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Motor Commands (motor + command)
Selected AbstractsInfluence of experience of treadmill exercise on visual perception while on a treadmillJAPANESE PSYCHOLOGICAL RESEARCH, Issue 2 2010YOSHIKO YABE Abstract A firm linkage exists between a motor command and its expected feedback. When we are exposed to a conflict between expected and actual feedback in a new context, we form a new linkage between action and perception, which may be further strengthened by prolonged experience. In this paper, we attempt to identify whether the linkage between treadmill locomotion and visual processing in relation to optic flow is strengthened in experienced users of treadmills. Yabe and Taga (2008) showed that ambiguous apparent motions are perceived to be moving downward more frequently when the stimuli are shown in front of the observers' feet on a treadmill when walking compared with when standing. Here, their experimental data was reanalyzed in relation to the experience of using the treadmill. The result revealed that habitual treadmill exercise reduced the difference in perceived direction of visual motion between the walking and standing conditions. It should be noted that the treadmill users showed perceptual "downward" bias for both the standing and walking conditions. The results suggest that treadmill users tend to activate the habitual linkage between treadmill locomotion and perception of optic ground flow even when they are just standing on a treadmill. [source] Muscle spindle signals combine with the sense of effort to indicate limb positionTHE JOURNAL OF PHYSIOLOGY, Issue 3 2005J. A. Winter Experiments were carried out to test the hypothesis that, in the absence of vision, position sense at the human forearm is generated by the combined input from muscle spindles in elbow flexor muscles and signals of central origin giving rise to a sense of effort. In a forearm position-matching task, to remove a possible contribution from the sense of effort, the reference arm was held supported at the test angle. Subjects were less accurate in matching elbow position of the supported forearm than when it was unsupported. Adding a 2 kg weight to the unsupported reference arm led subjects to make matching errors consistent with an increase in the effort signal. Evidence of a contribution from muscle spindles was provided by showing that the direction of position matching errors could be systematically altered by flexion or extension conditioning of the reference arm before its placement at the test angle. Such changes in errors with conditioning could be shown to be present when the reference arm was supported, unsupported, or unsupported and weighted. It is concluded that both peripheral signals from muscle spindles and signals of central origin, associated with the motor command required to maintain arm position against the force of gravity, can provide information about forearm position. [source] Computational motor control: feedback and accuracyEUROPEAN JOURNAL OF NEUROSCIENCE, Issue 4 2008Emmanuel Guigon Abstract Speed/accuracy trade-off is a ubiquitous phenomenon in motor behaviour, which has been ascribed to the presence of signal-dependent noise (SDN) in motor commands. Although this explanation can provide a quantitative account of many aspects of motor variability, including Fitts' law, the fact that this law is frequently violated, e.g. during the acquisition of new motor skills, remains unexplained. Here, we describe a principled approach to the influence of noise on motor behaviour, in which motor variability results from the interplay between sensory and motor execution noises in an optimal feedback-controlled system. In this framework, we first show that Fitts' law arises due to signal-dependent motor noise (SDNm) when sensory (proprioceptive) noise is low, e.g. under visual feedback. Then we show that the terminal variability of non-visually guided movement can be explained by the presence of signal-dependent proprioceptive noise. Finally, we show that movement accuracy can be controlled by opposite changes in signal-dependent sensory (SDNs) and SDNm, a phenomenon that could be ascribed to muscular co-contraction. As the model also explains kinematics, kinetics, muscular and neural characteristics of reaching movements, it provides a unified framework to address motor variability. [source] Mirror Neurons, the Motor System and Language: From the Motor Theory to Embodied Cognition and BeyondLINGUISTICS & LANGUAGE COMPASS (ELECTRONIC), Issue 6 2009Jonathan H. Venezia The motor theory of speech perception states that phonetic segments in the acoustic speech stream activate stored motor commands in the brain that give rise to perception of discrete speech sounds. The motor theory fell out of favor when growing evidence from lesion and behavioral studies led aspects of the theory to appear untenable. However, with the recent discovery of mirror neurons and their potential role in action understanding, interest in the motor theory of speech perception is renewed. We review the function and properties of mirror neurons in monkeys, and briefly describe the current literature that focuses on the role of a putative human mirror system in cognition and language processing. Further, we describe proposed evidence for the involvement of the motor system in perceptive speech processing, and point out ambiguities in the literature that arise from the tight coupling of sensory and motor processes in speech comprehension. An alternative theory proposing that sensory representations in superior temporal cortex are mapped onto frontal production networks is offered. We cite evidence that confirms the failure of the motor theory to accurately describe perceptive processes in speech, and promote the conclusion that speech representations are fundamentally sensory in nature. [source] Impact of gravity loading on post-stroke reaching and its relationship to weaknessMUSCLE AND NERVE, Issue 2 2007Randall F. Beer PhD Abstract The ability to extend the elbow following stroke depends on the magnitude and direction of torques acting at the shoulder. The mechanisms underlying this link remain unclear. The purpose of this study was to evaluate whether the effects of shoulder loading on elbow function were related to weakness or its distribution in the paretic limb. Ten subjects with longstanding hemiparesis performed movements with the arm either passively supported against gravity by an air bearing, or by activation of shoulder muscles. Isometric maximum voluntary torques at the elbow and shoulder were measured using a load cell. The speed and range of elbow extension movements were negatively impacted by actively supporting the paretic limb against gravity. However, the effects of gravity loading were not related to proximal weakness or abnormalities in the elbow flexor,extensor strength balance. The findings support the existence of abnormal descending motor commands that constrain the ability of stroke survivors to generate elbow extension torque in combination with abduction torque at the shoulder. Muscle Nerve, 2007 [source] Tests for presynaptic modulation of corticospinal terminals from peripheral afferents and pyramidal tract in the macaqueTHE JOURNAL OF PHYSIOLOGY, Issue 1 2006A. Jackson The efficacy of sensory input to the spinal cord can be modulated presynaptically during voluntary movement by mechanisms that depolarize afferent terminals and reduce transmitter release. It remains unclear whether similar influences are exerted on the terminals of descending fibres in the corticospinal pathway of Old World primates and man. We investigated two signatures of presynaptic inhibition of the macaque corticospinal pathway following stimulation of the peripheral nerves of the arm (median, radial and ulnar) and the pyramidal tract: (1) increased excitability of corticospinal axon terminals as revealed by changes in antidromically evoked cortical potentials, and (2) changes in the size of the corticospinal monosynaptic field potential in the spinal cord. Conditioning stimulation of the pyramidal tract increased both the terminal excitability and monosynaptic fields with similar time courses. Excitability was maximal between 7.5 and 10 ms following stimulation and returned to baseline within 40 ms. Conditioning stimulation of peripheral nerves produced no statistically significant effect in either measure. We conclude that peripheral afferents do not exert a presynaptic influence on the corticospinal pathway, and that descending volleys may produce autogenic terminal depolarization that is correlated with enhanced transmitter release. Presynaptic inhibition of afferent terminals by descending pathways and the absence of a reciprocal influence of peripheral input on corticospinal efficacy would help to preserve the fidelity of motor commands during centrally initiated movement. [source] | ||||||||||