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At least 19 recordsLinked to original sources
PubMed1998

The mode of movement selection. Movement-related cortical potentials prior to freely selected and repetitive movements.

In two previous studies, the readiness potential (RP) has been reported to be influenced by the mode of movement selection. Freely selected movements were found to have a higher RP amplitude than fixed repetitive movements. This was attributed to the higher demands on planning for the performance of freely selected movements. However, movements in the free mode are distinct from movements in the fixed mode in more than one respect. For example, they are also associated with a higher degree of alteration of the side and/or the finger of movement execution and hence serial "novelty" across blocks of trials. The aim of our study was to establish whether the greater novelty of movements in the free mode could also contribute to the enhanced RP amplitude of movements in the free mode of movement selection by comparing free versus fixed movements performed in long and short sequences that differ in terms of serial novelty. The RP was recorded in 31 healthy young subjects with electrodes placed over Fz, C3, Cz, C4 and Pz. Two types of movement were studied: randomly chosen button presses with right or left index or middle finger (free mode), and repetitive pressing of a predetermined button (fixed mode). We found that: (1) in confirmation of previous studies, the amplitude of the RP was higher for freely selected than free movements; (2) the effect of the mode of movement selection was present over central electrodes but was most pronounced for parietal electrode Pz, with movements in the free mode showing the earliest and greatest increase in negativity at this site; (3) this parietally enhanced negativity in free compared with the fixed mode was absent after the subjects had performed a block of long movement sequences, suggesting that serial novelty of movements also contributed to the effect of mode on the RP amplitude; (4) both the latency and the magnitude of the lateralized readiness potential (LRP) were altered by the mode of movement selection. Movements in the free mode showed an earlier onset of the LRP, which had a higher peak than the LRP prior to movements in the fixed mode. This effect was mainly due to an increased amplitude of the RP over the electrode contralateral to the side of movement prior to freely selected movements. These findings are discussed in relation to previous RP and positron emission tomography studies.

Adult↗
PubMed1995

Movement-related potentials preceding voluntary movement are modulated by the mode of movement selection.

In two experiments movement-related cortical potentials preceding voluntary movement were recorded. In experiment 1, subjects performed four motor tasks involving joystick movements. The four tasks differed in complexity (single vs sequential movements) and in the mode of movement selection, i.e., whether a movement or movement sequence was made in fixed or in self-determined directions. The choice of these tasks was based, firstly, on previous electrophysiological studies suggesting an effect of task-complexity on the amplitude of the readiness potential (RP) and, secondly, on previous positron emission tomography (PET) studies showing that activity of the supplementary motor area (SMA) is influenced by the mode of movement selection. The results show that, for single movements, RP amplitude is higher preceding freely selected movements than preceding movements in a fixed direction. In experiment 2 this effect was replicated using button presses instead of joystick movements. The results converge with PET evidence obtained in similar tasks and establish that the RP is modulated by the mode of movement selection. This modulation is probably related to differential involvement of the SMA.

Adult↗
PubMed1989

Neuromagnetic fields accompanying unilateral finger movements: pre-movement and movement-evoked fields.

Neuromagnetic fields accompanying voluntary flexions of the right index finger were studied in five subjects. In all subjects, slow magnetic fields were observed over the central scalp beginning about 1 second prior to movement onset. These fields displayed a similar time course to the electrically recorded "readiness potential", but with reversals of field direction over regions of the rolandic fissure over both hemispheres. Least-squares fitting of two current dipole sources for the pre-movement fields resulted in a consistent localization of one source in the region of the rolandic fissure contralateral to the side of movement in four subjects. Ipsilateral dipole sources fitted inconsistently at deeper locations or outside the head indicating the inability of a single dipole source to account for the ipsilateral fields. A large field reversal was also observed over the contralateral (left) hemisphere, 90-130 ms after onset of EMG activity in the active muscles. In some subjects, single dipole sources could be fitted to this "movement-evoked" field at locations slightly deeper and posterior to the pre-movement source locations in the contralateral hemisphere, possibly indicating unilateral activation of somatosensory cortex related to sensory feedback during the onset of this movement. Subtraction of pre-movement field activity from post-movement fields improved the ability to fit a single contralateral rolandic source for all subjects suggesting that pre-movement sources continue to be active during movement onset. These findings confirm previous reports that voluntary finger movements are preceded by slow magnetic fields.(ABSTRACT TRUNCATED AT 250 WORDS)

Adult↗
PubMed1999

Study of mandibular movements in mandibulectomy patients--border movements and functional movements during mastication, deglutition and speech.

In mandibulectomy patients who have not undergone surgical reconstruction, the remaining mandibular segment is unstable and often deviated. Its movements have low reproducibility during mastication, deglutition and speech. The purpose of this study was to clarify three-dimensionally the differences in mandibular movements for each of these oral functions in mandibulectomy patients with and without mandibular continuity. Four mandibulectomy subjects (Group I) without mandibular continuity and three subjects (Group II) with mandibular continuity were selected. Their mandibular movements were recorded using a jaw movement tracking device with six degrees of freedom. Each movement was assessed graphically at the virtual incisor point and the rotational angles of the mandible in the frontal, sagittal and horizontal plane were analyzed. The findings were as follows; 1. In Group I, the border movements at the virtual incisor point exhibited an irregular and asymmetric envelope deviated to the resected side in the frontal plane, whereas Group II exhibited a smooth and symmetric envelope. 2. In Group I, the rotational angles in the frontal plane during border movements and mastication, in all planes during speech, and in the frontal and horizontal plane during deglutition were significantly larger than in Group II. A comparison among border and all functional movements in mandibulectomy patients revealed characteristic movements in the rotation of the mandible in the frontal plane. It is suggested that the rotational angle of the mandible is a useful parameter for assessment of mandibular movements in mandibulectomy patients.

Aged↗
PubMed1994

Influence of heterologous tobamovirus movement protein and chimeric-movement protein genes on cell-to-cell and long-distance movement.

Sunn-hemp mosaic tobamovirus (SHMV) moves slowly from cell to cell in Nicotiana tabacum cv. Xanthi, but fails to move long distance. To determine the role of the SHMV movement protein (MP) in cell-to-cell and long-distance movement in tobacco, the SHMV MP gene was inserted into a TMV-cDNA clone that had approximately the 5'-half of the endogenous MP gene deleted. RNA transcripts inoculated onto tobacco induced systemic infections by 8 days postinoculation. Sequence analysis of the MP genes from purified virus isolated from systemically infected leaf tissue indicated that chimeric SHMV/TMV MP genes had been generated through RNA-RNA recombination within the 3'-termini of the MP gene sequences. When exchanged for the MP gene of TMV, three of four chimeric MP genes analyzed provided long-distance movement function for the hybrid viruses in tobacco. Two of the three hybrid viruses that moved long distance showed enhanced cell-to-cell movement relative to a recombinant TMV that expressed the intact SHMV MP gene. These observations suggest that the C-terminus of the TMV MP contains a determinant that can influence cell-to-cell movement in tobacco. A recombinant virus, TLSM, that expressed the intact SHMV MP gene exhibited cell-to-cell movement that was intermediate to SHMV and TMV, but failed to produce coat protein and was defective in long-distance movement. To further examine the role of the SHMV MP gene in long-distance movement, transgenic N. tabacum cv. Xanthi that expressed the wild-type SHMV MP gene were generated and found to facilitate rapid and efficient long-distance movement of a TMV mutant that contained a dysfunctional MP gene. Therefore, the inability of SHMV to systemically infect tobacco is a function of virus components and sequences other than those encoded by the SHMV MP gene.

Base Sequence↗
PubMed1988

Primate motor cortex and free arm movements to visual targets in three-dimensional space. III. Positional gradients and population coding of movement direction from various movement origins.

In one experiment, we studied the relations between the frequency of discharge of 274 single cells in the arm area of the motor cortex of the monkey and the actively maintained position of the hand in space. We found that the frequency of discharge of 63.9% of the cells studied was a multilinear function of the position of the hand in space according to the following equation (multiple linear regression): d = f + fxsx + fysy + fzsz, where d is the discharge rate of a single cell, f, fx, fy, fz are regression coefficients, and sx, sy, sz are the coordinates of the position of the hand. The equation above defines a positional gradient which implies that the frequency of cell discharge will increase at a maximum rate when the position of the hand changes along a certain direction; we call this direction of orientation of the positional gradient, and the rate of change in discharge rate along this orientation, the magnitude of the gradient. The orientations of the positional gradients were distributed throughout three-dimensional (3-D) space and their magnitudes differed among different cells. In a different experiment, we studied the changes in activity of 289 cells in the arm area of the motor cortex when the monkeys made equal-amplitude movements that started from different points in space, were in the same direction, and traveled along parallel trajectories in 3-D space. Four pairs of such movement directions (i.e., a total of 8 movement directions) were studied for every cell, and the changes in cell activity associated with movements within each pair were compared. We found that these changes in cell activity did not differ statistically for 68.4% of the movement pairs studied but did differ for the remaining 31.6%. The data from the whole population of cells studied in this experiment were analyzed using the population vector analysis described in the preceding paper (Georgopoulos et al., 1988). Thus, 8 population vectors were calculated, 1 for each of the 8 movement directions studied. We found that the direction of the population vector was close to the direction of the corresponding movement. These results indicate that the population vector provides unique information concerning the direction of the movement even when the point of origin of the movement varies in 3-D space.

Animals↗
PubMed1981

Peripheral movement, induced movement, and aftereffects from induced movement.

Substantial rotatory induced movement and aftereffects associated with induced movement were observed in a large statis patterned disc bounded at its periphery by a rotating patterned annulus. The area of the annulus was less than one tenth that of the disc, so its peripheral location seemed to be important in eliciting these phenomena. This was confirmed in two experiments comparing a peripheral annulus and a relatively central anulus in their ability to elicit induced movement and aftereffects in the same large static field. Aspects of the vection (induced self-movement) phenomenon may have been involved in generation of induced movement. This suggested that the motion-inducing properties of the peripheral annulus might have derived from: (i) its eccentric location in the perceiver's visual field; or (ii) its location with regard to the display itself. Two further experiments showed that (ii) was important for the elicitation of both induced movement and the aftereffects, and (i) was important for the elicitation of induced movement. Neurons responsive to relative movement in conjunction with lateral inhibition may provide a partial explanation for these effects. However, they do not explain why the visual system can assign considerable movement to a large static field under the conditions of these experiments.

Adult↗
PubMed1996

Movement preparation in Parkinson's disease. Time course and distribution of movement-related potentials in a movement precueing task.

Investigations of the effects of advance information on movement preparation in Parkinson's disease using reaction time (RT) measures have yielded contradictory results. In order to obtain direct information regarding the time course of movement preparation, we combined RT measurements in a movement precueing task with multi-channel recordings of movement-related potentials in the present study. Movements of the index and middle fingers of the left and right hand were either precued or not by advance information regarding the side (left or right hand) of the required response. Reaction times were slower for patients than for control subjects. Both groups benefited equally from informative precues, indicating that patients utilized the advance information as effectively as control subjects. Lateralization of the movement-preceding cerebral activity [i.e. the lateralized readiness potential (LRP)] confirmed that patients used the available partial information to prepare their responses and started this process no later than controls. In conjunction with EMG onset times, the LRP onset measures allowed for a fractionation of the RTs, which provided clues to the stages where the slowness of Parkinson's disease patients might arise. No definite abnormalities of temporal parameters were found, but differences in the distribution of the lateralized movement-preceding activity between patients and controls suggested differences in the cortical organization of movement preparation. Differences in amplitude of the contingent negative variation (CNV) and differences in the way in which the CNV was modulated by the information given by the precue pointed in the same direction. A difference in amplitude of the P300 between patients and controls suggested that preprogramming a response required more effort from patients than from control subjects.

Adult↗
PubMed1992

Movement features and H-reflex modulation. II. Passive rotation, movement velocity and single leg movement.

Modulation of soleus H-reflex magnitudes during pedalling, and their approximation when seated with appropriate joint positions and contractile activity was demonstrated in the previous paper. The present study investigated the modulation of H-reflexes during (A) pedalling movement in the absence of contractile activity, (B) different movement velocities and (C) movement of a single limb. Using a customized tandem cycle ergometer, seated subjects with trunk supported relaxed their leg muscles and allowed their legs to be rotated. Their feet were supported on the pedals with the ankle braced. Reflexes were collected at four phases in the movement cycle (with some at 13 phases) and with speeds of 5-60 revolutions per min (cycle times from 12 to 1 s). The results showed that (i) reflex magnitude substantially decreased with limb rotation (P less than 0.05). The degree of inhibition was dependent on the phase position. (ii) Increasing speed of passive rotation increased the inhibition at all positions, but was most pronounced near the fullest flexion of hip and knee. When subjects actively pedalled, the relationship between speed and inhibition remained. (iii) When the contralateral leg was moved and the target leg was stationary, crossed projection of reflex inhibition was clear. (iv) The reflex gain measured during active pedalling of one leg was similar to that observed during two legged pedalling. Again, a crossed effect from the contralateral leg could be observed. We conclude that the net influence of discharge from movement-elicited afference is inhibitory on this reflex path and that the reflex modulation during pedalling arises from overlaid sources.(ABSTRACT TRUNCATED AT 250 WORDS)

Adult↗
PubMed1989

[Study on grinding movements in chewing. 2. Relationship between grinding movement in chewing-like empty jaw movement and occlusal form of molar].

The purpose of this study is to clarify the relationship between the occlusal form of a molar and mandibular movement. For this purpose I measured the occlusal form of the upper first molar, and the 3-dimensional movement of the lower first molar during the grinding movement in chewing-similar to empty jaw movement. In this study the following three parameters were analyzed.; (1) the distance between the upper and lower first molars in the lateral occlusal position, (2) the inclination of the cusp-slope, (3) the inclination of the lower first molar path. Results were follows: 1) On the working side, the inclination of the cusp-slope is closely connected to that of the path, 2) On the non-working side, the correlation between the inclination of the cusp-slope, and that of the path was so weak, as to be statistically insignificant. 3) The distance between the molars tended to increase as the inclination of the path steepened. This tendency was marked on the non-working side. The results mentioned above proved that, in cases with steeper anterior guidance, the upper and lower first molars disclude more on both the working and non-working sides. On the working side, however, the steeper cusp-slope prevents excessive disclusion of molars.

Dental Occlusion↗
PubMed1989

[Study on grinding movements in chewing. 1. A comparison between grinding movement in chewing-like empty jaw movement and lateral excursion].

The purpose of this study is to clarify the relationship between grinding movements during chewing, and lateral excursions starting from the intercuspal position. For this purpose, I measured two different types of three-dimensional mandibular movement; lateral excursions and empty-jaw movement like chewing in 10 subjects, and compared these paths with each other in the lateral occlusal position, when the incisal point is 2.0 mm distant from the intercuspal position. The results can be summarized as follows: 1. The two positions of the incisal point were statistically coincident. 2. The position of both working and non-working side molars during chewing tended to be inferior to that during lateral excursion. 3. The moved distance of the working side condyle during chewing was significantly less than that during lateral excursion. 4. The position of the non-working side condyle during chewing tended to be medial to that during lateral excursion. 5. The difference in the condylar position was deeply related to that in the molar position. The differences mentioned above were considered to be originated from the difference in the masticatory muscle activity and the occlusal contact.

Dental Occlusion, Centric↗
PubMed1992

Role of primate basal ganglia and frontal cortex in the internal generation of movements. II. Movement-related activity in the anterior striatum.

In order to more comprehensively assess the role of the basal ganglia in the internal generation of movements, we studied the activity of neurons in the head of the caudate and in the rostral putamen in relation to the execution of movements. Monkeys performed self-initiated and stimulus-triggered arm reaching movements in separate blocks of trials. With stimulus-triggered movements, 217 striatal neurons increased their activity after the trigger stimulus (127 in caudate, 90 in putamen). Of these, 68 neurons showed time-locked responses to the trigger stimulus, with a median latency of 60 ms, that were independent of visual or auditory stimulus modalities. Three quarters of responses were conditional on a movement being performed. These responses may participate in neuronal processes through which the reception of a stimulus is translated into the execution of a behavioral reaction. Further, 44 neurons increased their activity before the earliest muscle activity without being clearly time-locked to the stimulus (148-324 ms before movement onset), 55 neurons were activated later before the movement, and 50 neurons were activated after movement onset. With self-initiated movements, 106 striatal neurons showed movement-related activity beginning up to 460 ms before movement onset (52 in caudate, 54 in putamen). Comparisons between the two types of movement were made on 53 neurons with premovement activity beginning more than 500 ms before self-initiated movements. Only one fifth of them also showed movement-related activity with stimulus-triggered movements, including trigger responses. Comparisons among 39 neurons with movement-related activity during self-initiated arm movements showed that about half of them also showed movement-related activity with stimulus-triggered movements. These data demonstrate a considerably segregated population of striatal neurons engaged in the internal generation of movements, whereas processes underlying the execution of movements appear to involve overlapping neuronal populations.

Animals↗
PubMed1992

Influences of hand movements on eye movements in tracking tasks in man.

We investigated horizontal smooth pursuit eye movements and hand movements in tracking tasks in order to find out whether hand movements influence eye movements and if so, in what ways. Externally controlled target movements were tracked either by the eyes alone or by the eyes and right hand together. Because a possible influence might depend on the stimulus, we used two classes of target movements: sinusoidal target movements (predictable target movements) and pseudo-random target movements (unpredictable target movements). Our data show that the eye movements contained only a few small saccades when sinusoidal target movements with frequencies higher than about 1 Hz were tracked by eyes and hand together. More and larger saccades were made when the same target movements were tracked by the eyes alone. The difference in smoothness of eye movements was highly significant between the two tracking conditions. Such a difference was not found during the tracking of a pseudo-random target motion. This suggests that the influence of hand movements is related to the predictability of the stimulus. In contrast to the gain of the smooth pursuit eye movements and the maximum of the cross-correlation function, the gain of the composite eye movements did not depend on the tracking condition. The delay of the eye movements with respect to the (sinusoidal) target movements also showed no dependence on the tracking condition. Visual feedback from the tracking hand was found not to play a role in the difference in eye movements for the two tracking conditions.

Feedback↗
PubMed2002

Movement-related potentials associated with self-paced, cued and imagined arm movements.

Self-paced movements, movement to a cue and imagined movement have all been reported to be preceded by a prolonged negativity on averaged electroencephalograph (EEG) recordings. Considerable evidence supports an important contribution from the supplementary motor area (SMA) to this potential and all three types of movement have been shown to be associated with SMA activation. This study was designed to compare the premovement component of these movement-related potentials (MRPs) in a group of subjects who performed each of these three types of movement. In addition, in view of the greater SMA activation in association with proximal arm movements, we studied movements at multiple joints in the right arm. All the potentials were largest at Cz. Self-paced movements were preceded by a negativity (mean onset 1.2 s prior to electromyographic activity) with two distinct phases - an early slow increase (early BP, Bereitschaftspotential) and a later, steeper phase (NS', negative slope). Proximal movements were associated with a larger peak amplitude (mean peak amplitude for shoulder 11.6 micro V, finger movement 9.0 micro V at Cz, n=14) due to a bigger NS' phase. Movements to a regular cue, but not to a randomly timed cue, were also preceded by a long duration negativity, but the NS' phase began earlier and was less distinct than for self-paced movements (mean peak amplitude for shoulder movement 9.1 micro V, finger 8.2 micro V at Cz, n=12). Imagining the movements to a regular cue was associated with a slow negativity, with no clear NS' phase (mean peak amplitude for shoulder movement 6.5 micro V, finger 6.2 micro V at Cz). Our results indicate that the MRPs prior to the three types of movement have distinct characteristics, most notably for the NS' phase. The MRP associated with movement to a regular cue may be analogous to the S2-related negativity of the contingent negative variation (CNV). We discuss the findings in the light of current evidence from functional imaging as to the cortical areas activated in similar movements.

Adult↗
PubMed1999

Mesial motor areas in self-initiated versus externally triggered movements examined with fMRI: effect of movement type and rate.

The human frontomesial cortex reportedly contains at least four cortical areas that are involved in motor control: the anterior supplementary motor area (pre-SMA), the posterior SMA (SMA proper, or SMA), and, in the anterior cingulate cortex, the rostral cingulate zone (RCZ) and the caudal cingulate zone (CCZ). We used functional magnetic resonance imaging (fMRI) to examine the role of each of these mesial motor areas in self-initiated and visually triggered movements. Healthy subjects performed self-initiated movements of the right fingers (self-initiated task, SI). Each movement elicited a visual signal that was recorded. The recorded sequence of visual signals was played back, and the subjects moved the right fingers in response to each signal (visually triggered task, VT). There were two types of movements: repetitive (FIXED) or sequential (SEQUENCE), performed at two different rates: SLOW or FAST. The four regions of interest (pre-SMA, SMA, RCZ, CCZ) were traced on a high-resolution MRI of each subject's brain. Descriptive analysis, consisting of individual assessment of significant activation, revealed a bilateral activation in the four mesial structures for all movement conditions, but SI movements were more efficient than VT movements. The more complex and more rapid the movements, the smaller the difference in activation efficiency between the SI and the VT tasks, which indicated an additional processing role of the mesial motor areas involving both the type and rate of movements. Quantitative analysis was performed on the spatial extent of the area activated and the percentage of change in signal amplitude. In the pre-SMA, activation was more extensive for SI than for VT movements, and for fast than for slow movements; the extent of activation was larger in the ipsilateral pre-SMA. In the SMA, the difference was not significant in the extent and magnitude of activation between SI and VT movements, but activation was more extensive for sequential than for fixed movements. In the RCZ and CCZ, both the extent and magnitude of activation were larger for SI than for VT movements. In the CCZ, both indices of activation were also larger for sequential than for fixed movements, and for fast than for slow movements. These data suggest functional specificities of the frontomesial motor areas with respect not only to the mode of movement initiation (self-initiated or externally triggered) but also to the movement type and rate.

Adult↗
PubMed1989

Distribution of neurons with set- and movement-related activity before hand and foot movements in the premotor cortex of rhesus monkeys.

Neuronal activity was studied in the premotor cortex (PM) of two rhesus monkeys, each of which performed both forelimb and hindlimb movements. On each trial, the monkey received a visual instruction stimulus (IS) that indicated whether a foot or a hand movement would be rewarded on that trial. After a delay period, during which the monkey withheld an overt movement, a visual trigger stimulus (TS) was presented to indicate that the monkey should execute a movement. Of 572 task-related neurons recorded in PM, 149 neurons showed set-related activity, defined as a significant increase or decrease in discharge rate throughout most of the instructed delay period, and 299 neurons showed movement-related activity, defined as a significant change in discharge rate between the TS and movement onset. Both set- and movement-related activity were subdivided into three patterns: activity modulation 1) before a foot movement only ("foot" neurons); 2) before a hand movement only ("hand" neurons); and 3) before both foot and hand movements ("mixed" neurons). The distribution of set-related neurons mostly overlapped with that of movement-related neurons, although set-related neurons were located in more restricted regions than movement-related neurons. "Foot" neurons with set- and movement-related activity were distributed near the superior precentral sulcus. "Hand" neurons were mainly located lateral to the "foot" neurons with some overlap. The results indicate that most PM set- and movement-related neurons contribute, respectively, to the preparation for and execution of specific limb movements, as opposed to movement per se. Further, the differential distribution of neurons with activity related to hindlimb vs. forelimb movement supports previous indications that PM is topographically organized.

Animals↗
PubMed1993

A cortical slow potential is larger before an isolated movement of a single finger than simultaneous movement of two fingers.

Movement-related cortical potentials (MRCPs) preceding voluntary, self-paced, simultaneous extension of the middle and index fingers (two finger movement) were compared with those preceding extension of the index or middle finger alone (single finger movement) of the right hand in 7 right-handed normal subjects. It was meant to double the number of muscles involved in the two finger movement as compared with the single finger movement and to activate only the motor cortex involving the movement of distal joints. The NS' (negative slope) amplitude with the isolated middle finger movement was significantly larger at the precentral area contralateral to the movement as compared with the two finger movement. The NS' amplitude with the index finger movement was also larger than that with the two finger movement at the contralateral precentral area, but the difference was not significant. It is postulated that greater activation of the primary hand sensorimotor area (HSMA) contralateral to the movement might be necessary for the isolated movement of a single finger than for the two finger movement, although a smaller area of HSMA is expected to be activated in the former than in the latter. The NS' may be related to central motor control processes independent of muscle mass activated. As the single finger movement is considered to be more discrete and fine as compared with the simultaneous two finger movement, it is concluded that the HSMA plays an especially important role in discrete and fine finger movement.

Adult↗
PubMed2000

Oscillatory cortical activity and movement-related potentials in proximal and distal movements.

OBJECTIVES: Event-related desynchronization (ERD) of alpha- and beta-rhythms, the post-movement beta-synchronization and the cortical movement-related potentials were analyzed in distal (finger) and proximal (shoulder) movements. METHODS: EEG was recorded in 7 healthy right-handed men using a 59-channel whole-head EEG system while subjects performed self-paced movements. RESULTS: The amplitude of the Bereitschaftspotential (BP) was greater over the central midline area and smaller over the contralateral sensorimotor hand area in shoulder than in finger movements. The maximal alpha- and beta-ERD was localized at parietal electrodes in shoulder movements and over the left and right sensorimotor hand area in finger movements. The post-movement beta-ERS was greater in shoulder than in finger movements, especially at the electrode located 3.5 cm left of the central midline electrode. A significant correlation between the slope of the terminal portion of the BP (negative slope) and amplitude of the post-movement beta-synchronization was observed in shoulder but not in finger movements. CONCLUSIONS: Enhancement of BP over the central midline electrode suggests increased activation of the supplementary motor area in proximal movements. The spatial distribution of the alpha- and beta-ERD and of the post-movement beta-ERS shows topographic differences which may refer to the somatotopic organization of the primary sensorimotor cortex with shoulder representation medial to hand and fingers. The correlation between the negative slope and the post-movement beta-ERS in proximal movements supports the view that the brief post-movement inhibition over the motor cortical area is related to the pre-movement activation of that area.

Adult↗