Changes in motor cortex activity during reaching movements with similar hand paths but different arm postures

1995 ◽  
Vol 73 (6) ◽  
pp. 2563-2567 ◽  
Author(s):  
S. H. Scott ◽  
J. F. Kalaska

1. Neuronal activity was recorded in the motor cortex of a monkey that performed reaching movements with the use of two different arm postures. In the first posture (control), the monkey used its natural arm orientation, approximately in the sagittal plane. In the second posture (abducted), the monkey had to adduct its elbow nearly to shoulder level to grasp the handle. The path of the hand between targets was similar in both arm postures, but the joint kinematics and kinetics were different. 2. In both postures, the activity of single cells was often broadly tuned with movement direction and static arm posture over the targets. In a large proportion of cells, either the level of tonic activity, the directional tuning, or both, varied between the two postures during the movement and target hold periods. 3. For most directions of movement, there was a statistically significant difference in the direction of the population vector for the two arm postures. Furthermore, whereas the population vector tended to point in the direction of movement for the control posture, there was a poorer correspondence between the direction of movement and the population vector for the abducted posture. These observed changes are inconsistent with the notion that the motor cortex encodes purely hand trajectory in space.

1994 ◽  
Vol 72 (5) ◽  
pp. 2280-2301 ◽  
Author(s):  
M. J. Prud'homme ◽  
J. F. Kalaska

1. We studied the activity of 254 cells in the primary somatosensory cortex (SI) responding to inputs from peripheral proprioceptors in a variety of tasks requiring active reaching movements of the contralateral arm. 2. The majority of cells with receptive fields on the proximal arm (shoulder and elbow) were broadly and unimodally tuned for movement direction, often with approximately sinusoidal tuning curves similar to those seen in motor and parietal cortex. 3. The predominant temporal response profiles were directionally tuned phasic bursts during movement and tonic activity that varied with different arm postures. 4. Most cells showed both phasic and tonic response components to differing degrees, and the population formed a continuum from purely phasic to purely tonic cells with no evidence of separate distinct phasic and tonic populations. This indicates that the initial cortical neuronal correlates of the introspectively distinguishable sensations of movement and position are represented in an overlapping or distributed manner in SI. 5. The directional tuning of the phasic and tonic response components of most cells was generally similar, although rarely identical. 6. We tested 62 cells during similar active and passive arm movements. Many cells showed large differences in their responses in the two conditions, presumably due to changes in peripheral receptor discharge during active muscle contractions. 7. We tested 86 cells in a convergent movement task in which monkeys made reaching movements to a single central target from eight peripheral starting positions. A majority of the cells (46 of 86, 53.5%) showed a movement direction-related hysteresis in which their tonic activity after movement to the central target varied with the direction by which the arm moved to the target. The directionality of this hysteresis was coupled with the movement-related directional tuning of the cells. 8. We recorded the discharge of 93 cells as the monkeys performed the task while compensating for loads in different directions. The large majority of cells showed a statistically significant modulation of activity as a function of load direction, which was qualitatively similar to that seen in motor cortex under similar task conditions. Quantitatively, however, the sensitivity of SI proprioceptive cells to loads was less than that seen in motor cortex but greater than in parietal cortex. 9. We interpret these results in terms of their implications for the central representation of the spatiotemporal form (“kinematics”) of arm movements and postures. Most importantly, the results emphasize the important influence of muscle contractile activity on the central proprioceptive representation of active movements.


2003 ◽  
Vol 89 (2) ◽  
pp. 1136-1142 ◽  
Author(s):  
Yoram Ben-Shaul ◽  
Eran Stark ◽  
Itay Asher ◽  
Rotem Drori ◽  
Zoltan Nadasdy ◽  
...  

Although previous studies have shown that activity of neurons in the motor cortex is related to various movement parameters, including the direction of movement, the spatial pattern by which these parameters are represented is still unresolved. The current work was designed to study the pattern of representation of the preferred direction (PD) of hand movement over the cortical surface. By studying pairwise PD differences, and by applying a novel implementation of the circular variance during preparation and movement periods in the context of a center-out task, we demonstrate a nonrandom distribution of PDs over the premotor and motor cortical surface of two monkeys. Our analysis shows that, whereas PDs of units recorded by nonadjacent electrodes are not more similar than expected by chance, PDs of units recorded by adjacent electrodes are. PDs of units recorded by a single electrode display the greatest similarity. Comparison of PD distributions during preparation and movement reveals that PDs of nearby units tend to be more similar during the preparation period. However, even for pairs of units recorded by a single electrode, the mean PD difference is typically large (45° and 75° during preparation and movement, respectively), so that a strictly modular representation of hand movement direction over the cortical surface is not supported by our data.


Author(s):  
M. Smith Allan ◽  
Dugas Clause ◽  
Fortier Pierre ◽  
Kalasha John ◽  
Picard Nathalie

ABSTRACT:The activity of single cells in the cerebellar and motor cortex of awake monkeys was recorded during separate studies of whole-arm reaching movements and during the application of force-pulse perturbations to handheld objects. Two general observations about the contribution of the cerebellum to the control of movement emerge from the data. The first, derived from the study of whole arm reaching, suggests that although both the motor cortex and cerebellum generate a signal related to movement direction, the cerebellar signal is less precise and varies from trial to trial even when the movement kinematics remain unchanged. The second observation, derived from the study of predictable perturbations of a hand-held object, indicates that cerebellar cortical neurons better reflect preparatory motor strategies formed from the anticipation of cutaneous and proprioceptive stimuli acquired by previous experience. In spite of strong relations to grip force and receptive fields stimulated by preparatory grip forces increase, the neurons of the percentral motor cortex showed very little anticipatory activity compared with either the premotor areas or the cerebellum.


1994 ◽  
Vol 6 (1) ◽  
pp. 29-37 ◽  
Author(s):  
Terence D. Sanger

Recent evidence of population coding in motor cortex has led some researchers to claim that certain variables such as hand direction or force may be coded within a Cartesian coordinate system with respect to extra personal space. These claims are based on the ability to predict the rectangular coordinates of hand movement direction using a “population vector” computed from multiple cells' firing rates. I show here that such a population vector can always be found given a very general set of assumptions. Therefore the existence of a population vector constitutes only weak support for the explicit use of a particular coordinate representation by motor cortex.


1999 ◽  
Vol 82 (5) ◽  
pp. 2705-2718 ◽  
Author(s):  
Andrew B. Schwartz ◽  
Daniel W. Moran

Activity was recorded extracellularly from single cells in motor and premotor cortex as monkeys traced figure-eights on a touch-sensitive computer monitor using the index finger. Each unit was recorded individually, and the responses collected from four hemispheres (3 primary motor and 1 dorsal premotor) were analyzed as a population. Population vectors constructed from this activity accurately and isomorphically represented the shape of the drawn figures showing that they represent the spatial aspect of the task well. These observations were extended by examining the temporal relation between this neural representation and finger displacement. Movements generated during this task were made in four kinematic segments. This segmentation was clearly evident in a time series of population vectors. In addition, the [Formula: see text] power law described for human drawing was also evident in the neural correlate of the monkey hand trajectory. Movement direction and speed changed continuously during the task. Within each segment, speed and direction changed reciprocally. The prediction interval between the population vector and movement direction increased in the middle of the segments where curvature was high, but decreased in straight portions at the beginning and end of each segment. In contrast to direction, prediction intervals between the movement speed and population vector length were near-constant with only a modest modulation in each segment. Population vectors predicted direction (vector angle) and speed (vector length) throughout the drawing task. Joint angular velocity and arm muscle EMG were well correlated to hand direction, suggesting that kinematic and kinetic parameters are correlated in these tasks.


1997 ◽  
Vol 77 (2) ◽  
pp. 826-852 ◽  
Author(s):  
Stephen H. Scott ◽  
John F. Kalaska

Scott, Stephen H. and John F. Kalaska. Reaching movements with similar hand paths but different arm orientations. I. Activity of individual cells in motor cortex. J. Neurophysiol. 77: 826–852, 1997. This study shows that the discharge of many motor cortical cells is strongly influenced by attributes of movement related to the geometry and mechanics of the arm and not only by spatial attributes of the hand trajectory. The activity of 619 directionally tuned cells was recorded from the motor cortex of two monkeys during reaching movements with the use of similar hand paths but two different arm orientations, in the natural parasagittal plane and abducted into the horizontal plane. Nearly all cells (588 of 619, 95%) showed statistically significant changes in activity between the two arm orientations [analysis of variance (ANOVA), P < 0.01]. A majority of cells showed a significant change in their overall level of activity (ANOVA, main effect of task, P < 0.01) between arm orientations before, during, and after movement. Many cells (433 of 619, 70%) also showed a significant change in the relation of their discharge with movement direction(ANOVA, task × direction interaction term, P < 0.01) during movement, including changes in the dynamic range of discharge with movement and changes in the directional preference of cells that were directionally tuned in both arm orientations. Similar effects were seen for the discharge of cells while the monkey maintained constant arm postures over the different peripheral targets with the use of different arm orientations. Repeated data files from the same cell with the use of the same arm orientation showed only small changes in the level of discharge or in directional tuning, suggesting that changes in cell discharge between arm orientations cannot be explained by random temporal variations in cell activity. The distribution of movement-related preferred directions of the whole sample differed between arm orientations, and also differed strongly between cells receiving passive input predominantly from the shoulder or elbow. The electromyographic activity of most prime mover muscles at the shoulder and elbow was also strongly affected by arm orientation, resulting in changes in overall level of activity and/or directional tuning that often resembled those of the proximal arm-related motor cortical cells. A mathematical model that represented movements in terms of movement direction centered on the hand could not account for any of the arm-orientation-related response changes seen in this task, whereas models in intrinsic parameter spaces of joint kinematics and joint torques predicted many of the effects.


2016 ◽  
Vol 2016 ◽  
pp. 1-10 ◽  
Author(s):  
Teresa Paolucci ◽  
Federico Zangrando ◽  
Giulia Piccinini ◽  
Federico Sciarra ◽  
Rocco Pallotta ◽  
...  

Background. The position sense of the shoulder joint is important during reaching.Objective. To examine the existence of additional competence of the shoulder with regard to the ability to measure extracorporeal space, through a novel approach, using the shoulder proprioceptive rehabilitation tool (SPRT), during reaching.Design. Observational case-control study.Methods. We examined 50 subjects: 25 healthy and 25 with impingement syndrome with a mean age [years] of 64.52 +/− 6.98 and 68.36 +/− 6.54, respectively. Two parameters were evaluated using the SPRT: the integration of visual information and the proprioceptive afferents of the shoulder (Test 1) and the discriminative proprioceptive capacity of the shoulder, with the subject blindfolded (Test 2). These tasks assessed the spatial error (in centimeters) by the shoulder joint in reaching movements on the sagittal plane.Results. The shoulder had proprioceptive features that allowed it to memorize a reaching position and reproduce it (error of 1.22 cm to 1.55 cm in healthy subjects). This ability was lower in the impingement group, with a statistically significant difference compared to the healthy group (p<0.05by Mann–Whitney test).Conclusions. The shoulder has specific expertise in the measurement of the extracorporeal space during reaching movements that gradually decreases in impingement syndrome.


1993 ◽  
Vol 69 (4) ◽  
pp. 1136-1149 ◽  
Author(s):  
P. A. Fortier ◽  
A. M. Smith ◽  
J. F. Kalaska

1. The responses of 262 motor cortex cells and 223 cerebellar neurons were recorded during whole-arm reaching movements toward targets lights in eight evenly distributed directions radiating from a common central starting position. The reaching movements were followed by a 2-s target hold period where a fixed arm posture was actively maintained to stabilize the hand over the target light. 2. Cerebellar neurons had a higher mean tonic discharge rate while holding over the starting position (22.9 imp/s) than did motor cortex cells (12.5 imp/s). The mean population response curve describing the changes in activities with movement direction was likewise shifted toward higher frequencies in the cerebellum compared with the motor cortex, but the amplitude of the two curves was about equal. Therefore, the baseline discharges of cerebellar neurons were higher, but their changes in activity during movement were similar to those of motor cortical cells. 3. Motor cortex neurons were more strongly related to active maintenance of different arm postures than were cerebellar units. This was shown by a larger posture-related population response curve in the motor cortex (half-wave amplitude of cosine function was 11.2 imp/s, compared with 7.0 imp/s for cerebellar neurons), which represented the average response curve calculated from all the cells of the population. Furthermore, the motor cortex population had a higher percentage of single cells with tonic responses while the hand was held over different targets (tonic and phasic-tonic cells composed 57% of motor cortex population, compared with 38% of cerebellar population). Proportionately more cerebellar cells were phasically related to the movements. 4. The majority of motor cortex cells (58%) showed reciprocal changes relative to the center-hold time activity where the activity increased for movements in the preferred direction and decreased for movements in the opposite direction. Most of the remaining cells (40%) showed graded changes where the activity increased gradually as reaching was directed closer to the preferred direction. In contrast, the most common cerebellar response pattern was graded (38%). Only 26% were reciprocal and 18% were non-directional. The remaining 2% of motor cortical cells and 18% of cerebellar neurons could not be readily assigned to any of these three response classes. 5. Sector widths were calculated to measure the dispersion of individual cerebellar and motor cortical cell activities about the eight movement directions. Sector widths calculated from the absolute activities were always broader for cerebellar neurons (i.e., the cells were more broadly tuned).(ABSTRACT TRUNCATED AT 400 WORDS)


2004 ◽  
Vol 98 (4-6) ◽  
pp. 498-506 ◽  
Author(s):  
Carsten Mehring ◽  
Martin Paul Nawrot ◽  
Simone Cardoso de Oliveira ◽  
Eilon Vaadia ◽  
Andreas Schulze-Bonhage ◽  
...  

2014 ◽  
Vol 10 (3) ◽  
pp. 181-186 ◽  
Author(s):  
A. Bergh ◽  
A. Egenvall ◽  
E. Olsson ◽  
M. Uhlhorn ◽  
M. Rhodin

Kinematic studies, using reflective skin markers, are commonly used to investigate equine joint motion in equitation science and for rehabilitation purposes. In order to interpret the registrations accurately, the degree of skin displacement has been described for the limbs and back, but not yet for the neck. The aim of the present study was to measure sagittal plane skin displacement in the equine neck. Radiopaque skin markers were applied to the skin over the first six cervical vertebrae of six healthy horses. Latero-lateral radiographs were taken in three standardised neck positions in the sagittal plane: control (horizontal neck), ‘on the bit’ and ‘nose to carpus’. The scales of the images were normalised and calculation of skin displacement was done by use of a coordinate system, dividing the displacement along an x-axis parallel to the vertebra's longitudinal axis and a y-axis perpendicular to the x-axis. Mixed models analysis was employed to study the differences in distances in x- and y-directions, and statistical significance was set to PÃ0.05. Between control and ‘nose to carpus’ positions, there were significant differences in skin marker locations, relative to the underlying vertebrae, in the x-direction for C1-6, and in y-direction for C3-6. Between normal and ‘on the bit’ positions, there were significant difference in both x- and y-directions for C6. Differences in marker locations along x- and y-axes, respectively, were 3±9 mm and 44±14 mm. The outcome of this study indicates that skin displacement should be considered when investigating equine neck motion with skin marker methodology.


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