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The purpose of this study was to examine aging and bimanual effects on finger spatial stability during precision grip. Twenty-one older and 21 younger adults performed precision grip tasks consisting of a single task (grip and lift an object with the thumb and index finger) and a dual task (the grip-lifting task with one hand and a peg board task with the other hand). The center of pressure (COP) trajectory and the grip force were evaluated using a pressure sensor with a high spatial resolution. In the COP trajectory, the main effects of age for the thumb (F1,140 = 46.17, p < 0.01) and index finger (F1,140 = 22.14, p < 0.01) and task difficulty for the thumb (F1,140 = 6.47, p = 0.01) were significant based on ANCOVA. The COP trajectory was statistically decreased in the older adults. The COP trajectory was also decreased in the dual task, regardless of age. The results suggest the existence of a safety strategy to prioritize the spatial stability in the elderly group and in the dual task. This study provides new insights into the interpretation of the COP trajectory.

Motor overflow, typically described in the context of unimanual movements, refers to the natural tendency for a ‘resting’ limb to move during movement of the opposite limb and is thought to be influenced by inter-hemispheric interactions and intra-cortical networks within the ‘resting’ hemisphere. It is currently unknown, however, how motor overflow contributes to asymmetric force coordination task accuracy, referred to as bimanual interference, as there is need to generate unequal forces and corticospinal output for each limb. Here, we assessed motor overflow via motor evoked potentials (MEPs) and the regulation of motor overflow via inter-hemispheric inhibition (IHI) and short-intra-cortical inhibition (SICI) using transcranial magnetic stimulation in the presence of unimanual and bimanual isometric force production. All outcomes were measured in the left first dorsal interosseous (test hand) muscle, which maintained 30% maximal voluntary contraction (MVC), while the right hand (conditioning hand) was maintained at rest, 10, 30, or 70% of its MVC. We have found that as higher forces are generated with the conditioning hand, MEP amplitudes at the active test hand decreased and inter-hemispheric inhibition increased, suggesting reduced motor overflow in the presence of bimanual asymmetric forces. Furthermore, we found that subjects with less motor overflow (i.e., reduced MEP amplitudes in the test hemisphere) demonstrated poorer accuracy in maintaining 30% MVC across all conditions. These findings suggest that motor overflow may serve as an adaptive substrate to support bimanual asymmetric force coordination.

This study investigated the asymmetry of bilateral interference in a bimanual isometric force pulse task and the relation of the degree of interference with the asymmetry of the force levels and the hand dominance. One hand produced force pulses with the same peak force target, while the other hand produced different peak forces in blocked conditions with force target ratios between the hands that ranged from 1:1 to 16:1. There was asymmetric interference between the hands in that the hand performing the same peak forces showed stronger (i.e., higher bias and variable error) interference with the hand performing the different peak force than vice versa. The force-time properties also correlated more strongly when the different peak forces were generated by the left non-dominant than the right dominant hand. With increasing peak force ratios, the extent of interference became stronger and plateaued around the force ratio of 8:1 indicating a boundary condition to the asymmetric interference between hands. The results extend to bimanual isometric force control the dependence of bilateral asymmetric interference on task demands and hand dominance and provide further evidence on the degree of bilateral interference with task asymmetry.

It is known that, in macaques, movements guided by somatosensory information engage anterior parietal and posterior precentral regions. Movements performed with both visual and somatosensory feedback additionally activate posterior parietal and anterior precentral areas. It remains unclear whether the human parieto-frontal circuits exhibit a similar functional organization. Here, we employed a directional interference task requiring a continuous update of sensory information for the on-line control of movement direction, while brain activity was measured by functional magnetic resonance imaging (fMRI). Directional interference arises when bimanual movements occur along different directions in joint space. Under these circumstances, the presence of visual information does not substantially alter performance, such that we could vary the amount and type of sensory information used during on-line guidance of goal-directed movements without affecting motor output. Our results confirmed that in humans, as in macaques, movements guided by somatosensory information engages anterior parietal and posterior precentral regions, while movements performed with both visual and somatosensory information activate posterior parietal and anterior precentral areas. We provide novel evidence on how the interaction of specific portions of the dorsal parietal and precentral cortex in the right hemisphere might generate spatial representations by integrating different sensory modalities during goal-directed movements.

Bimanual coordination is an essential feature of the motor system, yet interactions between the limbs during independent control remain poorly understood. Interference between the two hands, or the assimilation of movement characteristics between the two effectors, can be induced by perturbing one arm (e.g., via visuomotor rotation) and then measuring the effects in the contralateral limb. In this study, we sought to further determine the role adaptation plays in bimanual interference using a structural learning paradigm to alter feedback regulation in reaching. We trained healthy participants to counter 60 unique random rotations in right hand visual feedback over 240 reaches. Following this, we assessed feedforward and feedback measures of interference in a bimanual reaching task where the right hand was exposed to a fixed visual feedback rotation while the left hand reached without visual feedback. We found that participants who had been exposed to the structural training task in the right hand showed increased left hand interference during the first 20 trials of the test task. Moreover, interference was greater in feedback, rather than feedforward control parameters. The results further suggest that structural learning enhances bimanual interference via sensory feedback upregulation.

This reaction time study tested the hypothesis that in the case of finger movements skilled motor control involves the execution of learned hand postures. After delineating hypothetical control mechanisms and their predictions an experiment is described involving 32 participants who practiced 6 chord responses. These responses involved the simultaneous depression of one, two or three keys with either four right-hand fingers or two fingers of both hands. After practicing each of these responses for 240 trials, the participants performed the practiced and also novel chords with the familiar and with the unfamiliar hand configuration of the other practice group. The results suggest that participants learned hand postures rather than spatial or explicit chord representations. Participants practicing with both hands also developed a bimanual coordination skill. Chord execution was most likely slowed by interference between adjacent fingers. This interference seemed eliminated with practice for some chords but not for others. Hence, the results support the notion that skilled control of finger movements is based on learned hand postures that even after practice may be slowed by interference between adjacent fingers.

Current society has to deal with major challenges related to our constantly increasing population of older adults. Since, motor performance generally deteriorates at older age, research investigating the effects of different types of training on motor improvement is particularly important. Here, we tested the effects of contextual interference (CI) while learning a bimanual coordination task in both young and older subjects. Both age groups acquired a low and high complexity task variant following either a blocked or random practice schedule. Typical CI effects, i.e., better overall performance during acquisition but detrimental effects during retention for the blocked compared with the random groups, were found for the low complexity task variant in both age groups. With respect to the high complexity task variant, no retention differences between both practice schedules were found. However, following random practice, better skill persistence (i.e., from end of acquisition to retention) over a 1 week time interval was observed for both task complexity variants and in both age groups. The current study provides clear evidence that the effects of different practice schedules on learning a complex bimanual task are not modulated by age.

This work explores, for the first time, the electro-cortical activity related to the preparation of bimanual incompatible actions. To accomplish this aim, we recorded motor-related cortical potentials (MRCPs) in 16 healthy subjects, who were asked to draw lines and/or circles during three experimental conditions: Unimanual, Bimanually Compatible (either lines or circles with both hands) and Bimanually Incompatible (a line with one hand and a circle with the other hand). We show that the electro-cortical activity recorded during the preparation of the bimanually incompatible actions included a central positivity (CP) that began approximately 2.5s before movement onset and was localized in medial frontal areas. We then recorded a later (ca. 700ms before movement onset) negative activity in the supplementary motor area (consistent with Bereitschaftspotential). Finally, a strong frontal lateral positivity (FLP) emerged ca. 1.8s before the initiation of drawing that was localized in the dorsolateral prefrontal cortex. All components were bilateral. The CP component has not been described before. These data are discussed with regard to the “interference network” theory. •We showed the brain activity timing associated with bimanual incompatible movements.•We found novel electro-cortical activities preceding and following the movement.•These activities were localized in the prefrontal, premotor and parietal cortices.•The presence of the “interference network” for bimanual actions was confirmed.•The knowledge about this network has been extended including its timing.

Task-switching paradigms have generally been used to investigate cognitive processes involved in decision making or allocating attention. This work extended the task-switching paradigm into the motor domain in order to investigate the consequences of an unexpected environmental perturbation on reaction time and movement time. Typically, task-switching paradigms have investigated consequences of rearranging task sets from one trial to the next; this work explored rearranging planned movements within the context of a single trial. Of particular interest was how the motor system reorganizes coordination patterns when reaching amplitude congruency is manipulated between the two hands. Results for Experiment 1 and the far distance in Experiment 2 indicated that reaction time switch costs were the smallest during congruent task-switch trials, where reaching amplitudes between the two hands were the same. This implies that a planned movement parameter for one hand is accessible for the other hand in the circumstance of an unexpected task switch. However, the reversed congruency effects found for the near distance in Experiment 2 suggest that the ability to capitalize on stored parameter information to decrease reaction time is dependent on environmental factors and task instructions. Movement time results showed that even if a movement with one hand is aborted in mid-execution, it can still influence the performance of the other hand during a task switch. This suggests that bimanual coordination can affect prehensile performance even though only one hand has a goal to achieve.

When the left and right hands produce 2 different rhythms simultaneously, coordination of the hands is difficult unless the rhythms can be integrated into a unified temporal pattern. In the present study, the authors investigated whether a similar account can be applied to the spatial domain. Participants (N = 8) produced a movement trajectory of semicircular form in single-limb and bimanual conditions. In the bimanual tasks, 1 limb moved above the other in the frontal plane. Bimanual unified tasks were constructed so that the spatial paths to be produced by the 2 limbs could be easily conceptualized as parts of a unified circle pattern. Bimanual distinct tasks availed a less obvious spatial pattern that would unify the 2 tasks. Performance of the spatial patterns was more accurate in the unified task, despite similar demands placed on the coordination dynamics between the limbs in the 2 cases (e.g., the phase relations). The authors conclude that a dual task becomes a single task, and interlimb interference is reduced, when the spatial patterns produced by the 2 hands form a geometric arrangement that can be conceptualized as a unified representation.