of independence. We evaluated distinct visual and motor attention contributions to a cued saccade task to determine the extent to which aging selectively affects these processes.Methods. Nineteen healthy young (18–28 years) and 20 older (60–90 years) participants performed a cued saccade task under two conditions. We challenged motor attention by changing the number of possible saccade targets (1 or 6).Results. Older adults had difficulty in inhibiting unwanted eye movements and had greater eye movement inaccuracy in the hard condition when compared to the younger adults and to the easy condition. Also, an inverse relation existed between performance on the visual and motor components of the task in older adults, unlike younger adults.Conclusions. Older adults demonstrated difficulty in both inhibiting irrelevant saccade targets and selecting correct saccade endpoints during more complex tasks. The shift in relations among attention measures between the younger and older participants may indicate a need to prioritize attentional resources with age. These changes may impact an older adult’s ability to function in complex environments.



1995 ◽  
Vol 7 (3) ◽  
pp. 311-336 ◽  
Author(s):  
Peter Dominey ◽  
Michael Arbib ◽  
Jean-Paul Joseph

We present models that learn context-dependent oculomotor behavior in (1) conditional visual discrimination and (2) sequence reproduction tasks, based on the following three principles: (1) Visual input and efferent copies of motor output produce patterns of activity in cortex. (2) Cortex influences the saccade system in part via corticostriatal projections. (3) A reinforcement learning mechanism modifies corticostriatal synapses to link patterns of cortical activity to the correct saccade responses during trial-and-error learning. Our conditional visual discrimination model learns to associate visual cues with the corresponding saccades to one of two left-right targets. A visual cue produces patterns of neuronal activity in inferotemporal cortex (IT) that projects to the oculomotor region of the striatum. Initially random saccadic "guesses," when directed to the correct target for the current cue, result in increased synaptic strength between the cue-related IT cells and the striatal cells that participate in the correct saccade, increasing the probability that this cue will later elicit the correct saccade. We show that the model generates "inhibitory gradients" on the striatum as the substrate for spatial generalization. Our sequence reproduction model learns, when presented with temporal sequences of spatial targets, to reproduce the corresponding sequence of saccades. At any point in the execution of a saccade sequence, the current pattern of activity in pre-frontal cortex (PFC), combined with visual input and the motor efferent copy of the previous saccade, produces a new pattern of activity in PFC to be associated with the next saccade. Like IT, PFC also projects to the oculomotor region of the striatum. Correct guesses for the subsequent saccade in the sequence results in strengthening of corticostriatal synapses between active PFC cells and striatal cells involved in the correct saccade. The sequence is thus reproduced as a concatenation of associations. We compare the results of this model with data previously obtained in the monkey and discuss the nature of cortical representations of spatiotemporal information.



1995 ◽  
Vol 73 (3) ◽  
pp. 1101-1121 ◽  
Author(s):  
L. L. Chen ◽  
S. P. Wise

1. The supplementary eye field (SEF) has been viewed as a premotor cortical field for the selection and control of saccadic eye movements. Drawing on studies of the neighboring premotor cortex, we hypothesized that if the SEF participates in the selection of action based on arbitrary stimulus-response associations, then task-related activity in the SEF should change during the learning of such associations. 2. Rhesus monkeys were operantly conditioned to make a saccadic eye movement to one of four targets (7 deg up, down, left, and right from center) in response to a foveal instruction stimulus (IS). One and only one of those four possible responses was arbitrarily designated "correct" for each IS. The monkeys responded to familiar ISs, four stimuli that remained unchanged throughout training and recording, as well as to novel ISs, which the monkeys had not previously seen. The monkeys initially chose responses to novel stimuli by trial and error, with near chance levels of performance, but quickly learned to select the correct saccade. 3. We studied 186 SEF cells as monkeys learned new visuomotor associations. Neuronal activity was quantified in four task periods: during the presentation of the IS, during an instructed delay period (i.e., after the removal of the IS but before a trigger or "go" stimulus), just before the saccade, and after the saccade during fixation of the target location. The discharge rate in each task period was considered a separate case for analysis, compared with that in a reference period preceding the IS, and eliminated from further analysis if not significantly different. 4. We observed two main categories of activity change during learning, which we termed learning selective and learning dependent. Learning-selective cases showed a significant evolution in activity as the monkeys learned which saccade was instructed by a novel IS, but had no significant modulation during trials with familiar ISs. Many of these cells were virtually inactive on trials with familiar ISs. However, they initially showed dramatic modulation when tested with a novel IS. As the monkey chose the correct saccade (or target) with increasing reliability, the modulation often decremented until the cell was again relatively unmodulated, as observed during familiar-IS trials. These cells usually remained relatively inactive until the monkeys were challenged to start learning another new stimulus-response association. Learning-selective activity was observed in all task periods, and 33 (18%) of the 186 adequately tested SEF cells showed learning-selective activity in one or more task periods.(ABSTRACT TRUNCATED AT 400 WORDS)



1990 ◽  
Vol 64 (2) ◽  
pp. 575-581 ◽  
Author(s):  
J. Schlag ◽  
M. Schlag-Rey ◽  
P. Dassonville

1. If an eccentric, stationary target is flashed while a subject is performing an eye movement in the dark, can this subject make a saccade to the location in space where the target briefly appeared? Different predictions result from alternative hypotheses regarding the manner in which saccade goals are determined. Retinal error being defined as the vector from the eye position at the time of the flash to the position of the target, the retinal-error hypothesis predicts that the saccade vector will be equal to the retinal-error vector. This hypothesis assumes that the oculomotor system ignores the eye displacement between target presentation and saccade. If so, the target will be missed. In contrast, the spatial-error hypothesis predicts that the eye displacement is taken into account by the brain to calculate the target's physical location to which, therefore, a correct saccade could be aimed. 2. At issue is the generality of a fundamental principle of ocular targeting. Previous studies have established that, if the movement is saccadic, eye displacement is used by the oculomotor system to calculate the target's physical location. In the case of pursuit, perceptual experiments on humans suggest that eye displacement is taken into account although its velocity is underestimated. However, in a recent study McKenzie and Lisberger reported that saccade trajectories starting during pursuit conform to the retinal error hypothesis. In other words, velocity underestimation is close to 100%. 3. Although McKenzie and Lisberger's results are very clear, they might have depended on particular experimental conditions. The issue was reinvestigated in a situation facilitating the discrimination of stimuli.(ABSTRACT TRUNCATED AT 250 WORDS)



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