Motor Endplate Zone Research Articles

Anatomical analysis of the motor endplate zones of the suprascapular nerve to the infraspinatus muscle and its clinical significance in managing pain disorder.

Myofascial pain syndrome caused by myofascial trigger points is a musculoskeletal disorder commonly encountered in clinical practice. The infraspinatus muscle is the region most frequently involved in the myofascial pain syndrome in the scapular region. The characteristics of the myofascial trigger points are that they can be found constantly in the motor endplate zone. However, localizing myofascial trigger points within the motor endplate zone and establishing an accurate injection site of the infraspinatus muscle has been challenging because the anatomical position of the motor endplate zone of the infraspinatus muscle is yet to be described. Therefore, this cadaveric study aimed to scrutinize the motor endplate zone of the infraspinatus muscle, propose potential myofascial trigger points within the muscle, and recommend therapeutic injection sites. Twenty specimens of the infraspinatus muscle for nerve staining and 10 fresh frozen cadavers for evaluation of the injection were used in this study. The number of nerve branches penetrating the infraspinatus muscle and their entry locations were analyzed and photographed. Modified Sihler's staining was performed to examine the motor endplate regions of the infraspinatus muscle. The nerve entry points were mostly observed in the center of the muscle belly. The motor endplate was distributed equally throughout the infraspinatus muscle, but the motor endplate zone was primarily identified in the B area, which is approximately 20-40% proximal to the infraspinatus muscle. The second-most common occurrence of the motor endplate zone was observed in the center of the muscle. These detailed anatomical data would be very helpful in predicting potential pain sites and establishing safe and effective injection treatment using botulinum neurotoxin, steroids, or lidocaine to alleviate the pain disorder of the infraspinatus muscle.

Safe Needle Insertion Locations for Motor Point Injection of the Triceps Brachii Muscle: A Pilot Cadaveric and Ultrasonography Study.

Objective To determine the location of the motor endplate zones (MoEPs) for the three heads of the triceps brachii muscles during cadaveric dissection and estimate the safe injection zone using ultrasonography.MethodsWe studied 12 upper limbs of 6 fresh cadavers obtained from body donations to the medical school anatomy institution in Seoul, Korea. The locations of MoEPs were expressed as the percentage ratio of the vertical distance from the posterior acromion angle to the midpoint of the olecranon process. By using the same reference line as that used for cadaveric dissection, the safe injection zone away from the neurovascular bundle was identified in 6 healthy volunteers via ultrasonography. We identified the neurovascular bundle and its location with respect to the distal end of the humerus and measured its depth from the skin surface.ResultsThe MoEPs for the long, lateral, and medial heads were located at a median of 43.8%, 54.8%, and 60.4% of the length of the reference line in cadaver dissection. The safe injection zone of the medial head MoEPs corresponded to a depth of approximately 3.5 cm from the skin surface and 1.4 cm away from the humerus, as determined by sonography.ConclusionCorrect identification of the motor points for each head of the triceps brachii would increase the precision and efficacy of motor point injections to manage elbow extensor spasticity.

Motor endplate-targeted botulinum toxin injections of the gracilis muscle in children with cerebral palsy.

Intramuscular botulinum toxin-A (BoNT-A) injections reduce spasticity by blocking neurotransmission at the motor endplate (MEP). The goal of this study was to assess the reduction in spasticity achieved by injecting BoNT-A at different sites of the gracilis muscle. Thirty-four gracilis muscles, in 27 children (10 females and 17 males, mean age of 8.6y [SD 2.5y]) with spastic cerebral palsy (unilateral and bilateral, Gross Motor Function Classification System [GMFCS] levels I-IV), were randomly assigned to one of two groups. In one group BoNT-A was injected proximally (at a site 25% of the distance from the pubic tubercle and the medial epicondyle) and in the other it was injected at the MEP zones (half of the dose was administered at 30% of this distance and half at 60%). Spasticity was assessed before and after BoNT-A injection using simultaneous measurements of surface electromyography (sEMG) and angular velocity during passive muscle stretch applied at different velocities. The primary outcome measure included the velocity-dependent change in average root mean square electromyography (RMS-EMG). Secondary outcome was assessed with the Modified Ashworth Scale (MAS) and Modified Tardieu Scale (MTS). Spasticity decreased more in MEP-targeted muscles than in proximally injected muscles, as demonstrated by a larger reduction in average RMS-EMG values (p=0.04), though this difference was not found with the MAS or MTS. The results suggest that BoNT-A injection of the gracilis at sites with a high concentration of MEPs is effective at reducing spasticity. These preliminary findings should be confirmed by larger studies. In the case of long muscles, such as the gracilis, the injection site is important.

The clinical utility of botulinum toxin injections targeted at the motor endplate zone in cervical dystonia.

Cervical dystonia (CD) patients usually receive repeated botulinum neurotoxin (BoNT) injections. The aims of this study were to evaluate the feasibility of motor endplate zone (MEZ) detection of relevant cervical muscles in CD patients receiving chronic BoNT treatment and to compare the treatment effect of half-dosed, endplate-targeted injections to standard BoNT injections. In study 1, high-density surface electromyography (HD-sEMG) was recorded from the sternocleidomastoid (SCM) and splenius capitis (SC) muscles in 18 CD patients with ongoing BoNT treatment, by which the location of the MEZ was determined. In study 2, nine additional patients with rotational-type CD participated in a treatment effect study where they received either half of their regular BoNT dose through endplate-targeted injections or their normal BoNT dose through standard injections (crossover design). Dystonia severity was recorded before and 4weeks after each treatment session (Toronto Western Spasmodic Torticollis Rating Scale severity subscore). In the SCM muscle the MEZ was located at the lower border of the superior third part of the muscle, and in the SC muscle at half muscle length. Endplate-targeted, half-dosed BoNT injection resulted in a similar treatment effect to injecting the full dose in the standard technique. Half-dosed, endplate-targeted BoNT injections lead to a similar treatment effect to the standard BoNT injection protocol. MEZ detection confronts the clinician with some technical challenges, such as the ability of accurate and technically optimal placement of the electrode grid and correct interpretation of the HD-sEMG signal.

High-density Surface EMG: Techniques and Applications at a Motor Unit Level

Surface EMG comprises a variety of widely applied experimental tools in basic neuroscience, biomechanics and exercise physiology, but also in applied disciplines like clinical neuro-physiology, ergonomics and sports sciences. To increase the usefulness of surface EMG, we contributed to the introduction and application of a spatiotemporal variant of the usual single channel surface EMG techniques, called high-density surface EMG (HD-sEMG). In the present paper, we first discuss the background of the HD-sEMG technique and basic principles of recording and analysis. In a second part, we illustrate the usefulness of the technique on the basis of studies in which the analysis of HD-sEMG at a motor unit level is at hand. It concerns a precise analysis of the activity of the facial musculature that leads to a map of muscle fibre directions and the positions of motor endplate zones. Two other applications refer to neuromuscular pathology, being motor unit number estimation and the quantification of spontaneous motor unit activity, known as fasciculations.

Botulinum toxin has an increased effect when targeted toward the muscle’s endplate zone: A high-density surface EMG guided study

Objectives To compare the effect of endplate-targeted injections of a low Botulinum neurotoxin type A (BoNT-A) dose with that of injections at defined distances from the motor endplate zone. Methods In eight healthy volunteers, the main endplate zones of the right and left extensor digitorum brevis (EDB) muscles were localized using high-density surface EMG. On the study side BoNT-A was injected at fixed distances from the endplate zone. On the control side, BoNT-A was administered into the endplate zone. Compound muscle action potential (CMAP) prior to the injection and 2, 12, and 24 weeks later were recorded. Results On the control side, the mean CMAP reduction 2 weeks after BoNT-A injection was 79.3%. The difference in CMAP reduction between both EDB muscles was significantly related to the injection distance from the endplate zone. Increasing the injection distance by 1 cm reduced the effect of BoNT-A by 46%. Conclusions Guided injection of a reduced BoNT-A dose into the muscle’s endplate zone(s) is a promising strategy for optimizing the therapeutic effectiveness of BoNT-A and for minimizing side-effects such as unwanted weakness of adjacent muscles. Significance Precise endplate-targeted injections increase the effect of BoNT-A and may thus prove to reduce required dosage and treatment costs.

Localization of the motor endplate zone in human skeletal muscles of the lower limb: anatomical guidelines for injection with botulinum toxin

Botulinum toxin gives a local tone reduction by blocking neurotransmission at the motor endplate (MEP). The importance of using MEP-targeted injections is demonstrated in animal models and in a clinical human study. The goal of this review is to present the available data on the localization of the MEP zone of frequently injected muscles of the lower limb and to compare this with current practice. Current knowledge on the localization of the MEP zone is based on some older histological studies, and for some of the more frequently injected muscles also on more recent anatomical dissection. We find that for some muscles the MEP zone can be more precisely demarcated, and for many other muscles that its location is somewhat different than the currently injected areas in clinical practice. Optimal injection sites are presented for gastrocnemius, soleus, tibialis posterior, semitendinosus, semimembranosus, gracilis, biceps femoris, rectus femoris, adductor longus, brevis and magnus, and psoas muscles. We propose optimal injection sites in relation to external anatomical landmarks for the frequently injected muscles of the human lower limb to facilitate the efficiency of botulinum toxin injections.

Localization of motor nerve branches of the human psoas muscle

Endplate-targeted botulinum toxin injections can achieve optimal neuromuscular blockade. The goal of this study was to identify the motor endplate (MEP) zone in the human psoas muscle through dissection. In 24 human cadaver psoas muscles the nerve branches and their intramuscular course were followed by stereoscopic microscopic dissection as far as their terminal ramifications. From the lumbar plexus, an average of 3.7 (range 2-7) nerve branches enter the psoas muscle. The proximal and distal limit of the MEP-zone are situated at about 30% and 70%, respectively, of the distance between the twelfth thoracic vertebra (Th12) and the passing of the psoas under the inguinal ligament. In reference to the sacral promontory (P), these limits are respectively from 50% of the Th12-P distance to 20% of the P-pubis distance. This study of the MEP zone of the human psoas muscle can allow the clinician to inject BTX-A close to its site of action.

Studying motor end-plate topography by means of scanning-electromyography

This study investigates the anatomical and physiological causes of the temporal jumps between motor unit fractions observed in scanning-EMG recordings; i.e., temporal gaps in the distribution of the electrical activity of the motor unit within a transverse section of its territory. Scanning-EMG signals were extracted from the biceps brachii. Spatial and temporal aspects of motor unit fractions were characterized. Simulated motor unit potentials (MUPs) were generated under different distributions of the anatomical and physiological parameters. Complexity and latency of the MUPs were calculated. To obtain realistic simulated MUPs it was necessary to reduce the width of the motor end-plate zone and variability of the muscle fiber conduction velocity compared to the overall data available for the entire muscle. To simulate temporal jumps between fractions, motor end-plates must be distributed in sub-bands of narrow width with different mean positions, innervated by separate axonal branches. Differences in the motor end-plates positions, axonal branches lengths and conduction velocities explain the temporal jumps between fractions. Characterization of the motor unit fractions, observable by means of scanning-EMG, can be used to obtain valuable information about the motor end-plate topography and branching pattern of the axon innervating the motor unit.

Motor Points for the Neuromuscular Blockade of the Subscapularis Muscle

Harrison TP, Sadnicka A, Eastwood DM. Motor points for the neuromuscular blockade of the subscapularis muscle. Objective To locate the motor points of the subscapularis muscle in relation to palpable anatomic landmarks and hence suggest a technique for botulinum toxin injection into subscapularis applicable to patients of all ages. Design Anatomic dissection of the innervation of 20 subscapular muscles. Setting University dissecting room. Cadavers Ten formalin-preserved cadavers. Interventions Not applicable. Main Outcome Measure The location of motor points in relation to anatomic landmarks. Results The median number of motor points for the subscapularis was 5 (range, 3−6). All motor point measurements were related to surface points and converted into proportional values along reference lines. Motor points from the 20 dissections showed clustering in a band. A line of best fit was calculated ( y=1.48 x–0.743). Conclusions We describe an injection technique that would deliver botulinum toxin close to the motor points of the subscapularis, a surrogate marker of the motor endplate zones. By using proportional distances, this technique is applicable to an adult and pediatric population. This should lead to an increased efficacy and decreased side-effect profile in clinical practice, although clinical trials will need to confirm this.

Effects of intramuscular needle position on motor unit action potential metrics

It is unclear whether there are clinically significant differences in amplitude, duration, and numbers of turns and phases if an electromyographic (EMG) study is performed near to, or far from, the end-plate zone. The effects of temporal dispersion of arriving muscle-fiber action potentials on quantitative motor unit action potential (MUAP) metrics were assessed in simulated and biologic muscles. Two muscle simulation models were studied with electrode recording positions near the motor end-plate zone and 50-75 mm away. When the electrode was moved away from the end-plate zone, averages of 20 MUAPs significantly decreased in amplitude and area, and increased in numbers of turns and phases, but there was no significant change in duration. In biologic muscles (both normal and pathologic), similar changes in average metrics were observed, but to lesser degrees; few were statistically significant. Zones of innervation in biologic muscles are broadly distributed and, during routine electrode studies, distances between random electrode placements and end-plate zones are therefore relatively short, leading to clinically insignificant changes in quantitative MUAP metrics with distance from the end-plate zone. Thus, electrode position within a muscle is unlikely to affect clinical MUAP interpretation.

Three‐dimensional topography of the motor endplates of the rat gastrocnemius muscle

Spatial distribution of motor endplates affects the shape of the electrical activity recorded from muscle. In order to provide information for realistic models of action potential propagation within muscles, we assembled three-dimensional maps of the motor endplates of the rat medial gastrocnemius (MGM) and lateral gastrocnemius (MGL) muscles. The maps were assembled from histological cross sections stained for acetylcholinesterase activity. Within MGL, the motor endplates formed three columns along its longitudinal axis. Within MGM, the motor endplates were arranged in a leaf-like body that shifted obliquely from proximal to distal. As inferred from the proximo-distal distribution of the cross-sectional projection area, the majority of the motor endplates were concentrated in the middle of MGL and in the distal third of MGM. Regions of maximal motor endplate concentration are considered most suitable for injections of neuroactive substances, such as neuronal tracers. The assembled maps of the gastrocnemius muscles can be used as guides for such injections within the motor endplate zones.

Targeting the neuromuscular junction in skeletal muscles.

Botulinum neurotoxins selectively weaken skeletal muscle by presynaptic blockade of vesicles containing the neurotransmitter acetylcholine. Because the location of the neuromuscular junction (found in motor endplates) is most highly concentrated in a band within the midbelly of the muscle, injection of botulinum neurotoxins are hypothesized to be more potent when specifically targeted toward the motor endplate zones. Few studies have attempted to describe the distribution of motor endplate zones in skeletal muscles, and scant experimental data exist that directly tests this hypothesis. In this article, a rationale is presented for motor endplate targeting within specific limb muscles with respect to botulinum neurotoxin therapy.

Innervation of the levator ani and coccygeus muscles of the female rat.

In humans, the pelvic floor skeletal muscles support the viscera. Damage to innervation of these muscles during parturition may contribute to pelvic organ prolapse and urinary incontinence. Unfortunately, animal models that are suitable for studying parturition-induced pelvic floor neuropathy and its treatment are rare. The present study describes the intrapelvic skeletal muscles (i.e., the iliocaudalis, pubocaudalis, and coccygeus) and their innervation in the rat to assess its usefulness as a model for studies of pelvic floor nerve damage and repair. Dissection of rat intrapelvic skeletal muscles demonstrated a general similarity with human pelvic floor muscles. Innervation of the iliocaudalis and pubocaudalis muscles (which together constitute the levator ani muscles) was provided by a nerve (the "levator ani nerve") that entered the pelvic cavity alongside the pelvic nerve, and then branched and penetrated the ventromedial (i.e., intrapelvic) surface of these muscles. Innervation of the rat coccygeus muscle (the "coccygeal nerve") was derived from two adjacent branches of the L6-S1 trunk that penetrated the muscle on its rostral edge. Acetylcholinesterase staining revealed a single motor endplate zone in each muscle, closely adjacent to the point of nerve penetration. Transection of the levator ani or coccygeal nerves (with a 2-week survival time) reduced muscle mass and myocyte diameter in the iliocaudalis and pubocaudalis or coccygeus muscles, respectively. The pudendal nerve did not innervate the intrapelvic skeletal muscles. We conclude that the intrapelvic skeletal muscles in the rat are similar to those described in our previous studies of humans and that they have a distinct innervation with no contribution from the pudendal nerve.

Innervation of the levator ani muscles in the female squirrel monkey

Objective: The purpose of this study was to characterize the innervation of the levator ani muscles in the female squirrel monkey and to investigate its usefulness as an animal model of pelvic organ prolapse. Study Design: Eleven nulliparous female squirrel monkeys with no pelvic organ prolapse were used in this study. Detailed pelvic dissections were conducted (n = 3), and the Koelle stain for acetylcholinesterase was used to identify the motor endplate zone in the levator ani muscles (n = 2). Unilateral levator ani (n = 4) and pudendal (n = 2) neurectomies were performed; changes in levator ani muscle mass and myocyte diameter were examined 14 days after neurectomy. Nerve biopsy specimens from each animal were processed for microscopy. Results: The levator ani nerve originated from the S2 spinal root and entered the pelvic cavity adjacent to the pelvic nerve between the flexor caudalis brevis and iliocaudalis muscles. The levator ani nerve then projected caudally and bifurcated to penetrate the iliocaudalis and pubocaudalis. A single motor endplate zone in each muscle correlated with the point of levator ani nerve penetration. The pudendal nerve originated from the S1-S2 spinal roots to innervate the urethral and anal sphincters, clitoris, and perineum, but not the iliocaudalis or pubocaudalis. Significant atrophy and myocyte shrinkage occurred in the iliocaudalis and pubocaudalis ipsilateral to the levator ani nerve transection (P <.05). Pudendal neurectomy produced no levator ani muscle changes. Conclusion: Intrapelvic skeletal muscles in the female squirrel monkey are similar to humans and have distinct innervation with no contribution from the pudendal nerve. The squirrel monkey is likely to be a useful model of pelvic organ prolapse and warrants further study. (Am J Obstet Gynecol 2003;188:1141-7.)

Motor nerve transplantation

The motor nerve transplantation (MNT) technique is used to transfer an intact nerve into a denervated muscle by harvesting a neurovascular pedicle of muscle containing motor endplates from the motor endplate zone of a donor muscle and implanting it into a denervated muscle. Thirty-six adult New Zealand White rabbits underwent reinnervation of the left long peroneal (LP) muscle (fast twitch) with a motor nerve graft from the soleus muscle (slow twitch). The right LP muscle served as a control. Reinnervation was assessed using microstimulatory single-fiber electromyography (SFEMG), alterations in muscle fiber typing and grouping, and isometric response curves. Neurofilament antibody was used for axon staining. The neurofilament studies provided direct evidence of nerve growth from the motor nerve graft into the adjacent denervated muscle. Median motor endplate jitter was 13 μsec preoperatively, and 26 μsec at 2 months, 29.5 μsec at 4 months, and 14 μsec at 6 months postoperatively (p &lt; 0.001). Isometric tetanic tension studies showed a progressive functional recovery in the reinnervated muscle over 6 months. There was no histological evidence of aberrant reinnervation from any source outside the nerve pedicle. Isometric twitch responses and adenosine triphosphatase studies confirmed the conversion of the reinnervated LP muscle to a slow-type muscle. Acetylcholinesterase studies confirmed the presence of functioning motor endplates beneath the insertion of the motor nerve graft. It is concluded that the MNT technique achieves motor reinnervation by growth of new nerve fibers across the pedicle graft into the recipient muscle.

Neuromuscular specializations of the pharyngeal dilator muscles: I. Compartments of the canine geniohyoid muscle.

Little is known about the structure and innervation of the geniohyoid muscle (GH), which is an important pharyngeal dilator muscle activated in swallowing and respiration. The neuromuscular specializations of the canine GH were studied in detail by using a combination of histological, histochemical, and anatomical techniques. First, hematoxylin and eosin staining, Gomori's rapid one-step trichrome stain, and silver impregnation were used to determine the terminations of muscle fibers and existence of fibrous septa within the muscle (n = 8). Second, myofibrillar ATPase staining was employed to document the muscle fiber type distribution (n = 8). Finally, Sihler's stain (n = 10) and wholemount acetylcholinesterase staining (n = 8) were used to examine the distribution of the nerve supply within the muscle. The canine GH is divided into rostral and caudal compartments, which are arranged in series and separated by a transverse fibrous septum. Each compartment receives its own primary nerve branch, which supplies a separate motor endplate zone. The rostral compartment is innervated bilaterally, whereas the caudal compartment is innervated ipsilaterally. The rostral compartment was composed of significantly more type I (slow twitch) muscle fibers (56%) than the caudal compartment (25%). The canine GH is composed of two in-series neuromuscular compartments rather than a single muscle as traditionally believed. This anatomical finding suggests that these two compartments may function independently under different physiological conditions.

Motor nerve transplantation.

The motor nerve transplantation (MNT) technique is used to transfer an intact nerve into a denervated muscle by harvesting a neurovascular pedicle of muscle containing motor endplates from the motor endplate zone of a donor muscle and implanting it into a denervated muscle. Thirty-six adult New Zealand White rabbits underwent reinnervation of the left long peroneal (LP) muscle (fast twitch) with a motor nerve graft from the soleus muscle (slow twitch). The right LP muscle served as a control. Reinnervation was assessed using microstimulatory single-fiber electromyography (SFEMG), alterations in muscle fiber typing and grouping, and isometric response curves. Neurofilament antibody was used for axon staining. The neurofilament studies provided direct evidence of nerve growth from the motor nerve graft into the adjacent denervated muscle. Median motor endplate jitter was 13 microsec preoperatively, and 26 microsec at 2 months, 29.5 microsec at 4 months, and 14 microsec at 6 months postoperatively (p < 0.001). Isometric tetanic tension studies showed a progressive functional recovery in the reinnervated muscle over 6 months. There was no histological evidence of aberrant reinnervation from any source outside the nerve pedicle. Isometric twitch responses and adenosine triphosphatase studies confirmed the conversion of the reinnervated LP muscle to a slow-type muscle. Acetylcholinesterase studies confirmed the presence of functioning motor endplates beneath the insertion of the motor nerve graft. It is concluded that the MNT technique achieves motor reinnervation by growth of new nerve fibers across the pedicle graft into the recipient muscle.

Neurotization of the rat soleus muscle: A quantitative analysis of reinnervation

Neurotization--reinnervation of muscle by direct nerve implantation--has been the subject of several reports. The underlying neurobiology, however, has not been adequately studied. The use of a combined silver-acetylcholinesterase stain was used in this study to identify reinnervated motor endplates and to quantify motor endplates reinnervated by the neurotization process. This study examined the effect of distance between nerve implantation and native motor endplate zone on the formation of ectopic motor endplates and on the total number of motor endplates reinnervated. Experiments were performed on the rat soleus muscle. The transected tibial nerve was implanted directly into the motor endplate zone (near, n = 10) or distally, far from the motor endplate zone (far, n = 10). After a reinnervation interval, frozen sections were processed to demonstrate both axons and motor endplates. In the near group, a mean of 566 motor endplates were reinnervated in the native motor endplate zone and a mean of only 13 in distant locations. In the far group, a mean of 362 motor endplates were reinnervated in the native zone, while a mean of 477 were reinnervated in distant locations. Significantly more ectopic motor endplates were generated by far implantation, and native motor endplates were increased by near implantation. The total number of motor endplates was independent of implant location. These experiments demonstrate that the distance between implanted nerve and the native motor endplate zone influences the morphology of reinnervation.

Motor evoked potentials: appropriate positioning of recording electrodes for diagnosis of spinal disorders.

The interpretation of normal and pathological findings of motor evoked potential obtained by the use of transcranial magnetic stimulation depends on adequate examination technique, including the appropriate positioning of the recording electrodes over the muscle. On the basis of knowing the location of the motor end plate zones in muscles, magnetic stimulation of the motor cortex of 30 healthy adults was performed in order to explore the influence of the position of the surface recording electrodes on potential parameters and to establish the standard location of the recording electrodes over the biceps brachii, medial vastus, anterior tibial and abductor hallucis muscles for diagnostic use in spine disorders. The cortical latencies and peak-to-peak amplitudes of the evoked potentials were analysed by varying the location of the recording electrodes and the stimulus intensities. The latencies were significantly shorter when the different electrode lay more proximally over the muscle belly. Reproducible potentials with sharp negative onset and maximum amplitude were recorded with a separation of 5-7.5 cm between the different electrode, located over the motor end plate area, and the different electrode, located over the distal myotendinous junction. This implies that the parameters of evoked potentials depend on the position and separation distance of the recording electrodes over the muscles and that it is possible to record the potentials using a lower stimulus intensity and, above all, on relaxed muscles, which may prove to be applicable for intraoperative monitoring of the spinal cord using magnetic stimulation.(ABSTRACT TRUNCATED AT 250 WORDS)