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To investigate the decision-making process at the saccade programming we used modification of the "double step" experimental scheme, in which two short stimuli are presented successively in the opposite semifields (puls overshoot--scheme). The dependence of saccades to visual stimuli number, responses pattern (two saccades, or a single saccade to the second stimulus) and the value of saccade latency from the first stimulus duration (150 or 50 ms), the spatial stimuli arrangement and the individual characteristics of the subjects was shown. The findings suggest the relationship of attention and decision making processes at saccade programming and indicate to the possible influence of prognostic processes on the saccadic response "pattern" at the expectation period in the experimental "double step" scheme.

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Longer latency and duration of memory-guided saccades and their lower amplitude compared with visually-guided saccades testify to the slower programming of the former. Lateral distinctions in the latencies and durations of memory-guided and visually-guided saccades can reflect leading role of the right hemisphere in programming memory-guided saccades and leading role of the left hemisphere in programming visually-guided saccades. Topography and spatiotemporal dynamics of presaccadic potentials P-1 and N-1 within the last 100 ms of latent period suggest that the mechanisms of final stage of the programming of memory-guided and visually-guided saccades are different. Shorter latencies of the presaccadic P-1 and N-1 prior to memory-guided saccades testify to acceleration of the initiation of the memory-guided saccades. The acceleration of the initiation period of memory-guided saccades suggest that deceleration of memory-guided saccade programming occurs at the stages preceding saccade initiation.

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The difference in parameters of visually guided and memory-guided saccades was shown. Increase in the memory-guided saccade latency as compared to that of the visually guided saccades may indicate the deceleration of saccadic programming on the basis of information extraction from the memory. The comparison of parameters and topography of evoked components N1 and P1 of the evoked potential on the signal to make a memory- or visually guided saccade suggests that the early stage of the saccade programming associated with the space information processing is performed predominantly with top-down attention mechanism before the memory-guided saccade and bottom-up mechanism before the visually guided saccade. The findings show that the increase in the latency of the memory-guided saccades is connected with decision making at the central stage of the saccade programming. We proposed that wave N2, which develops in the middle of the latent period of the memory-guided saccades, is correlated with this process. Topography and spatial dynamics of components N1, P1 and N2 testify that the memory-guided saccade programming is controlled by the frontal mediothalamic system of selective attention and left-hemispheric brain mechanisms of motor attention.

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The latencies of visually-guided saccades of 47 right-handed subjects (32 with right leading and 15 with left leading eyes) were studied. Stimulation paradigm was spatially bidimentional, and stimuli were presented along horizontal, vertical and oblique axes. Three levels of visual space complicity and two traditional single-step GAP and OVERLAP temporal paradigms were used. A half of the left-leading-eye subjects had shorter latencies of the saccades directed towards the left (ipsilateral) hemifield, whereas only one fifth of the subjects demonstrated shorter latencies ofsaccades towards the right (contralateral) hemifield (53% vs 20%). Only one fourth of right-leading-eye subjects had shorter latencies of saccades towards the inpsilateral hemifield and one fifth of these subjects had shorter latencies of the saccades towards the contralateral hemifield (20% vs 25%). The interrelation between eye dominance and spatial asymmetry of saccadic latencies is revealed.

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In the review modern conceptions of the brain organization of visiomotor system are given. They based on neurophysiological and clinical researches which show reflection of attention processes at various levels of this system. Phenomenological data of saccadic eyes movements and existing models of saccade programming, which expressed on the basis of studying of saccades latent periods variation in different conditions of visual stimulation, are presented. Theoretical ideas of saccade programming stages according to "bloc" model of saccade programming are given. On the basis of literature data and own researches various views at the nature of "Gap-effect" and the express-saccades as a reflections of attention contribution in saccade programming are shown.

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A review. Recently published articles concerning the problem of attention are discussed, the most popular psychophysiological concepts and neurophysiological models of attention are described, and correlation of spatial attention and saccadic eyes movements is shown. The evidence for reflection of attention mechanisms and saccade preparation in intensity and topography of the visual evoked potentials and event-related potentials is given. On the basis of the results obtained by the authors and literature data, the contribution of attention to preparation of a saccade and its programming is shown. Different kinds of attention are reflected in a complex of EEG potentials of various duration and polarity. The analysis of parameters and topography of these potentials can serve a tool for investigation of the attention mechanisms.

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Fast negative EEG potentials preceding fast regular saccades and express saccades were studied by the method of backward averaging under conditions of monocular stimulation of the right and left eye. "Step" and "gap" experimental paradigms were used for visual stimulation. Analysis of parameters of potentials and their spatiotemporal dynamics suggests that, under conditions of the increased attention and optimal readiness of the neural structures, express saccades appear when the previously chosen program of the future eye movement coincides with the actual target coordinates. We assumed that the saccade latency decreases at the expense of the involvement of the main oculomotor areas of motor and saccadic planning in its initiation; an express saccade can be initiated also by means of direct transmission of the signal from the cortex to the brainstem saccadic generator passing by the superior colliculus. Moreover, anticipating release from the central fixation and attention distraction are necessary for the successful initiation of an express saccade.

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Parameters of saccadic eye movements were studied in patients with Parkinson's disease and control subjects. In parkinsonian patients, the number of slow regular saccades was shown to be increased, and the number of express saccades was shown to be decreased. As a result the mean of saccade latency in patients was longer than in the control group. Moreover, the percentage of multistep saccades in patients with Parkinson's disease. In this case, not one but two or three saccades were performed with smaller amplitude to the target. We point, that the multistep saccades occurred mainly among the express saccades. Obviously, the dopamine deficiency distinguishing parkinsonian patients takes the primary part in the development of saccadic disorders. Degeneration of the nigrostriatal dopamine pathway results in imbalance in activity of the direct and indirect output pathways of the striatum. We suppose that this leads to inhibition of neurons activity in the superior colliculus during the saccade performance, which results in the early saccade interruption. In support of this reasoning, the mean of saccade latency and the percentage of the multistep saccades decreased in patients with Parkinson's disease after dopamine D2/D3 agonist (piribedil) treatment, due to activity restoration of the indirect pathway.

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Three Macaca rhesus monkeys were used for studies of the performance of visually evoked saccades in single-step changes in the position of a stimulus using standard schemes for presentation of GAP-OVERLAP stimuli. Two spatial schemes were used: presentation of stimuli along the horizontal meridian (one-dimensional) and presentation of stimuli within a rectangular area of the visual field (two-dimensional). Asymmetrical foci of short-and long-latency saccades were found in the visual field. Dispersion factor analysis demonstrated that the dimensionality factor (one-dimensional versus two-dimensional stimulation schemes) had greater effects on the latent period of saccades than the lateralization factor (presentation on the left or right sides of the gaze point). The precision of the performance of visually evoked saccades decreased with increases in its eccentricity in both spatial stimulation schemes.

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The properties of visually-guided saccades were studied in three monkeys (Macaca rhesus). Traditional single-step GAP-OVERLAP temporal paradigms were used. Target stimuli were presented in accordance with two spatial stimulation schemes: (i) along the horizontal meridian (one-dimensional scheme) and (ii) within rectangle part of the visual field (two-dimensional scheme). We revealed asymmetric focuses of short- and long-latency saccades in the two-dimensional scheme of stimulation. The MANOVA revealed that the factor of dimensionality influenced saccadic latency to a greater extent than the factor of lateralization of stimuli (presenting in the right or left visual hemifields). Accuracy of saccades decreased with increasing in their eccentricity in both spatial schemes of stimulation.

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We used backward averaging method to study fast positive presaccadic EEG-potentials under conditions of the monocular stimulation of the leading and nonleading eye. Two schemes of the visual stimulus presentation ("no gap" and "overlap") were used. In the "no gap" condition, potential P1 dominated in the hemispere ipsilateral to a saccade direction. In the "overlap" condition, when the gaze was fixed at the central point, foci of this potential were localized in the sagittal derivations or in the same sites as in the "no gap" conditions. Irrespective on the stimulation scheme, the P2 foci were localized in the hemisphere contralateral to a saccade direction. We assume that the fast positive potentials involve both activation and inhibition processes in visuomotor structures and can be also associated with cognitive presaccadic processes (such as fixation disengage, attention lateralization and a preliminary extraction of motor programs from memory).

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Saccadic latency and averaged EEG-potentials connected with switching on of the set and cue visual stimuli were examined in 12 right-handed healthy subjects in M. Posner's "cost-benefit" experimental paradigm. It was shown that attention was reflected in parameters of positive potential P100 evoked by switching on of set and cue stimuli and P300 and slow positive wave PMP1 evoked by switching on of the set stimulus in the relevant conditions. The spatiotemporal pattern of P100 probably reflects the involvement of the frontoparietal network of spacial attention in the perception of a relevant stimulus. Prevalence of the P300 and PMP1 potentials in the right parietal cortex suggests that these potentials reflect processes of space attention and visual fixation. Late positive potentials in a 600-900-ms interval after switching on of the set stimulus were found. Their amplitude was higher in backward averaging and they were predominantly localized in the left frontal cortex. These findings suggest that the late potentials reflect the anticipation and motor attention processes.

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The EEG of 10 right-handed healthy subjects preceding saccade and antisaccade with mean values of latency in the eye fixations period were selected and averaged. The positive potential P2 appearing on the fixation stimuly switching on and slow positive wave following after it were more prominent before antisaccades than normal saccades. Space-temporal analyses of presaccadic potentials showed that right frontal cortex was activated more before antisaccades. These findings suggest that right cortical hemisphere dominate in spatial attention and inhibition of automatic saccades to visual stimuli in the period of antisaccades preparing. During the period of central fixations "intermediate" positivity potentials, developing in 600-400 ms prior to saccade or antisaccade onset, were find out. These potentials were predominantly recorded in the left frontal and frontosagittal cortical areas. The obtained evidence suggest that "intermediate" positive potentials a period related to the process of motor attention, anticipation and decision making in the period of eyes fixation.

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Latencies and other parameters of presaccadic potentials preceding antisaccades and normal saccades to visual stimuli were studied in 10 right-handed healthy subjects. The EEG was recorded in F3, F4, Fz, C3, C4, Cz, P3, P4, O1 and O2 derivation. EEG records preceding saccades and antisaccades with mean latencies were selected and averaged. The latencies of the leftward antisaccades were shorter than of the rightward antisaccades. The slow presaccadic negativity (in the period of central eye fixations) and fast N -2 and P -1 potentials within the latent period were more prominent before antisaccades than normal saccades. Spatiotemporal analyses of presaccadic potentials showed that the right frontal cortex was activated to a greater extent before antisaccades than before saccades. These findings suggest that right-hemispheric dominance in the spatial attention and inhibition of automatic saccades to visual stimuli in the period of antisaccades preparation.

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The EEG of 10 right-handed subjects preceding saccades with mean values of latent periods were selected and averaged. Two standard paradigms of presentation of visual stimuli (central fixation stimulus-peripheral target succession): with a 200-ms inerstimulus interval (GAP) and successive single step (SS). During the period of central fixation, two kinds of positive potentials were observed: fast potentials of "inermediate" positivity (IP) developing 600-400 ms prior to saccade onset and fast potentials of "leading" positivity (LP), which immediately preceded the offset of the central fixation stimulus. Peak latency of the LP potentials was 300 ms prior to saccade onset in the SS paradigm and 400 ms in the GAP paradigm. These potentials were predominantly recorded in the frontal and frontosagittal cortical areas. Decrease in the latency by 30-50 ms in the GAP paradigm was associated with more pronounced positive potentials during the fixation period and absence of the initiation potential P-1' (or decrease in its amplitude). The obtained evidence suggest that the fast positive presaccadic potentials are of a complex nature related to attention, anticipation, motor preparation, decision making, saccadic initiation, and backward afferentation.

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We studied the effect of bioactive peptide HLDF-6 on functional activity of the endogenous antinociceptive system in the offspring of morphine-tolerant animals. Disturbances in this system included changes in the thermonociceptive threshold and enkephalinase A activity in various brain structures. The peptide acted as a potent regulator of the homeostasis in systems responsible for the synthesis and catabolism of endogenous opioids. HLDF-6 effectively corrected disorders of the endogenous antinociceptive system.

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Saccadic latencies were studied in ten healthy subjects. Peripheral targets were presented monocularly to a leading and nonleading eyes in the right and left hemifields. SS (single step) and OVERLAP (200 ms) schemes of visual stimulation were used. Under OVERLAP conditions, the saccadic latency was longer by 30-39 ms and the number of long-latency saccades was higher than under SS conditions, especially in subjects with mixed asymmetry profiles. In the majority of subjects with right asymmetry profile, the latencies of saccades during stimulation of the leading eye were by 12 ms shorter than during stimulation of the nonleading eye, and the latencies of right saccades were by 24 ms shorter than that of the left saccades independently of the stimulated eye. The obtained results explain some characteristic features of hemyspheric asymmetry in organization of saccadic movements.

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