Evoked potentials of the auditory cortex on paired stimuli

Changes in the responsiveness of the auditory cortex to an acoustic click and to direct stimulation of the medial geniculate body were studied by the method of evoked potentials in an extended experiment on cats with implanted electrodes. It is shown that the minimum interval between two stimuli for which a second click produces an EP in the auditory cortex is from 30 to 50 msec. The relative refractory period consists of two parts. The first (50–100 msec) is characterized by a rapid recovery, and the second (about 500 msec) by a slow recovery. In contrast with a click, direct stimulation of the geniculate body does not produce a refractory condition but one of facilitation. The effects of Nembutal and chloralose anesthesia and the state of alertness on the recovery of auditory cortex responsiveness were investigated. The reason for the absence and the reduction of an EP from the auditory cortex to a testing click during absolute and relative refractory periods is not a passive decrease of excitability of the usual refractory kind, but an active interplay of excitatory and inhibitory processes in the cerebral cortex, geniculate bodies, and reticular formation of the brain stem.A. A. Bogomolets' Institute of Physiology, Academy of Sciences, Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 1, No. 1, pp. 54–64, July–August, 1969.     

Age-related changes in human middle latency auditory evoked potentials

We recorded middle latency auditory evoked potentials (MAEPs) in young (20–40 years) and elderly (60–80 years) subjects with normal hearing. The Pa component was prolonged in latency and markedly enhanced in amplitude in the elderly subjects. No changes were found in Na, or in the binaural interaction of the MAEP. Differences in Pa amplitude and latency were not due exclusively to changes in auditory thresholds, since they were not duplicated by changes in stimulus intensity, and persisted when MAEPs from selected young and old subjects were compared at similar SPL levels. The enhancement of Pa amplitude appears to reflect age-related central modifications in auditory processing.     

Possible overlapping potentials of the auditory P50 in humans: factor analysis of middle latency auditory evoked potentials

The auditory P50 in humans may consist of overlapping potentials. To test this hypothesis, we manipulated the conditions of stimulus discrimination and motor response difficulty and evaluated the data by factor analysis. Twenty right-handed males (mean age 27 years) performed the following 4 tasks: (1) a counting task, (2) an easy Go, No-Go task, (3) a difficult Go, No-Go task, and (4) a choice reaction task. Middle latency auditory evoked potentials were obtained with 100 times summation triggered by the onset of the auditory stimulus. Four factors were extracted by factor analysis for a 0–100 ms time period. Factor 1, the maximum factor loading at 91 ms, corresponded to N1, and factor 4, the maximum factor loading at 23 ms, appeared to correspond to P30. The latency of the maximum factor loading in factor 2 was adjacent to that in factor 3, the latency of factor 2 being 12 ms earlier than that of factor 3. Factor 2 and factor 3 latencies were approximately 55 ms which corresponded to the P50. Factor 3 started rising at the point that factor 2 reached the maximum factor loading, and the factor score demonstrated a significant group difference only when analyzed by motor response criteria. These results suggest that the P50 in humans consists of overlapping potentials and that a part of the potential might relate to a motor response process.     

Evoked potentials of the auditory cortex of the porpoise,Phocoena phocoena

Summary Evoked potential (EP) recordings in the auditory cortex of the porpoise,Phocoena phocoena, were used to obtain data characterizing the auditory perception of this dolphin. The frequency threshold curves showed that the lowest EP thresholds were within 120–130 kHz. An additional sensitivity peak was observed between 20 and 30 kHz. The minimal EP threshold to noise burst was 3·10^–4–10^/s-3 Pa. The threshold for response to modulations in sound intensity was below 0.5 dB and about 0.1% for frequency modulations. Special attention was paid to the dependence of the auditory cortex EP on the temporal parameters of the acoustic stimuli: sound burst duration, rise time, and repetition rate. The data indicate that the porpoise auditory cortex is adapted to detect ultrasonic, brief, fast rising, and closely spaced sounds like echolocating clicks.Abbreviation EP evoked potential     

Effect of repetition rate on middle latency auditory evoked potentials in humans

Middle Latency Auditory Evoked Potentials (MLAEPs) were recorded from 15 healthy subjects in order to evaluate the influence of different repetition rates on the latency and the amplitude of their main components Na, Pa and Nb. MLAEPs were obtained from Cz-ipsilateral ear lobe by averaging responses to 2000 monaural clicks delivered to both ears, at 65 dB SL of intensity, for each of 3 different repetition rates (1.1, 4.1, 8.1 Hz). Time base was 100 ms, analogical band-pass filter 5-1000 Hz (off-line digital bandpass: 20-100 Hz). The statistical analysis (repeated measures analysis of variance), demonstrated that, the latency and the amplitude of the Nb component were slightly influenced by repetition rate while Pa and Na were not. Moreover Nb showed the greatest interindividual variability (as already pointed out by other authors too); thus, we suggest that a stimulus rate of 8.1 Hz and the analysis of Na and Pa component only, can be regarded as the best assessment for MLAEPs evaluation when they are used for clinical purposes.     

Effect of stimulus mode on middle latency auditory evoked potentials in humans

Middle Latency Auditory Evoked Potentials (MLAEPs) were recorded in 35 healthy subjects; all underwent monaural stimulation and 18 of them additionally underwent binaural stimulation. The aim of the study was to determine the effect of stimulus mode on MLAEP Na, Pa and Nb components and to assess normative data for clinical purposes. MLAEPs were respectively obtained from Cz-ipsilateral ear lobe (monaural mode) and from Cz-A1 and Cz-A2 (binaural mode) by twice averaging 1000 responses to 65 dBHL alternating clicks delivered at a repetition rate of 8.1 Hz. Time base was 100 msec; analogical band-pass filter setting was 5-1000 Hz (off-line digital badpass: 20-100 Hz). The statistical analyses (paired t-test, repeated measures analysis of variance) were not able to demonstrate any differences that derived from differing sides of stimulation (monaural mode) or from differing recording derivations (binaural mode); on the contrary, we demonstrated a slight increase in waveform amplitudes when the binaural mode was employed. In particular, we observed an increase in Na-Pa peak-to-peak amplitude, whereas Pa-Nb amplitude was unmodified. This finding is explicable in terms of a binaural interaction effect. Finally, we propose some guidelines for the correct performance and evaluation of MLAEPs in clinical practice.     

Analysis of the middle latency evoked potentials to angular acceleration impulses in man

The middle latency vestibular evoked potential (ML-VsEP) recorded with scalp electrodes in man in response to impulses of angular acceleration is dominated by a forehead positive peak at about 15 ms and a negative peak at about 20 ms; the peak amplitude of this component is about 30 μV. This is followed by slower, smaller amplitude activity. The latency of this initial peak is similar to the latency of the vestibulo-ocular reflex (VOR) in monkeys. The present study was undertaken to elucidate the possible relation between the ML-VsEPs and VOR. This included recordings from forehead-mastoid electrodes (sites used to record VsEP) and other scalp electrodes and the recording of potentials due to eye movement: the electro-oculogram. Direct recording of eye movements was also conducted using an infra-red reflection device in those experiments in which the head was not moved. The recordings were conducted in man during vestibular stimulation eliciting VsEPs, during voluntary eye movements and during caloric and optokinetic stimulation. These experiments indicated that the 15–20 ms component of the ML-VsEP was not due to movements of the eye (corneoretinal dipole). The large amplitude 15–20 ms component of the ML-VsEP was similar in general magnitude, waveform, polarity, duration and rise time to the highly synchronous pre-saccadic spike (neural and/or myogenic) which precedes nystagnys and voluntary saccades. It therefore probably represents vestibular-initiated electrical activity in motor units of the extra-ocular muscles which then produce anti-compensatory saccades.     

体温过高对大鼠脑干听觉诱发电位和中潜伏期反应的影响

目的 :探讨体温过高对大鼠脑干听觉诱发电位 (BAEP)和听觉中潜伏期反应 (MLR )的影响。方法 :诱发电位仪颅表记录大鼠BAEP和MLR ;体表物理升温法逐步升高麻醉大鼠体温 ,传感探头式数字体温计监测大鼠直肠体温 ;主要观察BAEP和MLR的波峰潜伏期 (PL)、波峰间潜伏期 (IPL)和波幅随体温升高而发生的变化及它们消失的临界体温。结果 :BAEP各波PL及Ⅰ Ⅱ、Ⅰ Ⅲ、Ⅰ ⅣIPL随体温升高 ( 3 7～ 41.5℃ )而逐步缩短 ,但当体温升高至 42℃和超过 42℃时各波PL及Ⅰ Ⅱ、Ⅰ ⅣIPL不再继续缩短 ,并略有反向延长 ;MLR各波PL和P1 P3、P2 P3IPL也随体温升高 ( 3 7～ 43℃ )而缩短。随体温升高 ,BAEP和MLR波幅的主要表现为降低 ,特别是在体温升高至42℃以后。BAEP和MLR在体温 ( 4 3 .1± 0 .5)℃时出现不可逆性消失 ,且两者同步消失。结论 :体温过高对大鼠BAEP和MLR有相似的显著影响 ,体温过高至一临界值时会造成BAEP和MLR的不可逆性损害。     

Comparison of evoked potentials to tones and clicks recorded simulataneously by multiple electrodes from the auditory cortex in unanesthetized cats

Evoked potentials to tones and clicks were recorded simultaneously from seven points of the auditory cortex and one or two points of the somatosensory cortex in unanesthetized cats. Comparison of evoked potentials to tones of equal loudness in the 250–7000 Hz band showed no common pattern of cortical tonotopic distribution. However, an individual dependence of the components of the evoked potential on pitch and on localization of the recording point exists for each animal. With a change in stimulus intensity the absolute and relative values of these components of the evoked potential vary. The initial positive waves are the most variable; besides the two waves already known a third, intermediate wave, particulary sensitive to loudness, was discovered. The negative wave of the primary response increases proportionally to loudness. Evoked potentials to clicks are more uniform over the auditory cortex and more stable than those to tones. Responses appeared in the somatosensory cortex to loud stimuli, more regularly to clicks than to tones. It is concluded that the parameter of pitch is reflected in the cat cortex as a complex spatially-individual distribution of the amplitude and time parameters of the evoked potentials.I. P. Pavlov Institute of Physiology, Academy of Sciences of the USSR, Leningrad. Translated from Neirofiziologiya, Vol. 7, No. 2, pp. 115–125, March–April, 1975.     

Comparison in man of short latency averaged evoked potentials recorded in thalamic and scalp hand zones of representation

Recordings were performed in the thalamus of 13 patients suffering from either abnormal movements or intractable pain, with the aim of delimiting the region to be destroyed or stimulated in order to diminish the syndrome. In 11 of these patients averaged evoked potentials were recorded simultaneously from the scalp and specific thalamus (VP) hand area levels following median nerve stimulation. These recordings were done during the operation or afterwards when an electrode was left in place for a program of stimulation.The latencies of onsets and peaks on the scalp ‘P15’ were compared with those of the VP wave; a clear correspondence was found. Moreover, when increased stimulation was used, both waves began to develop in parallel. Thus in the contralateral ‘P15’ a component exists due to the field produced by the thalamic response. To explain the presence of an ipsilateral scalp ‘P15’ wave, we propose that a second wave having the same latency and a slightly shorter peak exists on the scalp due to a field produced by a brain-stem response. This double origin of ‘P15’ is also shown by the different changes which the ipsilateral and contralateral waves present during changes in alertness.The scalp ‘N18–N20’ is also composed of at least 2 components. The first peak appears on the scalp with a latency shorter than that of the negativity which develops in the thalamus. The N wave, moreover, increases in latency with rapid stimulus repetition. We propose with others that ‘N18’ is a cortical event reflecting the arrival of the thalamo-cortical volley. The second component, ‘N20,’ has a peak latency closely correlated to that of the thalamic negativity. This component was present alone in ‘N’ when rapid stimulation (> 4/sec) was used, which did not change the thalamic response. It must be a field produced by the thalamic negativity.     

Sequential mapping favours the hypothesis of distinct generators for Na and Pa middle latency auditory evoked potentials

The temporo-spatial organization of Na and Pa middle latency auditory components evoked by monaural clicks delivered separately to right and left ears was assessed by sequential mapping of scalp potentials. The potential field distribution was found to be different for the two components and was assessed by calculating the maximal potential differences in the Na/Pa time period. These data are compatible with the hypothesis that distinct generators are responsible for the two components. Scalp potential field configuration observed for Na suggests a deep generator, which could be situated at the mesencephalic or diencephalic level. Bilateral cortical generators tangentially orientated satisfactorily account for the distribution of the Pa potential field, which could be related to simultaneous activation of both supratemporal auditory cortices in response to monaural stimulation.     

Evoked potentials and unit activity in the cat somatosensory cortex

Investigation of unit activity of the cat somatosensory cortex has shown that the principal role in the genesis of the primary response, the response to stimulation of the thalamic relay nucleus, the callosal response, and certain other forms of evoked potentials (EPs) of the somatosensory cortex is played by neurons not usually responding by spike generation during EP development. The EPs reflect what the cortical neurons received from the afferent volley, and the level of their polarization, but they are not a reliable indicator of fast nervous processes in the cerebral cortex. The EPs reflect postsynaptic potentials (PSPs) of neurons not directly participating actively in the analysis of information reaching the cortex.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 2, No, 4, pp. 360–367, July–August, 1970.     

Intracranial and extracranial recordings of the auditory middle latency response

Simultaneous epidural and cortical depth recordings of the auditory middle latency reponse (MLR) were obtained from 18 anesthetized guinea pigs. Microelectrodes were advanced at a right angle to the cortical surface at sites shown to be optimal for recording surface MLRs.Transcortical polarity reversals of waves A (14 msec) and B (24 msec) of the MLR were recorded in depth penetrations initiated at sites on the temporal lobe with large amplitude surface potentials. In 6 of 18 penetrations yielding phase inversions, wave polarities changed abruptly as microelectrodes were advanced into the cortex. In the remaining penetrations, the reversals were preceded by gradual decreases in wave latencies at progressively deep sites. As electrodes were advanced beyond the depth at which polarity reversals were encountered, decreases in amplitude and only minor changes in latency were observed.Surface and depth MLR activity were temporarily eliminated immediately after electrolytic lesions were made at polarity reversal sites. Recovery of responses occurred within 30–60 min. Lesions produced in penetrations initiated at sites with no surface MLR activity had no effect. Histologic examination confirmed the location of the phase reversal sites as being within grey matter of the temporal lobe.These results are consistent with previous investigations in experimental animals which demonstrated transcortical polarity reversals, and provide evidence for dipolar generating systems of the early components of the MLR at the cortical level.