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At least 325 records · Page 18Linked to original sources

Movement in decline? Oscillatory movement displacement thresholds increase with ageing.

Displacement thresholds for continuous oscillatory movement were determined for ten subjects in each of three age groups--20-23, 40-55 and 60-80 years. Oscillation frequencies of 1, 2, 3, 5, 8, 13 and 20 Hz were used, all subjects having a corrected visual acuity of 6/5. A randomized block factorial design of analysis of variance revealed significant effects of both temporal frequency of oscillation (F6,189 = 4.10, p less than 0.001) and age (F2,189 = 46.98, p much less than 0.001). The deterioration in movement sensitivity occurs equally at both high and low temporal frequencies--no significant interaction effects being revealed (F12,189 = 0.45, p = not significant). The frequency effects are ascribed to underlying mechanisms mediating movement perception. Reasons for decreased movement sensitivity with increasing age are discussed.

Adult↗

Training reaction and movement times of moderately and severely mentally retarded persons in aiming movements.

The effect of information feedback of movement components on the reaction time (RT) and movement time (MT) of mentally retarded adults performing a discrete movement aiming task was investigated. We anticipated that specific training and informational feedback on the RT portion of the RT-MT task would more effectively reduce RT, despite aiming requirements of the movement. Results suggested that specific training and feedback on RT decreased both RT and MT components of the task, whereas specific training on MT reduced only MT. The data were discussed with respect to the differential effects of training on subject populations at varying levels of intellectual capacity.

Adult↗

Timing of bimanual movements and deafferentation: implications for the role of sensory movement effects.

In a repetitive tapping task, the within-hand variability of intertap intervals is reduced when participants tap with both hands instead of single-handedly. This bimanual advantage has been attributed to timer as opposed to motor variance (according to the Wing-Kristofferson model; Helmuth and Ivry 1996) and related to the additional sensory consequences of the movement of the extra hand in the bimanual case (Drewing et al. 2002). In the present study the effect of sensory feedback of the movement on this advantage was investigated by comparing the results of a person (IW) deafferented below the neck with those of age-matched controls. IW showed an even more pronounced bimanual advantage than controls, suggesting that the bimanual advantage is not due to actual sensory feedback. These results support another hypothesis, namely that bimanual timing profits from the averaging of different central control signals that relate to each effector's movements.

Adult↗

Haptic texture affects the kinematics of pointing movements, but not of eye movements.

Discrepant findings on the degree of eye-hand coupling suggest its dependence on the task. One task characteristic modulating this coupling may be the relevance of certain target attributes for each motor system. We tested this assumption by comparing eye and hand movements towards targets of different haptic texture, a target attribute which is behaviourally relevant only to the hand, not the eye. Pointing to a slippery target (fur) resulted in longer hand movement time than to a rougher target (sandpaper). This effect was due to an increased ratio of time spent in deceleration. In contrast, eye movement time was invariant across different haptic target textures. Thus, information about target texture is used differently by eye and hand.

Adult↗

Movement correction of the kidney in dynamic MRI scans using FFT phase difference movement detection.

To measure cortical and medullary MR renograms, regions of interest (ROIs) are placed on the kidney in images acquired using dynamic MRI. Since native kidneys move with breathing, and breath-holding techniques are not feasible, movement correction is necessary. In this contribution we compare three correction methods, based on image matching, phase difference movement detection (PDMD), and cross-correlation, respectively. The PDMD-based method showed the best performance and was able to determine kidney movement in our test series in 68% of the scans with no visible deviation, and in 88% of the scans if a one-pixel deviation is considered acceptable.

Algorithms↗

A kinematic theory of rapid human movements. Part I. Movement representation and generation.

This paper proposes a kinematic theory that can be used to study and analyze rapid human movements. It describes a synergy in terms of the agonist and antagonist neuromuscular systems involved in the production of these movements. It is shown that these systems have a log-normal impulse response that results from the limiting behavior of a large number of interdependent neuromuscular networks, as predicted by the central limit theorem. The delta log-normal law that follows from this model is very general and can reproduce almost perfectly the complete velocity patterns of an end-effector. The theory accounts for the invariance and rescalability of these patterns, as well as for the various observations that have been reported concerning the change in maximum and mean velocities, time to maximum velocity, etc., under different experimental conditions. Movement time, load effects, and control strategies are discussed in a companion paper.

Algorithms↗

[A contribution to the physiology of movement of gregarines: elements and modus of cellular movement (author's transl)].

1. Cytochalasin B (= CCB, Phomin) in several concentrations inhibits the visible movement of gregarines. The fine structure of the cell is simultaneously changed, fibrillar bundles are desorganized. These fibrils are regarded as myonemes. 2. These myonemes are directed peripherally of the cell longitudinal and transverse to its axis. The longitudinal myonemes are organized in separated strings stretching along the top of the epicyte folds, between the plasmalemm and the secondary membranous layer. Fibrils under this layer serve as skeleton and as thus antagonist. The skeleton fibrils remain unaltered after CCB inhibition. They are located in a parallel direction to the myonemes. Their number corresponds together in one epicyte fold. The transverse myonemata surround the central plasma nearby the basal lamella, which cannot be found in some of the regarded species. 3. The co-work of skeleton-fibrils, stiff pellicle and myonemes allows to describe the modus of all known types of movement. Only change of coordination yields the multitude of these kinds of movement.

Animals↗

Guidelines for the therapeutic use of botulinum toxin in movement disorders. Italian Study Group for Movement Disorders, Italian Society of Neurology.

Since its introduction in the early '80s the use of botulinum toxin has improved the quality of life of the patients affected by movement disorders. Toxin's neuromuscular blocking action allows a symptomatic treatment of those clinical conditions characterised by excessive muscular activity. Although the dosages used are safe and the side-effects are reversible, a correct use of botulinum toxin depends on the knowledge of its clinical pharmacology and of the anatomy of the body segments to be injected. In addition, the treatment of more complex conditions, i.e. laringeal dystonia, imposes an inter-disciplinary approach and specialised injection techniques. In this review, the Italian Study Group on Movement Disorders presents the consensus guidelines for the therapeutic use of botulinum toxin in movement disorders. The main toxin types, their use and administration modalities, and the training guidelines will be presented.

Botulinum Toxins↗

Movement-dependent positioning errors in human elbow joint movements.

Healthy adult humans performed elbow movements in a horizontal plane under a small external extending torque (2.1-3.3 Nm). Test movements (TMs) consisted of slow ramp-and-hold flexions in the absence of visual feedback, with the target joint angle to be remembered from a preceding conditioning movement (CM). The CM was produced by matching two beams on the monitor screen: (1) command representing the target position (a straight line); and (2) a signal from the sensor of the elbow joint angle. Two kinds of CM were applied, which had the same target position (50 degrees in most experiments) but differed in initial positions: (1) fully extended joint (0 degrees, P1 CMs); (2) flexed joint (100 degrees, P2 CMs). In a group of 25 subjects, the target in TMs was usually overshot, with the position errors depending on the CMs: 2.7 +/- 0.6 degree (mean +/- SEM) for P1 CMs, and 10.9 +/- 0.7 degree (P < 0.001) for P2 CMs. Vibration of the elbow flexors substantially diminished the difference between the position errors, amounting to--0.31 +/- 0.5 degree and 2.33 +/- 0.6 degrees, respectively. It is suggested that the observed position errors resulted from after-effects in the activity of muscle spindles in agonist and antagonist muscles, but influence of differences in dynamic components of the afferent signals during oppositely directed approaches to the target cannot be excluded.

Adult↗

Bereitschaftspotential in a simple movement or in a motor sequence starting with the same simple movement.

The Bereitschaftspotential (BP) recorded from 3 derivations (vertex, left and right precentral areas) in 20 right-handed, normal young subjects was compared in 2 kinds of motor task: a simple movement (task A) and a motor sequence (task B) starting with the simple movement (A). Differences in the onset time and amplitude of the BP were observed: the onset was earlier and the amplitude was larger in the sequential motor task (B) than in the simple one (A). These differences were more important at the vertex (Cz) and in the right precentral area (C4) than in the left contralateral precentral area (C3). These results suggest that the preparatory processes involved in a motor sequence do not exclusively concern the initial movement but also the remainder of the motor task and that the BP is dependent upon the duration or the complexity of the motor task to be executed. The BP seems on temporal grounds to be a global and not a partial expression of a motor task. The changes in the onset time and amplitude of the BP are maximal at the vertex and this could be related to a greater and perhaps earlier activation of SMA in complex sequential motor tasks.

Adult↗

Mental representations of movements. Brain potentials associated with imagination of hand movements.

The present study was designed in order to contribute towards the understanding of the physiology of motor imagery. DC potentials were recorded when subjects either imagined or executed a sequence of unilateral or bilateral hand movements. The sequence consisted of hand movements in 4 directions, forwards, backwards, to the right and to the left, and varied from trial to trial. The sequence had been cued by visual targets on a computer screen and had to be memorized before the trial was initiated. Changes of DC potentials between task execution and imagination were localized in central recordings (C3, Cz, C4) with larger amplitudes when executing the task than when imagining to do so. Stimulation of peripheral receptors associated with task execution or a different level of activation of the cortico-motoneural system could account for this finding. The main result of the present study was that with unilateral performance, the side of the performing hand (right, left) had localized effects in recordings over the sensorimotor hand area (C3, C4) which were qualitatively the same with imagination and execution and quantitatively similar (i.e., without significant difference). Performance of the right hand augmented negative DC potentials in C3, performance of the left hand augmented amplitudes in C4. This result is consistent with the assumption that the primary motor cortex is active with motor imagery. Finally, the question has been addressed whether motor imagery may involve the left hemisphere to a larger extent than the execution of the movement. It is shown that a particular contribution of the left hemisphere associated with motor imagery may only show up under strictly controlled conditions.

Adult↗

Effects of brefeldin A on the localization of Tobamovirus movement protein and cell-to-cell movement of the virus.

It has been demonstrated that the subcellular location of Tobamovirus movement protein (MP) which was fused with green fluorescent protein (MP:GFP) changed during the infection process. However, the intracellular route through which MP is transported and its biological meaning are still obscure. Treatment with brefeldin A (BFA), which disrupts ER-to-Golgi transport, inhibited the formation of irregularly shaped and filamentous structures of MP. In this condition, MP was still targeted to plasmodesmata in leaf cells. Furthermore, the viral cell-to-cell movement was not inhibited by BFA treatment. These data indicated that the targeting of viral replication complexes (VRCs) to plasmodesmata is mediated by a BFA-insensitive pathway and that the ER-to-Golgi transport pathway is not involved in viral intercellular movement.

Antiviral Agents↗

The impairments in reaching and the movements of compensation in rats with motor cortex lesions: an endpoint, videorecording, and movement notation analysis.

Reaching for food by rats, with the limb contralateral to limb area motor cortex damage, was analyzed using end-point scores, videoanalysis, and Eshkol-Wachmann Movement Notation (EWMN). End point results from groups of rats with small, medium, and large lesions showed reaching success and amount of food grasped per reach decreased with increases in lesion size. Videoanalysis and EWMN showed that the impairments were attributable to: (1) an inability to pronate the paw over the food by abduction of the upper arm, and (2) an inability to supinate the paw at the wrist to orient the food to the mouth. There were no obvious impairments in locating food using olfaction, in positioning the body in order to initiate a reach, or in clasping the digits to grasp food. There were only mild impairments in lifting, aiming, and advancing the limb. In rats with medium and large lesions, loss of pronation and supination were compensated for by a variety of whole body movements. These findings are discussed in reference to neural and behavioral mechanisms underlying recovery of function and the contribution of the motor cortex to skilled movements in the rat and other species.

Animals↗

Early onset of post-movement beta electroencephalogram synchronization in the supplementary motor area during self-paced finger movement in man.

A voluntary finger movement is accompanied by an event-related desynchronization followed by a short burst of beta oscillations or event-related synchronization. These beta bursts are dominant over the contralateral hand representation area, but also appear over the midcentral area overlaying the supplementary motor area (SMA) and the foot representation area. We show that the induced midcentral beta oscillations following movement-offset display not only slightly higher frequency components, but have also a significantly earlier onset. These beta oscillations arise likely from the SMA. Assuming that the short-lasting beta synchronizations at frequencies below 35 Hz after termination of a movement reflect a state of localized cortical inhibition, we propose that the induced midcentral oscillations reflect the inhibition of networks within the SMA. This assumed resetting or inhibitory process within the SMA precedes that of the networks within the primary motor hand area.

Beta Rhythm↗

Cerebral control of eye movements. II. Timing of anticipatory eye movements, predictive pursuit and phase errors in focal cerebral lesions.

Smooth pursuit eye movements are known to be driven by a mixture of visual feedback and predictive strategies. Prediction in pursuit allows humans to track predictable stimuli with minimal phase lag. But in certain disease states and focal neurological lesions, normal phase relationships are lost and humans track with increased phase errors. Using a sinusoidal pursuit paradigm, we sorted patients into those with large phase errors and those without. Then, working on the premise that large phase errors may have resulted from lack of prediction, we compared predictive and non-predictive ocular pursuit in patients with large phase errors, patients with normal phase errors and control subjects. Subjects sat in darkness and pursued an intermittently illuminated target moving with constant velocity to the right or left. When the movements were in alternate directions and predictable, all the groups possessed the ability to preprogramme appropriate anticipatory eye movements before target onset, and to use this for predictive pursuit. The difference between patients with large phase errors and normal subjects was not an absolute lack or possession of predictive ability but a difference in the timing at which a preprogrammed motor behaviour was initiated or terminated. The timing variability was wide and formed a graded continuum, the control subjects initiating anticipatory pursuit earlier, and the patients with large phase errors initiating much later. In a second experiment, subjects pursued a predictable ramp stimulus presented at various fixed frequencies. We found that in patients where anticipatory pursuit seemed abolished at one frequency of target presentation, changing the frequency of presentation elicited an anticipatory response. Patients adjusted their pursuit latencies to match the temporal demands of target presentation. At target frequencies above 0.8 Hz, there was a significant positive correlation between latencies in ramp pursuit and phase lags in sinusoidal pursuit. None of our patients showed complete loss of prediction irrespective of how large the phase errors were. Even when severe time delays in the system made it impossible for a subject to initiate anticipatory pursuit before target onset, prediction could still be demonstrated by the significant velocity and timing advantage the subject had in the pursuit of a predictable target stimulus or by the technique of unexpectedly blanking the target.

Adolescent↗

Rapid eye movement sleep periodic leg movements in patients with spinal cord injury.

We describe three spinal cord injury cases exhibiting periodic leg movements (PLMs) in both rapid eye movement (REM) and nonrapid eye movement (NREM) sleep. The difference in the average periodicity in REM and NREM sleep was modest, but was generally shorter in REM than in NREM sleep. However, the variability associated with the PLMs was nearly three to six times smaller in REM than in NREM sleep, suggesting that the periodicity of the PLMs in REM sleep was more precise than in NREM sleep. The finding of PLMs in these patients suggests that a spinal cord injury may permit the expression of a spinal PLM generator, which may be an unusual presentation of a spinal locomotor generator. The PLM generator would be displayed when the descending inhibitory spinal pathways are interrupted by a spinal injury. The rapid periodicity of the PLM generator in REM sleep, compared with NREM sleep, may result from an increase in sympathetic activity normally accompanying this sleep state. Alternative explanations for the occurrence of PLMs in spinal injury are the influence of adverse sleeping position, age, an increase in circulating catecholamines and peripheral perfusion. We conclude that the presence of PLMs may be an important, but neglected, sleep disorder in spinal cord patients. Therefore, health care professionals should be aware of the possibility of sleep-related PLMs when these patients have sleep and/or waking complaints.

Adult↗

A dysfunctional movement protein of tobacco mosaic virus interferes with targeting of wild-type movement protein to microtubules.

The Tobacco mosaic virus (TMV) movement protein (MPTMV) mediates cell-to-cell viral trafficking by altering properties of the plasmodesmata (Pd) in infected cells. During the infection cycle, MPTMV becomes transiently associated with endomembranes, microfilaments, and microtubules (MT). It has been shown that the cell-to-cell spread of TMV is reduced in plants expressing the dysfunctional MP mutant MPNT-1. To expand our understanding of the MP function, we analyzed events occurring during the intracellular and intercellular targeting of MPTMV and MPNT-1 when expressed as a fusion protein to green fluorescent protein (GFP), either by biolistic bombardment in a viral-free system or from a recombinant virus. The accumulation of MPTMV:GFP, when expressed in a viral-free system, is similar to MPTMV:GFP in TMV-infected tissues. Pd localization and cell-to-cell spread are late events, occurring only after accumulation of MP:GFP in aggregate bodies and on MT in the target cell. MPNT-1:GFP localizes to MT but does not target to Pd nor does it move cell to cell. The spread of transiently expressed MPTMV:GFP in leaves of transgenic plants that produce MPNT-1 is reduced, and targeting of the MPTMV:GFP to the cytoskeleton is inhibited. Although MPTMV:GFP targets to the Pd in these plants, it is partially impaired for movement. It has been suggested that MPNT-1 interferes with host-dependent processes that occur during the intracellular targeting program that makes MP movement competent.

Cucumis sativus↗

Brain pathology, eye movement disorders, and basic science of ocular movement.

Diagnosis of eye movement disorders is an important step in evaluation of patients with developmental or acquired brain lesions. A better understanding of the various pathologies requires both a detailed clinical examination and the analysis of eye movement recordings (nystagmus of various types, saccade, and pursuit anomalies). Basic science studies help to interpret these eye movement disorders.

Brain↗