Relationships between the changes in compound muscle action potentials and selective injuries to the spinal cord and spinal nerve roots.

OBJECTIVE: Compound muscle action potentials (CMAPs) evoked by transcranial electrical stimulation have been widely introduced to monitor motor function during spinal surgery. They may reflect segmental injuries as well as injuries to motor-related tracts in the spinal cord. However, we have experience with some patients who developed postoperative segmental motor weakness without any potential changes during surgery. To evaluate the efficacy of this method, we used a cat model to observe the relationships between potential changes and selective injuries to the white and gray matters of the spinal cord and spinal nerve roots. METHODS: Ten CMAPs were obtained before and after injury to the spinal cord and spinal nerve roots in 20 cats. Changes in the amplitude, latency, and duration of CMAPs were analyzed. RESULTS: CMAPs decreased in amplitude significantly after the insult to the motor-related tracts in the spinal cord in all cats, while the potentials did not always change when the insult was restricted to a limited area in the anterior horn of the spinal cord or to the single spinal nerve root. CONCLUSIONS: CMAPs may not exactly reflect segmental injury, and careful attention should be paid to the interpretation of CMAPs.     

Bit-mapped colour imaging of the potential fields of propagated and segmental subcortical components of somatosensory evoked potentials in man

Early somatosensory evoked potentials (SEPs) to median or ulnar nerve stimulation were recorded with non-cephalic reference from neck, oesophagus and scalp in normal young adults. Transit times and durations were estimated for different components. SEP fields were mapped with up to 24 skin electrodes around the neck or along the midline neck and scalp, and projected onto a 2-dimensional plane for bit-mapped colour imaging. The posterior neck N11 is a near-field potential propagated caudorostrally in the dorsal column, associated with a positive P11 far field beyond termination of the cuneate bundle. A true phase reversal of the posterior neck N13 into an anterior neck P13 is substantiated, identifying a segmental generator with horizontal axis in dorsal horn. The N13-P13 represents postsynaptic excitatory potentials in interneurones of layers IV-V of the dorsal horn. It is not reflected in any scalp far field. The duration and onset latency of N13-P13 are in line with this interpretation. A new montage of posterior-to-anterior neck can enhance this component without introducing extraneous potentials. The P14 far field does not extend below the inion and presents distinct features. Neck-to-front scalp montages confound the SEP components generated in the spinal cord and above the foramen magnum respectively, but may serve to estimate N11 onset latency.     

STUDIES ON THE HUMAN EVOKED ELECTROSPINOGRAM

The propagation velocity of the ascending volleys along the dorsal funiculus of the human spinal cord was studied in 31 normal volunteers. Intrathecal recordings from lower cervical and lower thoracic intervertebral levels were made after the supramaximal stimulation of the posterior tibial nerves. When the electrode tip was behind the cord dorsum at the cervical level, it was easily possible to obtain very clear triphasic compound action potential on stimulation of the posterior tibial nerve of one leg or both legs. This "Tractus Potential" was found to originate mainly from the dorsal funiculus fibres, i.e. Fasciculus gracilis. The maximal conduction velocity of the ascending afferent volley from the leg was then calculated to be, on average, 37 meters/sec between lumbar and cervical spinal enlargements. Intrathecal stimulation and recording of the spinal cord gave the distinct triphasic wave with low threshold. This was also found to be related to dorsal funiculus activity. In these intraspinal stimulations and recordings, very early small and some late long-lasting deflections appeared, especially in the lateral position of the intrathecal electrode.     

Origin of components P 11 and P 13 in short latency somato-sensory evoked potentials (SSEP): correlative study of SSEP and intraoperative evoked potentials

In 15 patients with cervical or posterior fossa lesion, SSEPs were recorded between the skull and the non-cephalic reference electrodes during the surgical operation and compared with the evoked potentials directly recorded at the same time from the surface of the cervical spinal cord and the brain stem. The directly recorded evoked potential consisted of three main components appeared within about 25 ms., they were a small negative spike wave, a large positive spike wave and a subsequent slow potential. The positive spike wave of the evoked potentials recorded from the surface of the dorsal column was not only coincided in latency with component P 11 of SSEP, but also showed the greatest amplitude at the lower cervical level. Moreover, the positive spike wave gradually delayed in latency and reduced in amplitude from lower to upper cervical segments. The amplitude of the positive spike wave was greater at the surface of the dorsal column ipsilateral to the stimulated median nerve than that of contra-lateral recording. No polarity change was observed between the anterior and posterior surface of the spinal cord. Similarly, the positive spike wave of the evoked potentials, recorded from the surface of the brain stem, showed fairly same latency with P 13 and a maximal amplitude at the surface of the cuneate tuberculum ipsilateral to the median nerve stimulated, and those positive spike wave traveled to contra-lateral ventral surface of the pons, presumably from ipsilateral cuneate nucleus to the contra-lateral medial lemniscus.(ABSTRACT TRUNCATED AT 250 WORDS)     

Evoked electrospinogram in spinal cord and peripheral nerve disorders

Spinal cord evoked potentials have been studied by means of intrathecal application in 80 patients with various spinal cord and peripheral nerve disorders.
The segmental spinal cord potentials are normal in acute motor polyneuropathy, generalized anterior horn cell disease and in discrete lesions of dorso-lumbar segments. On the other hand, the first component of the segmental response is delayed, reduced and sometimes dispersed or lost in chronic sensory-motor polyneuropathy and in hereditary spinocerebellar degeneration. the reduction in amplitude is also present in multiple sclerosis with clinical signs of dorsal funiculus involvement.
In compressive lesions of the cauda-conus, recordings of lower thoracic intervertebral level show that the segmental responses are delayed with marked amplitude reduction.
The potentials recorded from lumbo-sacral segments show a greater the amplitude of the second component proportionally to the first one as the duration of second component is longer in spastic paraplegia regardless of its etiology.
The cervical tractus response is seen to be markedly slowed with a reduction of amplitude or is often absent in chronic polyneuropathy, spinocerebellar degeneration and in multiple sclerosis.
The primary sensory neurones lying both in periphery and in the dorsal column are assumed to be responsible for the segmental evoked potentials especially for the first component. the late slow component is related to the activation of interneurones situated within the segmental gray matter and segmental collaterals of the dorsal root fibres carrying impulses to those cells. Cervical tractus responses are mostly formed by the dorsal column fibres and their physiological action upon demyelination is similar to that of the peripheral nerves.     

Topographical organization of group II afferent input in the rat spinal cord

The organization of neurons in the lumbar enlargement of the rat spinal cord processing information conveyed by group II afferents of hind-limb muscle nerves has been investigated by using cord dorsum and intraspinal field potential recording. Group II afferents of different muscle nerves were found to evoke their strongest synaptic actions in specific segments of the lumbar cord. Group II afferents of quadriceps and deep peroneal nerves evoked potentials mainly at the rostral end of the lumbar enlargement (L1-rostral L3), whereas group II afferents of gastrocnemius-soleus and hamstring nerves evoked their main synaptic actions at the caudal end of the lumbar enlargement (L5). In the central lumbar segments (caudal L3–L4), the largest group II potentials were produced by afferents of tibialis posterior and, to a lesser degree, flexor digitorum longus. Field potentials evoked by group II afferents of quadriceps, tibialis posterior, and flexor digitorum longus were largest in the dorsal horn (up to 600 μV), but also occurred in the ventral horn where they were sometimes preceded by group I field potentials. In contrast, field potentials evoked by group II afferents of gastrocnemius-soleus and hamstring nerves were restricted to the dorsal horn. These results indicate that neurons in different segments of the rat lumbar spinal cord process information from group II afferents of different hind-limb muscles. Furthermore, the topographical organization of group II neuronal systems in the rat is similar in several respects to that in the cat and may therefore represent a general organizational feature of the mammalian spinal cord. J. Comp. Neurol. 394:357–373, 1998. © 1998 Wiley-Liss, Inc.     

Crossed and uncrossed projections to the cat sacrocaudal spinal cord: III. Axons expressing calcitonin gene-related peptide immunoreactivity

We have investigated the projection patterns of peptidergic small-diameter primary afferent fibers to the cat sacrocaudal spinal cord, a region associated with midline structures of the lower urogenital system and of the tail. Calcitonin gene-related peptide (CGRP)-immunoreactive (CGRP-IR) primary afferent fibers were observed within the superficial laminae, rostrally as the typical inverted U-shaped band that capped the separate dorsal horns (S1 to rostral S2) and caudally as a broad band that spanned the entire mediolateral extent of the fused dorsal horns (caudal S2 and caudal). Within the dorsal gray commissure, labeling was seen as a periodic vertical, midline band. CGRP-IR labeling was prevalent in an extensive mediolateral distribution at the base of the dorsal horn, originating from both lateral and medial collateral bundles that extend from the superficial dorsal horn. Some bundles, in part traveling within the dorsal commissure, conspicuously crossed the midline. In addition to the robust projection to the superficial dorsal horn, there was a more extensive distribution of CGRP-IR fibers within the deeper portions of the cat sacrocaudal dorsal horn than has been reported for other regions of the cat spinal cord. Presumably, these deep projections convey visceral information to projection or segmental neurons at the neck of the dorsal horn and in the region of the central canal. This deep distribution overlaps the reported projections of the pelvic and pudendal nerves. In addition, the contralateral projections of CGRP-IR fibers may form an anatomical substrate of the bilateral receptive fields for selective dorsal horn neurons. The density and variety of CGRP-IR projection patterns is a reflection of the functional attributes of the innervated structures.     

Spinal evoked potential in the monkey

Computer-averaged evoked potential responses (EPs) to stimulation of the sciatic nerve and cervical spinal cord were recorded from the dura and skin over the cauda equina and spinal cord in seven monkeys, three with chronic spinal cord lesions. Sciatic EPs consisted of predominantly negative triphasic propagated potentials recorded at all spinal levels and greatest in amplitude over the cauda equina and caudal spinal cord. The conduction velocity of this EP was faster over the cauda equina and rostral spinal cord than over caudal cord segments. Triphasic potentials were succeeded by small negative potentials over the cauda equina and larger negative potentials over the lumbar enlargement. Sciatic EPs over the upper lumbar and thoracic cord were more sensitive to asphyxia than the initial triphasic potentials recorded over cauda equina and caudal cord but resisted changes from increasing the rate of stimulation up to 100 per second. Propagated thoracic EPs were preceded by nonpropagated potentials. The longer latency negative potentials occurring locally over the cauda equina and lower lumbar enlargement were abolished at levels of asphyxia and were attenuated at rates of stimulation that did not affect the preceding triphasic potentials. Following complete spinal cord transection, nonpropagated sciatic EPs were recorded in leads rostral to the section. In preparations with chronic partial cord hemisection involving dorsal and lateral quadrants, ipsilateral sciatic EPs had increased latency, reduced amplitude, and poor definition in the vicinity of and rostral to the lesion. Direct cervical cord stimulation elicited caudally propagated potentials which were followed by large, broad potentials over the lumbar enlargement.     

Cortical potentials evoked by epidural stimulation of the cervical and thoracic spinal cord in man

Scalp somatosensory evoked potentials (SEPs) were recorded after electrical stimulation of the spinal cord in humans. Stimulating electrodes were placed at different vertebral levels of the epidural space over the midline of the posterior aspect of the spinal cord. The wave form of the response differed according to the level of the stimulating epidural electrodes. Cervical stimulation elicited an SEP very similar to that produced by stimulation of upper extremity nerves, e.g., bilateral median nerve SEP, but with a shorter latency. Epidural stimulation of the lower thoracic cord elicited an SEP similar to that produced by stimulation of lower extremity nerves. The results of upper thoracic stimulation appeared as a mixed upper and lower extremity type of SEP. The overall amplitudes of SEPs elicited by the epidural stimulation were higher than SEPs elicited by peripheral nerve stimulation. In 4 patients the CV along the spinal cord was calculated from the difference in latencies of the cortical responses to stimulation at two different vertebral levels. The CVs were in the range of 45-65 m/sec. The method was shown to be promising for future study of spinal cord dysfunctions.     

引起顽固性呃逆、呕吐的视神经脊髓炎的临床表现和影像学研究

目的 探讨引起顽固性呃逆、呕吐(IHN)的视神经脊髓炎(NMO)患者的临床表现和脑干、脊髓MRI特点.方法 收集中山大学附属第三医院神经科17例NMO患者的临床资料,对其中8例合并IHN的NMO患者临床表现及MRI特点进行分析.结果 IHN在NMO患者中常见,本组17例NMO中有8例合并IHN,临床上表现为IHN、复视、眼球震颤,其中6例表现有线样延髓征(LML)或线样延髓脊髓征(LMSL).脊髓纵向MRI显示病灶常常大于3个椎体节段,且以脊髓中央管为中心;轴位脊髓MRI表现为部分性或横贯性,以脊髓的后角或侧角为主,前角受累较少. 结论 引起IHN的NMO临床上多伴有复视和眼球震颤,延髓脊髓MRI常常可见LML或LMSL征,而且病灶以脊髓中央管为中心,后角或侧角受累为主,这些可与多发性硬化相鉴别.     

Posterior spinal cord infarction presenting Brown-Séquard syndrome]

We report a 56 year-old-woman with spinal cord infarction. She experienced left-sided girdle pain without precipitating symptoms and she developed monoparesis of her left leg and urinary retention. She also presented the segmental loss of total sensations in the Th10-11 area of the left trunk, the disturbance of position and vibration senses in the left leg and the disturbance of pain and temperature senses in the right leg. T2-weighted MR imagings showed high signal intensity lesion in the left half of the spinal posterior column at Th9-10 vertebral levels. Somatosensory evoked potentials confirmed that the loss of position and vibration senses was unilateral. Though she became able to walk with canes two months later, her sensory disturbance showed no improvement. This is a rare case of unilateral posterior spinal cord infarction presenting Brown-Séquard syndrome.     

Conduction properties of epidurally recorded spinal cord potentials following lower limb stimulation in man

Spinal somatosensory evoked potentials were recorded in 35 neurologically normal patients undergoing surgery for scoliosis. During posterior procedures the recording electrodes were placed in the dorsal epidural space and during anterior operations in the intervertebral discs. Stimulation was of the tibial nerve in the popliteal fossa and the posterior tibial and sural nerves at the ankle. At thoracic levels the response consisted of at least 3 components with different peripheral excitation thresholds and spinal conduction velocities (range 35-85 m/sec). All components were conducted mainly in tracts ipsilateral to the stimulus, component 1 being most laterally located. At low stimulus intensity only the fastest activity was recorded but this was markedly delayed over low thoracic segments and was recorded as a repetitive discharge rostrally. Higher intensities elicited additional components which were conducted at a slower but relatively uniform velocity; consequently they might overlap with or even overtake the fast activity at mid-to-low thoracic levels. Component 1 was much less prominent when the posterior tibial nerve was stimulated at the ankle and absent from the (cutaneous) sural nerve response; remaining potentials were conducted at velocities similar to those of components 2 and 3 following tibial nerve stimulation at the knee. Small 'stationary' potentials were recorded at all thoracic levels, probably due to the change in conductivity as the volley entered the spinal cord. Efferent activity was recorded at and below the thoraco-lumbar junction, possibly related to the H-reflex or F-wave. Similar, although smaller, afferent potentials were recorded from the anterior side of the vertebral column. Component 1 is likely to be due to the stimulation of group 1 muscle afferents which terminate in the dorsal horn and activate second order neurones, many of whose axons go to form the ipsilateral dorsal spinocerebellar tract. Components 2 and 3 are believed to be largely cutaneous in origin and to be conducted mainly in the dorsal columns.     

Paraspinal stimulation to elicit somatosensory evoked potentials: an approach to physiological localization of spinal lesions

Somatosensory evoked potentials (SEPs) were elicited by stimulation of the paraspinal region. Simultaneous bilateral stimulation, 2 cm lateral to the midline, sufficient to induce a visible muscle twitch, was applied opposite vertebral levels L3, T12, T6 and T1 and intervening segments in some subjects. The potentials were recorded over the scalp (Cz-Fz). The stimulus excludes most of the peripheral nervous system; the volley being initiated in the cutaneous branches of the primary dorsal root rami with some contribution from paraspinal muscle Ia afferents. In normal subjects, paraspinal evoked SEPs are easily elicitable and measurable. Mean spinal cord conduction velocity between T12 and T1 measured 64.1 m/sec (N = 25). The upper thoracic cord propagated faster than the lower thoracic cord which conducted faster than the lumbar segment. The technique was used to confirm the approximate level of radiologically visible spinal lesions that were surgically treated and to identify diffuse, focal or multisegmental spinal conduction slowing in patients devoid of radiologically visible lesions. The method has potential for intraoperative spinal cord monitoring.     

Lumbar cord potentials evoked by stimulation of the nerves of the lower limb in man

Lumbar cord potentials evoked by electrical stimulation of the posterior tibial and sural nerves at the ankle were recorded with monopolar epidural electrodes, at T11-T12 level in 20 subjects and were compared with surface recorded potentials. Two quadriplegic patients with spinal section were included in this group. Curare was given in two cases. Xylocaine block of peripheral nerve was carried out in 4 cases. Double shock study was done in 5 cases. The lumbar cord evoked potentials show two successive components: a 'primary' negative-positive spike response with a latency of 19-35 msec, and the 'secondary' waves with latencies up to 200 msec. The 'primary' response is mainly produced by the afferent volley in the fibres of the dorsal roots and of their intramedullary prolongations. There is no evidence which suggests that it is correlated with presynaptic inhibition. The secondary components may be divided into the early and the late waves. The early waves (40-90 msec) are related to the polysynaptic activities from the afferent fibres of small diameters. The late waves are under the influence of supraspinal mechanism and may be related to long-loop reflexes. The clinical implications of these evoked potentials are discussed.     

Effect of spinal cord irradiation with a low-intensity laser on synaptic transmission characteristics in the dorsal horn

The effect of the monochromatic red light irradiation on the inhibition dynamics of repetitively evoked spinal cord potentials was studied in cats. It is suggested that the radiation increases the intensity of transmitter replenishment processes in the synapses of neurons involved into the generation of observed potentials (N1 component of the cord dorsum potential and monosynaptically evoked discharges of dorsal horn units).     

The P18 component of the median nerve SEP recorded from a posterior to anterior neck montage

Objective

To investigate the P18 component in the posterior to anterior neck montage after median nerve stimulation.

Methods

Somatosensory evoked potentials, through electrical wrist stimulation, were collected. In 12 subjects, the presence of the P18 component was evaluated in the posterior to anterior neck montage. In 10 subjects, the effects of simultaneous vibration of the hand were evaluated. In five subjects, responses after double-pulse stimulation (ISI 20 ms) were evaluated.

Results

The P18 component was identified in all subjects. Vibration reduced the amplitude of all components except the P18 and N18. Double-pulse stimulation reduced the amplitude of the P18 and the N18 components without significantly changing the amplitude of the other components.

Conclusions

The posterior to anterior neck montage allows for recording the P18 component. The amplitude reduction of all components during vibration, except N18 and P18, is interpreted as reflecting inhibitory activities at the cuneiform nucleus and at the segmental dorsal horn of the spinal cord, respectively. The reduction in the P18 component after double-pulse stimulation is compatible with previous observations on the positive component of cord dorsum potentials.

Significance

Studying this component may add to the knowledge of the function of the spinal cord in humans.     

The origins of lumbosacral spinal evoked potentials in humans using a surface electrode recording technique.

Somatosensory evoked potentials were recorded over the lumbar spine and scalp in 12 normal subjects after stimulating the posterior tibial nerve at the knee and ankle and the sural nerve at the ankle. The H-reflex from the soleus muscle was recorded at the same time. The effects of stimulus intensity, frequency of stimulation and vibration were assessed. It was concluded that when the posterior tibial nerve was stimulated in the popliteal fossa, three negative peaks were recorded over the lumbosacral area. They arose from activity in the dorsal roots, the dorsal horn of the spinal cord (SD) and the ventral roots. In contrast when the posterior tibial nerve and the sural nerve were stimulated at the ankle only two negative peaks were recorded, a dorsal root potential and a spinal cord dorsum potential. In addition the data suggested that the peripheral nerve fibres that are involved with generating the surface recorded spinal potential with mixed nerve stimulation are primarily muscle afferents.     

Electrophysiological characteristics of lumbosacral evoked potentials in patients with established spinal cord injury

Surface electrodes positioned over the S1 and T12 vertebrae and referenced to T6 were used to record spinal potentials evoked by unilateral stimulation of the posterior tibial nerve at the knee. Data were collected on 24 patients who received spinal cord injuries 2 months to 31 years previously. The recording sites were below the level of spinal injury. The lumbosacral evoked potentials (LSEPs) were compared with the results of measurements obtained from 19 neurologically healthy subjects. Additional data were collected on each patient to characterize segmental reflex responses and preservation of sensory and motor functions associated with the L5 through S2 segments of the spinal cord. Assuming that the LSEP reflects the activity of spinal cord interneurons, the results demonstrate a degree of spinal cord dysfunction caudal to the area of injury in a substantial number of the patients with spinal cord injury which we studied.     

Fiber composition of the posterior lateral-line nerve of goldfish, investigated by electrophysiological and microscopical techniques

The trunk of the posterior lateral-line nerve of goldfish was stimulated electrically, and the evoked compound spike potential was recorded from the proximal cut end of the nerve. The spike potential consisted of four components which were distinguished from each other by differences of excitability, refractory period and conduction velocity. They were named F-1, F-2, F-3 and S, in the order of decreasing conduction velocity. All of these components could generally be elicited by stimulation of the small nerve branches innervating canal organs. By means of light- and electron-microscopical examination, the fiber diameter spectrum of the posterior lateral-line nerve was obtained. The observed compound spike potentials were reconstructed successfully from this fiber spectrum. It is concluded that the three subgroups, F-1, F-2 and F-3 components are thick myelinated fibers and the S component is thin myelinated fibers.     

Spinal somatosensory evoked potentials in infants and children with spinal cord lesions

Spinal somatosensory evoked responses to peroneal nerve stimulation were examined in 23 control subjects and 8 patients with pathological lesions of the spinal cord or peripheral nerve. In the control subjects, the response was found as a triphasic potential increasing in latency rostrally at the lumbar spinous recording location. Another negative potential following this triphasic potential appeared at the L1 to T10 spinous recording locations, which might reflect synaptic and/or post-synaptic activity in the spinal cord. This negative response then progressively increased in latency rostrally. The spinal conduction velocity was higher at the upper thoracic leads than at the lower leads. Three patients with spinal cord atrophy showed disappearance of the spinal evoked potential at the spinous recording location corresponding to the pathological lesion. However, since the triphasic potential at the lumbar spinous lead was undetectable in the patients with lesions of the peripheral nerve or cauda equina, the spinal cord function could not be estimated well in these patients.