This study examines the roles of somatosensory and vestibular information in the coordination of postural responses. The role of somatosensory information was examined by comparing postural responses of healthy control subjects prior to and following somatosensory loss due to hypoxic anesthesia of the feet and ankles. The role of vestibular information was evaluated by comparing the postural responses of control subjects and patients with bilateral vestibular loss. Postural responses were quantified by measuring 1) spatial and temporal characteristics of leg and trunk EMG activation; 2) ankle, knee, and hip joint kinematics, and 3) surface forces in response to anterior and posterior surface translations under different visual and surface conditions. Results showed that neither vestibular nor somatosensory loss resulted in delayed or disorganized postural responses. However, both types of sensory deficits altered the type of postural response selected under a given set of conditions. Somatosensory loss resulted in an increased hip strategy for postural correction, similar to the movement strategy used by control subjects while standing across a shortened surface. Vestibular loss resulted in a normal ankle strategy but lack of a hip strategy, even when required for the task of maintaining equilibrium on a shortened surface. Neither somatosensory nor vestibular loss resulted in difficulty in utilizing remaining sensory information for orientation during quiet stance. These results support the hypothesis that cutaneous and joint somatosensory information from the feet and ankles may play an important role in assuring that the form of postural movements are appropriate for the current biomechanical constraints of the surface and/or foot. The results also suggest that vestibular information is necessary in controlling equilibrium in a task requiring use of the hip strategy. Thus, both somatosensory and vestibular sensory information play important roles in the selection of postural movement strategies appropriate for their environmental contexts.

In a previous study (Ivry and Keele, in press), cerebellar patients were found to be impaired on both a motor and a perceptual task which required accurate timing. This report presents case study analyses of seven patients with focal lesions in the cerebellum. The lesions were predominantly in the lateral, hemispheric regions for four of the patients. For the remaining three patients, the lesions were centered near the medial zone of the cerebellum. The clinical evaluation of the patients also was in agreement with the different lesion foci: lateral lesions primarily impaired fine motor coordination, especially apparent in movements with the distal extremities and medial lesions primarily disturbed balance and gait. All of the patients were found to have increased variability in performing rhythmic tapping when tapping with an effector (finger or foot) ipsilateral to the lesion in comparison to their performance with a contralateral effector. Separable estimates of a central timekeeper component and an implementation component were derived from the total variability scores following a model developed by Wing and Kristofferson (1973). This analysis indicated that the poor performance of patients with lateral lesions can be attributed to a deficit in the central timing process. In contrast, patients with medial lesions are able to accurately determine when to make a response, but are unable to implement the response at the desired time. A similar dissociation between the lateral and medial regions has been observed on a time perception task in patients with cerebellar atrophy. It is concluded that the lateral regions of the cerebellum are critical for the accurate functioning of an internal timing system.

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1. The objective was to investigate in cerebellar patients with dysmetria the kinematic and electromyographic (EMG) characteristics of large and small movements at the elbow, wrist, and finger and thereby to determine the nature of cerebellar dysmetria at distal as well as proximal joints. Flexions were made as fast as possible by moving relatively heavy manipulanda for each joint to the same end position through 5, 30, and 60 degrees. 2. In normal subjects flexions at all joints were accompanied by similar triphasic EMG activity. Movements of increasing amplitude were made with increasing movement durations and increasing durations and magnitudes of initial agonist EMG activity. Antagonist activity often appeared to have two components: one coactive with the initial agonist burst but starting later, the other reaching its peak at about peak velocity. 3. Cerebellar patients with dysmetria showed hypermetria followed by tremor at all three joints when movements were made with the manipulanda. Hypermetria was most marked for aimed movements of small amplitude (5 degrees) at all joints. 4. A characteristic of cerebellar disordered movements, which could be present at all amplitudes and all joints, was an asymmetry with decreased peak accelerations and increased peak decelerations compared to normal movements. Both the asymmetry and the hypermetria for small amplitude movements could be used clinically as sensitive indicators of cerebellar dysfunction. 5. The EMG abnormalities accompanying hypermetria and asymmetry were a more gradual buildup and a prolongation of agonist activity and delayed onset of antagonist activity.(ABSTRACT TRUNCATED AT 250 WORDS)

We used positron emission tomography (PET) to localize a cerebellar timing function. Six healthy volunteers estimated time differences by comparing a test interval (defined by two tones) with a standard interval. In the timing condition, subjects lifted their right index finger if the test interval was shorter and their right middle finger if it was longer than the standard interval. In the control condition, the two intervals were identical and subjects had to alternate between lifting their index and middle fingers. We examined regional cerebral blood flow (rCBF) using the standard C15O2 inhalation technique. Comparison of control and rest conditions revealed significant increases of rCBF during the control condition in the inferior parts of the ipsilateral cerebellar hemisphere, reflecting finger movements. Comparison of timing and control conditions showed additional activations of the cerebellar vermis and hemispheres bilaterally during the timing condition, reflecting the cerebellar timing process. We conclude that the cerebellum is involved in time-critical perception ("timing"). This nonmotor task can be separated from a motor task (finger movement).