EMG responses to maintain stance during multidirectional surface translations.

To characterize muscle synergy organization underlying multidirectional control of stance posture, electromyographic activity was recorded from 11 lower limb and trunk muscles of 7 healthy subjects while they were subjected to horizontal surface translations in 12 different, randomly presented directions. The latency and amplitude of muscle responses were quantified for each perturbation direction. Tuning curves for each muscle were examined to relate the amplitude of the muscle response to the direction of surface translation. The latencies of responses for the shank and thigh muscles were constant, regardless of perturbation direction. In contrast, the latencies for another thigh [tensor fascia latae (TFL)] and two trunk muscles [rectus abdominis (RAB) and erector spinae (ESP)] were either early or late, depending on the perturbation direction. These three muscles with direction-specific latencies may play different roles in postural control as prime movers or as stabilizers for different translation directions, depending on the timing of recruitment. Most muscle tuning curves were within one quadrant, having one direction of maximal activity, generally in response to diagonal surface translations. Two trunk muscles (RAB and ESP) and two lower limb muscles (semimembranosus and peroneus longus) had bipolar tuning curves, with two different directions of maximal activity, suggesting that these muscle can play different roles as part of different synergies, depending on translation direction. Muscle tuning curves tended to group into one of three regions in response to 12 different directions of perturbations. Two muscles [rectus femoris (RFM) and TFL] were maximally active in response to lateral surface translations. The remaining muscles clustered into one of two diagonal regions. The diagonal regions corresponded to the two primary directions of active horizontal force vector responses. Two muscles (RFM and adductor longus) were maximally active orthogonal to their predicted direction of maximal activity based on anatomic orientation. Some of the muscles in each of the synergic regions were not anatomic synergists, suggesting a complex central organization for recruitment of muscles. The results suggest that neither a simple reflex mechanism nor a fixed muscle synergy organization is adequate to explain the muscle activation patterns observed in this postural control task. Our results are consistent with a centrally mediated pattern of muscle latencies combined with peripheral influence on muscle magnitude. We suggest that a flexible continuum of muscle synergies that are modifiable in a task-dependent manner be used for equilibrium control in stance.

[1]  C. Sherrington Integrative Action of the Nervous System , 1907 .

[2]  W. Smith The Integrative Action of the Nervous System , 1907, Nature.

[3]  F. Plum Handbook of Physiology. , 1960 .

[4]  N. A. Bernshteĭn The co-ordination and regulation of movements , 1967 .

[5]  M. L. Root,et al.  Normal and abnormal function of the foot , 1977 .

[6]  C D Marsden,et al.  Rapid postural reactions to mechanical displacement of the hand in man. , 1983, Advances in neurology.

[7]  F. Horak,et al.  Parsimony in Neural Calculations for Postural Movements , 1984 .

[8]  W. Rymer,et al.  Characteristics of synergic relations during isometric contractions of human elbow muscles. , 1986, Journal of neurophysiology.

[9]  F. Horak,et al.  Central programming of postural movements: adaptation to altered support-surface configurations. , 1986, Journal of neurophysiology.

[10]  J M Macpherson,et al.  Strategies that simplify the control of quadrupedal stance. II. Electromyographic activity. , 1988, Journal of neurophysiology.

[11]  F. Horak,et al.  Influence of stimulus parameters on human postural responses. , 1988, Journal of neurophysiology.

[12]  F. Horak,et al.  Influence of central set on human postural responses. , 1989, Journal of neurophysiology.

[13]  Fay B. Horak,et al.  The effect of prior leaning on human postural responses , 1993 .

[14]  F E Zajac,et al.  Human standing posture: multi-joint movement strategies based on biomechanical constraints. , 1993, Progress in brain research.

[15]  T. Nichols,et al.  Cat hindlimb muscles exert substantial torques outside the sagittal plane. , 1993, Journal of neurophysiology.

[16]  F. Horak,et al.  Modification of postural responses and step initiation: evidence for goal-directed postural interactions. , 1994, Journal of neurophysiology.

[17]  J. F. Soechting,et al.  Spatial/temporal characteristics of a motor pattern for reaching. , 1994, Journal of neurophysiology.

[18]  J M Macpherson,et al.  Changes in a postural strategy with inter-paw distance. , 1994, Journal of neurophysiology.

[19]  L. Rowell,et al.  Exercise : regulation and integration of multiple systems , 1996 .

[20]  D. Winter,et al.  Unified theory regarding A/P and M/L balance in quiet stance. , 1996, Journal of neurophysiology.

[21]  J. Macpherson,et al.  Two functional muscle groupings during postural equilibrium tasks in standing cats. , 1996, Journal of neurophysiology.

[22]  F B Horak,et al.  Prediction and set-dependent scaling of early postural responses in cerebellar patients. , 1997, Brain : a journal of neurology.

[23]  F. Horak,et al.  Postural perturbations: new insights for treatment of balance disorders. , 1997, Physical therapy.

[24]  F B Horak,et al.  Control of stance during lateral and anterior/posterior surface translations. , 1998, IEEE transactions on rehabilitation engineering : a publication of the IEEE Engineering in Medicine and Biology Society.