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At least 451 records · Page 25Linked to original sources
PubMed1984

Maintenance of equilibrium point control during an unexpectedly loaded rapid limb movement.

Two experiments investigated whether the equilibrium point hypothesis or the mass-spring model of motor control subserves positioning accuracy during spring loaded, rapid, bi-articulated movement. For intact preparations, the equilibrium point hypothesis predicts response accuracy to be determined by a mixture of afferent and efferent information, whereas the mass-spring model predicts positioning to be under a direct control system. Subjects completed a series of load-resisted training trials to a spatial target. The magnitude of a sustained spring load was unexpectedly increased on selected trials. Results indicated positioning accuracy and applied force varied with increases in load, which suggests that the original efferent commands are modified by afferent information during the movement as predicted by the equilibrium point hypothesis.

Humans↗
PubMed1984

Responses of prepositus hypoglossi neurons to optokinetic and vestibular stimulations in the rat.

The responses of 47 nucleus prepositus hypoglossi neurons to vestibular optokinetic stimulations in the horizontal plane were recorded in immobilized, pigmented rats. During sinusoidal vestibular stimulation in the dark, type II (62%) and type I (38%) responses were recorded. In addition to the sinusoidal modulation of firing rate, units often showed fast rhythmic increases or decreases in firing (nystagmic modulation). The mean phase of the response relative acceleration measured at 0.025 and 0.2 Hz were 19 and 84 deg., respectively. Some units (25%) showed larger phase-lags. The sensitivities of unit responses at 0.025 and 0.2 Hz were 1.6 and 0.5 spikes X s-1/deg X s-2, respectively. The responses of NPH neurons to binocular optokinetic stimulation were divided in 2 classes: (i) neurons with unidirectional responses (18%) were excited by stimuli moving towards the side of recording and showed no change in firing on oppositely directed stimulation; all of them showed a type II pattern during vestibular stimulation; (ii) bidirectional responses showed an increase in one direction and a decrease in firing for stimulation in the opposite direction. In every case the optokinetic responses were synergistic with the vestibular responses, which consisted of both type I and type II units. On the basis of the directionality of their optokinetic response, the value of their time constants and the shape of their velocity tuning curves, it is suggested that unidirectional type II NPH neurons could serve as relays in the optokinetic pathways between NRTP (or PT) and vestibular neurons. Some other neurons, having time constants particularly long and different for the rising and falling of the response, probably serve other functions.

Animals↗
PubMed1986

Joint angle signaling by muscle spindle receptors.

Nerve impulses were recorded from sensory fibers supplying the tibialis anterior and soleus muscles of anesthetized cats as the ankle joint was moved from one end of the flexion-extension axis to the other and back again in steps of 6-7 degrees. The rate of movement from one position to the next was 40 deg/s and each position was held for 16-18 s. Plots were made of receptor discharge frequency as a function of ankle joint angle during joint movement (dynamic input-output (I-O) functions) as well as 2 and 15 s after movement terminated (2 and 15 s static I-O functions). Only receptors with a sustained (5s) static response within the physiological range were studied. A total of 229 tibialis anterior receptors met this criterion, of which 11 were identified as tendon organs. One hundred and five soleus receptors were studied, of which 6 were tendon organs. Thus tendon organ activity accounted for only a small part of the muscle afferent signal under passive conditions. The spindle receptors in soleus and tibialis anterior divided the ankle flexion-extension range about equally between them, those in soleus signaling over the flexion half of the range and those in tibialis anterior over the extension half. At angles where the receptors in a particular muscle did not signal joint angle, the tendon of the muscle was observed to be slack. Thus the total muscle afferent discharge in a relaxed animal is high at one end of the range, declines progressively as the ankle is displaced to an intermediate position, and then increases again as the joint moves toward the opposite end of the range. The spindle receptors within an individual muscle were recruited rather early as the muscle came under tension so that over most of a muscle's signaling range joint angle could have been coded by changes in receptor discharge frequency but not by which spindle receptors were active. To evaluate the information signaled by individual muscle spindle receptors, the following measurements were made from plots of impulse frequency vs joint angle: dynamic response, defined as the frequency difference between the dynamic and 2 s static I-O functions during muscle lengthening; adaptation, defined as the frequency difference between the 2 and 15 s static I-O functions during muscle lengthening.(ABSTRACT TRUNCATED AT 400 WORDS)

Adaptation, Physiological↗
PubMed1986

Classification of muscle spindle receptors.

The conduction velocities of muscle spindle afferent fibers have a bimodal distribution, and classifications of spindle receptors based on afferent fiber diameter have therefore divided these receptors into two groups, the well known primary and secondary endings. However, measures of spindle function that are likely to be important for kinesthetic sensibility such as dynamic response, adaptation and linear directionality (hysteresis) are distributed rather uniformly. Therefore, from this functional perspective it might be argued that muscle spindle receptors should not be subdivided at all. On the other hand, different receptors demonstrate these properties to varying degrees, and there are simple, linear correlations among log (dynamic response), log (adaptation), linear directionality and conduction velocity. Thus, the receptors can be divided into as many as 5-10 different subpopulations that differ significantly in one or more of these properties.

Adaptation, Physiological↗
PubMed1989

The role of location indexes in spatial perception: a sketch of the FINST spatial-index model.

This paper hypothesizes a resource-limited mechanism, called a FINST, for individuating or indexing visual features, as distinct from encoding their type or location. FINSTs have the property that they index features in a way that is transparent to their retinal location, and hence under certain conditions succeed in "pointing to" scene locations. The basic assumption is that no operation upon sets of features can occur unless all the features to which the operation applies are first FINSTed. A number of applications of this hypothesis are explored in this paper, including applications to phenomena such as the spatial stability of visual percepts, the ability to track several independently moving targets in parallel, the ability to detect a class of spatial relations requiring the use of "visual routines", various mental imagery phenomena, and the ability to encode complex shapes for recognition. In addition, the possibility is examined that such indexes might be used to bind perceived locations to arguments in motor commands, thereby allowing some forms of perceptual-motor coordination. Several additional assumptions are introduced for this purpose, including the postulation of other indexes (called ANCHORS) for non-visually sensed locations. It is assumed that ANCHORS can be bound to FINSTs, thus allowing cross-referencing of visually detected locations to locations given within a proprioceptive or motor-command frame of reference.

Attention↗
PubMed1989

Human DC scalp potentials during vestibular and optokinetic stimulation: non-specific responses?

In normal subjects transient horizontal body rotation in the dark (vestibular stimulation) elicited a DC potential change with the maximum at Cz. The response appeared to covary with stimulus velocity, which is the most relevant stimulus parameter transferred by the horizontal semicircular canal system. A similar response was obtained during optokinetic stimulation. However, the following findings suggested that the responses are related to 'high' perceptual functions rather than representing a visuo-vestibular evoked cortical potential: (a) the visual response was found independent of whether the subjects perceived, as a task, self-motion in a stationary environment or 'object' motion about the stationary body; its amplitude depended on the subjects' subjective compliance to the task; (b) when presenting various combinations of optokinetic and vestibular stimuli, the response amplitude depended on the subjective and objective intersensory conflict in the combinations; (c) sinusoidal stimulation yielded a negative shift of the DC potential, but the potential was not modulated along with the waxing and waning of stimulus velocity or of the self-motion sensation evoked; (d) patients with loss of vestibular functions showed a similar Cz response during body rotation in the dark.

Cerebral Cortex↗
PubMed1984

Influence of vision on vibration-induced illusions of limb movement.

Illusory motion of the unseen stationary forearm can be elicited by vibration of the biceps brachii or triceps brachii muscle. We have studied in 12 individuals how sight of part of the arm alone or in relation to other objects affects such vibration-induced, illusory motion of the forearm. Our findings indicate a complex but systematic influence of vision in attenuating apparent motion of the forearm. They show, too, that the seen and felt positions of the forearm can be dissociated and that physically impossible spatial configurations of the arm can be experienced. These findings have implications for physiological theories of position sense.

Eye Movements↗