Developmental changes in shortening of pro-saccade reaction time while maintaining neck flexion position.

BACKGROUND: We investigated developmental changes in shortening of pro-saccade reaction time while maintaining neck flexion. METHODS: Subjects comprised 135 children (3-14 years) and 29 young adults (19-23 years). Children were divided into six groups in 2-year age strata. Pro-saccade reaction tasks for 30 s were performed in neck rest and flexion positions. Reaction times under each position were averaged in every 10-s period. RESULTS: Under neck rest position, reaction time in the 0-10 s period was significantly longer in the 3- to 4-year-old group than in the 5- to 6-year-old group and above. No significant age effect was found for reaction time in the 0-10 s period in the 5- to 6-year-old group and above. Although a significant effect of neck flexion was not observed until the 9- to 10-year-old group, significant shortening of reaction time with neck flexion was found in the 11- to 12-year-old group and above. Furthermore, this shortening was maintained until the first 20-s period in the 11- to 12-year-old group and during the entire 30 s in the 13- to 14-year-old and above. CONCLUSIONS: These results suggest that brain activation with the maintenance of neck flexion, related to shortening of the pro-saccade reaction time, was found from a later age of approximately 11 years and above, compared with the age at which information-processing function in the pro-saccade was enhanced. In addition, brain activation with the maintenance of neck flexion was sustained longer with age.

Timings of attentional switching to perturbation and postural preparation during transient forward or backward floor translation.

BACKGROUND: Relationships between the timings of attentional switching and postural preparation were investigated using a choice-reaction paradigm with transient floor translation (S2), with the direction indicated by a warning auditory signal (S1). METHODS: Thirteen healthy young adults participated in this study. S2 started 2 s after S1 onset while standing on the platform. The platform moved forward when S1 was a high tone, and backward when S1 was a low tone. In the S1-S2 period, attentional switching was evaluated by P3 component of event-related potential. RESULTS: A shift in the center of pressure in the anteroposterior direction (CoPap) or a continuous increase in postural muscle activation toward S2 was recognized as postural preparation. Changes in postural muscle activation were found just before the CoPap shift. P3 was observed about 250-650 ms after S1. Onset of postural preparation was significantly later (about 200 ms) than latency of P3 (p < 0.001) and correlated strongly with P3 latency (forward: r = 0.81, backward: r = 0.74, p < 0.01). CONCLUSION: Postural preparation for S2 was demonstrated to start after attentional switching from S1 to S2.

Activation timing of postural muscles of lower legs and prediction of postural disturbance during bilateral arm flexion in older adults.

BACKGROUND: Activation timings of postural muscles of lower legs and prediction of postural disturbance were investigated in young and older adults during bilateral arm flexion in a self-timing task and an oddball task with different probabilities of target presentation. Arm flexion was started from a standing posture with hands suspended 10 cm below the horizontal level in front of the body, in which postural control focused on the ankles is important. METHODS: Fourteen young and 14 older adults raised the arms in response to the target sound signal. Three task conditions were used: 15 and 45% probabilities of the target in the oddball task and self-timing. Analysis items were activation timing of postural muscles (erector spinae, biceps femoris, and gastrocnemius) with respect to the anterior deltoid (AD), and latency and amplitude of the P300 component of event-related brain potential. RESULTS: For young adults, all postural muscles were activated significantly earlier than AD under each condition, and time of preceding gastrocnemius activation was significantly longer in the order of the self-timing, 45 and 15% conditions. P300 latency was significantly shorter, and P300 amplitude was significantly smaller under the 45% condition than under the 15% condition. For older adults, although all postural muscles, including gastrocnemius, were activated significantly earlier than AD in the self-timing condition, only activation timing of gastrocnemius was not significantly earlier than that of AD in oddball tasks, regardless of target probability. No significant differences were found between 15 and 45% conditions in onset times of all postural muscles, and latency and amplitude of P300. CONCLUSION: These results suggest that during arm movement, young adults can achieve sufficient postural preparation in proportion to the probability of target presentation in the oddball task. Older adults can achieve postural control using ankle joints in the self-timing task. However, in the oddball task, older adults experience difficulty predicting the timing of target presentation, which could be related to deteriorated cognitive function, resulting in reduced use of the ankle joints for postural control.

Postural control and contingent negative variation during transient floor translation while standing with the ankle fixed.

BACKGROUND: Adaptation changes in postural muscle activity and anticipatory attention were investigated with the ankle joint fixed to change postural control strategies during transient floor translation. METHODS: For 15 healthy young adults, 40 transient floor translations (S2) in the anterior direction were applied 2 s after an auditory warning signal (S1), under conditions with or without fixation of the ankle. Activity of the frontal postural muscles (tibialis anterior (TA), rectus femoris (RF), rectus abdominis) and contingent negative variation (CNV, brain potential) were analyzed for 20 trials each of the early and latter halves under each fixation condition. RESULTS: With fixation, peak amplitude of muscle activity after S2 was significantly decreased in TA and increased in RF. These muscles showed marked adaptive decreases. The early component of CNV reduced with adaptation, particularly under fixation condition. Only in RF, background activity increased just before S2, with adaptation under fixation. A significant correlation was found between timings of CNV peak and RF activation just before S2 only after adaptation under fixation. CONCLUSION: These results suggest that the main activation muscle changes from TA to RF with fixation. Under such condition, attention would be focused on the knee with adaptation, and the need for heightening attention in the early stage may have declined. Correspondingly, the timing to heighten stiffness of the RF became later, and attention would have been paid to RF activation just before S2.

Event-related brain potential and postural muscle activity during standing on an oscillating table while the knee, hip, and trunk are fixed.

BACKGROUND: In this study, a cast brace was used to immobilize the knee, hip, and trunk, and relations between the event-related brain potential (ERP) and postural muscle activity were investigated while standing on an oscillating table. METHODS: Twelve healthy young adults maintained a standing posture for 1 min per trial while oscillating in the anteroposterior direction at 0.5 Hz with a 2.5-cm amplitude. Trials were performed without and with the cast brace (no-fixation and fixation condition, respectively) until the subject had adapted to the floor oscillation. The ERP from the Cz electrode, postural muscle activity, and joint movement range were analyzed for the first and last two trials (before and after adaptation, respectively). RESULTS: Movement range of the hip and knee was lower in the fixation condition than in the no-fixation condition, and postural control was achieved by pivoting at the ankle. Peak muscle activity was largest in the gastrocnemius (GcM) in both conditions. GcM activity significantly increased after fixation and then decreased with adaptation. The time of peak erector spinae (ES) activity in the fixation condition was significantly earlier than in the no-fixation condition and was not significantly different from the time of the anterior reversal and peak of triceps surae activity. The negative ERP peaked approximately 80 ms after the anterior reversal. Significant correlations between the time of the peak negative ERP and the peak GcM, soleus, and ES activity were observed only after the adaptation, and were greater in the fixation condition (r = 0.83, 0.84, and 0.83, respectively) than in the no-fixation condition (r = 0.62, 0.73, and 0.51, respectively). CONCLUSION: All joints of the leg and trunk except for the ankle were rigidly fixed by the cast brace, and the phase differences between body segments were very small in the fixation condition. High correlations between the time of the peak negative ERP and the peak GcM, soleus, and ES activity after adaptation in the fixation condition suggest that attention would be more focused on anticipatory processing of muscle sensory information from the triceps surae and/or ES, particularly GcM, which had the greatest activation.

Postural responses to various frequencies of vibration of the triceps surae and forefoot sole during quiet standing.

The purpose of this study was to determine the role of somatosensory input to the sensory reference system in quiet standing. We applied vibration (0.5 mm amplitude, 1-60 Hz) to the triceps surae and the forefoot sole to stimulate the muscle spindles and the mechanoreceptors, respectively, and evaluated postural responses. Thirteen young healthy adults who showed backward-lean and forward-lean responses to vibration at high and low frequencies, respectively, participated in the full experiment. The lowest vibration frequencies inducing backward-lean responses (B-LF) were 15-55 Hz for the triceps surae and 16-60 Hz for the forefoot sole. The highest frequencies inducing forward-lean responses (F-HF) were 3-18 Hz for the triceps surae and 1-20 Hz for the forefoot sole. When vibration was simultaneously applied to the triceps surae and forefoot sole at F-HF, no response was induced in 70% of trials. A forward-lean response was induced in the remaining 30% of trials. Simultaneous vibration of the triceps surae and forefoot sole at B-LF induced backward-lean responses in all trials. All postural responses occurred 0.5-4.3 s after vibration onset. Postural responses to high-frequency vibration conceivably occur as a compensatory movement to the illusionary perception that standing position is deviating forward from quiet standing, which must be a reference position. Postural responses to low-frequency vibration possibly occur to equalize the positional information that is received from the triceps surae and the forefoot sole. Both postural responses are likely to involve the sensory reference system, which is located in the supraspinal nervous system.

Postural control during transient floor translation while standing with the leg and trunk fixed.

Postural movement was restricted above the ankle, and contingent negative variation (CNV) and postural muscle activity were investigated during a transient floor translation (S2) 2s after an auditory warning signal (S1). For 13 healthy young adults, the joints of the knee, hip, and trunk were fixed using a cast brace. Under no-fixation and fixation, a set of 10 translations was repeated at least 4 times, and center of pressure in the anteroposterior direction (CoPap), posterior postural muscle activity of the body (elector spinae (ES), biceps femoris (BF), gastrocnemius (GcM) and soleus (Sol)), and late CNV at Cz were analyzed in the initial two sets (initial set) and last two sets (late set). In the no-fixation, CoPap forward displacement after S2 gradually decreased. In the first trial of the fixation, it had significantly increased, and then rapidly decreased across subsequent trials. CNV peak amplitude was largest in the late set of the fixation. The activity of postural muscles increased just before S2 and in the late set the start time showed high correlations with CNV peak time in all muscles (ES (r=0.88), BF (0.92), GcM (0.80), and Sol (0.89)) under the no-fixation, but exclusively in the GcM (0.84) and Sol (0.88) under the fixation. When postural control was restricted mainly to the ankle, attention would have been focused mainly on processing sensory information from the triceps surae just before the floor translation.

Effect of time pressure on attentional shift and anticipatory postural control during unilateral shoulder abduction reactions in an oddball-like paradigm.

BACKGROUND: The effect of time pressure on attentional shift and anticipatory postural control was investigated during unilateral shoulder abduction reactions in an oddball-like paradigm. METHODS: A cue signal (S1) - imperative signal (S2) sequence was repeated with various S2-S1 intervals (1.0, 1.5, and 2.0 s). S2 comprised target and non-target stimuli presented at the position (9° to the left or the right) indicated by S1. Right shoulder abduction was performed only in response to target stimuli, which were presented with a 30% probability. The P1, N1, N2, and P3 components of event-related potentials were analyzed, and onset times of postural muscles (electromyographic activity of erector spinae and gluteus medius) were quantified with respect to middle deltoid activation. RESULTS: There was no significant effect of S2-S1 interval on the latency or amplitude of P1, N1, or N2. The percentage of subjects with bimodal P3 peaks was significantly smaller and the slope of the P3 waveform in the 100 ms after the first peak was significantly steeper with a 1.0-s S2-S1 interval than with a 1.5- or 2.0-s S2-S1 interval. The onset of postural muscle activity was significantly later in the shorter interval conditions. CONCLUSIONS: These results suggest that with a shorter S2-S1 interval, that is, higher time pressure, attention was allocated to hasten the latter part of cognitive processing that may relate to attentional shift from S2 to next S1, which led to insufficient postural preparation associated with arm movement and anticipatory attention directed to S2.

Adaptation changes in dynamic postural control and contingent negative variation during repeated transient forward translation in the elderly.

BACKGROUND: Adaptation changes in postural control and contingent negative variation (CNV) for the elderly were investigated during repeated forward floor translation. METHODS: Fifteen healthy elderly persons, living in the suburban area of Kanazawa City, Japan, underwent backward postural disturbance by a forward-floor translation (S2) 2 s after an auditory warning signal (S1). A set with 20 trials was repeated until a negative peak of late CNV was recognized in the 600-ms period before S2, and the last set was defined as the final set. Electroencephalograms, center of foot pressure in the anteroposterior direction (CoPap), and electromyograms of postural muscles were analyzed. RESULTS: CoPap displacement generated by the floor translation was significantly decreased until the twelfth trial in the first set, and mean CoPap displacement was smaller in the second and final sets than in the first set. The mean displacement was significantly smaller in the final set than the previous set. A late CNV with a negative peak was not recognized in the first and second sets. However, most subjects (13/15) showed a negative peak by the fourth set, when the late CNV started to increase negatively from about 1,000 ms after S1 and peaked at about 300 ms before S2. At about 160 ms before the CNV peak, the CoPap forward shift started. The increase in timing of the gastrocnemius activity related to the CoPap shift was significantly correlated with the CNV peak timing (r = 0.64). After S2, peak amplitudes of the anterior postural muscles were significantly decreased in the final set compared to the first set. CONCLUSIONS: It was demonstrated that even for the elderly, with so many repetitions of postural disturbance, a late CNV with a negative peak was recognized, leading to accurate postural preparation. This suggests the improvement of frontal lobe function (e.g., anticipatory attention and motor preparation) in the elderly.

Postural responses accompanying Achilles tendon vibration stimulation during various phases of sit-to-stand movement.

The aim of this study was to determine the postural response accompanying Achilles tendon vibration stimulation during various phases of the sit-to-stand movement. Twelve healthy young adults performed the sit-to-stand movement in response to an auditory signal 2 s after a first one. Vibration stimulation with a 100 Hz frequency was applied to both Achilles tendons during the following phases: (1) 10 s of sitting before standing up; (2) 10 s plus a period until the standing position was achieved; and (3) 5 s after standing. The postural response after standing was analyzed with the center of foot pressure in the anteroposterior direction. Forward-leaning responses were identified in 78.3% and 63.3% of trials under conditions 1 and 2, respectively. Backward-leaning responses were identified in 93.3% of the trials under condition 3. Response latency (+/- standard deviation) was significantly longer under conditions 1 and 2 than under condition 3 (1: 872 +/- 576, 2: 1026 +/- 542, and 3:555 +/- 322 ms; ps < 0.05). Sensory information at the standing point might be anticipated based on sensory information received while sitting. Consequently, postural response as a compensatory movement would occur via the sensory reference system within the supraspinal nervous system.

The effects of neck flexion on cerebral potentials evoked by visual, auditory and somatosensory stimuli and focal brain blood flow in related sensory cortices.

BACKGROUND: A flexed neck posture leads to non-specific activation of the brain. Sensory evoked cerebral potentials and focal brain blood flow have been used to evaluate the activation of the sensory cortex. We investigated the effects of a flexed neck posture on the cerebral potentials evoked by visual, auditory and somatosensory stimuli and focal brain blood flow in the related sensory cortices. METHODS: Twelve healthy young adults received right visual hemi-field, binaural auditory and left median nerve stimuli while sitting with the neck in a resting and flexed (20° flexion) position. Sensory evoked potentials were recorded from the right occipital region, Cz in accordance with the international 10-20 system, and 2 cm posterior from C4, during visual, auditory and somatosensory stimulations. The oxidative-hemoglobin concentration was measured in the respective sensory cortex using near-infrared spectroscopy. RESULTS: Latencies of the late component of all sensory evoked potentials significantly shortened, and the amplitude of auditory evoked potentials increased when the neck was in a flexed position. Oxidative-hemoglobin concentrations in the left and right visual cortices were higher during visual stimulation in the flexed neck position. The left visual cortex is responsible for receiving the visual information. In addition, oxidative-hemoglobin concentrations in the bilateral auditory cortex during auditory stimulation, and in the right somatosensory cortex during somatosensory stimulation, were higher in the flexed neck position. CONCLUSIONS: Visual, auditory and somatosensory pathways were activated by neck flexion. The sensory cortices were selectively activated, reflecting the modalities in sensory projection to the cerebral cortex and inter-hemispheric connections.

Adaptation changes in dynamic postural control and contingent negative variation during backward disturbance by transient floor translation in the elderly.

BACKGROUND: We investigated adaptation changes in dynamic postural control and contingent negative variation (CNV) in 13 young and 12 elderly adults. Subjects repeatedly underwent backward postural disturbance by a forward floor translation (S2) 2 s after an auditory warning signal (S1). Initial and second sets were conducted, each set with 20 trials. Posterior peak position of the center of pressure in the anteroposterior direction (CoPy) after S2 was identified. Electroencephalograms from Cz were averaged for each set, and the CNV negative peak was identified. RESULTS: Compared with the first trial, the posterior peak position of CoPy changed significantly forward from the 12th trial in the young and from the 19th trial in the elderly during the initial set. The mean of the posterior peak position was more forward in second set than in the initial set for both groups and was significantly backward in the elderly compared to the young for both sets. These findings indicate that subjects in both groups adapted better to the postural disturbance in the second set than in the initial set, and the adaptation was later in the elderly. Late CNV in the young started to increase negatively from the middle of the S1-S2 period and peaked just before S2. Peak CNV amplitude was larger in the second set than in the initial set. In contrast, late CNV in the elderly exhibited no negative increase as in the young and peaked in the middle of the S1-S2 period, which was followed by gradual decreasing toward S2. No adaptive changes were found in late CNV for the elderly. CONCLUSIONS: It is conceivable that reduced activation of the frontal lobe may be one of the factors contributing to the decrease in postural adaptability in the elderly. The elderly may use various brain regions for the adaptation of dynamic postural control compared with the young.

Contingent negative variation and activation of postural preparation before postural perturbation by backward floor translation at different initial standing positions.

We investigated the effects of balance difficulty on contingent negative variation (CNV) and postural preparation against perturbation. Thirteen subjects were perturbed by a backward floor translation (S2) after an auditory warning stimulus. To alter balance difficulty, subjects maintained standing posture from four initial positions before perturbation. The position of the center of pressure in the anteroposterior direction (CoPy) was expressed as a percentage distance of foot length (%FL) from the heel: 10%FL anterior to extreme backward leaning; quiet standing (QS); and 20%FL and 10%FL posterior to extreme forward leaning. CNV, CoPy, and electromyography (EMG) of the lower leg muscles were analyzed. Balance difficulty was represented by the relative distance of the forward peak position of CoPy after S2 from the QS position. Balance difficulty was higher with a more anterior initial position. The late CNV peaked just before S2 (latency: -76 to -306 ms), then started becoming small. CNV peak was earlier and larger with increasing balance difficulty. CoPy backward shift and a continuous EMG increase were observed as the strategy for postural preparation, and were significantly earlier (61 ms and 42 ms, respectively) than the CNV peak. CNV peak time correlated closely with onset times of CoPy backward shift (r=0.78) and continuous EMG increase (r=0.71). These findings suggest that as balance difficulty increases, attentional allocation to sensory information and/or postural preparation starts earlier just before the perturbation.

Relationship between quiet standing position and perceptibility of standing position in the anteroposterior direction.

We investigated the relationship between an individual's center of pressure in the anteroposterior direction in quiet standing (QS) and perceptibility of different standing positions. The position of the center of pressure in the anteroposterior direction (CoPy position) while standing was represented as the percentage distance (%FL) from the hindmost point of the heel in relation to foot length. CoPy position in QS was located from 31 to 58%FL. Perceptibility of standing position was evaluated by the difference between the reference position and the subject's attempt to reproduce that position. Subjects were tested for their ability to reproduce reference positions selected randomly from a total of 13 positions at 5%FL increments from 20 to 80%FL. Using an approximation formula curve, we identified the relationship between reference position and reproduction absolute error. The standing position range with reproduction error exceeding 90% of the difference between the maximum and minimum errors was defined as the low perceptibility range of standing position. The approximation curve had one peak near QS. CoPy positions in QS were located in the low perceptibility range, except for five subjects with a more posterior location. The correlation coefficient between CoPy positions in QS (x) and reference position (y) showing maximum error was 0.70 and the regression line was y=0.464x+28.2; the intersection point with y=x was 53%FL. Reproduction absolute errors in reference positions at 20-30%FL and 70-80%FL were significantly smaller than those at 40-60%FL (p<0.05). We concluded the following. (1) Standing positions showing the lowest perceptibility are located close to the QS position; however, in subjects whose QS position is located more posteriorly, the standing position showing maximum error is more anterior. (2) Perceptibility of extreme forward- and backward-leaning positions is very high and independent of individual QS position.

Effects of anti-saccade training with neck flexion on eye movement performance, presaccadic potentials and prefrontal hemodynamics in the elderly.

Anti-saccade performance, with strong contributions from frontal brain regions, reportedly deteriorates with age and maintenance of neck flexion and is known to cause brain activation. We investigated the effects of anti-saccade training on eye movement performance and frontal activity, and synergistic effects of training with neck flexion in the elderly. Thirty elderly individuals were divided into three equal groups: training group at neck resting position (NRT); training group at 20° neck flexion position (NFT); and untrained group. NRT and NFT performed approximately 200 anti-saccades (a block of 10-12 anti-saccades for 30 s × 20 blocks) per day over 3 weeks. Before and after training, horizontal eye movement, presaccadic potentials, and oxygenated hemoglobin concentration (oxy-Hb) in the prefrontal cortex during anti-saccades were tested in neck resting and 20° neck flexion conditions. In NRT and NFT, reaction time (-50 ms), percentage of erroneous saccades (-24%), and period between peak of presaccadic negativity and onset of spike potential (-16 ms) were significantly decreased through training. Only in NFT, after training, slight shortening of reaction time associated with neck flexion was recognized (-10 ms), and peak amplitude of presaccadic negativity was increased in both test neck conditions. Oxy-Hb was not significantly affected by trainings and test neck conditions. We demonstrated that in the elderly, anti-saccade training with both neck postures improved performance and facilitated related neural pathways. Moreover, training with neck flexion showed small but synergistic effects on performance and frontal activity. However, these trainings would be insufficient for elderly individuals to automatically control anti-saccade.

Eye movement performance and prefrontal hemodynamics during saccadic eye movements in the elderly.

No previous study has investigated age-related changes in prefrontal hemodynamics during saccade tasks in a large number of elderly adults. The purpose of this study was to evaluate prefrontal activity related to the performance of anti-saccade in the elderly using near-infrared spectroscopy (NIRS). Ninety-six elderly adults and 22 young adults performed pro- and anti-saccade tasks. Measures included reaction times of both saccades, error rate during anti-saccade, and concentration of oxyhemoglobin (Deltaoxy-Hb) in the prefrontal cortex during both saccades. Saccade performance, especially error rate, was significantly poorer in the elderly than the young. In the elderly, error rates were widely distributed from 5% to 100%. In about half (48%) of the elderly, error rates were distributed under the mean+3 standard deviations (48%) for the young, and Deltaoxy-Hb did not differ significantly from that in the young. Elderly subjects whose anti-saccade reaction time was over the regression line (of reaction time in anti-saccade to that in pro-saccade in the young)+2 standard errors showed a strong positive correlation (r=0.79) between Deltaoxy-Hb and error rate, as did those whose error rate exceeded 48%. In the elderly subjects whose error rates exceeded 90%, Deltaoxy-Hb was extremely small and deviated greatly from the correlation between Deltaoxy-Hb and error rate. Based on these findings, we propose a method of evaluating inhibitory function and attention allocation in anti-saccade performance, which is mainly related to the prefrontal cortex, in the elderly, using NIRS.

Changes in muscle thickness of gastrocnemius and soleus associated with age and sex.

BACKGROUND AND AIMS: Gastrocnemius and soleus in the triceps surae have functional and histological differences.We therefore investigated age-related changes in muscle thickness of these two muscles, as well as the difference in these changes between men and women. METHODS: Participants comprised 847 healthy adults aged 20 to 79 years. A B-mode ultrasound scanner, with participants sitting on a chair, was used to measure muscle thickness from the midpoint of the gastrocnemius medialis muscle at the level of maximum girth (target point). The ratio of muscle thickness to height was calculated. The inter-rater and intra-rater reliability of measuring muscle thickness with the ultrasound scanner and the validity of the target point were demonstrated before the examination. RESULTS: Gastrocnemius was significantly thinner in women aged 60 or older and in men aged 50 or older, compared with their counterparts in their 20s. For soleus, no significant differences in thickness were found among the age groups in either sex. Decline in muscle thickness from age 40-79 was greater for gastrocnemius than for soleus. CONCLUSIONS: These results confirm that gastrocnemius starts to deteriorate earlier and atrophies at a faster pace than soleus. A significant sex difference was found only in the onset age of gastrocnemius deterioration, which was earlier in men than in women.