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PubMed1996

Control of remembered reaching sequences in monkey. II. Storage and preparation before movement in motor and premotor cortex.

Single-neuron responses in motor and premotor cortex were recorded during a movement-sequence delay task. On each trial the monkey viewed a randomly selected sequence of target lights arrayed in two-dimensional space, remembered the sequence during a delay period, and then generated a coordinated sequence of movements to the remembered targets. Of 307 neurons studied, 25% were tuned specifically for either the first or the second target, but not both. In particular, for neurons tuned during both target presentations, tuned activity related to a particular first target direction were maintained during the presentation of a second target in a different direction. During the delay period, 32% of the neurons were tuned for upcoming movement in a single direction. These delay period responses often reflected activity patterns that first developed during target presentations and may therefore act to maintain target period information during the delay. Neurons with tuned activity during both the delay and movement periods exhibited two patterns: the first exhibited tuned responses during the delay that were correlated with the tuning of first-movement responses, while the second pattern showed delay-period tuning that was better correlated with tuned responses during second movements. This indicates that, before movement, distinct neural populations are correlated with specific movements in a sequence. About half the neurons studied were not directionally tuned during the initiation, target, or delay periods, but did show systematic changes in activity during task performance. Some (34%) were exclusively tuned during movement and appear to be involved in the direct control of movement. Others (17%) showed changes in firing rate from period to period within a trial but showed no directional preference for a particular direction of movement. Population analyses of tuned activity during the target and delay periods indicated that accurate directional information about both first and second movements was available in the neuronal ensemble well before reaching began. These results extend the idea that both motor and premotor cortex play a role in reaching behavior other than the direct control of muscles. While some early neural responses resembled muscle activation patterns involved in maintaining fixed postures before movement, others probably relate to the sensory-to-motor transformations, information storage in short-term memory, and movement preparation required to generate accurate reaching to remembered locations in space.

Animals↗
PubMed1992

Single-unit activity in the globus pallidus and neostriatum of the rat during performance of a trained head movement.

Single-unit extracellular neuronal recordings were obtained from the globus pallidus (GP) and the neostriatum (NS) of rats while they performed a learned head movement in response to an auditory cue. In both GP and NS, units that altered their discharge rate in association with head movements and with the cues that triggered these head movements were prevalent. Frequently, the responses were directionally-specific (i.e., the magnitude or direction of change in firing rate of these neurons was substantially different for trials in which head movements were made to the left vs. the right). For some units, firing rates were altered only in response to the movement cue or only in association with head movements. However, the majority of neurons exhibited responses with both cue-related and movement-related components. Neuronal responses to the auditory cue usually were context-dependent, in that they did not occur if the same stimulus was presented when the animal was not performing the task. At least a small proportion of GP and NS neurons also appeared to exhibit context-dependent movement-related activity, in that responses occasionally were observed that were associated either with sensory-triggered head movements or with spontaneous head movements, but not with both. These data are consistent with previous suggestions that the activity of basal ganglia neurons during movement performance is highly dependent on the conditions associated with movement initiation. The data also indicate that the response characteristics of both GP and NS neurons in the rat are generally similar to those that have been described for basal ganglia neurons in primates and cats during sensory-triggered movement tasks. However, the proportion of task-related neurons that exhibited responses with both movement-related and cue-related components was greater than has generally been reported in studies of cats and primates, suggesting that neurons with these response properties may be more predominant in the rat basal ganglia.

Acoustic Stimulation↗
PubMed1994

Inaccuracy and instability of sequential movements in Parkinson's disease.

Animal studies suggest that the basal ganglia (BG) provide internal cues to trigger submovements in a movement sequence, with Parkinson's disease (PD) involving a deficiency in this cueing mechanism. However, it is not clear why defective internal cues can produce slow movements, or the extent to which slow movements are indeed the basic movement abnormality or are perhaps a compensatory mechanism for some other primary deficit. In this study we examined a number of the kinematic indices of matched fast movements between PD patients and age-matched controls, performed with and without reductions in visual cues for guidance, in order to delineate the relationship between the internal cue and the kinematic characteristics of these movements. Fourteen patients with PD, and their matched controls, used an electronic pen, which sampled pen-tip position at 200 Hz, and performed a sequence of drawing movements to nine targets upon a WACOM SD 420 graphics tablet. Subjects were trained to perform the movement sequence at a fast speed and were then required to perform the same movement at the same speed with reduced visual cues. Kinematic analysis indicated that, when visual cues were reduced, movements of PD patients became spatially and temporally unstable as they were progressively performed down the sequence. The instability was associated with an abnormal force profile increase in peak movement velocity and target overshoot, which became additive as the submovements progressed. We suggest that defective cue production is the basic deficit in parkinsonian hypokinesia. The defective cue leads to problems synchronising preparatory activity, which then results in abnormalities in movement forces which are characterised by unpredictable and inaccurate movement endpoints. When movements are strung together in a sequence the inaccuracy is additive leading to motor instability.

Aged↗
PubMed1981

Relation of automatic postural responses and reaction-time voluntary movements of human leg muscles.

This study contrasts the properties of compensatory postural adjustments in response to movements of the support surface with those of reaction-time voluntary movements in human subjects. Subjects stood upon a six degrees-of-freedom movable platform and performed tone and movement-triggered voluntary sways about the ankle joints both under conditions of postural stability and instability. These triggered movements could be executed as rapidly as postural adjustments to support surface perturbations (80-120 ms), but only when the former were well practiced, single-choice (direction) and were performed under conditions of postural stability. Evaluation of the properties of postural adjustments and reaction-time voluntary movements revealed a number of clear organizational differences between the two categories of movement, but most interesting was the finding that, when reaction-time movements were triggered by or at the onset of platform movement, the postural adjustments always occurred first. Only when subjects were given a tone trigger 50 ms in advance of platform movement were they able to execute the reaction-time movement first. We found that the dichotomous voluntary/reflexive classification of movements was not consistent with all of the identified properties of postural adjustments and reaction-time movements. Instead, we find a system which classifies movements by function, as either stabilizating or orientational adjustments, to be more useful. In the context of whole-body movement then, intentional focal components would be closely associated with others directed towards postural stabilization.

Electromyography↗
PubMed1982

Sigma-movement and optokinetic nystagmus elicited by stroboscopically illuminated stereopatterns.

Sigma-movement is an apparent movement seen when a stationary periodic visual pattern of the period PS is illuminated stroboscopically at the flash frequency fS and smooth gaze pursuit eye movements are performed across the pattern at an angular velocity Ve = PS X fS deg X S-1. Sigma-movement leads to an optokinetic nystagmus (Sigma OKN) which in turn sustains Sigma-movement perception. (1) Sigma-movement was also seen in an apparent three-dimensional periodic stripe pattern generated by two periodic monocular stimulus patterns with a certain degree of horizontal binocular disparity. (2) Sigma-movement perception and Sigma-OKN were also elicited by a stroboscopically illuminated, stationary, random dot stereostripe pattern. The periodicity PS of this pattern is generated on the cyclopean retina (Julesz 1971). The equation described above was also valid. When the time delay delta t between left eye and right eye flashes was varied, the apparent depth of the random dot stereostripe pattern decreased with increasing delta t, but the Sigma-effects were not affected. (3) Sigma-movement illusion and Sigma-pursuit movements can also be induced when real three-dimensional objects composed of periodic components are stroboscopically illuminated and adequate gaze or eye pursuit movements are induced. Sigma-movement is related to gaze movement and is therefore elicitable by eye, head or body movements. (4) Sigma-movement is presumably caused by the interaction of efference copy signals (generated in a cortical gaze pursuit system) and afferent visual signals. The present data indicate that neuronal mechanisms for this interaction are located--at least in part--at or beyond the level of binocular fusion and stereopsis.

Adult↗
PubMed1994

Accuracy of planar reaching movements. II. Systematic extent errors resulting from inertial anisotropy.

This study examines the source of direction-dependent errors in movement extent made by human subjects in a reaching task. As in the preceding study, subjects were to move a cursor on a digitizing tablet to targets displayed on a computer monitor. Movements were made without concurrent visual feedback of cursor position, but movement paths were displayed on the monitor after the completion of each movement. We first examined horizontal hand movements made at waist level with the upper arm in a vertical orientation. Targets were located at five distances and two directions (30 degrees and 150 degrees) from one of two initial positions. Trajectory shapes were stereotyped, and movements to more distant targets had larger accelerations and velocities. Comparison of movements in the two directions showed that in the 30 degrees direction responses were hypermetric, accelerations and velocities were larger, and movement times were shorter. Since movements in the 30 degrees direction required less motion of the upper arm than movements in the 150 degrees direction, we hypothesized that the differences in accuracy and acceleration reflected a failure to take into account the difference in total limb inertia in the two directions. To test this hypothesis we simulated the initial accelerations of a two-segment limb moving in the horizontal plane with the hand at shoulder level when a constant force was applied at the hand in each of 24 directions. We compared these simulated accelerations to ones produced by our subjects with their arms in the same position when they aimed movements to targets in the 24 directions and at equal distances from an initial position. The magnitudes of both simulated and actual accelerations were greatest in the two directions perpendicular to the forearm, where inertial resistance is least, and lowest for movements directed along the axis of the forearm. In all subjects, the directional variation in peak acceleration was similar to that predicted by the model and shifted in the same way when the initial position of the hand was displaced. The pattern of direction-dependent variations in initial acceleration did not depend on the speed of movement. It was also unchanged when subjects aimed their movements toward targets presented within the workspace on the tablet instead of on the computer monitor. These findings indicate that, in programming the magnitude of the initial force that will accelerate the hand, subjects do not fully compensate for direction dependent differences in inertial resistance.(ABSTRACT TRUNCATED AT 400 WORDS)

Acceleration↗
PubMed1995

Influence of joint interactional effects on the coordination of planar two-joint arm movements.

We have examined EMG-movement relations in two-joint planar arm movements to determine the influence of interactional torques on movement coordination. Explicitly defined combinations of elbow movements (ranging from 20 to 70 degrees) and wrist movements (ranging from 20 to 40 degrees) were performed during a visual, step-tracking task in which subjects were specifically required to attend to the initial and final angles at each joint. In all conditions the wrist and elbow rotated in the same direction, that is, flexion-flexion or extension-extension. Elbow movement kinematics were only slightly influenced by motion about the wrist. In contrast, the trajectory of the wrist movement was significantly influenced by uncompensated reaction torques resulting from movement about the elbow joint. At any given wrist amplitude, wrist movement duration increased and peak velocity decreased as elbow amplitude increased. In addition, as elbow amplitude increased, wrist movement onset was progressively delayed relative to this elbow movement. Surprisingly, the changes between joint movement onsets were not accompanied by corresponding changes between agonist EMG onsets at the elbow and wrist joints. The mean difference in onset times between elbow and wrist agonists (22-30 ms) remained unchanged across conditions. In addition, a basic pattern of muscle activation that scaled with movement amplitude was observed at each joint. Phasic agonist activity at the wrist and elbow joints remained remarkably similar across conditions and thus the changes in joint movement onset could not be attributed to changes in the motor commands.(ABSTRACT TRUNCATED AT 250 WORDS)

Adult↗
PubMed2005

Identifying brain regions for integrative sensorimotor processing with ankle movements.

The objective of this study was to define cortical and subcortical structures activated during both active and passive movements of the ankle, which have a fundamental role in the physiology of locomotion, to improve our understanding of brain sensorimotor integration. Sixteen healthy subjects, all right-foot dominant, performed a dorsi-plantar flexion task of the foot using a custom-made wooden manipulandum, which enabled measurements of the movement amplitude. All subjects underwent a training session, which included surface electromyography, and were able to relax completely during passive movements. Patterns of activation during active and passive movements and differences between functional MRI (fMRI) responses for the two types of movement were assessed. Regions of common activation during the active and passive movements were identified by conjunction analysis. We found that passive movements activated cortical regions that were usually similar in location to those activated by active movements, although the extent of the activations was more limited with passive movements. Active movements of both feet generated greater activation than passive movements in some regions (such as the ipsilateral primary motor cortex) identified in previous studies as being important for motor planning. Common activations during active and passive movements were found not only in the contralateral primary motor and sensory cortices, but also in the premotor cortical regions (such as the bilateral rolandic operculum and contralateral supplementary motor area), and in the subcortical regions (such as the ipsilateral cerebellum and contralateral putamen), suggesting that these regions participate in sensorimotor integration for ankle movements. In future, similar fMRI studies using passive movements have potential to elucidate abnormalities of sensorimotor integration in central nervous system diseases that affect motor function.

Adult↗
PubMed2006

Optimizing rapid aiming behaviour: Movement kinematics depend on the cost of corrective modifications.

Recent studies have shown that the initial impulse associated with goal-directed aiming movements typically brings the limb to a position short of the target. This is because target overshooting is associated with greater temporal and energy costs than target undershooting. Presumably these costs can be expected to vary not only with the muscular forces required to move the limb, but also the gravitational forces inherent in the aiming task. In this study we examined the degree to which primary movement endpoint distributions depend on the direction of the movement with respect to gravity. We hypothesized that the magnitude of an undershoot bias would be greatest for downward movements because target overshooting necessitates a time and energy consuming movement reversal against gravity. Participants completed rapid aiming movements toward targets located above and below, as well as proximal and distal to a central home position. Movements were made both with and without additional mass attached to the limb. Although movement time did not vary with experimental condition, primary movement endpoint distributions were consistent with our predictions. Specifically, both greater undershooting and greater endpoint variability was associated with downward aiming movements. As well, a greater proportion of the overall movement time was spent in the corrective phase of the movement. These results are consistent with models of energy minimization that posit an inherent efficiency of control and hold that movements are organized to minimize movement time and energy expenditure and maximize mechanical advantages.

Adult↗
PubMed1999

Comparison of variability of initial kinematics and endpoints of reaching movements.

The accuracy of reaching movements to memorized visual target locations is presumed to be determined largely by central planning processes before movement onset. If so, then the initial kinematics of a pointing movement should predict its endpoint. Our study examined this hypothesis by testing the correlation between peak acceleration, peak velocity, and movement amplitude and the correspondence between the respective spatial positions of these kinematic landmarks. Subjects made planar horizontal reaching movements to targets located at five different distances and along five radially arrayed directions without visual feedback during the movements. The spatial dispersion of the positions of peak acceleration, peak velocity, and endpoint all tended to form ellipses oriented along the movement trajectory. However, whereas the peaks of acceleration and velocity scaled strongly with movement amplitude for all of the movements made at the five target distances in any one direction, the correlations with movement amplitude were more modest for trajectories aimed at each target separately. Furthermore, the spatial variability in direction and extent of the distribution of positions of peak acceleration and peak velocity did not scale differently with target distance, whereas they did for endpoint distributions. Therefore, certain features of the final kinematics are evident in the early kinematics of the movements as predicted by the hypothesis that they reflect planning processes. However, endpoint distributions were not completely predetermined by the Initial kinematics. In contrast, multivariate analysis suggests that adjustments to movement duration help compensate for the variability of the initial kinematics to achieve desired movement amplitude. These compensatory adjustments do not contradict the general conclusion that the systematic patterns in the spatial variability observed in this study reflect planning processes. On the contrary, and consistent with that conclusion, our results provide further evidence that direction and extent of reaching movements are planned and determined in parallel over time.

Adult↗
PubMed1997

Analysis of an optimal control model of multi-joint arm movements.

In this paper, we propose a model of biological motor control for generation of goal-directed multi-joint arm movements, and study the formation of muscle control inputs and invariant kinematic features of movements. The model has a hierarchical structure that can determine the control inputs for a set of redundant muscles without any inverse computation. Calculation of motor commands is divided into two stages, each of which performs a transformation of motor commands from one coordinate system to another. At the first level, a central controller in the brain accepts instructions from higher centers, which represent the motor goal in the Cartesian space. The controller computes joint equilibrium trajectories and excitation signals according to a minimum effort criterion. At the second level, a neural network in the spinal cord translates the excitation signals and equilibrium trajectories into control commands to three pairs of antagonist muscles which are redundant for a two-joint arm. No inverse computation is required in the determination of individual muscle commands. The minimum effort controller can produce arm movements whose dynamic and kinematic features are similar to those of voluntary arm movements. For fast movements, the hand approaches a target position along a near-straight path with a smooth bell-shaped velocity. The equilibrium trajectories in X and Y show an "N' shape, but the end-point equilibrium path zigzags around the hand path. Joint movements are not always smooth. Joint reversal is found in movements in some directions. The excitation signals have a triphasic (or biphasic) pulse pattern, which leads to stereotyped triphasic (or biphasic) bursts in muscle control inputs, and a dynamically modulated joint stiffness. There is a fixed sequence of muscle activation from proximal muscles to distal muscles. The order is preserved in all movements. For slow movements, it is shown that a constant joint stiffness is necessary to produce a smooth movement with a bell-shaped velocity. Scaled movements can be reproduced by varying the constraints on the maximal level of excitation signals according to the speed of movement. When the inertial parameters of the arm are altered, movement trajectories can be kept invariant by adjusting the pulse height values, showing the ability to adapt to load changes. These results agree with a wide range of experimental observations on human voluntary movements.

Arm↗
PubMed1981

Characteristics of the ipsilateral movement-related neuron in the motor cortex of the monkey.

The characteristics of the precentral neuron activity related to ipsilateral movements were studied while the monkey was performing finger, wrist and arm movements on either side. Out of 197 task-related neurons, 134 discharged in association with contralateral movements, but not with any one of 3 ipsilateral movements. Fifty neurons discharged with bilateral movements. Thirteen neurons discharged in association with ipsilateral movements (ipsi-neurons). Ten were recorded from the trunk or shoulder area of the motor cortex and were accompanied by contraction of those muscles by intracortical stimulation (ICS). The remaining 3 were related to elbow or wrist, but no ipsi-neurons were related to finger muscle contractions. In ipsilateral task performance, 7 ipsi-neurons discharged in association with finger and/or wrist movements in addition to arm movement. Five others were associated with arm movement. The last one discharged with wrist movement. Most of the units showed similar response to contralateral movement. Ipsi-neurons were classified into two groups. One group was recorded around the sulcus precentralis superior, had the lower threshold current and was mostly associated with finger, wrist and arm movements. The other was recorded in the rostral motor cortex, and had the higher threshold current and was related to arm movement. Among 185 neurons to which pyramidal tract stimulation was delivered, 2 out of the 80 PTNs and 11 out of the 105 non-PTNs were ipsi-neurons. EMGs were recorded from various muscles involved in the forelimb movements. Arm and finger muscles showed no activity when the monkey used the ipsilateral hand, while most of the shoulder and trunk muscles showed tonic or moderate transient changes in the activity during the ipsilateral tasks. The ipsi-neuron activity was discussed in consideration with EMGs.

Animals↗
PubMed1995

Long-lasting inhibition of the human soleus H reflex pathway after passive movement.

Human soleus H reflexes are attenuated during passive pedalling movements. This depression occurs within 70 ms of movement onset. We hypothesized that the reflex gain would return to control values with a similar brevity following movement. However, H reflexes sampled following a slow (10 rpm) passive pedalling movement of a single leg remained below control values for the duration of a 200 ms collection period, for all four pedal positions tested. The extent of the attenuation after movement was position dependent in a manner similar to that observed during movement. This position effect was more precisely defined by sampling reflexes 200 ms post-movement at 10 pedal crank positions. Also, the full course of reflex recovery was investigated by sampling up to 8 s post-movement at four pedal positions. Reflex gain remained reduced 1-4 s post-movement, in a position dependent manner. There was a subsequent facilitation of the reflex. Thus, following a locomotor-like movement there is sustained attenuation of the soleus H reflex. The early post-movement period is likely the continued expression of movement-induced reflex inhibition while the later period may arise from descending influences consequent to the termination of movement. Presynaptic inhibition is implicated, as reflexes still showed the gain modulation when sampled while soleus was tonically contracted, both following and during the passive movement.

Adult↗
PubMed1987

Movements of cats on a rotating cylinder: role of the substantia nigra pars reticulata and the deeper layers of the superior colliculus.

Recently it has been shown that the substantia nigra pars reticulata (SNR) is required for adjusting the body position. In this study the role of the SNR in the execution of movements was investigated. Therefore, the effects of bilateral SNR injections of picrotoxin (500 ng/0.5 microliter) and muscimol (200 ng/1 microliter) were investigated on movements of cats which were trained to cross a rotating cylinder. SNR injection of picrotoxin suppressed the movements that were executed by cats injected with distilled water (0.5 microliter), i.e. 'normal movements'. While crossing the rotating cylinder, picrotoxin-injected cats mainly executed movements that almost never occurred in distilled water treated cats. Picrotoxin-injected cats executed 'special movements', i.e. forward locomotion in which the hindlimbs were affected, and 'counter-movements'. While executing the latter movements no forward locomotion occurred at all; the cats solely executed lateral fore- and hindlimb movements opposite to the direction in which the cylinder rotated. SNR application of muscimol enhanced the execution of 'normal movements'. Since the SNR sends information to the deeper layers of the superior colliculus (dl-SC) via GABAergic fibers, it was also investigated whether pharmacological stimulation (muscimol) and inhibition (picrotoxin) of the GABAergic dl-SC activity affected these movements on the rotating cylinder: no changes were observed after injecting otherwise effective doses of muscimol (75 ng/1 microliter) and picrotoxin (100 ng/0.5 microliter). In order to compare the function of the SNR and dl-SC in programming a different type of movements, the effects of GABAergic agents in the dl-SC (picrotoxin 100 ng/0.5 microliter and muscimol 75 ng/1 microliter) and the SNR (picrotoxin 500 ng/0.5 microliter and muscimol 200 ng/1 microliter) were investigated on the feline ability to execute goal-directed movements in an experimental set-up that prevented the occurrence of targeting movements which were continuously guided by external, i.e. auditory, visual, tactile and olfactory stimuli. For that purpose cats were trained to step out of a startbox on a rotating cylinder, i.e. the target. Dl-SC injection of muscimol or SNR application of picrotoxin prevented the cats from stepping out of the startbox on the rotating cylinder. In contrast, cats injected with muscimol into the SNR or picrotoxin into the dl-SC stepped out of the startbox, although dl-SC application of picrotoxin elicited forelimb misplacements: frequently the cats placed their forelimbs alongside of, but not on the cylinder when trying to leave the startbox.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗
PubMed1984

Neural substrates of two different rhythmical vibrissal movements in the rat.

Normal rats show two types of rhythmical vibrissal movement, one synchronized precisely with alpha waves (about 9 Hz) of the thalamocortical system, and the other often synchronized with theta waves (about 7 Hz) of the septohippocampal system. The alpha-synchronized vibrissal movements appear while the rat stands still with a slow respiratory pattern, and are of small amplitude (a fine tremor). The theta-synchronized vibrissal movements appear during exploratory sniffing behavior, and are of large amplitude. Thus, a group of facial motoneurons which constitute the final common pathway for vibrissal movement apparently receive input convergently from these two neural systems. In the present study, we observed the following: (1) the two types of movement rarely, if ever, appeared simultaneously and the same was true of the two brain wave patterns. Topographically, the predominant appearance of the alpha waves was in the frontal (sensorimotor) cortex, whereas that of the theta waves was in the occipital cortex and hippocampus. (2) Bilateral ablation of either the entire neocortex or just its anterior (but not posterior) half eliminated the vibrissal alpha-tremor movement while leaving vibrissal theta-sniffing movement normal. In anterior decorticate rats, the tremor movements started to recover by 1-4 months, and were abolished again by the removal of the remaining posterior cortex. (3) Lesions of the medial septum or the fornix eliminated hippocampal theta waves, but had no effect on vibrissal sniffing movement or alpha wave-vibrissal tremor. (4) Cerebellectomy and, to a lesser extent, pharmacological lesions of the inferior olive slowed, but did not block, alpha waves. In addition, vibrissal tremor movement became intermittent and less vigorous. The same manipulations, however, did not affect theta wave-vibrissal sniffing movement. (5) Harmaline (30 mg/kg, i.p.) did not induce alpha-tremor, which, in combination with the results with cerebellectomy and inferior olive lesions, indicates that alpha-tremor is generated by a neural mechanism that is different from that for harmaline-induced generalized tremor of 10 Hz. These findings confirmed that there exist two patterns of synchrony between vibrissal movement and rhythmical brain activity in the rat, i.e. alpha wave-vibrissal tremor movement and theta wave-vibrissal sniffing movement, and suggest that the two patterns reflect a rhythmical mode of functioning of two different neural systems, probably the thalamocortical and the septohippocampal system, respectively.

Animals↗
PubMed2006

Post-movement beta rebound is generated in motor cortex: evidence from neuromagnetic recordings.

Voluntary movements are accompanied by amplitude changes in cortical rhythms presumably as a result of functional activation of sensorimotor areas. Recently, the location of the neural generators involved in increasing power within the beta (15-30 Hz) frequency band following movement (post-movement beta rebound, PMBR) has come into question [Parkes, L.M, Bastiaansen, M.C.M, Norris, D.G., 2006. Combining EEG and fMRI to investigate the post-movement beta rebound. NeuroImage 29, 685-696.]. We used the synthetic aperture magnetometry (SAM) spatial filtering method to identify the time course and location of oscillatory changes within the beta and mu (8-14 Hz) frequency bands during the performance of voluntary movements. Neuromagnetic activity was recorded from 10 adult subjects during abduction of the right index finger. Changes in beta and mu source power were calculated for periods during and following movement, relative to pre-movement baseline activity. Decreases in beta band activity (event-related desynchronization, ERD) were observed during movement, with a strong increase (PMBR) beginning 230+/-170 ms following movement, lasting for 680+/-170 ms. Mu band ERD was observed both during and following movement, with little to no post-movement rebound. Beta and mu ERD were localized bilaterally to the hand region of postcentral gyrus whereas PMBR was localized bilaterally to the hand region of precentral gyrus (motor cortex). Both PMBR and beta ERD were strongest contralateral to the side of movement. These results provide further evidence that movement influences independent cortical rhythms in sensorimotor areas, and confirm previous reports of precentral generators of PMBR in the region of motor cortex, with postcentral generators of beta and mu ERD during movement.

Adult↗
PubMed2000

Human lateral pterygoid muscle activity on the return phase of contralateral and protrusive jaw movements.

Normal function of the lateral pterygoid muscle is not well understood. The principal aim of this study was to determine whether there is a progressive decrease in lateral pterygoid activity as the condyle moves posteriorly and superiorly during the return phase of a contralateral or protrusive jaw movement, as would be expected if the muscle is involved in controlling or stabilizing the condyle during the return phase of these movements. In seven humans, electromyographic activity was recorded in the superior (SHLP) and inferior (IHLP) heads of the lateral pterygoid, the masseter, anterior temporal, posterior temporal and submandibular group of muscles, together with condylar movement, during contralateral and protrusive jaw movement. In most individuals, there was a progressive decrease in rectified and smoothed IHLP activity in relation to condylar movement during the return phase of contralateral and protrusive jaw movement. However, this pattern usually was not seen when SHLP activity was studied in relation to condylar movement. Further, there was a high correlation coefficient between condylar displacement and the rectified and smoothed IHLP and anterior temporal muscle activities during the return phase of contralateral or protrusive jaw movement, while SHLP presented a much lower correlation. For example, the mean (+/-SD) correlation coefficient between posterior condylar movement (along anteroposterior axis) and IHLP activity during the return phase of a protrusive jaw movement was -0.73+/-0.36 (for contralateral movement: -0.71+/-0.56), for the anterior temporal 0.69+/-0.21 (contralateral: 0.81+/-0.09), and for the submandibular muscles, -0. 77+/-0.15 (contralateral: -0.34+/-0.71). For the SHLP, masseter and posterior temporal, values were -0.34+/-0.61 (contralateral: -0. 48+/-0.37), -0.24+/-0.57 (contralateral: 0.16+/-0.80), and 0.16+/-0. 77 (contralateral: 0.64+/-0.14), respectively. These findings suggest an important role for the IHLP and anterior temporal in controlling the movement of the condyle to the glenoid fossa on the return phase of contralateral and protrusive jaw movements. Further studies are needed to clarify the function of the lateral pterygoid muscle during these and other jaw movements.

Adult↗
PubMed2003

Eye movement-related modulation of trigeminal neuron activity during active sleep and wakefulness.

The amplitude of electrically-evoked mass action potentials recorded in the spinal cord and brainstem has been reported to decrease only during eye movement events of active sleep. In contrast, we have reported that the response of trigeminal sensory neurons to peripheral stimuli is modulated throughout the behavioral state of active sleep. It is unclear whether eye movement events contribute to the modulation of trigeminal sensory neuron activity during active sleep. In the present study, eye movement events were demarcated in order to investigate how these events affect peripheral input to trigeminal sensory neurons in chronic, intact, behaving cats. When compared with wakefulness, the mean response of 45 trigeminal sensory neurons to low-intensity electrical stimulation of the canine tooth pulp was significantly suppressed by 28% during periods of active sleep where no eye movement activity was present and by 41% during periods of active sleep with eye movement events. Hence, during active sleep, tooth pulp-evoked responses were significantly decreased by 16% during eye movement events when compared with non-eye movement active sleep. To investigate whether presynaptic inhibition played a role in this phenomenon, the excitability of eight individual tooth pulp afferent terminals during eye movement periods was compared with non-eye movement periods of active sleep. No evidence of eye movement-related depolarization of tooth pulp terminals was detected. When compared to wakefulness, the responses of six trigeminal sensory neurons to air puff stimulation of facial hair mechanoreceptors were significantly increased by 96% during periods of active sleep where no eye movement activity was present but were significantly decreased by 15% during eye movement events when compared with non-eye movement active sleep. The results of the present study indicate that neuronal responses to both tooth pulp and facial hair mechanoreceptor stimulation are significantly attenuated during eye movement events of active sleep.

Animals↗