EMG Levels Research Articles

Central efferent pathways mediating shivering thermogenesis

Shivering is a remarkable thermogenic response when body temperature needs to be defended from environmental cold challenges as well as during the development of fever. The preoptic area (POA) receives both environmental thermal information from the skin and pyrogenic signals from the immune system activated by infection and the POA sends descending signals that induce shivering in skeletal muscles. However, the efferent pathway from the POA that is responsible for shivering is unknown. In this study, we examined the involvement of several brain regions in the cooling‐evoked or febrile shivering response in isoflurane‐anesthetized rats. Cooling the trunk skin or nanoinjecting prostaglandin E2 (PGE2) into the POA evoked an increase in the EMG level recorded from the nuchal muscle. Both cooling‐ and PGE2‐evoked EMG increases were blocked by bilateral injections of muscimol, a GABAA receptor agonist, into the dorsomedial hypothalamic nucleus (DMH). In addition, injection of muscimol or 8‐OH‐DPAT, a 5‐HT1A receptor agonist, into the rostral raphe pallidus nucleus (rRPa) also blocked the EMG increase. These results suggest that the DMH and rRPa are essential synaptic integration sites in the efferent neuronal pathway from the POA that mediates the shivering responses to skin cooling and to pyrogens and that this pathway can be modulated by serotonergic inputs to the medullary raphe. Supported by NIH and MEXT Japan.

Corticospinal contribution to arm muscle activity during human walking

When we walk, our arm muscles show rhythmic activity suggesting that the central nervous system contributes to the swing of the arms. The purpose of the present study was to investigate whether corticospinal drive plays a role in the control of arm muscle activity during human walking. Motor evoked potentials (MEPs) elicited in the posterior deltoid muscle (PD) by transcranial magnetic stimulation (TMS) were modulated during the gait cycle in parallel with changes in the background EMG activity. There was no significant difference in the size of the MEPs at a comparable level of background EMG during walking and during static PD contraction. Short latency intracortical inhibition (SICI; 2 ms interval) studied by paired-pulse TMS was diminished during bursts of PD EMG activity. This could not be explained only by changes in background EMG activity and/or control MEP size, since SICI showed no correlation to the level of background EMG activity during static PD contraction. Finally, TMS at intensity below the threshold for activation of corticospinal tract fibres elicited a suppression of the PD EMG activity during walking. Since TMS at this intensity is likely to only activate intracortical inhibitory interneurones, the suppression is in all likelihood caused by removal of a corticospinal contribution to the ongoing EMG activity. The data thus suggest that the motor cortex makes an active contribution, through the corticospinal tract, to the ongoing EMG activity in arm muscles during walking.

Oblique abdominal muscle activity in response to external perturbations when pushing a cart

Cyclic activation of the external and internal oblique muscles contributes to twisting moments during normal gait. During pushing while walking, it is not well understood how these muscles respond to presence of predictable (cyclic push-off forces) and unpredictable (external) perturbations that occur in pushing tasks. We hypothesized that the predictable perturbations due to the cyclic push-off forces would be associated with cyclic muscle activity, while external perturbations would be counteracted by cocontraction of the oblique abdominal muscles. Eight healthy male subjects pushed at two target forces and two handle heights in a static condition and while walking without and with external perturbations. For all pushing tasks, the median, the static (10th percentile) and the peak levels (90th percentile) of the electromyographic amplitudes were determined. Linear models with oblique abdominal EMGs and trunk angles as input were fit to the twisting moments, to estimate trunk stiffness. There was no significant difference between the static EMG levels in pushing while walking compared to the peak levels in pushing while standing. When pushing while walking, the additional dynamic activity was associated with the twisting moments, which were actively modulated by the pairs of oblique muscles as in normal gait. The median and static levels of trunk muscle activity and estimated trunk stiffness were significantly higher when perturbations occurred than without perturbations. The increase baseline of muscle activity indicated cocontraction of the antagonistic muscle pairs. Furthermore, this cocontraction resulted in an increased trunk stiffness around the longitudinal axis.

Creep and Fatigue Development in the Low Back in Static Flexion

In vivo measurements of low back flexion posture and muscle activity before, during, and after static flexion. To identify the occurrence of creep and muscle fatigue development in the low back during static upper body deep flexion that resembled an above ground work posture. Static lumbar flexion has been related to the development of low back disorders, and its injury mechanism has been focused on the changes in passive spinal tissues. Potential influences of muscle fatigue of extensor muscles have not been explored. A total of 20 asymptomatic subjects performed submaximal isometric trunk extension exertions and an isokinetic trunk flexion before and immediately after 5-minute static flexion while the trunk sagittal flexion angle and the myoelectric activities (electromyography [EMG]) of back extensor muscles were recorded simultaneously. Changes in the flexion-relaxation onset angle, maximum flexion angle, muscle activity level, and the median power frequency of EMG associated with the static flexion were evaluated. Flexion-relaxation onset angle in isokinetic flexion and EMG amplitude of isometric extension were significantly greater after static flexion, indicating creep of spinal tissues in static flexion. Median power frequency of lumbar erector spinae EMG during isometric extension was significantly lower after static flexion, suggesting the development of muscle fatigue. Consistent but low level of EMG was observed together with sporadic muscle spasms during the static flexion period. Fatigue of low back extensor muscles may occur in static flexion due to prolonged passive stretching of the muscles. Low back extensor muscles are required to generate more active forces in weight holding or lifting after static flexion to compensate for the reduced contribution of creep deformed passive tissues in maintaining spinal stability and the posture. The degraded force generating capacity of the fatigued muscles can be a significant risk factor for low back pain.

Relation between electrical stimulus intensity, masseteric exteroceptive reflex and sensory perception

The purpose of this study was to characterize the relation between stimulus intensity, masseteric exteroceptive suppression (ES), and sensory perception as a possible quantitative or qualitative tool in the diagnosis of the masticatory system for prosthodontic treatment. From 12 males and 12 females (22-41 years), surface EMG was recorded from the left masseter muscle. Visual feedback allowed the subjects to maintain a constant clenching level of 30% maximal voluntary contraction. Thirteen fixed stimulus intensities from 5 to 35 mA in 2.5 mA increments were applied at random. A computer program calculated the duration of ES, based on the 50% level of the mean pre-stimulus EMG. The stimulation intensity at which early (ES1) or late (ES2) exteroceptive suppressions appeared first and at which subjects answered as being painful were defined as the reflex threshold (RT1 or RT2) and pain threshold (PT), respectively. The relation between sensory perception and ES was evaluated using stimulus-response (S-R) curve analysis. Significant differences were found between PT and RT1, and between RT1 and RT2 (P<0.001). After S-R curve analysis, the maximum duration of ES1 and ES2 was estimated at 9.6 ms and 33.5 ms, and appearance was rated as 6.2 and 4.0 on numeric rating scale (NRS), saturation was 7.6 and 6.9, and slope was 7.0 and 11.2, respectively. All parameters for changes in ES following increasing incremental stimulus intensity could be analyzed. The construction of S-R curves in relation to sensory perception and ES parameters characterized the difference between ES1 and ES2.

Modulation of recurrent inhibition from knee extensors to ankle motoneurones during human walking

The neural control for muscle coordination during human locomotion involves spinal and supraspinal networks, but little is known about the exact mechanisms implicated. The present study focused on modulation of heteronymous recurrent inhibition from knee extensors to ankle motoneurones at different times in the gait cycle, when quadriceps (Quad) muscle activity overlaps that in tibialis anterior (TA) and soleus (Sol). The effects of femoral nerve stimulation on ankle motoneurones were investigated during treadmill walking and during tonic co-contraction of Quad and TA/Sol while standing. Recurrent inhibition of TA motoneurones depended on the level of background EMG, and was similar during walking and standing for matched background EMG levels. On the other hand, recurrent inhibition in Sol was reduced in early stance, with respect to standing, and enhanced in late stance. Reduced inhibition in Sol was also observed when Quad was coactivated with TA around the time of heel contact, compared to standing at matched background EMG levels in the two muscles. The modulation of recurrent inhibition of Sol during walking might reflect central and/or peripheral control of the Renshaw cells. These modulations could be implicated in the transition phases, from swing to stance to assist Sol activation during the stance phase, and from stance to swing, for its deactivation.

Potential value of vestibular evoked myogenic potentials in paediatric neuropathies

Showing the interest of vestibular evoked myogenic potentials in paediatric neurological vestibulospinal pathology detection and followup. The vestibular evoked myogenic potentials testing apparatus presented is now commonly used in ENT clinics for patients from 1 month of age. Our system and protocol permits control to evoke and select the best EMG level and makes possible a comparison of data from different sides or level of stimulation or different sessions. Normal vestibular evoked myogenic potentials latencies obtained with tone bursts were remarkably stable (P: 13 +/- 0.8 ms, N: 19.6 +/- 1.6 ms). The reported case illustrates abnormal vestibular evoked myogenic potentials latencies in neuropathy. A 6 y.o. child with progressive imbalance was referred to the ENT department for vestibular functional evaluation. Abnormally long latencies in the vestibular evoked myogenic potentials and neurological examination oriented the diagnosis towards Guillain-Barre syndrome and immediate referral to a neurology department. Vestibular evoked myogenic potentials also helped to monitor the neurological recovery. The present case shows the potential value of vestibular evoked myogenic potentials in diagnosis and evaluation of descending brainstem pathways in neuropathies like Guillain-Barre syndrome in complement to neurological evaluation.

Rapid muscle activation and force capacity in conditions of chronic musculoskeletal pain

Background The association between musculoskeletal pain and decreased maximal muscle strength capacity has been extensively studied, but knowledge about functional rapid force capacity in conditions of chronic musculoskeletal pain is lacking. The objective of this study is to investigate rapid muscle activation and force capacity of chronically painful muscles. Methods Cross-sectional study with 42 women with chronic trapezius myalgia, and 20 healthy matched controls. Maximal capacity was determined as peak torque and peak EMG amplitude of the painful trapezius and painfree deltoid muscles during the stable high-force phase of maximal voluntary shoulder abduction, whereas rapid capacity was determined as the steepest slope of the torque–time and EMG–time curves, defined as rate of torque development and rate of EMG rise. Intensity of pain was registered prior to the test on a visual-analogue-scale. Findings Peak torque was 18% lower at 115° shoulder joint angle in women with myalgia compared with healthy controls ( P < 0.001), with a corresponding 29% lower level of peak EMG specifically of the painful trapezius muscle ( P < 0.001). Rate of torque development was 33–54% lower ( P < 0.001), with a corresponding 21–35% lower level of rate of EMG rise of both the painful trapezius and painfree deltoid ( P < 0.0001). Intensity of pain showed higher association with parameters of rapid capacity ( R = −0.33 to −0.53, P < 0.001–0.05) than with maximal capacity ( R = −0.15 to −0.41, P < 0.01-ns). Interpretation In conditions of chronic musculoskeletal pain, the ability to rapidly activate painful and painfree synergistic muscles is more severely impaired than maximal muscle activation. These findings have clinical relevance for rehabilitation of chronically painful muscles.

Co-contraction in RA patients with a mobile bearing total knee prosthesis during a step-up task

It was hypothesized that rheumatoid arthritis (RA) patients with a total knee prosthesis that allows axial rotation of the bearing (MB) will show more co-contraction to stabilize the knee joint during a step-up task than RA patients with a fixed bearing total knee prosthesis (FB) where this rotational freedom is absent while having the same articular geometry. Surface EMG, kinematics and kinetics about the knee were recorded during a step-up task of a MB group (n = 5), a FB group (n = 4) and a control group (n = 8). Surface EMG levels of thigh muscles were calibrated to either knee flexion or extension moments by means of isokinetic contractions on a dynamometer. During the step-up task co-contraction indices were determined from an EMG-force model. Controls showed a higher active ROM during the step-up task than the patient group, 96° versus 88° (P = 0.007). In the control group higher average muscle extension, flexion and net moments during single limb support phase were observed than in the patient group. During the 20–60% interval of the single limb support, MB patients showed a significant higher level of flexor activity, resulting in a lower net joint moment, however co-contraction levels were not different. Compared to the control group arthroplasty patients showed a 40% higher level of co-contraction during this interval (P = 0.009). Control subjects used higher extension moments, resulting in a higher net joint moment. Visual analysis revealed a timing difference between the MB and FB group. The FB group seems to co-contract approximately 20% later compared to the MB group. RA patients after total knee arthroplasty show a lower net knee joint moment and a higher co-contraction than controls indicating avoidance of net joint load and an active stabilization of the knee joint. MB and FB patients showed no difference in co-contraction levels, although timing in FB is closer to controls than MB subjects. Since visual analysis revealed a timing difference between the MB and FB group, this may express compensation by coordination. Rehabilitation programs for RA patients should include besides muscle strength training, elements of muscle-coordination training.

Modulation Of Hamstring Muscle H-reflex During Human Gait

Peripheral inputs from muscle, joints and skin play a major role in the control of locomotion by the central nervous system. Assessing their influences has shown that afferent inputs are modulated with the level of motoneuron activity but also exhibit task/phase dependent modulations. Tendon taps and spinal cord electrical stimulation have shown that hamstring muscle afferent responses follow motoneuron activity. However, problems in controlling for the stimulation and recording electrode positions in such large movements impairs the interpretation of the data in regards to the assessment of the task/phase dependent modulation. PURPOSE: To test the feasibility of lumbosacral roots stimulation during human gait to elicit M and H-reflexes responses in hamstring muscles. METHODS: Participants with no know neurological disorders were tested while walking on a treadmill set to their comfortable walking speed. The lumbosacral roots were stimulated percutaneously at 12 different times within the gait cycle with a diffusing electrode placed over the L5 spinous process and the stimulating electrode placed at a 6 inch distance (45 deg downward angle, distal and lateral) away. Timing of the lumbosacral root stimulation was controlled by recording from a footswitch taped under the right heel. EMG of biceps femoris was recorded using a surface electrode and differential amplifier placed over the belly of the muscle. Stimulation intensities were applied pseudo-randomly until a stimulus-response curve was elicited for each of the 12 gait cycle bins. RESULTS: H-reflexes were successfully elicited using lumbosacral root stimulation. In all subjects (n=6) it was possible to elicit a Maximal M wave during walking (amplitude: 2.99+/-1.53 mV). In a subset of participants (n=2), the maximal H-reflex amplitude is modulated within the gait cycle (range: 20.3-81.1% of Mmax) with a moderate correlation to the background EMG (r=0.65 and-0.07). CONCLUSIONS: The results from this study show that it is feasible to use lumbosacral stimulation to record maximal M and H responses from Hamstring muscles during walking. Furthermore, it seems that the modulation of the hamstring maximal H-reflex is not simply dependent on the background EMG levels but might also be modulated in a task/phase dependent manner.

Dynamic influence of wrist flexion and extension on the intracortical inhibition of the first dorsal interosseus muscle during precision grip

This work questioned further the influence of wrist movements on the control of precision grip. Seated subjects wearing a full-arm orthosis with the wrist and hand free were instructed to maintain a thumb/index finger opposition corresponding to 15% of maximal voluntary contraction for the first dorsal interosseus (FDI). Paired-pulse transcranial magnetic stimulation eliciting conditioned MEPs of FDI was used to determine the modulation of short intracortical inhibition (SICI) during cyclic active and passive wrist flexion and extension and during a static condition (no wrist movement, hand in the neutral position). The FDI active motor threshold (AMT) and the conditioning stimulus (0.8 AMT) were assessed in each series of FDI SICI measurements and the test stimulus (TS) was adjusted to match the amplitudes of test FDI MEPs across conditions. An increase of FDI background EMG during active wrist flexion compared to extension in some subjects did not influence FDI SICI as tested at matched EMG levels in the static condition. FDI SICI was reduced during wrist flexion (whether active or passive) compared to wrist extension, the latter being of equivalent FDI SICI as in the static condition. We suggest that wrist flexion and precision grip could be linked in a functional proximo-distal synergy. Indeed, coupling the activity between M1 sites of wrist flexors and FDI muscle via cortico-cortical disinhibition of FDI site may help recruit the interjoint synergy. Also, the salience of afferent information from wrist muscles may contribute to the phase-dependent modulation of SICI in the preactivated FDI muscle.

Task-Specific Depression of the Soleus H-Reflex After Cocontraction Training of Antagonistic Ankle Muscles

Ballet dancers have small soleus (SOL) H-reflex amplitudes, which may be related to frequent use of cocontraction of antagonistic ankle muscles. Indeed, SOL H-reflexes are depressed during cocontraction compared with plantarflexion at matched background EMG level. We investigated the effect of 30-min training of simultaneous activation of ankle dorsi- and plantarflexor muscles (cocontraction task) on the SOL H-reflex in 10 healthy volunteers. Measurements were taken during cocontraction. After training, there was a significant improvement in the ability of the subjects to perform a stable cocontraction. SOL H-reflex recruitment curves and H-max/M-max ratios were decreased after cocontraction training but not after 30 min of static dorsi or plantarflexion. The decreased H-reflex size correlated with improved motor performance. No changes in SOL and tibialis anterior (TA) EMG activity or EMG power were observed, suggesting that increased presynaptic inhibition of Ia afferents is a likely mechanism for H-reflex depression. In different sessions we measured SOL and TA motor-evoked potentials (MEPs) by using transcranial magnetic stimulation (TMS), TMS-elicited suppression of SOL EMG, and coherence between electroencephalographic (EEG) activity (Cz) and TA and SOL EMG. SOL and TA MEPs were depressed, whereas TMS-elicited suppression of SOL EMG and coherence were increased after training. Decreased excitability of corticospinal neurons due to increased intracortical inhibition seems a likely explanation of these observations. Our results indicate that the depression in H-reflex observed during a cocontraction task can be trained and that repeated performance of tasks involving cocontraction may lead to prolonged changes in reflex and corticospinal excitability.

Muscle responses to transcranial stimulation in man depend on background oscillatory activity.

Muscle responses to transcranial stimulation show high sweep-to-sweep variability, which may reflect an underlying noise process in the motor system. We examined whether response amplitude correlated with the level of prestimulus background EMG, and network oscillations. Transcranial magnetic or electrical stimulation was delivered to primary motor cortex whilst human subjects performed a precision grip task known to promote beta-band ( approximately 20 Hz) cortical oscillations. Responses were recorded from two intrinsic hand muscles. Response magnitude correlated significantly with the level of background EMG (mean r(2) = 0.20). Using a novel wavelet method, we quantified the amplitude and phase of oscillations in prestimulus sensorimotor EEG. Surprisingly, response magnitude showed no significant correlation with EEG oscillations at any frequency. However, oscillations in the prestimulus EMG were significantly correlated with response size; the correlation coefficient had peaks around 20 Hz. When oscillations in one muscle were used to predict response amplitude in a different muscle, correlations were substantially smaller. Finally, for each recording, we calculated the best possible prediction of response size obtainable from up to 20 measures of prestimulus EEG and EMG oscillations. Such optimal predictions had low correlation coefficients (mean r(2) = 0.2; 76% were below 0.3). We conclude that prestimulus oscillations, mainly in the beta-band, do explain some of the variability in responses to transcranial stimulation. Oscillations may likewise increase the noise of natural motor processing, explaining why this form of network activity is usually suppressed prior to dynamic movements. However, the majority of the variation is determined by other factors, which are not accessible by noninvasive recordings.

Task‐related changes in propriospinal excitation from hand muscles to human flexor carpi radialis motoneurones

This study addresses whether there is excitation from human hand muscles to flexor carpi radialis (FCR) motoneurones mediated through propriospinal circuits and, if so, whether it is used in specific motor tasks. Electrical stimuli to the ulnar nerve at wrist level produced an excitation in FCR motoneurones with characteristics typical of a propriospinally mediated effect: low threshold (0.6 x motor threshold (MT)), a group I effect that was not reproduced by purely cutaneous stimuli, long central delay (4.1 +/- 0.4 ms in single units), suppression when the stimulus intensity was increased, and facilitation of the corticospinal excitation at the premotoneuronal level. Ulnar-induced propriospinally mediated excitation was compared during selective voluntary contractions of the FCR and, at equivalent level of FCR EMG, during tasks in which the FCR was activated automatically in postural contractions rather than voluntarily (grip, pinching and pointing). The excitation was significantly greater during grip (and pinching) than during voluntary FCR contractions and pointing, whether measured in single motor units or tonic EMG activity, or whether the response to motor cortex stimulation was assessed as the compound motor-evoked potential or the corticospinal peak in single units. The discrepancy between the tasks appeared with ulnar intensities above 0.8 x MT and was then present across a wide range of stimulus intensities. This suggests a reduction in the corticospinal control of 'feedback inhibitory interneurones' mediating peripheral inhibition to propriospinal neurones during grip and pinching. The resulting more effective background excitation of propriospinal neurones by the peripheral input from hand muscles could contribute to stabilizing the wrist during grip.

Neural regulation of rhythmic arm and leg movement is conserved across human locomotor tasks

It has been proposed that different forms of rhythmic human limb movement have a common central neural control ('common core hypothesis'), just as in other animals. We compared the modulation patterns of background EMG and cutaneous reflexes during walking, arm and leg cycling, and arm-assisted recumbent stepping. We hypothesized that patterns of EMG and reflex modulation during cycling and stepping (deduced from mathematical principal components analysis) would be comparable to those during walking because they rely on similar neural substrates. Differences between the tasks were assessed by evoking cutaneous reflexes via stimulation of nerves in the foot and hand in separate trials. The EMG was recorded from flexor and extensor muscles of the arms and legs. Angular positions of the hip, knee and elbow joints were also recorded. Factor analysis revealed that across the three tasks, four principal components explained more than 93% of the variance in the background EMG and middle-latency reflex amplitude. Phase modulation of reflex amplitude was observed in most muscles across all tasks, suggesting activity in similar control networks. Significant correlations between EMG level and reflex amplitude were frequently observed only during static voluntary muscle activation and not during rhythmic movement. Results from a control experiment showed that strong correlation between EMG and reflex amplitudes was observed during discrete, voluntary leg extension but not during walking. There were task-dependent differences in reflex modulation between the three tasks which probably arise owing to specific constraints during each task. Overall, the results show strong correlation across tasks and support common neural patterning as the regulator of arm and leg movement during various rhythmic human movements.

Cortical topography of human first dorsal interroseus during individuated and nonindividuated grip tasks

Neural activity in the motor cortex and its descending projections is modulated in a task-related manner. Several TMS studies have shown that when normal human subjects execute different manual tasks requiring similar contraction levels in first dorsal interroseous (FDI) there is a task-related modulation of the amplitude of FDI motor evoked potentials (MEPs). Not all studies of task-related changes show the same pattern of results, however. One reason for this might be methodological. Studies have assessed task-related changes by stimulating a single site, which can provide information about task-related changes in the excitability of the cortex at that site, but which is not sensitive to excitability changes throughout the muscle's cortical representation. We investigated how the execution of an individuated versus a nonindividuated isometric grasping task affected the excitability of FDI's entire cortical representation. We examined FDI MEP amplitudes while subjects grasped an object between their thumb and index finger, or when they grasped the same object between their thumb and all four fingers, keeping the background level of EMG in FDI constant for the two tasks. We found no overall task-related change in the excitability of FDI or its cortical topography, possibly due to behavioral differences of individual subjects. The stability of FDI's cortical representation during two different manual tasks expands the possibilities for studying cortical reorganization in the context of active muscle contraction, which will enable us to better understand whether changes in the motor system observed when muscles are at rest are also present during voluntary muscle recruitment.

Fatigue effects on tracking performance and muscle activity

It has been suggested that fatigue affects proprioception and consequently movement accuracy, the effects of which may be counteracted by increased muscle activity. To determine the effects of fatigue on tracking performance and muscle activity in the M. extensor carpi radialis (ECR), 11 female participants performed a 2-min tracking task with a computer mouse, before and immediately after a fatiguing wrist extension protocol. Tracking performance was significantly affected by fatigue. Percentage time on target was significantly lower in the first half of the task after the fatigue protocol, but was unaffected in the latter half of the task. Mean distance to target and the standard deviation of the distance to target were both increased after the fatigue protocol. The changed performance was accompanied by higher peak EMG amplitudes in the ECR, whereas the static and the median EMG levels were not affected. The results of this study showed that subjects changed tracking performance when fatigued in order to meet the task instruction to stay on target. Contrary to our expectations, this did not lead to an overall higher muscle activity, but to a selective increase in peak muscle activity levels of the ECR.

The effect of background muscle activity on computerized detection of sEMG onset and offset

The performance of two computerized algorithms for the detection of muscle onset and offset was compared. The standard deviation (SD) method, a commonly used algorithm, and the approximated generalized likelihood ratio (AGLR) method, a more recently developed algorithm, were evaluated at different levels of background surface EMG (sEMG) activity. For this purpose, the amplitude ratio between the period of muscle inactivity and activity was varied from 0.125 to 1 in artificially assembled sEMG traces. In addition, 1230 real sEMG signals, obtained from various trunk muscles during quick release, were raised to a power of 3 to change their relative amplitude ratio. As the relative level of background activity increased, both the SD and AGLR methods produced longer latencies and detected fewer muscle responses, suggesting that a detection artifact can be introduced if the subject populations being compared have different levels of background muscle activity. Of the two methods, AGLR appears to be the least affected by background activity. However, above the ratio 0.8, results from AGLR are also unreliable, particularly in detecting offsets. Average latency artifacts near this ratio were 8 ms for AGLR and 46 ms for SD.

Priming of Head Premotor Circuits During Oculomotor Preparation

Large, rapid gaze shifts necessitate intricate coordination of the eyes and head. Brief high-frequency bursts of activity within the intermediate and deeper layers of the superior colliculus (dSC) encode desired gaze shifts regardless of component movements of the eyes and head. However, it remains unclear whether low-frequency activity emitted by oculomotor neurons within the dSC and elsewhere has any role in eye-head gaze shifts. Here we test the hypothesis that such low-frequency activity contributes to eye-head coordination by selectively priming head premotor circuits. We exploited the capacity for short-duration (10 ms, 4 pulses) dSC stimulation to evoke neck muscle responses without compromising ocular stability, stimulating at various intervals of a "gap-saccade" task. Low-frequency neural activity in many oculomotor areas (including the dSC) is known to increase during the progression of the gap-saccade task. Stimulation was passed during either a fixation-interval while a central fixation point was illuminated, a 200-ms gap-interval between fixation point offset and target onset, or a movement-interval following target onset. In the two monkeys studied, the amplitude of evoked responses on multiple neck muscles tracked the known increases in low-frequency oculomotor activity during the gap-saccade task, being greater following stimulation passed at the end of the gap- versus the fixation-interval, and greater still when the location of stimulation during the movement interval coincided with the area of the dSC generating the ensuing saccade. In one of these monkeys, we obtained a more detailed timeline of how these results co-varied with low-frequency oculomotor activity by stimulating, across multiple trials, at different times within the fixation-, gap- and movement-intervals. Importantly, in both monkeys, baseline levels of neck EMG taken immediately prior to stimulation onset did not co-vary with the known pattern of low-frequency oculomotor activity up until the arrival of a transient burst associated with visual target onset. These baseline results demonstrate that any priming of the head premotor circuits occurs without affecting the output of neck muscle motoneurons, We conclude that low-frequency oculomotor activity primes head premotor circuits well in advance of gaze shift initiation, and in a manner distinct from its effects on the eye premotor circuits. Such distinctions presumably aid the temporal coordination of the eyes and head despite fundamentally different biomechanics.

H-Reflex Operant Conditioning in Mice

Rats, monkeys, and humans can alter the size of their spinal stretch reflex and its electrically induced analog, the H-reflex (HR), when exposed to an operant conditioning paradigm. Because this conditioning induces plasticity in the spinal cord, it offers a unique opportunity to identify the neuronal sites and mechanisms that underlie a well-defined change in a simple behavior. To facilitate these studies, we developed an HR operant conditioning protocol in mice, which are better suited to genetic manipulation and electrophysiological spinal cord study in vitro than rats or primates. Eleven mice under deep surgical anesthesia were implanted with tibial nerve stimulating electrodes and soleus and gastrocnemius intramuscular electrodes for recording ongoing and stimulus-evoked EMG activity. During the 24-h/day computer-controlled experiment, mice received a liquid reward for either increasing (up-conditioning) or decreasing (down-conditioning) HR amplitude while maintaining target levels of ongoing EMG and directly evoked EMG (M-responses). After 3-7 wk of conditioning, the HR amplitude was 133 +/- 7% (SE) of control for up-conditioning and 71 +/- 8% of control for down-conditioning. HR conditioning was successful (i.e., > or =20% change in HR amplitude in the appropriate direction) in five of six up-conditioned animals (mean final HR amplitude = 139 +/- 5% of control HR for successful mice) and in four of five down-conditioned animals (mean final HR amplitude = 63 +/- 8% of control HR for successful mice). These effects were not attributable to differences in the net level of motoneuron pool excitation, stimulation strength, or distribution of HR trials throughout the day. Thus mice exhibit HR operant conditioning comparable with that observed in rats and monkeys.