SUMMARY1. Discharges of Purkinje cells and of presumed mossy fibres were extracellularly recorded from vermal lobules VI and VII of two monkeys during saccadic eye movements and fixation. Among the units showing changes in activity in relation to either saccades or eye position, eighty-four units were identified as mossy fibres and ninetyone units were Purkinje cells.2. Based on the discharge patterns associated with saccades, mossy fibre units were classified into long-lead burst, burst, and burst-tonic units. The long-lead burst units (twenty-eight units) started firing long before the saccades, the discharge consisting of a prelude (average lead time: 160 msec) and a burst (average lead time: 16 msec). In twenty-two units the saccade-related bursts showed a directional preference. The burst units (thirty-seven units) started firing slightly before the saccade onset (average lead time: 7-4 msec) and thirteen units showed directional preference. The bursts in burst-tonic units (thirteen units) had an average lead time of 0-2 msec.3. Among the ninety-one Purkinje cells, eighty-eight cells showed bursts associated with saccades. Three units paused for all directions of saccades.4. Seventy-one units out of the eighty-eight burst Purkinje cells showed bursts beginning approximately at the saccade onset (average lead time: 0 6 msec) and lasting throughout the saccade. The durations of bursts and saccades were highly correlated (correlation coefficients ranging from 0 70 to 0.88).5. In the remaining seventeen burst Purkinje cells, the bursts followed the saccade onset (average delay: 32 msec). The bursts started approximately 40 msec before the end of a saccade and persisted on the average 70 msec after its completion. Peak firing rate occurred with a close temporal relation to the end of the saccade.6. The tonic activity in nineteen mossy fibres and five Purkinje cells changed with eye positions. In the nineteen mossy fibres, there were thirteen burst-tonic and six tonic units. The activity in the five Purkinje cells was a linear function of horizontal eye position.
Changes in oculomotor behaviors with aging were studied in normal young and elderly subjects. Saccadic eye movements induced by presentation of a visual target were analyzed. Elderly subjects commonly showed an elongation of the time to locate the target, accompanied by an increase in reaction times (mean increase, 100 ms) and a decrease in saccadic velocities. The decrease in the velocity was particularly notable when a large-amplitude saccade was executed. In spite of the slowed motor responses, most elderly subjects preserved the function necessary to execute a correct saccade toward the visual target. The saccadic slowing was accompanied by an increase in saccade duration. Although a longer time was necessary for elderly subjects to locate the target, the accuracy of the initial saccades was not different from that of young subjects. One group of elderly subjects showed extremely long reaction times. These subjects, displaying no abnormal neurological symptoms, were not able to locate the visual target with initial saccades. They had to execute multistep saccades typically seen in patients with degenerative neurological diseases.
This study demonstrated that CCT was significantly decreased in the presence of mild/moderate NPDR in the no treatment group, suggesting that a continuously high blood sugar state caused by insufficient treatments for DM may facilitate vascular damage in the choroid in the early stage of DR.
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