Mechanisms of interpersonal sway synchrony and stability

Here we explain the neural and mechanical mechanisms responsible for synchronizing sway and improving postural control during physical contact with another standing person. Postural control processes were modelled using an inverted pendulum under continuous feedback control. Interpersonal interactions were simulated either by coupling the sensory feedback loops or by physically coupling the pendulums with a damped spring. These simulations precisely recreated the timing and magnitude of sway interactions observed empirically. Effects of firmly grasping another person's shoulder were explained entirely by the mechanical linkage. This contrasted with light touch and/or visual contact, which were explained by a sensory weighting phenomenon; each person's estimate of upright was based on a weighted combination of veridical sensory feedback combined with a small contribution from their partner. Under these circumstances, the model predicted reductions in sway even without the need to distinguish between self and partner motion. Our findings explain the seemingly paradoxical observation that touching a swaying person can improve postural control.This work was supported by two BBSRC grants (BB/100579X/1 and an Industry Interchange Award)

Ingestion of sodium bicarbonate (NaHCO3) following a fatiguing bout of exercise accelerates post-exercise acid-base balance recovery and improves subsequent high-intensity cycling time to exhaustion.

This study evaluated the ingestion of sodium bicarbonate (NaHCO3) on post-exercise acid-base balance recovery kinetics and subsequent high-intensity cycling time to exhaustion. In a counterbalanced, crossover design, nine healthy and active males (age: 23±2 years, height: 179±5 cm, body mass: 74±9 kg, peak mean minute power (WPEAK) 256±45 W, peak oxygen uptake (V̇O2PEAK) 46±8 ml.kg-1.min-1) performed a graded incremental exercise test, two familiarisation and two experimental trials. Experimental trials consisted of cycling to volitional exhaustion (TLIM1) at 100% WPEAK on two occasions (TLIM1 and TLIM2) interspersed by a 90 min passive recovery period. Using a double blind approach, 30 min into a 90 min recovery period participants ingested either 0.3 g.kg-1 body mass sodium bicarbonate (NaHCO3) or a placebo (PLA) containing 0.1 g.kg-1 body mass sodium chloride (NaCl) mixed with 4 ml.kg-1 tap water and 1 ml.kg-1 orange squash. The mean differences between TLIM2 and TLIM1 was larger for PLA compared to NaHCO3 (-53±53 vs. -20±48 s; P=0.008, d=0.7, CI=-0.3, 1.6), indicating superior subsequent exercise time to exhaustion following NaHCO3. Blood lactate [BLa-] was similar between treatments post TLIM1, but greater for NaHCO3 post TLIM2 and 5 min post TLIM2. Ingestion of NaHCO3 induced marked increases (P<0.01) in both blood pH (+0.07±0.02, d=2.6, CI=1.2, 3.7) and bicarbonate ion concentration [HCO3-] (+6.8±1.6 mmo.l-1, d=3.4, CI=1.8, 4.7) compared to the PLA treatment, prior to TLIM2. It is likely both the acceleration of recovery and the marked increases of acid-base after TLIM1 contributed to greater TLIM2 performance compared to the PLA condition.The authors received no external funding for this research. Mr. Steven Rimmer received a small undergraduate research bursary from the University of Derby to fund his contribution to the study

Rebuttal from Raymond Reynolds, Callum Osler, Linda Tersteeg and Ian Loram.

This work was supported by BBSRC grant BB/I00579X/

Effects of mental fatigue on static upright stance and functional balance in older adults

Cognitive influences on balance control may contribute to greater instability and falls in older adults. In support of this, old age exacerbates the effects of a concurrent cognitive task on balance. Mental fatigue is a psychobiological state experienced following prolonged demanding cognitive activity. However, its effects on static upright stance and functional balance in older adults is unclear. It is also unclear how the effects of mental fatigue and a concurrent task interact. Balance was assessed in ten younger and ten older participants before and immediately after 25 min of the incongruent Stroop colour-word test (mental fatigue) and leisurely reading (control), presented in a randomized counterbalanced order on separate days. Static and functional balance was assessed using the centre of pressure path length when standing still and the ‘Timed Up & Go’ test, respectively. These balance assessments were completed with and without a concurrent backward counting task (i.e. dual-task and single-task, respectively). Under subjectively-confirmed conditions of mental fatigue, sway path length when standing still was 32% greater than the control condition in older adults but unchanged in younger adults. This age-dependant effect of mental fatigue on static balance was similar in single-task and dual-task trials. Mental fatigue did not significantly affect functional balance performance in either age group. These findings are the first to show mental fatigue to impair static balance control in older adults. Therefore, whether due to everyday activities or a symptom of disease, mental fatigue may contribute to poor balance in older adults.University of Derby Vice-Chancellor's Ideas Foru

Crosstalk opposing view: Fear of falling does not influence vestibular-evoked balance responses

This work was supported by BBSRC grant BB/I00579X/

Postural reorientation does not cause the locomotor after-effect following rotary locomotion

After a period of stepping on a rotating platform, blindfolded subjects demonstrate a tendency to unconsciously turn when stepping in place, an after-effect known as podokinetic after-rotation (PKAR). Recent studies have also reported a change in postural orientation following the adaptive period and have suggested that this is causally related to PKAR. Here, we assess changes in trunk orientation following platform adaptation and determine their relationship to PKAR. Specifically, we determine whether a reorganized standing posture causes PKAR. Ten subjects stepped on a platform rotating at 60deg/s for 10 min, with a cadence of 100 steps/min. Following adaptation, a significant PKAR response was seen, with a mean yaw rotation velocity of 6.0 ± 2.2deg/s. In addition to this dynamic after-effect, there was a significant twist of the trunk with respect to the feet when standing still (6.9 ± 4.5deg; mean ± SD), confirming the presence of a postural reorientation after-effect. However, the magnitudes of the two after-effects did not correlate (r = 0.06, p = 0.87). Furthermore, in a second experiment, a prolonged passive twist of the trunk was used to induce postural reorientation. However, in this case, PKAR was not induced. These results demonstrate that PKAR is not an automatic consequence of reorganized standing posture

Dynamic transformation of vestibular signals for orientation

The same pattern of vestibular afferent feedback may signify a loss of balance or a change in body orientation, depending upon the initial head posture. To resolve this ambiguity and generate an appropriate motor response, the CNS must transform vestibular information from a head-centred reference frame into relevant motor coordinates. But what if the reference frame is continuously moving? Here, we ask if this neural transformation process is continuously updated during a voluntary change in head posture. Galvanic vestibular stimulation (GVS) was used to induce a sensation of head roll motion in blindfolded subjects marching on the spot. When head orientation was fixed, this caused unconscious turning behaviour that was maximal during neck flexion, minimal with the head level and reversed direction with neck extension. Subjects were then asked to produce a continuous voluntary change in head pitch, while GVS was applied. As the neck moved from full flexion into extension, turn velocity was continuously modulated and even reversed direction, reflecting the pattern observed during the head-fixed condition. Hence, an identical vestibular input resulted in motor output which was dynamically modulated by changes in head pitch. However, response magnitude was significantly reduced, suggesting possible suppression of vestibular input during voluntary head movement. Nevertheless, these results show that the CNS continuously reinterprets vestibular exafference to account for ongoing voluntary changes in head posture. This may explain why the head can be moved freely without losing the sense of balance and orientation