Saccadic reaction times during isometric voluntary contraction of the shoulder girdle elevators and vibration stimulation to the trapezius.

We investigated the effect of increases in muscle afferent information from the shoulder girdle elevators on saccadic reaction time. Saccadic reaction time was measured under conditions of isometric voluntary contraction of the shoulder girdle elevators and vibratory stimulation of the trapezius. Saccadic reaction time was defined as the latency until the beginning of eye movement toward the lateral target, which was moved at random time-intervals in jumps of 20 degress amplitude. Eye movement was measured using the electro-oculogram technique. Muscle contraction force was set in 10% increments from 0% to 30% of maximal voluntary contraction (MVC), and vibration frequency was maintained at 100 Hz. Under voluntary contraction, the saccadic reaction time gradually shortened up to 30% MVC. Under vibration stimulation at 0% MVC, the reaction time shortened to the same degree as that under voluntary contraction at 30% MVC. Under conditions of combined vibratory stimulation and voluntary contraction, the reaction time was essentially identical to these values; namely, no additive effect in shortening of the reaction time was recognized. The results demonstrated that saccadic reaction times were remarkably shortened by increases in muscle afferent information from the neck extensors. We have discussed reasons for the lack of an additive effect and factors limiting shortening of reaction times.

Modality of postural movement in men and women with both arms flexed during standing.

We investigated postural movement associated with bilateral arm flexion in response to a light signal during standing in 179 healthy men and women to assess whether individual and sex differences arc evident in the postural movement pattern. The following results were obtained. (a) A correlation of -.87 was noted between movement angles of the foot-leg and leg-trunk. (b) Individual differences in movement angle were approximately twice as large in the hip joint as in the ankle and knee joints, and the movement angle of the leg trunk showed approximately half the number of extension as flexion movements. (c) The postural movement pattern was categorized on the basis of the movement angle of the foot leg and leg trunk into the following three patterns: hip flexion, backward leaning, and hip extension. The percentages of subjects showing these patterns were 59.2%, 33.5%, and 7.3%, respectively. (d) The inclination angle reflecting the righting response showed a gradual increase in size in the order of trunk, head, and neck. However, the righting response was not controlled precisely enough to enable subjects to maintain the inclination angle in a quiet standing posture. (e) We identified a significant sex difference in the relative frequency of subjects in the postural movement pattern.

Starting position of movement and perception of angle of trunk flexion while standing with eyes closed.

The present study attempted to investigate the effect of position on the perception of angle of trunk flexion while standing. For this purpose, the range effect was factored out by setting the constant target angle at 10 degrees, with varied starting positions of trunk flexion. We found that subjects underestimated angle of trunk flexion when the starting position was close to a quiet standing posture, overestimated when close to maximum trunk flexion, and correctly perceived it when at the middle position. Less perceptual distortion was observed at the positions close to maximum trunk flexion in the present study than in our previous one, in which various target angles of trunk flexion were reproduced from a quiet standing posture. The reduced distortion in the present study was believed to have resulted from factoring out the range effect. The flexion angle of the hip joint changed in tandem with that of the trunk, while very little movement was observed in the ankle, knee, and neck joints. Judging from the changing pattern of hip-joint angle, the muscle activity of the erector spinae and biceps femoris increased gradually to 90 degrees trunk flexion. In contrast, the actual increment of muscle activity reached zero or a minimum value at the middle angles as the angle of trunk flexion increased. It was assumed that the abrupt change in kinesthetic information associated with muscle activity exerted a great influence on the perception of trunk flexion.