Control Of Saccadic Eye Movements Research Articles

P2-71. Saccadic eye movements in Spinocerebellar Degeneration – study of saccades in eight directions

Objectives The cerebellum is implicated in the control of saccadic eye movement but it is unknown how it differs for vertical and horizontal saccades, since vertical saccades have been rarely studied. To clarify the role of the cerebellum we studied saccades in hereditary spinocerebellar degeneration in two dimensional directions. Methods We compared saccade performance in 16 patients (SCA31 and SCA6) with that in 19 normal age-matched controls. We used the visual guided (VGS) and memory guided tasks (MGS) in which targets were presented in eight directions with 45 degrees separation, and recorded saccades with a video-based eye tracker. Results In SCA patients, latency of VGS was significantly delayed compared with normal subjects in vertical and oblique directions, which correlated with SARA scores. MGS latency was significantly delayed only in the oblique direction. Hypermetria was prominently detected in the vertical and oblique directions, but less in the horizontal directions. Conclusion Abnormal latency and dysmetria are easily detected for directions having vertical component. The cerebellum may be more involved in vertical than in horizontal saccade system, or vertical saccade system may be more susceptible to diseases than horizontal saccades. Further study of other diseases will be helpful to differentiate between these possibilities.

The active construction of the visual world.

What we see is fundamentally dependent on where we look. Despite this seemingly obvious statement, many accounts of the neurobiology underpinning visual perception fail to consider the active nature of how we sample our sensory world. This review offers an overview of the neurobiology of visual perception, which begins with the control of saccadic eye movements. Starting from here, we can follow the anatomy backwards, to try to understand the functional architecture of neuronal networks that support the interrogation of a visual scene. Many of the principles encountered in this exercise are equally applicable to other perceptual modalities. For example, the somatosensory system, like the visual system, requires the sampling of data through mobile receptive epithelia. Analysis of a somatosensory scene depends on what is palpated, in much the same way that visual analysis relies on what is foveated. The discussion here is structured around the anatomical systems involved in active vision and visual scene construction, but will use these systems to introduce some general theoretical considerations. We will additionally highlight points of contact between the biology and the pathophysiology that has been proposed to cause a clinical disorder of scene construction – spatial hemineglect.

Developing clinically practical transcranial direct current stimulation protocols to improve saccadic eye movement control.

Recent research indicates that anodal transcranial direct current stimulation (tDCS) applied over the frontal eye field (FEF) can improve saccadic eye movement control in healthy young adults. The current research set out to determine whether similar results can be produced using a clinically practical protocol, whether tDCS applied over the dorsolateral prefrontal cortex (DLPFC) might also afford benefits, and whether benefits extend to older adults. Twenty young and 10 older adults completed two active (FEF and DLPFC) and one sham stimulation session. To aid clinical translation, the method of positioning the electrodes entailed simple measurements only. Saccadic performance following anodal tDCS applied over the FEF or DLPFC did not differ from the sham condition in either age group. Additionally, saccadic performance contralateral to the active electrodes showed no evidence of benefits over ipsilateral performance. These results call into question whether the protocol utilized can be applied effectively using only simple measurements to localize the relevant frontal subregion. Future efforts to develop a clinically practical tDCS protocol to improve saccadic eye movement control should include a sham control condition and consider adjusting the tDCS electrode montage and current strength to optimize the chances of conferring benefits in the population under study.

Second stage development of an early screening tool for detection of vulnerability to schizophrenia, as an example of empathic action

Statement of the Problem: The concept of empathy in psychiatry infers an understanding, concern or interest in a person’s emotional state or experience. The experience of psychosis that usually precedes schizophrenia is often frightening; destabilizing a person’s sense of self and confidence in reality. Empathic action calls for ways to diminish the likelihood of a person experiencing psychosis. Methodology & Theoretical Basis: The current research tests the theory that vulnerability to developing this type of psychosis can be identified by an early-screening-tool (Schizophrenia-Traits-Questionnaire, STQ) in teenage, in a second stage of development by Flourish Australia. Originally developed in a PhD by the author, it is based on the neurodynamic/ psychobiological theory of Robert Miller. Originally, 600 adults participated in the STQ to test both the theory and its power to predict whether someone would fit into the schizophrenia category or not. The current research trial is on teenagers. Findings: The factor analysis supported the underlying theory and thirteen (13) of the items in combination, in the original sample, accurately predicted schizophrenia to 85% accuracy with no mention of psychotic symptoms. With early-detection and the appropriate education and resources, not only can the STQ potentially stop a psychotic episode from occurring, it also identifies the types of occupations to avoid, to prevent being overwhelmed by stimuli/environments that challenge.

Cognitive Control of Saccadic Eye Movements in Children with Developmental Coordination Disorder.

The ability to use advance information to prepare and execute a movement requires cognitive control of behaviour (e.g., anticipation and inhibition). Our aim was to explore the integrity of saccadic eye movement control in developmental coordination disorder (DCD) and typically developing (TD) children (8–12 years) and assess how these children plan and inhibit saccadic responses, the principal mechanisms within visual attention control. Eye movements and touch responses were measured (separately and concurrently) in Cued and Non-Cued conditions. We found that children with DCD had similar saccade kinematics to the TD group during saccade initiation. Advance information decreased hand movement duration in both groups during Cued trials, but decrements in accuracy were significantly worse in the DCD group. In addition, children with DCD exhibited greater inhibitory errors and inaccurate fixation during the Cued trials. Thus, children with DCD were reasonably proficient in executing saccades during reflexive (Non-Cued) conditions, but showed deficits in more complex control processes involving prediction and inhibition. These findings have implications for our understanding of motor control in children with DCD.

Short-latency allocentric control of saccadic eye movements.

We found that the saccade end point was shifted from the actual target position toward the direction expected from allocentric coding when a large frame in the background was transiently shifted during the period of target presentation. The effect occurred within 150 ms. The present study provides direct evidence that the brain rapidly uses allocentric coding of a target to control immediate saccades.

What do we know about eye movements in Alzheimer's disease? The past 37 years and future directions.

What do we know about eye movements in Alzheimer's disease? The past 37 years and future directions.

Kinesthetic information facilitates saccades towards proprioceptive-tactile targets

Saccades to somatosensory targets have longer latencies and are less accurate and precise than saccades to visual targets. Here we examined how different somatosensory information influences the planning and control of saccadic eye movements. Participants fixated a central cross and initiated a saccade as fast as possible in response to a tactile stimulus that was presented to either the index or the middle fingertip of their unseen left hand. In a static condition, the hand remained at a target location for the entire block of trials and the stimulus was presented at a fixed time after an auditory tone. Therefore, the target location was derived only from proprioceptive and tactile information. In a moving condition, the hand was first actively moved to the same target location and the stimulus was then presented immediately. Thus, in the moving condition additional kinesthetic information about the target location was available. We found shorter saccade latencies in the moving compared to the static condition, but no differences in accuracy or precision of saccadic endpoints. In a second experiment, we introduced variable delays after the auditory tone (static condition) or after the end of the hand movement (moving condition) in order to reduce the predictability of the moment of the stimulation and to allow more time to process the kinesthetic information. Again, we found shorter latencies in the moving compared to the static condition but no improvement in saccade accuracy or precision. In a third experiment, we showed that the shorter saccade latencies in the moving condition cannot be explained by the temporal proximity between the relevant event (auditory tone or end of hand movement) and the moment of the stimulation. Our findings suggest that kinesthetic information facilitates planning, but not control, of saccadic eye movements to proprioceptive-tactile targets.

The Impact of Same- and Other-Race Gaze Distractors on the Control of Saccadic Eye Movements.

Two experiments were aimed at investigating whether the implementation of voluntary saccades in White participants could be modulated more strongly by gaze distractors embedded in White versus Black faces. Participants were instructed to make a rightward or leftward saccade, depending on a central directional cue. Saccade direction could be either congruent or incongruent with gaze direction of the distractor face. In Experiment 1, White faces produced greater interference on saccadic accuracy than Black faces when the averted-gaze face and cue onset were simultaneous rather than separated by a 900-ms asynchrony. In Experiment 2, two temporal intervals (50 ms vs. 1,000 ms) occurred between the initial presentation of the face with direct-gaze and the averted-gaze face onset, whereas the averted-gaze face and cue onset were synchronous. A greater interference emerged for White versus Black faces irrespective of the temporal interval. Overall, these findings suggest that saccadic generation system is sensitive to features of face stimuli conveying eye gaze.

Saccade reprogramming in Friedreich ataxia reveals impairments in the cognitive control of saccadic eye movement

Although cerebellar dysfunction has known effects on motor function in Friedreich ataxia (FRDA), it remains unclear the extent to which the reprogramming of eye movements (saccades) and inhibition of well-learned automatic responses are similarly compromised in affected individuals. Here we examined saccade reprogramming to assess the ability of people with FRDA to respond toward unexpected changes in either the amplitude or direction of an “oddball” target. Thirteen individuals with genetically confirmed FRDA and 12 age-matched controls participated in the study. The saccade reprogramming paradigm was used to examine the effect of an unpredictable “oddball” target on saccade latencies and accuracy when compared to a well-learned sequence of reciprocating movements. Horizontal eye movements were recorded using a scleral search coil eye tracking technique. The results showed a proportionally greater increase in latencies for reprogrammed saccades toward an oddball-direction target in the FRDA group when compared to controls. The FRDA group were also less accurate in primary saccade gain (i.e. ratio of saccade amplitude to target amplitude) when reprogramming saccades toward an unexpected change in direction. No significant group differences were found on any of the oddball-amplitude targets. Significant correlations were revealed between latency and disease severity as measured by the Friedreich Ataxia Rating Scale. These findings provide further support to the view that cognitive changes in FRDA may arise from disruption of cerebellar connections to cortical structures.

Effects of unilateral deactivations of dorsolateral prefrontal cortex and anterior cingulate cortex on saccadic eye movements

The dorsolateral prefrontal cortex (dlPFC) and anterior cingulate cortex (ACC) have both been implicated in the cognitive control of saccadic eye movements by single neuron recording studies in nonhuman primates and functional imaging studies in humans, but their relative roles remain unclear. Here, we reversibly deactivated either dlPFC or ACC subregions in macaque monkeys while the animals performed randomly interleaved pro- and antisaccades. In addition, we explored the whole-brain functional connectivity of these two regions by applying a seed-based resting-state functional MRI analysis in a separate cohort of monkeys. We found that unilateral dlPFC deactivation had stronger behavioral effects on saccades than unilateral ACC deactivation, and that the dlPFC displayed stronger functional connectivity with frontoparietal areas than the ACC. We suggest that the dlPFC plays a more prominent role in the preparation of pro- and antisaccades than the ACC.

Production, Control, and Visual Guidance of Saccadic Eye Movements

Primate vision is served by rapid shifts of gaze called saccades. This review will survey current knowledge and particular problems concerning the neural control and guidance of gaze shifts.

Learning and switching between stimulus-saccade associations in Parkinson’s disease

Making flexible associations between what we see and what we do is important for many everyday tasks. Previous work in patients with focal lesions has shown that the control of saccadic eye movements in such contexts relies on a network of areas in the frontal cerebral cortex. These regions are reciprocally connected with structures in the basal ganglia although the contribution of these sub-cortical structures to oculomotor control in complex tasks is not well understood. We report the performance of patients with idiopathic Parkinsons disease (PDs) in a test which required learning and switching between arbitrary cue-saccade rules. In Experiment 1 feedback was given following each response which reliably indicated which of the two possible rules was correct. PDs were slower to learn the first cue-saccade association presented, but did not show increased error or reaction time switch costs when switching between two rules within blocks. In a follow up experiment the feedback given by the computer was adjusted to be probabilistic such that executing a response based upon the “correct” rule only resulted in positive feedback on 80% of trials. Under these conditions patients were impaired in terms of response latencies and number of errors. In all conditions PDs showed multi-stepping/hypometria of saccades consistent with a motoric deficit in executing actions based on cognitive cues. The findings are consistent with a role for the nigrostriatal dopamine system in the reinforcement of saccade-response-outcome associations. Intact performance of PDs when associations are not stochastically reinforced suggests that striatal learning systems are complemented by cognitive representations of task rules which are unaffected in the early stages of PD.

Shared attention for smooth pursuit and saccades.

Identification of brief luminance decrements on parafoveal stimuli presented during smooth pursuit improves when a spot pursuit target is surrounded by a larger random dot cinematogram (RDC) that moves with it (Heinen, Jin, & Watamaniuk, 2011). This was hypothesized to occur because the RDC provided an alternative, less attention-demanding pursuit drive, and therefore released attentional resources for visual perception tasks that are shared with those used to pursue the spot. Here, we used the RDC as a tool to probe whether spot pursuit also shares attentional resources with the saccadic system. To this end, we set out to determine if the RDC could release attention from pursuit of the spot to perform a saccade task. Observers made a saccade to one of four parafoveal targets that moved with the spot pursuit stimulus. The targets either moved alone or were surrounded by an RDC (100% coherence). Saccade latency decreased with the RDC, suggesting that the RDC released attention needed to pursue the spot, which was then used for the saccade task. Additional evidence that attention was released by the RDC was obtained in an experiment in which attention was anchored to the fovea by requiring observers to detect a brief color change applied 130 ms before the saccade target appeared. This manipulation eliminated the RDC advantage. The results imply that attentional resources used by the pursuit and saccadic eye movement control systems are shared.

Deficits of cortical oculomotor mechanisms in cerebellar atrophy patients

Commonly, the cerebellum is not associated with cortical components of saccadic eye movement programming. The present study investigates cerebellar effects on visually guided saccades in reflexive tasks (step, gap, overlap) and on internally driven saccades in intentional tasks (anti, memory, short memory sequences of four targets) in five patients with isolated cerebellar atrophy. The cerebellar dysfunction led to impairments in both reflexive and intentional saccades. Cerebellar atrophy patients showed an increase in the gain variability and an increase in the saccade latency. Furthermore, in the memory and anti task, suppression and pro-saccade errors were more frequent in the atrophy group compared to the control group. In the sequence task, patients had difficulties reproducing all four target locations in the order of the displayed sequence. The high variability of the saccade gain is a common observation in cerebellar atrophy patients and can be explained by the general variability present in the saccadic system. The increase in the saccade latency could be due to a cerebellar contribution to cortical processes related to fixation and target selection preceding the initiation of a saccade. Furthermore, the frequent occurrence of saccade errors in the memory and anti task suggests a cerebellar involvement in frontal inhibition of unwanted reflexive saccades. The impaired reproduction of saccade sequences in atrophy patients points to a deficit in short-term memory processes. Thus, this study provides further evidence that the cerebellum is involved in different cortical mechanisms related to the control of saccadic eye movements.

Cerebellar Activation Related to Saccadic Inaccuracies

Using functional MRI, we assessed activity in the human cerebellum related to the properties of post-saccadic visual errors that drive the plasticity of saccadic eye movements. In the scanner subjects executed blocks of saccadic eye movements toward a target that could be randomly displaced during the saccade. Such an intra-saccadic shift was randomly forward or backward, and could be either small or large. Post-saccadic visual errors induced activation in several cerebellar areas. These areas included, but were not limited to, the oculomotor vermis which is known for its role in saccadic control. Large errors yielded more activation in the cerebellar hemispheres, whereas small errors induced more activation in the vermis. Forward shifts induced more activation than backward shifts. Our results suggest that the differences in cerebellar activation patterns for different sizes and directions of post-saccadic errors could underlie the behavioral differences observed between various saccadic adaptation paradigms. In addition, the outcome argues for an extended range of cerebellar target areas in electrophysiological studies on saccadic eye movement control.

The role of working memory and attentional disengagement on inhibitory control: effects of aging and Alzheimer's disease

Patients with Alzheimer's disease have an impairment of inhibitory control for reasons that are currently unclear. Using an eye-tracking task (the gap-overlap paradigm), we examined whether the uncorrected errors relate to the task of attentional disengagement in preparation for action. Alternatively, the difficulty in correcting for errors may be caused by the working memory representation of the task. A major aim of this study was to distinguish between the effects of healthy aging and neurodegenerative disease on the voluntary control of saccadic eye movements. Using the antisaccade task (AST) and pro-saccade task (PST) with the 'gap' and 'overlap' procedures, we obtained detailed eye-tracking measures in patients, with 18 patients with probable Alzheimer's disease, 25 patients with Parkinson's disease and 17 healthy young and 18 old participants. Uncorrected errors in the AST were selectively increased in Alzheimer's disease, but not in Parkinson's disease compared to the control groups. These uncorrected errors were strongly correlated with spatial working memory. There was an increase in the saccade reaction times to targets that were presented simultaneously with the fixation stimulus, compared to the removal of fixation. This 'gap' effect (i.e. overlap-gap) saccade reaction time was elevated in the older groups compared to young group, which yielded a strong effect of aging and no specific effect of neurodegenerative disease. Healthy aging, rather than neurodegenerative disease, accounted for the increase in the saccade reaction times to the target that are presented simultaneously with a fixation stimulus. These results suggest that the impairment of inhibitory control in the AST may provide a convenient and putative mark of working memory dysfunction in Alzheimer's disease.

Role of the Lateral Intraparietal Area in Modulation of the Strength of Sensory-Motor Transmission for Visually Guided Movements

The lateral intraparietal area (LIP) has been implicated as a salience map for control of saccadic eye movements and visual attention. Here, we report evidence to link the encoding of saccades and saliency in LIP to modulation of several other sensory-motor behaviors in monkeys. In many LIP neurons, there was a significant trial-by-trial correlation between the firing rate just before a saccade and the postsaccadic or presaccadic pursuit eye velocity. Some neurons also showed trail-by-trial correlations of the firing rate of LIP neurons with the speed of "glissades" that occur at the end of saccades to stationary targets. LIP-pursuit correlations were spatially specific and were strong only when the target appeared in the receptive/movement field of the neuron under study. We suggest that LIP is a component of a salience representation that modulates the strength of visual-motor transmission for pursuit, and that may play a similar role for many movements, beyond its traditional roles in guiding saccadic eye movements and localizing attention.

EFFECTS OF MULLER-LYER ILLUSION ON THE ACCURACY OF PRIMARY SACCADES AND SMOOTH PURSUIT EYE MOVEMENTS

The goal of the present investigation was to evaluate the effect of visual Muller-Lyer (M-L) illusion on the control of saccadic and smooth pursuit eye movements and compare it with the results obtained during perceptual judgment of the length of the shaft of M-L illusion. Experimental investigation revealed that the primary saccades elicited in the reflexive mode were mostly affected by the M-L illusion. The position errors of the primary saccades elicited in the reflexive mode were affected by 4% for wings-in illusion and by 3.6% for wings-out illusion comparing with the 0.25% and 0.1% for the saccades elicited in the voluntary mode. The position errors of complete saccades (0.14% and 0.02%) and tracking errors obtained during the smooth pursuit (0.11% and 0.05%) were negligibly small. Nevertheless, experimental results obtained during perceptual judgment of M-L illusion were substantially larger - 14% and 10% respectively. The obtained results have demonstrated that vision for perception and vision for action were executed by different neural networks and supported the two-visual-system hypothesis.DOI: http://dx.doi.org/10.5755/j01.itc.41.1.763

A test of spatial temporal decoding mechanisms in the superior colliculus

Population coding is a ubiquitous principle in the nervous system for the proper control of motor behavior. A significant amount of research is dedicated to studying population activity in the superior colliculus (SC) to investigate the motor control of saccadic eye movements. Vector summation with saturation (VSS) has been proposed as a mechanism for how population activity in the SC can be decoded to generate saccades. Interestingly, the model produces different predictions when decoding two simultaneous populations at high vs. low levels of activity. We tested these predictions by generating two simultaneous populations in the SC with high or low levels of dual microstimulation. We also combined varying levels of stimulation with visually induced activity. We found that our results did not perfectly conform to the predictions of the VSS scheme and conclude that the simplest implementation of the model is incomplete. We propose that additional parameters to the model might account for the results of this investigation.