Far-field potentials in muscle

Far-field potentials have been predicted by computer simulations as well as demonstrated in both animals and humans with respect to the peripheral and central nervous systems. Computer simulations have also predicted far-field potentials originating at the termination of muscle tissue. This investigation demonstrates the occurrence of 2 far-field potentials in the human biceps muscle resulting from action potential termination at the musculotendonous junctions. A monophasic potential is produced at both the muscle's origin and insertion, and the polarity is entirely dependent upon the recording montage. Sequential stimulation of the biceps muscle at 2.5-cm increments resulted in the 2 far-field potentials and their respective latencies changing proportional to the distance between the stimulus site and the 2 musculotendonous junctions. Various stimulation and recording montages are used to investigate the properties of these far-field potentials. The leading/trailing dipole model is utilized to explain the production and polarity of far-field potentials generated by muscle tissue.     

Far-field potentials in circular volumes: evidence to support the leading/trailing dipole model.

The leading/trailing dipole model explains the production of far-field potentials as an asymmetry in the leading and trailing dipole moments of a propagating action potential detected by a referential montage. This investigation documents the production of far-field potentials produced by a pure dipole generator in a circular volume conductor. Multiple equipotential waveforms are recorded in an adjoining circular volume conductor attached to the one in which the dipole generator is located. This finding substantiates the "wick electrode" effect that explains the equipotential and instantaneous distribution of far-field potentials over relatively large distances in volume conductors. The present findings support a number of the leading/trailing dipole model proposals which explain far-field potential generation.     

Median/ulnar premotor potential identification and localization

A small negative waveform is known to precede the median and ulnar compound muscle action potentials when recorded with surface or concentric needle electrodes. This investigation documents that there are two distinct waveforms preceding the median compound muscle action potential (CMAP) depending upon the type of recording electrodes used (concentric needle versus surface) and their respective locations. The negative waveform originally described with a concentric needle electrode positioned within the substance of the distal thenar eminence and having a restricted zone of detection is referred to as the intramuscular nerve action potential (INAP). This potential is shown to be distinct from the premotor potential (the small negative waveform preceding surface recorded ulnar and median CMAPs). Detection of the median and ulnar premotor potentials at multiple locations about the hand with the same respective onset/peak latencies and amplitudes substantiates that this potential is a far-field potential. The median and ulnar premotor potentials most likely originate from a dipolar moment imbalance generated by digital sensory nerve action potentials as they cross the first and fifth metacarpophalangeal junctions, respectively. Applying far-field principles permits the documentation of additional far-field potentials as they are generated at the second through fourth metacarpophalangeal junctions following median nerve stimulation. Also, because the premotor potential is a far-field potential, caution must be exercised with respect to its diagnostic utility as joint position and other unknown factors may affect amplitude and onset/peak latency. The INAP following median nerve excitation, however, is documented to be a near-field potential distinct from the premotor potential arising from the recurrent branch of the median nerve. Therefore, although the median intramuscular nerve action potential and premotor potentials both precede the compound muscle action potential, they are different potentials with unique generator sites. © 1995 John Wiley & Sons, Inc.     

Far-field Potentials as a Method of Monitoring Acute and Chronic Spinal Cord Injury

Far-field potentials (FFPs) were studied in monkeys to determine the utility of such responses in evaluating acute and chronic spinal cord injury. Monkeys (Macaca fascicularis) were anesthetized with 70% N₂O 30% O₂, immobilized with pancuronium bromide, and maintained on a respirator. Spinal cord transections were made at level T₃-T₄ and included bilateral dorsal columns or anterolateral columns, right or left hemisection, or central cord lesions. Percutaneous stimulation of both posterior tibial nerves was performed at a frequency of 3 Hz using 3-4 mA for 0.3 msec duration. Potentials were recorded from chronically implanted epidural electrodes (right ear reference) through a 300-3,000 Hz band pass filter. Each far-field potential represents the average of 256 individual responses recorded for a duration of 25 msec before and after cord lesion for up to 8 weeks.

Seven reproducible components in the far-field potential could be identified. Following dorsal column transection all components were reduced in amplitude. After anterolateral column transection only latencies were altered. Right or left hemisections caused both attenuation of component amplitudes and latency alteration. Central cord lesions resulted in no detectable amplitude or latency disturbances. Control records likewise showed no changes. No major alterations, following day 1 posttransection, were observed, attesting to the relative stability of far-field potentials over long periods of time. Far-field potentials therefore may be useful in monitoring spinal cord injury.     

Far-field potentials generated by action potentials of isolated frog sciatic nerves in a spherical volume.

Previous results in cylindrical volumes have shown that action potentials generate far-field potentials when experimental conditions are such that quadrupolar components of the action potential are reduced to an equivalent dipole. We now show that the same conclusions are also reached within a spherical volume, again recording far-field potentials from isolated bullfrog nerves. A mathematical proof is given that shows that in a sphere, antipodal electrodes primarily detect far-field potentials from dipole generators and not quadrupole generators. A revised conception of the 'far-field' in evoked responses is discussed which equates far-field recordings with dipole detection.     

Electrophysiologic Studies of Cervical Vagus Nerve Stimulation in Humans: II. Evoked Potentials

Evidence from studies of experimental animals indicates that electrical stimulation of the vagus nerve not only can alter the EEG but evokes activity in specific brain areas. We report effects of electrical stimulation of the vagus nerve in 9 patients with medically intractable seizures as part of a clinical trial of chronic vagal stimulation for control of epilepsy. The left vagus nerve in the neck was stimulated with a programmable implanted stimulator. Effects of stimulus amplitude, duration, and rate were studied. Noncephalic reference recording of the vagus nerve evoked potential showed some unusual properties: a scalp negative component occurred with a latency of 12 ms, very high amplitude (< or = 60 microV), and widespread scalp distribution. Field distribution studies indicated that this potential was myogenic in origin and generated in the region of the stimulating electrodes in the neck area. Chemically induced muscle paralysis confirmed this observation. Bipolar scalp recording showed several small-amplitude topographically distinct potentials occurring in 30 ms. No effect, either acute or chronic, could be detected on pattern-reversal evoked potentials, auditory brainstem evoked potentials, auditory 40-Hz potentials, or cognitive evoked potentials.     

Stationary waves recorded at the shoulder after median nerve stimulation

A new recording method with a reference electrode on the stimulated arm defined two discrete far-field potentials just before the propagated near-field nerve action potential was recorded at Erb's point. Both potentials were stationary waves with the same latency at all recording sites. The first potential had the same onset and peak latencies as the propagated wave at the axilla; it corresponded to the first component of the P9 far-field potential recorded with scalp to noncephalic reference montages. The latency of the second potential coincided with that of the propagated wave entering the neck and corresponded to the peak of the P9 potential. The occurrence of these potentials where there are significant changes in the morphology of the volume conductor suggests that the P9 far-field potential is due to a change in the conducting medium that surrounds the nerve.     

Subcortical, thalamic and cortical somatosensory evoked potentials to median nerve stimulation

Subcortical and cortical somatosensory evoked potentials (SEPs) to median nerve stimulation were studied in 16 normal controls, 3 patients with Parkinson's disease, and 2 patients with thalamic lesions. Multiple electrodes were placed over the scalp and cervical spines and connected with a hand electrode or Fz in grid II. Thalamic SEPs were recorded directly from the Vim nucleus in 3 patients with Parkinson's disease during the stereotaxic operation. SEPs recorded from the scalp-hand derivations were composed of 4 negative (N9, N11, N16, N18) and 3 positive potentials (P8, P10, P12), whereas, at the scalp-Fz electrode, only one negative peak was identified (N20). N18 is of higher amplitude on the parieto-occipital areas and corresponds to N20. On the other hand, N16 can be identified more clearly on the fronto-central areas at scalp-hand derivations because of intermixture with N18 on the posterior head areas and disappears at scalp-scalp derivation. This suggests that N16 represents a subcortical component that is picked up as a far-field potential at the scalp electrodes. Components preceding N16 at scalp-hand derivations are also interpreted as far-field potentials because of their short latency and wide distribution over the scalp. The peak latency of N16 is not significantly different from the major negativity recorded directly from the thalamus, whereas N18 (N20) occurs significantly later. From this we conclude that N16 is most probably generated in the thalamus with the potentials of shorter latency originating caudal to the thalamus and N18 rostral to the thalamus.     

Auditory event-related potentials in the squirrel monkey: Parallels to human late wave responses

Event-related potentials (ERPs) were recorded from the brain surface in squirrel monkeys during the presentation of two auditory stimulus paradigms which have previously been utilized to elicit scalp-recorded ERPs in humans. In the first paradigm, inter-stimulus interval (ISI) was systematically varied during the presentation of a series of tone pips. The tones produced a negative (70 ms)-positive (130 ms) sequence of components similar in morphology to the human scalp-recorded N1-P2 'vertex' potential. The amplitude of the N70 and P130 components recorded from midline electrodes decreased with decreasing ISI, as previously shown for the human vertex potential. However, this amplitude change with ISI was not observed in ERPs recorded from lateral frontal and temporal electrodes. These results agree with previous studies of monkeys and humans which suggest at least two different sources contribute to N1-P2 components recorded in response to tones. The effects of stimulus probability and novelty on ERP morphology and amplitude were studied in the second paradigm. ERPs elicited by frequent (P = 0.92) and infrequent (P = 0.08) tone pips presented in an unpredictable order were compared. N70 - P130 components were produced by both stimuli, and the infrequent stimuli also elicited a broad, long latency (300 ms) positive complex that decreased in amplitude with repeated presentations. In humans the same infrequent auditory stimuli produce a frontally distributed late positive component that has been interpreted as indicating the activation of orientation mechanisms or of a 'mismatch detector'. These data suggest that in these paradigms squirrel monkeys exhibit ERPs which are similar in several respects to ERPs recorded to identical stimuli in humans.     

Cervical somatosensory evoked potentials in the healthy subject: analysis of the effect of the location of the reference electrode on aspects of the responses

Cervical SEPs were recorded in 111 normal subjects following stimulation of the median nerve at the wrist, using 3 different sites for the reference electrode (Fz, earlobe, shoulder). It was shown that cephalic reference electrodes (Fz or earlobe) modify the wave form of the cervical response, because they pick up far-field SEPs (P9, P11, P13, P14) originating from cervical roots, spinal cord and brainstem. These far-field SEP components are injected as negativities in the activity recorded by the cervical electrode. The responses recorded with cephalic reference differ from those recorded at the same cervical site, with a non-cephalic reference in 3 main points: (1) the amplitude of negative components N11 and N13 is increased; (2) the onset latency of N11 is significantly shorter; (3) an N14 negativity is added, the origin of which is probably in the brainstem; this component may occupy the peak of the cervical negativity; thus the central conduction time, calculated as the time interval between N14 and N20, does not take into account the time for spinal propagation of the somatosensory afferent inputs. A topographic study of cervical responses in 10 normal subjects showed an increase of the onset latency of N11 (mean 0.89) from the lower cervical region to the cervico-occipital junction, provided that a non-cephalic reference is used. This result suggests that N11 corresponds to the travelling of action potentials in the ascending spinal somatosensory pathways. The use of a medio-frontal (Fz) reference electrode results in: (1) a masking of the latency shift of N11 latency because of the subtraction of the far-field Fz-recorded P11 component, the onset of which was found to be synchronous with the entry of afferent volleys in the lower cervical spinal cord; (2) a modification of the spatial organization of the responses, due to the subtraction of far-field scalp-recorded positivities P9, P11, P13 and P14, that creates negative N9, N11, N13 and N14 potentials far below the level where cervical roots enter the spinal cord.     

Far-field potentials in cylindrical and rectangular volume conductors

The occurrence of a transient dipole is one method of producing a far-field potential. This investigation qualitatively defines the characteristics of the near-field and far-field electrical potentials produced by a transient dipole in both cylindrical and rectangular volume conductors. Most body segments of electrophysiologic interest such as arms, legs, thorax, and neck are roughly cylindrical in shape. A centrally located dipole generator produces a nonzero equipotential region which is found to occur along the cylindrical wall at a distance from the dipole of approximately 1.4 times the cylinder's radius and 1.9 times the cylinder's radius for the center of the cylinder. This distance to the equipotential zone along the surface wall expands but remains less than 3.0 times the cylindrical radius when the dipole is eccentrically placed. The magnitude of the equipotential region resulting from an asymmetrically placed dipole remains identical to that when the dipole is centrally located. This behavior is found to be very similar in rectangular shallow conducting volumes that model a longitudinal slice of the cylinder, thus allowing a simple experimental model of the cylinder to be utilized. Amplitudes of the equipotential region are inversely proportional to the cylindrical or rectangular volume's cross-sectional area at the location of dipolar imbalance. This study predicts that referential electrode montages, when placed at 3.0 times the radius or greater from a dipolar axially aligned far-field generator in cylindrical homogeneous volume conductors, will record only equipotential far-field effects.     

Motor unit action potential components and physiologic duration.

Motor unit action potentials (MUAPs) recorded from the same motor unit at two distances along the biceps brachii muscle with monopolar needle electrodes at high amplifier gains (20 microV/division) and averaged 2000-3000 times reveal total potential durations of 39.6 +/- 4.6 ms. In addition, the terminal segment for each of these two MUAPs contained a late far-field potential with a mean duration of 23.8 +/- 4.1 ms. Computer simulations of MUAPs suggest that this long-duration positive far-field mirrors the true morphology of the intracellular action potential (IAP), which is monophasic positive, possessing a terminal repolarization phase approaching 30 ms. This investigation suggests that the MUAP's physiologic duration is directly proportional to the muscle fiber length and the IAP's duration, which becomes manifest as a positive far-field potential when the IAP encounters the musculotendinous junction and slowly dissipates. The leading/trailing dipole model is used to explain qualitatively this study's quantitative clinical and computer simulation findings.     

Morphological characteristics of the scalp far-field potentials evoked by median nerve stimulation in infants and children.

We investigated the somatosensory evoked potentials (SEPs) produced by median nerve stimulation in normal infants, children and adults, focussing upon the wave forms of the scalp far-field potentials (FFPs). In adolescents and adults, 3 or 4 positive FFPs preceded the widespread N18 component on the scalp, corresponding to P9, P11, P13 and P14 (or P13-14). In infants and children, however, the scalp FFPs often included 5 positive waves, the initial three of which were characteristically sharp and brief. This distinctive wave form, with 5 positive FFPs, was correlated with an Erb's potential having a bipeaked negative phase. We studied the temporal relationship of the 5 positive FFPs to the Erb's potential and the cervical SEPs and concluded that the initial 3 brief positive waves were produced by overlapping of a bipeaked "P9" and bipeaked "P11." Both "P9" and "P11" are stationary waves that are thought to originate in the first-order afferents, so they probably reflect the bipeaked appearance of the compound nerve action potential.     

Sensory and movement-related cortical potentials in nociceptive and auditory reaction time tasks

The processing of a sensory stimulus leading to a simple motor command was studied with scalp-recorded long latency cortical potentials in humans. Two sensory modalities were tested in their ability to activate descending motor pathways: auditory stimuli and painful cutaneous stimuli produced by a CO2 laser. Subjects were asked to react to stimuli with voluntary index finger movements. The stimulus-related and movement-related cortical potentials were recorded simultaneously with five midline electrodes on the scalp. The auditory reaction time, measured from the stimulus to the onset of electromyogram (EMG), was faster (150 ms) than the laser reaction time (350 ms). The onset of EMG of finger movements occurred only after the first negative components following auditory or laser stimuli but before the positive components. The latency from the auditory negativity to the onset of EMG was about 50 ms and the latency from the laser negativity to the onset of EMG was about 110 ms. This finding indicates that not only the peripheral afferent conduction but also central processing takes longer in a pain-related somatosensory task than in an auditory task. The frontal peak of Motor Potential (fpMP), a cortical potential related to the sensory feedback from movement, occurred with a constant latency after the onset of EMG (100 ms) and was unaffected by the task.     

Auditory input to the pedunculopontine nucleus: I. Evoked potentials

The pedunculopontine nucleus (PPN) has been implicated in sleep-wake control, arousal responses, and motor functions. The PPN also has been implicated in the generation of the 1311 middle-latency auditory-evoked potential. The present study was undertaken to determine the topographical distribution, threshold, and response properties of depth-recorded potentials following auditory click stimulation. Experiments were conducted in both decerebrate cat and rat, with a view towards determining the presence of P1-like middle-latency auditory-evoked potentials in the midbrain of both species. These results demonstrate a) the presence in and around the PPN of a P1-like potential in the decerebrate rat similar to that described in the accompanying article as the P13 in the intact rat; b) the presence in and around the PPN of a P1-like potential in the decerebrate cat similar to that previously described by others as wave A in the intact cat; c) although thresholds for these potentials were similar to those of intact preparations, following frequencies were higher in the decerebrate preparations, i.e., responsiveness to repetitive stimulation was higher, and d) depth-recorded somatosensory-evoked potentials also were studied in the cat and found to show an evoked potential at a similar latency as middle-latency auditory depth-recorded potentials. These findings suggest that click stimulus-evoked, depth-recorded potentials are present in and around the PPN in the decerebrate rat and cat, i.e., in the absence of cortex, at a similar latency as in intact preparations.     

Experimental study on the origins of far-field SEP to median nerve stimulation in the cat

Results of various experimental and clinical studies on the origins of somatosensory evoked potentials (SEP) suggested that the far-field and early near-field potentials are generated primarily from sources within the dorsal column-medial lemniscal system. However, there are a few studies where direct depth recordings of SEP were performed and they were compared with surface-recorded SEP components. The purpose of this investigation is to determine the origins of somatosensory far-field and early near-field evoked potentials in cat by the analysis of distribution mode of surface-recorded SEPs, the comparison of depth recorded with surface-recorded SEPs and by the study of SEP changes caused by serial destruction of the structures relating to sensory pathway. A complex patterns of evoked potentials were recorded from cerebral epidural surface in cat by forelimb median nerve stimulation. The largest positive to negative slope was recorded from the epidural electrode on the sensory cortex contralateral to the stimulation. Five small positive potentials could be identified on the positive slope. We labeled these potentials as I, II, IIIA, IIIB, IV according to the report by Iragui-Madoz. The largest positive potential recorded from the VPL was coincident with the surface-recorded IIIB in latency at different interstimulus intervals. After transection of the midbrain-pons junction, IIIA remained unchanged, and the following waves disappeared. However, IIIA decreased in latency and markedly decreased in amplitude after transection of the pons at its rostral level. IIIA seems to be generated from the medial lemniscus at the level of osseous cerebellar tentorium.(ABSTRACT TRUNCATED AT 250 WORDS)     

Origin of the "N10" stationary-field potential after median nerve stimulation.

The scalp far-field potentials after median nerve stimulation at the wrist consist of P9, P11, P13, and P14 positive components. Earlier, Emerson et al. (1984) identified the "N10" negative potential in-between the P9 and P11 and claimed that this was not merely a passive return to the baseline after the P9 positive deflection but a distinct component reflecting a proximal brachial plexus volley. They thought N10 was a far-field potential having widespread distribution with a fixed latency. In this study we found that N10 was of higher amplitude after median nerve stimulation at the elbow than after stimulation at the wrist. Indeed the N10 latency was fixed from the lower anterior neck to the scalp, and its amplitude was maximum at the anterior lower neck. The latency of N10 was about 0.3 milliseconds longer than the Erb's potential and 0.15 milliseconds longer than the potential recorded from the lateral neck on the side of stimulation. The N10 amplitude increased in parallel with increased stimulus intensity. In order to explore the origin of the N10 stationary field potential, we designed a paired stimuli paradigm applied to the wrist (S1) and to the elbow (S2). The interstimulus interval between S and S2 was adjusted so that the timing of S2 was immediately after the traveling impulse produced by the S1 stimulus as it passed through the S2 stimulus site. This technique allowed stimulation of the anterior interosseous nerve selectively at the elbow while the median nerve originating from the wrist was undergoing refractory period. The response of (S1 + S2) - S1 showed only the N10 with absence of cervical and cortical responses, implying that N10 was activated, predominantly by the interosseous nerve, i.e., an antidromic motor volley, when the median nerve was stimulated at the elbow.     

Cognitive evoked potentials to anticipated oesophageal stimulus in humans: quantitative assessment of the cognitive aspects of visceral perception

Evoked potential studies provide an objective measure of the neural pathways involved with perception. The effects of cognitive factors, such as anticipation or awareness, on evoked potentials are not known. The aim was to compare the evoked potential response to oesophageal stimulation with the cortical activity associated with anticipation of the same stimulus. In 12 healthy men (23.5 +/- 4 years), oesophageal electrical stimulation (15 mA, 0.2 Hz, 0.2 msec) was applied, and the evoked potentials recorded using scalp electrodes. A computerized model of randomly skipped stimuli (4:1 ratio) was used to separately record the evoked potentials associated with stimulation and those associated with an anticipated stimulus. The electrical stimulus represented the nontarget stimulus and the skipped impulse the target (anticipatory) stimulus. This anticipatory evoked potential was also compared to auditory P300 evoked potentials. Reproducible evoked potentials and auditory P300 responses were elicited in all subjects. Anticipatory evoked potentials (peak latency 282.1 +/- 7.9 msec, amplitude 8.2 +/- 0.7 microV, P < 0.05 vs auditory P300 evoked potential) were obtained with the skipped stimulus. This anticipatory evoked potential was located frontocentrally, while the auditory P300 potential was located in the centro-parietal cortex. The anticipatory evoked potential associated with expectation of an oesophageal stimulus, although of similar latency to that of the auditory P300 evoked response, originates from a different cortical location. The recording of cognitive evoked potentials to an expected oesophageal stimulus depends on attention to, and awareness of, the actual stimulus. Anticipatory evoked potentials to GI stimuli may provide an objective electrophysiological tool for the assessment of the cognitive factors associated with visceral perception.     

The cervical somatosensory evoked potential in man: far-field, conducted and segmental components

Somatosensory evoked potentials (SEPs) to median nerve stimulation were recorded from neck and scalp electrodes in 23 normal adults using cephalic and non-cephalic (knee) references simultaneously. With a cephalic reference, the neck SEP consisted of several 'negative' potentials that had the same latency at all recording locations. Simultaneous recordings from neck-scalp, neck-knee and scalp-knee derivations demonstrated that scalp far-field potentials significantly contributed to neck-to-scalp recordings and obscured the cervical SEPs. With a non-cephalic reference, the neck SEP consisted of a prominent positive wave (P9) followed by a large negative component (N13). A small positive potential, P10, seen in the lower neck, gradually increased in latency and amplitude from lower to upper neck and appeared as a P11 potential at upper cervical levels. In lower neck recordings, a negative wave, N11, was also present and in some subjects exhibited a latency shift from lower to upper neck. P9, P11 and N11 had a short refractory period suggesting a presynaptic origin whereas N13 had a longer refractory period indicating a postsynaptic generator. The consensus that P9 originates in the peripheral nervous system is consistent with its rapid recovery cycle. The bipolar characteristics of N11 and P11 as well as their latency shift and their short recovery cycle suggest that they reflect activity in the cervical dorsal columns. N13, that displayed no latency shift and had a longer recovery cycle, may originate in spinal cord dorsal horn interneurons.     

Far-field potentials in circular volumes: the effect of different volume sizes and intercompartmental openings.

Preliminary investigations of circular volume conductors suggested that far-field potential magnitude declines progressively slower with increasing radial distance from a current source and follows a cosine function with angular displacement of the recording electrode from the electrical generator's axis. Using circular volumes of 6 differing radii, the mathematical relationship between angle, radii, and far-field potential amplitude is determined. Previous theoretical relationships of amplitude versus dipolar spacing, current, and distance from a dipole generator in a bounded volume conducting medium are verified for the near-field. Far-field potentials in circular volumes are found to become constant at radii greater than 75% of the bounded volume's radius. Additionally, an adjoining volume conductor acts simply as a passive fluid-filled electrode (wick electrode) to the circular volume containing the generator until the intercompartmental opening to the circular volume exceeds 20% of its circumference. This finding was clinically supported by recording similar P9 somatosensory-evoked far-field potentials generated caudal to the foramen magnum from various portions of the cranium, whose connections to the torso, foramen magnum, and neck, average 6.2% and 17.8%, respectively. Finally, 3 circular volume conductors were connected in series by channels less than 20% of the volume conductor's circumference. Both adjoining circular volumes were equipotential to the far-field potential present at the boundary of the first circular volume containing the dipole generator. This observation supports the clinical finding of far-field potential transmission through multiple human bodies in conductive contact.