Biceps EMG Activity Research Articles

Neurodevelopment of Posture-movement Coordination from Late Childhood to Adulthood as Assessed From Bimanual Load-lifting Task: An Event-related Potential Study

In a bimanual task, proprioception provides information about position and movement of upper arms. Developmental studies showed improvement of proprioceptive accuracy and timing adjustments of muscular events from childhood to adulthood in bimanual tasks. However, the cortical maturational changes related to bimanual coordination is not fully understood. The aim of this study was to investigate cortical correlates underlying motor planning and upper limb stabilization performance at left (C3) and right (C4) sensorimotor cortices using event-related potential (ERP) analyses. We recruited 46 participants divided into four groups (12 children: 8–10 years, 13 early adolescents: 11–13 years, 11 late adolescents: 14–16 years and 10 young adults: 20–35 years). Participants performed a bimanual load-lifting task, where the left postural arm supported the load and the right motor arm lifted the load. Maximal amplitude of elbow rotation (MA%) of the postural arm, reaction time (RT) and EMG activity of biceps brachii bilaterally were computed. Laplacian-transformed ERPs of the electroencephalographic (EEG) signal response-locked to motor arm biceps EMG activity onset were analyzed over C3 and C4. We found a developmental effect for behavioral and EEG data denoted by significant decrease of MA% and RT with age, earlier inhibition of the biceps brachii of the postural arm in adults and earlier EEG activation/inhibition onset at C3/C4. Amplitude of the negative wave at C4 was higher in children and early adolescents compared to the other groups. In conclusion, we found a maturational process in cortical correlates related to motor planning and upper limb stabilization performance with interhemispheric lateralization appearing during adolescence. Findings may serve documenting bimanual performance in children with neurodevelopmental disorders.

The Effects of a 28-Hz Vibration on Arm Muscle Activity during Isometric Exercise

The aim of this study was to evaluate activation and coactivation of biceps and triceps muscles during isometric exercise performed with and without superimposing a vibration stimulation. Twelve healthy volunteers (age = 22.7 +/- 2.6 yr) participated in this study. The subjects performed five trials of isometric elbow flexion and five trials of elbow extension with increasing levels of force in two conditions: vibration (V) and normal loading (C). V stimulation was characterized by a frequency of 28 Hz. Surface EMG activity of biceps and triceps muscles was simultaneously measured by bipolar surface electromyography and assessed by the estimation of the root mean square (RMS) of the electrical recordings over a fixed 5-s interval. Frequency analysis was adopted to estimate the RMS related to muscle activation and to exclude the harmonics generated by movement artifacts due to V. The analysis of the recordings revealed a significant EMG RMS increase when V was applied. On average, the EMG RMS of biceps and triceps during elbow flexion was, respectively, 26.1% (P < 0.05) and 18.2% (P = 0.15) higher than C. During elbow extension, the EMG RMS of biceps and triceps was 77.2% and 45.2% (P < 0.05) higher than C, respectively. The coactivation was assessed as the ratio between the activation of antagonist and agonist muscles during arm flexion and extension tasks. The results revealed an increase of coactivation during V exercise, especially for lighter loads. This study shows that V exercise at 28 Hz produces an increase of the activation and the coactivation of biceps and triceps. This exercise modality seems therefore suitable for various applications.

Braking of elbow extension in fast overarm throws made by skilled and unskilled subjects

A previous computer simulation study of overarm throws in 2D showed that reversal of elbow torque by antagonist muscle action late in the throw led to increased wrist flexion velocity and to increased ball speeds. We tested the hypothesis that the skill of making fast overarm throws in 3D involves deceleration (braking) of elbow extension before ball release, and that this is an active mechanism. Skilled and unskilled throwers were instructed to throw baseballs at a fast speed. Arm segment angular positions in 3D at 1,000 Hz were recorded with the search-coil technique (which records angular motions). In skilled throws, but not in unskilled throws, there was a period (mean 17 ms) of rapid elbow extension deceleration before ball release. However, there was relatively little biceps EMG activity associated with the very large magnitude of elbow deceleration. This finding and other work suggests that elbow extension deceleration results in part from interaction torques associated with late-occurring shoulder rotations, and only in part from elbow flexor contraction. During the period when elbow extension was decelerating, the forearm in space was undergoing angular acceleration (because of internal rotation at the shoulder) which would be expected to produce a torque at the wrist in the extensor (not flexor) direction. The results show that elbow extension deceleration occurs before ball release in fast (skilled) 3D throws, and that it does not produce forearm angular deceleration. Whether it produces forearm translational deceleration, which could increase wrist flexion velocity, remains to be determined.

Brainstem influences on biceps reflex activity and muscle tone in the anaesthetized rat

This study analyzes the effect of electrical stimulation of the locus coeruleus (LC) and adjacent brainstem structures on the tonic reflex (TVR), the tonic stretch reflex (TSR) and on muscle tone (MT) in anaesthetized rat. Increases in TVR. TSR and MT of the m. biceps were evoked from regions rostrally and ventrally of LC, the caudal pontine reticular nucleus, the cuneiform nucleus and from the ventral parts of the colliculus inferior. Stimulation of the LC did not influence biceps EMG activity. The results indicate that the observed facilitation of muscle activity is due to stimulation of parts of the mesencephalic locomotor region. It is discussed that the recorded increase in TVR, TSR and MT possibly is due to an excitatory action on α motoneurones on one hand and to an enhanced fusimotor drive on the other.

EMG and motor performance changes with practice of a forearm movement by children.

The purpose of this research was to investigate changes in the control of movement, using EMG and kinematic variables, over practice by children. Children in three age groups, 7, 9, and 11 yr., performed 60 trials of an elbow-flexion movement. Correct movements consisted of a 60 degrees angular movement of the forearm in 800 msec. The analysis of biceps brachii and triceps brachii muscle EMG activity, movement displacement and timing error, and movement velocity patterns indicated changes in motor performance with practice. All age groups improved performance with practice and also exhibited a decrease in biceps EMG activity with practice. Only movement-time error and time to peak triceps muscle activity differed between the age groups. The 11-yr.-old group significantly altered the timing of the antagonistic response to stop the movement over the practice session. This change is suggested to be related to the greater information-processing ability of these children and the development of appropriate movement strategies to perform the movement task successfully. Other changes observed in the EMG data appear similar to changes observed in studies of adults.

Postural forearm changes induced by predictable in time or voluntary triggered unloading in man.

Human subjects sitting in a chair were asked to maintain their right forearm in a horizontal position in half supination. The forearm was loaded with a constant weight of one kilogram. Vertical force at the wrist level, angular position of the elbow and EMG activity of biceps, brachio-radialis and triceps muscles were recorded. Unloading was tested under four different conditions, the first two having been used in a previous study (Hugon et al. 1982): Voluntary unloading by the subject's other hand. An "anticipatory" deactivation of the load bearing forearm flexors is observed preventing the elbow rotation of that arm. Unpredictable passive unloading. This results in an upward forearm rotation which provokes the classical "unloading reflex". Two new conditions were tested in the present paradigm: Imposed unloading predictable in time (tone signal preceding unloading by a fixed interval). Unloading being actively triggered when the subject presses a key. Under the two latter conditions, no anticipatory deactivation of the flexor supporting muscles preceding the onset of unloading as in situation A was observed. During the first 120 ms after the onset of unloading, the forearm rotation was the same as in situation B (unpredictable passive unloading). Thereafter, the rotation was smaller in some subjects, apparently due to an ameliorated reflex action. It is concluded that temporal information concerning the precise time of the unloading or the triggering of the load release by a voluntary movement (key press) was not by itself able to induce the anticipatory deactivation of the forearm flexors that was seen with a coordinated voluntary release of the load by the contralateral arm.

EMG patterns in antagonist muscles during isometric contraction in man: relations to response dynamics.

We studied the EMG activity of biceps and triceps in human subjects during isometric force adjustments at the elbow. Rapid targeted force pulses exhibited stereotyped trajectories in which peak force was a linear function of the derivatives of force and the time to peak force was largely independent of its amplitude. These responses were associated with an alternating triphasic pattern of EMG bursts in agonist and antagonist muscles similar to that previously described for rapid limb movements. When the instructions demanded rapid force pulses, initial agonist bursts were of constant duration, and their magnitude was strongly related to peak force achieved. The timing of EMG bursts in antagonist pairs was closely coupled to the dynamics of the force trajectory, and the rising phase of the force was determined by both agonist and antagonist bursts. When peak force was kept constant and rise time systematically varied, the presence and magnitude of antagonist and late agonist bursts were dependent on the rate of rise of force, appearing at a threshold value and then increasing in proportion to this parameter. It is proposed that antagonist activity compensates for nonlinearity in muscle properties to enable the linear scaling of targeted forces which characterizes performance in this task.

Anticipatory postural changes induced by active unloading and comparison with passive unloading in man.

Normal human subjects, sitting in a chair, were required to maintain stable elbow flexion against loads of 0.5 kg or 1.0 kg. Unloading was affected either 'passively' by the experimenter, or 'actively' with the subject's own contralateral arm. Elbow angle, force exerted by the load, and electromyographic activity (EMG) of biceps and triceps muscles of both arms were recorded and averaged. 'Passive' unloading was followed by a reduction of biceps EMG activity, starting 50--80 ms after weight lift, and by an upward deflection of the forearm. With 'active' unloading, however, a reduction of the biceps EMG activity slightly preceded the onset of unloading (0--30 ms). This reduction of the 'actively' unloading arm occurred at about the same time as the activity of the contralateral unloading arm. In this experiment, the unloaded forearm maintained an almost stable position. Thus, the anticipatory adjustment of elbow posture, observed when unloading was performed by the subject, appears to optimize limb stability during the mechanical perturbation.

Coordination of arm and wrist motion during a reaching task

An analysis of arm movements involving forward projection of the hand in order to reach for and grasp a target at different orientations is presented. The reaching movements required shoulder flexion, elbow extension, and wrist pronation or supination. The relation between elbow and shoulder instantaneous angular position proved to be consistent from trial to trial of each task, independent of movement speed. Further, this relation was not influenced by the presence or absence of a concomitant wrist rotation. During the deceleratory phase of the movement, the slope of elbow angular velocity to shoulder angular velocity was constant and independent of target orientation. Wrist motion was instead highly variable in timing, course, and duration. Supinatory movements tended to be fractionated. On average, the duration of wrist movements was shorter than that of shoulder and elbow motions. The pattern of biceps EMG activity during supinatory and pronatory movements was different. Since motion at the shoulder and elbow was virtually identical in the two cases, net flexor torque at the elbow was also little different. It is concluded that other elbow flexors and extensors also exhibit a task-dependent patterning of activity so as to produce the same net torque. The results are discussed in the context of the internal constraints present during the movements that we examined. These constraints are the inertial coupling between shoulder and elbow motion and those which derive from the bifunctional nature of many of the muscles participating in the movement.

Changes in short and long latency stretch responses during the transition from posture to movement

Experiments were performed in 18 normal subjects to estimate the time course of changes in the gains of pathways mediating short- and long-latency responses to muscle stretch during the transition from a maintained posture against a steady load to a rapid ballistic movement. Subjects were instructed to rapidly flex or extend their forearm in response to a tone from an initial position of 90° of elbow flexion. Torque pulses stretching the biceps muscle were applied to the forearm at 8 different times before and after the signal to initiate the movement, and the gains of short- and long-latency pathways were estimated from averages of rectified biceps EMG activity for 20 trials at each time interval between the onsets of the tone and torque pulse. The findings demonstrate that changes in the magnitude of long-latency responses (M2, M3) occur during the period between the onset of the auditory signal and the voluntary motor response. However, the magnitude of the short-latency response (M1) remains unchanged until after the onset of voluntary motor activity. The differences in the timing of short- and long-latency stretch responses suggests that activity in long-latency pathways may play an important preparatory role in facilitating the transition from posture to movement.

Muscle reaction to passive shortening in normal man

We have studied in 32 healthy subjects the EMG activity of biceps and triceps brachii, wrist flexors and wrist extensors, triceps surae and tibialis anterior, sterno-cleido-mastoideus (SCM) and splenius, during their passive shortening. A shortening reaction was observe more frequently in wrist extensors, SCM and tibialis anterior than in biceps and triceps brachii. The response appeared only when the joint reached a specific angle regardless of the starting point or the speed used to reach this position. During a muscle ischaemia which abolished the tendon reflex the reaction was not modified. During a joint ischaemia produced distal to the examined muscle its amplitude was strongly reduced. Our results support the hypothesis that joint receptors could play a role in its origin, perhaps through a long-loop reflex.