Positive potentials of the human brain at different stages of preparation of a visually triggered saccade

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.     

Lateralization of saccadic latency during monocular presentation of stimuli to a leading and non-leading eye

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.     

Slow Cortical Potentials Preceeding Visually Guided Saccades in Schizophrenics

The parameters of saccades and presaccadic slow potentials were studied in right-handed men with a dominant right eye, including 19 schizophrenics and 12 healthy subjects. For visual stimulation, three light-emitting diodes were used, which were located in the center of the visual field (the central fixation stimulus) and 10° to the right and left of it (peripheral stimuli). Two stimulation protocols were used: with a simultaneous switching off of the central fixation stimulus and switching on of the peripheral stimuli (test 1) and with an interstimulus gap of 200 ms (test 2). According to the latency, saccades were divided into anticipatory, express, and regular. Slow EEG potentials preceding regular saccades were analyzed. It was found that the proportion of anticipatory saccades is considerably higher than the normal value in schizophrenia. The analysis of the presaccadic potentials demonstrated a significant decrease in the amplitude of negative potentials in the vertex region at early stages of presaccadic preparation and its increase in the occipital region at late stages. Test 2 in the patients demonstrated an increase in the positivity focus in the frontal region of the right hemisphere. It was assumed that the alterations found in schizophrenia result from the deficit of frontal cortical fields.     

Potential of the human cerebral cortex prior to antisaccades

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.     

Cortical positive potentials in the period of eye fixation prior to saccades and antisaccades

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.     

Cortical slow negative potentials during eye fixation and preparing of visually triggered saccades in a man

In 10 right-handed healthy subjects EEGs preceding saccades with mean latent periods were selectively averaged. Two standard schemes of visual stimulation were used: with immediate presentation of a peripheral target stimuli after the central fixation stimulus (a single step paradigm) and with the interval between the stimuli in 200 ms (GAP paradigm). Two waves of slow premotor negativity (early PMN1 and late PMN2) that appeared 930 +/- 79 and 609 +/- 82 ms, respectively, prior to a saccade onset were observed. The PMN2 was followed by the negative potentials N-3, N-2, and N-1 (saccadic initiation potential). It was found that in GAP stimulation condition the PMN1 was less pronounces and N-1 was increased as compared to the single step. These findings suggest that disengage of attention from the central point during the GAP period clears the saccadic system for decision making and initiation of a saccade. Under such conditions, the expectation of a visual target does not require a high level of nonspecific activation and motor attention.     

Asymmetry of the latent periods of saccades in human depending on visual space complicity

Saccadic latencies of visually-guided saccades of 10 right-handed subjects with right-leading eyes were studied. Stimulation paradigm was spatially bidimentional, and stimuli were shown along horizontal and vertical meridians. Three traditional single step GAP - NO DELAY - OVERLAP temporal paradigms were used. In the first experiment, each paradigm was applied separately (simple visual space). In the second experiment, all the three paradigms were varied pseudo-random order and equiprobably, which complicated the time parameters of visual stimulation (complicated visual space). Asymmetry of visually-guided saccades along the vertical and horizontal meridians was revealed. The character of this asymmetry varied between subjects. MANOVA showed that the factor of visual space complicity (simple or complicated visual space) affected the latent period of saccades to a greater extent than the factor of stimulus lateralization (stimulus presentation in the left/right or upper/lower visual hemifields).     

The Frontal Eye Field Is Involved in Visual Vector Inversion in Humans – A Theta Burst Stimulation Study

In the antisaccade task, subjects are requested to suppress a reflexive saccade towards a visual target and to perform a saccade towards the opposite side. In addition, in order to reproduce an accurate saccadic amplitude, the visual saccade vector (i.e., the distance between a central fixation point and the peripheral target) must be exactly inverted from one visual hemifield to the other. Results from recent studies using a correlational approach (i.e., fMRI, MEG) suggest that not only the posterior parietal cortex (PPC) but also the frontal eye field (FEF) might play an important role in such a visual vector inversion process. In order to assess whether the FEF contributes to visual vector inversion, we applied an interference approach with continuous theta burst stimulation (cTBS) during a memory-guided antisaccade task. In 10 healthy subjects, one train of cTBS was applied over the right FEF prior to a memory-guided antisaccade task. In comparison to the performance without stimulation or with sham stimulation, cTBS over the right FEF induced a hypometric gain for rightward but not leftward antisaccades. These results obtained with an interference approach confirm that the FEF is also involved in the process of visual vector inversion.     

The effects of simulated microgravity on characteristics of slow presaccadic potentials

The parameters of saccades and presaccadic slow potentials were studied in seven right-handed male volunteers with a dominant right eye before and after exposure to 6-day dry immersion. Visual stimuli were presented using three light diodes, which were located in the center of the visual field (the central fixation stimulus) and 10° to the right and left of it (peripheral stimuli (PSs)). The subjects performed a test with simple saccades to a PS and a test with antisaccades to the point located symmetrically in the opposite visual field. The EEG (19 monopolar leads) and electrooculogram were recorded. To isolate slow potentials, backward EEG averaging was performed, with the moment of switching on the PS serving as a trigger for the averaging. It was found that the characteristics of saccadic eye movements did not substantially change after exposure to immersion. However, both tests revealed a change in topography and a decrease in the amplitude of presaccadic slow negative potentials (PSNPs) during immersion. Characteristically, the focus of presaccadic negativity shifted to the right hemisphere so that the PSNP amplitude sharply decreased in the left and increased in the right hemisphere. A significant decrease in the PSNP amplitude on day 6 of immersion was found in the midline and left-hemispheric frontal and parietal leads. It may be suggested that, because of support unloading and a decrease in proprioceptive input, exposure to microgravity causes a decrease in the activity of the left hemisphere and prefrontal and parietal cortices, initially involved in preparation and realization of motor responses. The activation of the right hemisphere could be of compensatory character.     

The influence of eye dominance on saccade characteristics and slow presaccadic potentials

Characteristics of saccades and presaccadic slow potentials were studied in 36 right-handed men with right (the RE group) and left (the LE group) eye dominance. Three light-emitting diodes located in the center of the visual field (the central fixation stimulus, CFS) and 10 deg to the left and to the right of the center (peripheral stimuli, PSs) were used for stimulation. The subjects performed a task with simple saccades to a PS and a task with antisaccades to the horizontal mirror position of the PS. Monopolar EEGs at 19 derivations and electrooculograms (EOGs) were recorded. Back averaging of the EEG time-locked to the PS onset or the saccade onset was used to obtain slow presaccadic potentials. The saccade characteristics in the RE and LE groups were similar. Differences between them were found only in the antisaccade task. The amplitude of negative presaccadic potentials (NPPs) time-locked to the PS in the frontal cortex was lower in the LE group compared to the RE group. Analysis of potentials time-locked to the saccade onset showed that changes in the slow potentials during the last 50 s before the saccade depended on the saccade direction and reflected the activation of the hemisphere opposite to the saccade direction. The activation of the right hemisphere before left-side saccades was higher in the LE than the RE group. In addition, the amplitude of NPPs was decreased in the frontal area and increased in the left posterior temporal area in the LE group compared to the RE group. The obtained results indicate that the involvement of the frontal cortex in cognitive and motor processes is decreased in subjects with the left eye dominance.     

The influence of support withdrawal on presaccadic EEG potentials in subjects with different asymmetry profiles

Characteristics of saccades and parameters of slow presaccadic potentials were studied in 12 volunteers, including seven subjects with a leading right eye (the RE group) and five subjects with a leading left eye (the LE group) before and on the sixth day of dry immersion. For visual stimulation, three light-emitting diodes were used; one of them was located in the center of the visual field, and two other, 10° away from the horizontal axis to the right and left of the first one. The subjects performed an anti-saccade test, which included making saccades at the spot that was symmetrically located in the visual field opposite to the stimulus. The EEG (19 standard unipolar derivations) and electrooculogram were recorded. To obtain slow presaccadic potentials (PSPs), backward averaging triggered by switching on a peripheral stimulus was performed. Before the immersion, there were no significant differences in the characteristics of saccades in both groups of subjects. At the same time, the amplitude of presaccadic negativity (PSN) in the LE group was decreased, especially in the frontal region, and had considerable asymmetry during the analysis. During the immersion, the latent periods of the saccades and the percentage of incorrect reactions did not change in RE subjects and were increased in LE subjects. Both groups demonstrated a decrease in the PSN amplitude and its shift to the right hemisphere; intergroup differences decreased in immersion conditions. The characteristic feature of the RE group was a significant decrease in PSN in frontal leas at immersion, apparently caused by sensory disintegration and a decrease in the tonic afferent input. In the LE group, the maximal amplitude of PSN was observed in the central region.     

Startle Auditory Stimuli Enhance the Performance of Fast Dynamic Contractions

Fast reaction times and the ability to develop a high rate of force development (RFD) are crucial for sports performance. However, little is known regarding the relationship between these parameters. The aim of this study was to investigate the effects of auditory stimuli of different intensities on the performance of a concentric bench-press exercise. Concentric bench-presses were performed by thirteen trained subjects in response to three different conditions: a visual stimulus (VS); a visual stimulus accompanied by a non-startle auditory stimulus (AS); and a visual stimulus accompanied by a startle auditory stimulus (SS). Peak RFD, peak velocity, onset movement, movement duration and electromyography from pectoralis and tricep muscles were recorded. The SS condition induced an increase in the RFD and peak velocity and a reduction in the movement onset and duration, in comparison with the VS and AS condition. The onset activation of the pectoralis and tricep muscles was shorter for the SS than for the VS and AS conditions. These findings point out to specific enhancement effects of loud auditory stimulation on the rate of force development. This is of relevance since startle stimuli could be used to explore neural adaptations to resistance training.     

The effect of selective attention on pattern-specific visual evoked potentials

In a complex choice reaction time experiment, patterned stimuli without luminance change were presented, and pattern-specific visual evoked potentials to lower half-field stimulation were recorded. Two experimental conditions were used. The first was the between-field selection, where square patterns were presented in either the lower or the upper half of the visual field. In a given stimulus run one of the half-fields was task-relevant, and the subjects' task was to press a microswitch to stimuli of higher duration value (GO stimuli), while they had to ignore shorter ones, i. e. stimuli of lower apparent spatial contrast (NOGO stimuli). They had to ignore the stimuli appearing in the irrelevant half-field (IRR stimuli). In order to ensure proper fixation, the subjects had to press another microswitch at the onset of a dim light at the fixation point (CRT stimuli). Our second experimental condition was the within-field selection, where the GO, NOGO, and IRR stimuli appeared in the lower half of the visual field. GO and NOGO were square patterns while IRR stimuli were constructed of circles, or vice versa. (The CRT stimuli were the same as in the previous condition.) Three pattern-specific visual evoked potential components were identified, i. e. CI (70 ms latency), CII (100 ms latency), and CIII (170 ms latency). There were marked selective attention effects on both the CI-CII and CII-CIII peak-to-peak amplitudes. In both experimental conditions, responses with the highest amplitude were evoked by the GO type of stimuli, while the IRR stimuli evoked the smallest responses. According to these results, attention effects on the pattern-specific visual evoked potentials in the first 200 ms cannot be attributed to a simple stimulus set kind of selection.     

Asymmetry of the amplitude-temporal properties of visually-guided saccades in monkeys depending on the complexity of the spatial scheme of the visual stimulation

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.     

Precisely timed oculomotor and parietal EEG activity in perceptual switching

Blinks and saccades cause transient interruptions of visual input. To investigate how such effects influence our perceptual state, we analyzed the time courses of blink and saccade rates in relation to perceptual switching in the Necker cube. Both time courses of blink and saccade rates showed peaks at different moments along the switching process. A peak in blinking rate appeared 1,000 ms prior to the switching responses. Blinks occurring around this peak were associated with subsequent switching to the preferred interpretation of the Necker cube. Saccade rates showed a peak 150 ms prior to the switching response. The direction of saccades around this peak was predictive of the perceived orientation of the Necker cube afterwards. Peak blinks were followed and peak saccades were preceded by transient parietal theta band activity indicating the changing of the perceptual interpretation. Precisely-timed blinks, therefore, can initiate perceptual switching, and precisely-timed saccades can facilitate an ongoing change of interpretation.     

The effect of the visual stimulation of the leading and nonleading eye on the value of the saccadic latency period and on the peak latency of rapid presaccadic potentials]

Visual targets were presented monocularly to the leading and nonleading eyes. The complex of rapid positive and negative potentials was studied using the reverse summation from the onset of saccades. The latencies of saccades and peak latencies of the averaged presaccadic potentials were measured. The dependence of the saccade latencies and peak latencies of the complex of potentials on stimulation of the leading or nonleading eye and saccade direction was not simple and was largely determined by the individual profile of asymmetry. It is suggested that during stimulation of the leading eye the processes of attention fixation and switching as well as of the space visual processing are faster than during stimulation of the nonleading eye. Thus, the leading role of the right eye is reflected not only in fixation processes but also in movement anticipation.     

Modulation of backward pattern masking by focal visual attention

The effect of focal visual attention on backward pattern masking was investigated using an orientation discrimination task. The results show that attention reduces primarily the effect of interruption masking, the later component of pattern masking, which occurs when the delay between the target and mask onset is about 50-150 ms. The strongest spatial cueing effect, i.e. the strongest reduction of the orientation discrimination threshold due to focal attention, was observed at intermediate (approximately 100 ms) target-to-mask stimulus onset asynchrony (SOA). There was a weak effect of cueing at shorter SOAs, and no or a very weak attentional effect was present at longer target-to-mask SOAs, where the pattern masking effect is absent. The dynamics of attentional modulation of backward pattern masking correlates closely with the dynamics of the attentional modulation of neuronal responses in the early visual cortex.     

Amplitude-temporal parameters of the evoked potentials of the visual and motor areas in the visual perception and mental representation of an image

Amplitude-temporal analysis was carried out of the EP components of the visual and motor areas elicited by neutral (diffuse light) and structural (checker board pattern) stimuli in different situations, defined by instruction. Interserial comparisons showed that at any instruction, the latency of the first EP component of the motor areas is reduced; as a result it can appear here simultaneously with the EP of the visual areas. At the instruction involving the subject in the process of active change of perception, activation of the right hemisphere, including the motor area, is manifest by EP parameters, while the right occipital area is activated in response to the structural stimulus, and the left one--in response to the neutral stimulus. At complication of the stimulus or instruction, the period is prolonged when the latency of EP components of the motor area is shorter than the latency of the isopolar components of the visual area--from 120 to 150 ms in response to the neutral stimuli and the neutral with their counting; from 90 to 150 ms in response to the structural stimuli; from 80 to 210 ms in response to the neutral stimuli with mental representation of the structural one.     

Reaction time and interhemispheric interaction

The study was made on healthy adult subjects. The reaction time of the hand (RT) was measured under two conditions: 1) the choice of reaction (right or left hand) is determined by the nature of the warning stimulus; 2) decision on the choice is taken, depending on the second, trigger stimulus. Stimuli are presented at random sequences to different visual fields. The reaction time to the visual signal presented to the visual field ipsilateral to the hand is significantly shorter (by 15 to 26 msec) than to the stimulus in the contralateral visual field. In a simple motor reaction, when no discrimination of trigger stimulus and the decision on the choice of reaction is required, a hemispheric asymmetry of reaction time is manifested: the left hemisphere only responds differently to direct visual stimulation and to that mediated through the contralateral hemisphere.     

Song switching and agonistic stimulation in the song sparrow (Melospiza melodia): five tests

Male song sparrows in southeastern Ontario have repertoires of five to 11 distinct song types. The singer repeats each song type a variable number of times before switching to another type. Analysis of territorial singing suggested that rate of switching song types is positively correlated with intensity of agonistic stimulation, where ‘agonistic’ signifies conflict-related. The song-switching hypothesis was tested with playback experiments which varied stimulus intensity in five different ways: (1) presence or absence of song stimuli; (2) addition of visual to auditory stimuli; (3) location of the song stimulus 20 m inside or outside territory; (4) nesting phases of the subjects; and (5) switching rate and rate of novel song type production of the playback (i.e. stimulus versatility). The subjects' switching rates and flight rates consistently increased with greater stimulation, although song rate tended to remain unaffected. The signalling of response intensity through adjustments in switching rate exemplifies how song repertoires function in agonistic communication.