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PubMed2000

Electromyographic responses to a mechanical perturbation applied during impending arm movements in different directions: one-joint and two-joint conditions.

Directional tuning is a common finding for many physiological features of arm movements and related neuronal activity. We investigated whether the electromyographic response to a brief (30 ms) torque perturbation prior to voluntary movement depends on the direction of the impending movement. Pointing movements with the elbow joint alone and those involving both the shoulder and elbow joints were studied in separate experiments. Target direction was varied between flexion and extension for the one-joint experiments and among four spatial directions for the two-joint experiments. Movement trials in which a perturbation stretched the flexor muscles just prior to the pointing movement were randomly interspersed among unperturbed movement trials in each experiment. A small pre-load ensured some background activity of the flexor muscles. Results were remarkably similar for the one- and two-joint conditions. The short-latency reflex response of the stretched muscles (in a 30-60 ms window after perturbation onset) was not modulated with direction of target-reaching movement in a statistically significant manner, which confirms earlier findings for one-joint movements and extends these to the two-joint condition. Beyond the short-latency window, the perturbation provoked earlier onsets of target-reaching muscle activities for the agonist muscles, whether or not the muscle had been stretched by the perturbation. The onset of the braking activity of the antagonist muscles also occurred earlier in the presence of the brief perturbation prior to movement, irrespective of whether the muscle had been stretched or not. The magnitude of target-reaching muscle activity, in general, was greater for the perturbed trials, though not consistently for all muscles or all directions. These results suggest that, when movement is about to be initiated, in either single- or multi-joint conditions, the long-latency effects of the stretch strongly depend on the intended direction of movement. The dependence is such that the response serves to hasten and augment the intended movement, but not necessarily to oppose the perturbation.

Adult↗
PubMed1998

Hand and joint paths during reaching movements with and without vision.

This study examines whether the kinematics of pointing movements are altered by the sensory systems used to select spatial targets and to guide movement. Hand and joint paths of visually guided reaching movements of human subjects were compared with two non-visual conditions where only proprioception was available: (1) movements of the same subjects with blindfolds, and (2) movements by congenitally blind subjects. While hand-path curvatures were overall quite small, sighted subjects wearing a blindfold showed a statistical increase in hand-path curvature compared with their visually guided movements. Blindfolded subjects also showed greater hand-path curvature than blind subjects. These increases in hand-path curvature for blindfolded subjects did not always lead to a decrease in joint-path curvature. While there were differences between blind subjects and sighted subjects using vision for some movement directions, there was no systematic difference between these two groups. The magnitude of joint-path curvature showed much greater variation than hand-path curvature across the movement directions. We found variation in joint-path curvature to be correlated to two factors, one spatial and one geometrical. For all subject groups, joint-path curvature tended to be smaller for sagittal-plane movements than for transverse or diagonal movements. As well, we found that the magnitude of joint-path curvature was also related to the relative motion at each joint. Joint-path curvature tended to increase when movements predominantly involved changes in shoulder angle and was minimal when movements predominantly involved elbow motion. The consistently small curvatures of hand trajectory across blind and sighted subjects emphasize the powerful tendency of the motor system to generate goal-directed reaching movements with relatively straight hand trajectories, even when deprived of visual feedback from very early in life.

Adult↗
PubMed2000

Reaction time differences in spatially constrained bilateral and unilateral movements.

Previous investigations of bilateral-unilateral reaction time (RT) differences have reported equivocal findings. Studies where bilateral RT has been found longer than unilateral RT have often emphasized movement precision, while studies reporting non-significant differences have placed little emphasis on precision. To test the hypothesis that movement precision is an important factor in the bilateral unilateral difference, we investigated the influence of changes in spatial accuracy constraints on RT for unilateral and bilateral movements. Ten self-declared right-handed subjects performed fast and accurate 45 degrees unilateral and bilateral elbow flexion movements to small (1.5 degrees) and large (12.0 degrees) targets. For bilateral movements, spatial accuracy was emphasized for only one arm (the "aiming" arm), while the contralateral ("mirroring") arm performed a simultaneous flexion movement with no emphasis on movement accuracy. We found that while changes in target size had no significant effect on movement latency, changing the hand (right vs left) for which accuracy was emphasized did. When subjects performed right-arm aiming, bilateral movements, unilateral and bilateral RT did not differ significantly. In contrast, when subjects performed left-arm aiming, bilateral movements, RT was significantly longer than for unilateral movements. We conclude that while spatial accuracy per se (i.e., target size) does not differentiate bilateral and unilateral movements, the role of the left hand (i.e., aiming vs mirroring) does. Differences in the hemispheric control of right- and left-hand aiming movements are discussed.

Adult↗
PubMed2004

Three digestive movements in Hydra regulated by the diffuse nerve net in the body column.

The mammalian digestive tract undergoes various digestive movements such as peristalsis and segmentation movement. How those digestive movements and the underlying mechanisms appeared in evolution remains unraveled. A widely accepted view has been that, early in evolution, the digestive process was static based upon diffusion, and later it became dynamic involving digestive movements. Here, we report digestive movements which occur in Hydra, a member of the phylum Cnidaria. We find that the body column of Hydra undergoes a series of movements when fed with Artemia. Comparison of the movements to those in mammals showed similarities in appearance to esophageal reflex, segmentation movement, and defecation reflex. When nerve cells were eliminated, polyps showed only a weak segmentation movement, demonstrating that the diffuse nerve net in the body column of Hydra primarily regulates the movements just as the netlike enteric nervous system does in mammals. Elimination of both secretory gland cells and nerve cells resulted in the complete loss of movement, suggesting that the gland cells are involved in the weak movement. Overall, these observations suggest that the digestive process in Hydra is dynamic and that the diffuse nerve net regulates the digestive movements as a primitive form of enteric nervous system.

Animals↗
PubMed1994

Slowness of movement in melancholic depression.

We studied 10 subjects each with melancholic depression evidencing significant motor retardation (RM), Parkinson's disease (PD) with bradykinesia, and normal healthy controls (NC), matched closely for age and gender, on measurements of motor function and depression, and their performance of simple and complex ballistic movements. The simple movements involved the execution of 10 degrees, 20 degrees, and 40 degrees angular movements using a methodology adapted from Hallett and Khoshbin (1980). The complex movements involved the performance by the right arm and hand of a squeeze and a flexion movement, both sequentially and simultaneously, using a methodology adopted from Benecke et al (1986, 1987). The RM and PD groups demonstrated a smaller increase in the angular velocity as the angle of the movement increased from 10 degrees to 40 degrees than did the NC group. Many PD and RM subjects showed multiple electromyographic (EMG) bursts during the ballistic movements. The RM and PD subjects tended take longer to perform the simultaneous and sequential movements, but nonsignificantly so. The RM group performed the squeeze movement slower when executed as part of the simultaneous movement than when performed as a simple movement. The pause time between the movements when performed sequentially was longer (nonsignificantly) for the RM subjects. Our study demonstrated a disturbance in the execution of simple and complex movements by RM subjects that resembled the disturbance seen in PD. This argues for a common pathophysiological basis for at least some aspects of motor retardation in the two disorders. Reduced dopamine function is one common abnormality that may partially account for these findings.

Basal Ganglia Diseases↗
PubMed1979

Cerebral potentials preceding unilateral and simultaneous bilateral finger movements.

Cerebral potentials preceding voluntary bilateral simultaneous finger movements were investigated in 19 right-handed young adult subjects, and were compared with unilateral right-sided finger m n the same experiment. With bilateral movements, the Bereitschaftspotential (BP) was not symmetrical or larger over the dominant hemisphere, but surprisingly, it was larger over the minor hemisphere. The BP averaged -3.66 microV (S.D. 1.96) over the left precentral region and -4.82 microV (S.D. 3.73) over the right precentral region in this condition. The difference was significant at 2P less than 0.01. This difference was pronounced in precentral leads but very small and almost missing in parietal leads. The pre-motion positivity (PMP) was well developed and even larger with bilateral than with unilateral (right-sides) movements. At the vertex it averaged +1.33 microV (S.D.4.16) with bilateral movements and only +0.15 microV (S.D. 1.42) with right-sided unilateral movements (2P less than 0.05). With bilateral movements the PMP could be observed in any record, but with unilateral movements it was missing at the left precentral lead, in accordance with previous publications (Deecke et al. 1969, 1976). The motor potential (MP), measured in a bipolar record from left and right precentral leads, was larger with unilateral (-1.25 microV, S.D. 1.33) than with bilateral movements (-0.36 microV, S.D. 0.92). Onset time differences of the BP preceding unilateral and bilateral movements were very small. However, there was a tendency towards earlier onset with unilateral than with bilateral movements (1031 msec, S.D. 358, as compared with 951 msec, S.D. 305). The averaged EMG revealed differences in movement onset. Muscular contraction tended to be earlier in the right than in the left m. flexor indicis in our right-handed subjects, on the average by 16 msec (S.D. 15). With unilateral right-sided movements, the left m. flexor indicis was not silent but showed an abortive mirror activity in the EMG, without visible movement. This activity occurred on the average 50 msec (S.D. 39) later on the non-moving side.

Adult↗
PubMed1986

Cortical potentials preceding voluntary movement: evidence for three periods of preparation in man.

We have recorded movement-related cortical potentials (MRCPs) to voluntary middle finger extension from 10 young and 10 old subjects free of neurological disease using the method of detecting EMG onset associated with each movement described by Barrett et al. (1985). The slow potential shifts preceding movement were measured by fitting a linear regression line to the wave forms to obtain a measure of their slope. Three separate potential shifts were identified. The first had a scalp distribution and onset latency similar to the Bereitschaftspotential (BP) first reported by Kornhuber and Deecke (1964, 1965). The potential shift immediately preceding movement corresponded with the NS' of Shibasaki et al. (1980). We identified, for the first time, a third shift intervening between BP and NS' and named it the intermediate shift (IS). The onset of BP occurred about 1.6 sec before EMG onset and was followed by IS which began about 875 msec before movement. The onset of NS' occurred 300 msec before EMG onset and terminated about 90 msec before this event. The slope of BP preceding right finger movement was steeper than that preceding left hand movement in all our right-handed subjects. The distribution of BP was symmetric about the midline. The IS potential shift had a slope which was steeper on the average preceding left finger movement than right. The distribution of IS was symmetric about the midline preceding left finger movement but had a contralateral tendency preceding right hand movement. NS' had a maximum slope at contralateral electrodes over the hand motor area and parietal areas. It was suggested that the BP potential shift originates in the supplementary motor area on the medial surface of the cerebral cortex. The differing distribution of the IS shift for the two hands suggests that this potential may be generated bilaterally preceding left finger movement but from the contralateral hemisphere only preceding movement of the right finger. The most likely origin of this potential was thought to be superior premotor cortex. NS' was considered to originate in primary motor cortex with possible contributions from other cortical areas associated with movement.

Adult↗
PubMed1995

Neuronal correlates of the specification of movement direction and force in four cortical areas of the monkey.

Single-neuron activity was recorded in several areas of the cerebral cortex when monkeys performed a movement-precueing reaction time task. In such a task, information provided by a first signal ('preparatory signal', PS) refers to what has to be done in response to a second signal ('response signal', RS). Two monkeys were trained to rotate a handle by performing wrist flexion/extension movements while two levels of frictional resistance were applied to the manipulandum. The PS provided complete, partial or no prior information about movement direction (flexion or extension) and/or the level of the frictional force (weak or strong). Since providing partial prior information about either movement parameter shortened reaction time (RT)--RT being shorter when movement direction than movement force was precued--, as compared to the condition in which no prior information was provided, the analysis of changes in neuronal activity during the preparatory period (PP), i.e., the instructed delay between PS and RS, makes the study of the neuronal mechanism underlying the specification of movement parameters possible. The activity of 411 neurons of the primary motor (MI), premotor (PM), somatosensory (SI) and parietal (PA) cortex was recorded during task performance. Many more neurons changed selectively their activity in relation to movement direction than in relation to movement force, not only during PP, but also during RT and movement time (MT). The number of purely direction-related neurons increased, whereas the number of purely force-related neurons decreased from SI to PA, then to MI and finally to PM. During PP, selective activity changes were related only to one movement parameter, whereas during RT and MT, a large population of neurons changed its activity in relation to both movement direction and force, especially in MI. These data provide further evidence for the clustering of distinct neuronal populations responsible for programming movement direction and force.

Animals↗
PubMedDate not supplied

Control of simple arm movements in elderly humans.

Eight elderly subjects (aged 68-95 years) and 6 young adults (aged 21-24 years) performed elbow flexion and extension movements in a visual step-tracking paradigm. Movement amplitudes ranging from 10 degrees-80 degrees were made under two instructions: "move at own speed" and "move fast and accurate." In a second experiment, 5 elderly subjects practiced 30 degrees movements for a total of 180 flexion and 180 extension movements under the instruction to increase movement speed, while maintaining accuracy, during practice. Movement trajectories became more variable as both movement amplitude and speed increased. Trajectory variability was greater in the elderly subjects for both the acceleratory and deceleratory phases of movements. This was due primarily to a greater rate of increase in trajectory variability during the acceleration phase in the elderly. With practice, elderly subjects could substantially reduce trajectory variability with little change in movement speed. The agonist burst initiating movements was qualitatively normal in the elderly subjects. However, there was considerable tonic cocontraction of agonist and antagonist muscles prior to and during movement. Phasic antagonist EMG activity was obviously abnormal in many elderly subjects. There was often no clear antagonist burst associated with deceleration of the movements or, if present, it was timed inappropriately early. With practice, combined agonist-antagonist EMG variability decreased. A clear antagonist burst also developed during practice in most elderly subjects, but its inappropriate timing remained in all but one subject. The results show that movement trajectories are less accurately controlled in the elderly.(ABSTRACT TRUNCATED AT 250 WORDS)

Adult↗
PubMed1991

Reconstruction of shifting elbow joint compliant characteristics during fast and slow movements.

The purpose of this study was to experimentally investigate the applicability of the equilibrium-point hypothesis to the dynamics of single-joint movements. Subjects were trained to perform relatively slow (movement time 600-1000 ms) or fast (movement time 200-300 ms) single-joint elbow flexion movements against a constant extending torque bias. They were instructed to reproduce the same time pattern of central motor command for a series of movements when the external torque could slowly and unpredictably increase, decrease, or remain constant. For fast movements, the total muscle torque was calculated as a sum of external and inertial components. Analysis of the data allowed reconstruction of the elbow joint compliant characteristics at different times during execution of the learned motor command. "Virtual" trajectories of the movements, representing time-varying changes in a central control parameter, were reconstructed and compared with the "actual" trajectories. For slow movements, the actual trajectories lagged behind the virtual ones. There were no consistent changes in the joint stiffness during slow movements. Similar analysis of experiments without voluntary movements demonstrated a lack of changes in the central parameters, supporting the assumption that the subjects were able to keep the same central motor command in spite of externally imposed unexpected torque perturbations. For the fast movements, the virtual trajectories were N-shaped, and the joint stiffness demonstrated a considerable increase near the middle of the movement. These findings contradict an hypothesis of monotonic joint compliant characteristic translation at a nearly constant rate during such movements.

Adult↗
PubMed2004

Discrete and cyclical movements: unified dynamics or separate control?

In the literature on motor control, three theoretical perspectives on the relation between discrete and cyclical movements may be discerned: (a) cyclical movements are concatenated discrete movements; (b) discrete movements are a limiting case of cyclical movements, and (c) discrete and cyclical movements are motor primitives that may be combined but are irreducible to each other. To examine the tenability of these perspectives, 16 participants performed cyclical and discrete (flexion and extension) reaching movements of various amplitudes to differently sized targets. The kinematic properties of the recorded movements were analyzed and compared in detail. The cyclical, ongoing movements differed markedly from the discrete movements as well as from the first and last half-cycles of a bout of cyclical movements, especially in terms of their symmetry ratio. These effects were largely independent of amplitude, target size and movement direction (flexion-extension). The results obtained ruled out perspective (a) and, in principle, left open perspectives (b) and (c). However, the observed kinematic features were not readily accounted for by the specific dynamical models that have been proposed under perspectives (b) and (c). Future modeling attempts should explicate the dynamics of initiation and abortion of both discrete and cyclical movements.

Adult↗
PubMed2004

Modeling facial movement: I. A dynamic analysis of differences based on skeletal characteristics.

PURPOSE: To introduce a novel approach to analyze and model facial movements; and to quantify variations in facial movement caused by the extent of skeletal differences between the maxilla and mandible and the middle to lower facial heights. The hypothesis was that there are differences in facial movement related to the underlying facial skeleton which may be explained by the shape of the face rather than the pattern of movement. PATIENTS AND METHODS: The study sample consisted of 43 subjects (23 men, 20 women) with a mean age of 18.5 years (SD = 11.90). Measures of the facial skeletal differences were made from lateral cephalometric radiographs, and subjects were classified as Class I and Class II, and normal to decreased lower anterior face height, respectively. Facial movements were recorded by a video-based tracking system. Descriptive and inferential statistics were performed on principal component scores generated from the movement data. A linear mixed-effects model was used to test for significant differences in movement among the different skeletal types. RESULTS: A dynamic modeling of facial movements was described that has numerous potential clinical applications. Also, differences in movement were found during the lip purse movement. Specifically, skeletal Class I individuals showed greater forward and upward movement during lip purse compared with individuals with severe skeletal Class II who moved their lips straight forward with less magnitude of movement. CONCLUSION: For most of the movements, apart from the lip purse, differences in motion were explained by static facial shape.

Adolescent↗
PubMed2004

Modeling facial movement: II. A dynamic analysis of differences caused by orthognathic surgery.

PURPOSE: The purpose of this study was to determine the facial movement characteristics of patients who underwent orthognathic surgery. The specific aims were to determine the presurgery versus postsurgery differences in facial movements; to determine whether the presurgery facial movements were similar among patients with different dentofacial deformities; and to determine whether patients have a more similar post- than presurgery dentofacial morphology and soft tissue movement. The hypothesis was that there are differences between the pre- and postsurgery facial movements. PATIENTS AND METHODS: The sample consisted of 19 patients (11 women, 8 men) with a mean age of 20.6 years (SD +/- 8.34). Facial movement and lateral cephalometric data were collected at presurgery, and at 6 and 12 months postsurgery. Measures of the facial skeletal differences were made from lateral cephalometric radiographs and facial movements were recorded by a video-based tracking system. Descriptive and inferential statistics were performed on principal component scores generated from the movement data. A linear mixed-effects model was used to test for significant differences in movement. RESULTS: Differences were found between the presurgery and 12-month postsurgery visits for the instructed smile, lip purse, eye closure, grimace, and mouth opening movements as well as the natural smile. Also, there were significant differences at presurgery among the dentofacial groups for the lip purse movement but no differences were found at postsurgery for any of the movements. CONCLUSION: These findings suggest that facial movements are effected by skeletal malocclusion and orthognathic surgical procedures.

Adult↗
PubMed1999

Cortical distribution of Bereitschaftspotential and negative slope potential preceding mouth-opening movements in humans.

Cortical potentials associated with the voluntary movement of various body parts are known as movement-related cortical potentials, which allow evaluation of the cortical efferent function and other higher functions controlling voluntary movement. The cortical potentials have three main components: the Bereitschaftspotential (or 'readiness potential'), the negative slope and the motor potential. Here, the cortical potentials preceding mouth-opening movements were recorded to investigate which of these components could be observed. Electroencephalograms (EEGs) were recorded from 11 electrodes placed over the scalp (F3, Fz, F4, T3, C3, Cz, C4, T4, P3, Pz and P4) according to the international 10-20 system. Electromyograms (EMGs) were recorded from the anterior belly of the digastric and the masseter. The 10 healthy participants were requested to make brisk and self-paced mouth-opening movements. All data were digitized with a sampling frequency of 200 Hz and stored for off-line analysis. Movement-related cortical potentials were obtained by averaging the EEG, using the digastric EMG onset as a trigger signal. The Bereitschaftspotential was recorded as a gradually increasing, bilaterally widespread negativity starting 1.7 s (mean) +/-0.23 s (S.D.) before the onset of the opening movement. The amplitude, which was measured at movement onset, was maximum at Cz (3.8 +/- 1.3 microV). The negative slope was observed 500-600 ms before the movement onset, and the motor potential was not clearly identified, because of postmotion artefacts. The cortical maps of the Bereitschaftspotential and negative slope combined together before to the mouth opening showed a symmetrical distribution with a maximum at the vertex region. The study reveals that the Bereitschaftspotential and the negative slope, two components of the movement-related cortical potentials, can be observed preceding mouth-opening movements and are similar to those associated with other voluntary movements. Findings such as distribution, amplitude and onset of the potentials could provide important information for studying the cortical control of mandibular movements.

Adult↗
PubMed2006

Intracerebral ERD/ERS in voluntary movement and in cognitive visuomotor task.

In order to study cerebral activity related to preparation and execution of movement, evoked and induced brain electrical activities were compared to each other and to fMRI results in voluntary self-paced movements. Also, the event-related desynchronization and synchronization (ERD/ERS) were studied in complex movements with various degrees of cognitive load. The Bereitschaftspotential (BP) and alpha (8-12 Hz) and beta (16-24 Hz) ERD/ERS rhythms in self-paced simple movements were analyzed in 14 epilepsy surgery candidates. In previous studies, the cortical sources of BP were consistently displayed contralateral to the movement in the primary motor cortex and somatosensory cortex, and bilateral in the supplementary motor area (SMA) and in the cingulate cortex. There were also small and inconstant BP generators in the ipsilateral sensorimotor, premotor, and dorsolateral prefrontal cortex. Alpha and beta ERD/ERS were also observed in these cortical regions. The distribution of contacts showing ERD or ERS was larger than of those showing BP. In contrast to BP, ERD, and ERS frequently occurred in the orbitofrontal, lateral and mesial temporal cortices, and inferior parietal lobule. The spatial location of brain activation for self-paced repetitive movements, i.e., writing simple dots, was studied using event-related functional MRI (fMRI) in 10 healthy right-handed subjects. We observed significant activation in regions known to participate in motor control: contralateral to the movement in the primary sensorimotor and supramarginal cortices, the SMA and the underlying cingulate, and, to a lesser extent, the ipsilateral sensorimotor region. When the fMRI was compared with the map of the brain areas electrically active with self-paced movements (intracerebral recordings; Rektor et al., 1994, 1998, 2001b, c; Rektor, 2003), there was an evident overlap of most results. Nevertheless, the electrophysiological studies were more sensitive in uncovering small active areas, i.e., in the premotor and prefrontal cortices. The BP and the event-related hemodynamic changes were displayed in regions known to participate in motor control. The cortical occurrence of oscillatory activities in the alpha-beta range was clearly more widespread. Four epilepsy surgery candidates with implanted depth brain electrodes performed two visuomotor-cognitive tasks with cued complex movements: a simple task--copying randomly presented letters from the monitor; and a more complex task--writing a letter other than that which appears on the monitor. The second task demanded an increased cognitive load, i.e., of executive functions. Alpha and beta ERD/ERS rhythms were evaluated. Similar results for both tasks were found in the majority of the frontal contacts, i.e., in the SMA, anterior cingulate, premotor, and dorsolateral prefrontal cortices. The most frequent observed activity was ERD in the beta rhythm; alpha ERS and ERD were also present. Significant differences between the two tasks appeared in several frontal areas--in the dorsolateral and ventrolateral prefrontal and orbitofrontal cortices (BA 9, 45, 11), and in the temporal neocortex (BA 21). In several contacts localized in these areas, namely in the lateral temporal cortex, there were significant changes only with the complex task--mostly beta ERD. Although the fMRI results fit well with the map of the evoked activity (BP), several discrepant localizations were displayed when the BP was compared with the distribution of the oscillatory activity (ERD-ERS). The BP and hemodynamic changes are closely related to the motor control areas; ERD/ERS represent the broader physiological aspects of motor execution and control. The BP probably reflects regional activation, while the more widespread ERD/ERS may reflect the spread of task-relevant information across relevant areas. In the writing tasks, the spatial distribution of the alpha-beta ERD/ERS in the frontal and lateral temporal cortices was partially task dependent. The ERD/ERS occurred there predominantly in the more complex of the writing tasks. Some sites were only active in the task with the increased demand on executive functions. In the temporal neocortex only, the oscillatory, but not the evoked, activity was recorded in the self-paced movement. The temporal appearance of changes of oscillatory activities in the self-paced movement task as well as in the cued movement task with an increased load of executive functions raises the interesting question of the role of this region in cognitive-movement information processing.

Adolescent↗
PubMed2001

A higher-order mechanism overrules the automatic grip-load force constraint during bimanual asymmetrical movements.

The aim of the present study was to examine grip-load force regulation during unimanual and bimanual movements. Two protocols were included which manipulated the object's weight and covered distance. Results showed that grip-load ratio was adapted to the task requirements. During unimanual and bimanual symmetrical movements, an increased grip-load force ratio for long versus short amplitude movements as well as for light versus heavy weight movements was noted. These findings could be related to the observed movement speed variations associated with the tasks. During bimanual asymmetrical movements, the grip-load force ratio became comparable for both sides. When transporting different object's weights to constant distances, the grip-load force ratio of light weight movements decreased towards that of heavy weight movements. As movement speed was reduced, it indicates that grasping forces were adapted accordingly. When transporting constant object's weights to different distances, the grip-load force ratio of short amplitude movements increased towards that of long amplitude movements. Since movement speed was decreased, it suggests that a bimanual coordinative command overruled the automatic grip-load coupling. In conclusion, these data show that interlimb coupling induced a rescaling towards a common control structure, leading to similar grasping forces during bimanual movements with dissimilar actions.

Functional Laterality↗
PubMed1998

Cardiac response induced by voluntary self-paced finger movement.

Cardiac responses induced by slow and brisk voluntary self-paced index finger movements of the dominant and non-dominant hand were investigated in a group of 12 right-handed subjects. Since subjects synchronised movement and respiration, initiating movement preferably during inspiration, a novel method of evaluating the movement-induced cardiac response was used. This method allows one to distinguish the differential effects on the cardiac response due to movement and respiration. The effect of type of movements (slow vs. brisk) and hand (right vs. left) were analysed. Slow movements induced a monophasic cardiac response, consisting of cardiac deceleration preceding and accompanying movement. Brisk movements induced a biphasic cardiac response, consisting of preparatory deceleration followed by slight post-movement cardiac acceleration. Hand-dominance did not influence the movement-induced cardiac response. The results suggest that neocortical structures involved in planning and execution of voluntary movement impinge upon brainstem cardiovascular nuclei. Vagal cardiac outflow is affected and gives rise to movement-induced changes in cardiac chronotropism.

Adult↗
PubMed2003

Time-series analyses of mandibular and perioral soft tissue movements during mastication.

Masticatory movements are rhythmically repeated and coordinated movements of the jaw, tongue and facial muscles. Thus, we considered that the elucidation of movements that are specific to perioral soft tissue, as a result of perioral facial muscle activities, should be useful for evaluation of the smoothness of masticatory movements. The aim of this study was to evaluate the smoothness of masticatory movements from the component of movements that are specific to perioral soft tissue during mastication by the application of time-series analysis. The subjects were 15 healthy persons with complete natural dentition. The experimental food used for mastication in this study was sufficiently softened chewing gum. The results showed that the component of movements that are specific to perioral soft tissue during mastication are the equal repetition spatially and stable movements temporally, and that these movements have the same accurate rhythm as that of mandibular movements and cooperate with mandibular movements temporally. Moreover, the results suggested, from the viewpoint of kinematics, that the innervation of the central pattern generator was concerned with the neural basis of rhythm generation of perioral facial muscles. Therefore, the component of movements that are specific to perioral soft tissue during mastication is useful for evaluation of the smoothness of masticatory movements.

Adult↗