Effect of forward masking on evoked potentials of auditory cortex in guinea pigs

Thresholds of the event-related potentials (ERPs) appearance were measured for one stationary and four moving auditory images presented in silence or under forward masking conditions. The difference between thresholds in silence and after noise masker was considered as masking level. Under the forward masking, the amplitude of the ERP to the first click in the test series decreased in guinea pig auditory cortex. Masking level decreased with the time lag between signal and masker and didn't depend on the fused auditory image localization that corresponded to the first click in different test signals. This fact can support the hypothesis that for the long test signals the initial part can be masked more than the final one. The ERPs amplitude to next clicks in test series depended on interaction of two factors: forward masking in the "masker-signal" system and interaction of separate ERPs in the series evoked by the test signal.     

The effect of the rate of movement of a sound image on human long-latency auditory evoked potentials

In 10 healthy subjects, studies have been made on changes in amplitude-temporal characteristics of N1-P2 components at different rates of movement of a sound image (3.14, 1.57 and 0.78 rad/s). It was shown that only movement of the sound image from the right ear to the median line of the head with sufficiently high rate (3.14 rad/s) results in the increase in total peak amplitude of N1-P2 components relatively similar parameters obtained during the effect of a resting sound image lateralized at the same ear. Latent periods of N1 component in both hemispheres are longer during the effect of the moving sound image than during the effect of the resting lateralized one, although with the decrease in the rate the difference becomes less significant. It is suggested that the right hemisphere is more sensitive to changes in the rate of movement of the sound image.     

Changes in components of the auditory long-latency evoked potentials at different stages of the slow-wave sleep

In accordance with the present views, during sleep, analysis of external stimuli continues at the subconscious level, because the need to estimate the biological significance of external stimuli in order to maintain a flexible contact of a sleeping subject with the environment persists during sleep. It is known that new components of the auditory evoked potentials (AEP) appear as sleep deepens. However, the common procedure of analysis of event-related potentials averaged for a group of subjects has some drawbacks because of the interindividual variability of the event-related potentials. Therefore, an additional analysis of the interindividual variability of the AEP shape and component structure can simplify the detection of individual components of group-averaged AEP at different stages of the slow-wave sleep. The AEPs were recorded in healthy volunteers (n = 26) during falling asleep in the evening from eight EEG derivations (F3, F4, C3, C4, P3, P4, O1, O2) in reference to a linked mastoid electrode. Computer-generated sound stimuli (50 ms-pulses with the frequency of 1000 Hz, 60 dB HL) were presented binaurally through earphones with interstimulus intervals of 20-40 s. Selective summation of AEPs for all the subjects was performed for each stage of the slow-wave sleep individually for each of the eight derivations. It was shown that the account made for interindividual variability of the AEP shape facilitated the identification of individual components of the group-averaged AEP typical of wakefulness (P1, N1, P300) and those which appeared during sleep onset and at different stages of the slow-wave sleep (P2, N350, P450, N550, N900).     

The psychoacoustic phenomenon of masking level differences in the human subject studied by auditory evoked potentials

Auditory brainstem responses (ABRs), middle latency responses (MLRs), and slow cortical potentials (SCPs) were recorded in normal-hearing adults to trains of low-frequency acoustic signals delivered binaurally against a background of a continuous masking noise. Two stimulus conditions, labelled as binaural homophasic and binaural antiphasic paradigms, respectively, were systematically compared. In the homophasic paradigm both the signals and the masker were in-phase at two ears. In the antiphasic paradigm the signals were 180 degrees out-of-phase at two ears, while the masker was in-phase. The psychoacoustic release from masking in the antiphasic vs. the homophasic paradigm was regularly accompanied by an increase in amplitudes and a shortening in peak latencies of the SCPs. In contrast, no differences were evidenced between the homophasic and the antiphasic paradigms with respect to the ABRs and the MLRs. Considering the generation loci of the studied electric responses, it is concluded that the binaural psychoacoustic phenomenon, referred to as the masking level difference, is operated primarily at the cortical level.     

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.     

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.     

Habituation of auditory evoked potentials and emotional state

"Fast" and "slow" habituation of N1 and N1-P2 components of auditory evoked potentials was studied in healthy subjects and in depressed patients. In patients, initially more low amplitudes of N1 and N1-P2 were revealed, as well as slowing down of habituation in the beginning of stimuli series and acceleration to its end (in healthy people--the greatest habituation in the initial part of the series and amplitude increase at its end), the absence of power effect in the component N1 at reaching, in the process of habituation, of the same minimum parameters as in healthy subjects. This points to weakening of dishabituation process parallel with well expressed "slow" habituation in patients and allows to suggest at expressed negative emotions a deficit of attention processes as a result of "internal abstraction".     

Physiology-based modeling of cortical auditory evoked potentials

Evoked potentials are the transient electrical responses caused by changes in the brain following stimuli. This work uses a physiology-based continuum model of neuronal activity in the human brain to calculate theoretical cortical auditory evoked potentials (CAEPs) from the model’s linearized response. These are fitted to experimental data, allowing the fitted parameters to be related to brain physiology. This approach yields excellent fits to CAEP data, which can then be compared to fits of EEG spectra. It is shown that the differences between resting eyes-open EEG and standard CAEPs can be explained by changes in the physiology of populations of neurons in corticothalamic pathways, with notable similarities to certain aspects of slow-wave sleep. This pilot study demonstrates the ability of our model-based fitting method to provide information on the underlying physiology of the brain that is not available using standard methods.     

Nicotine receptor subtype-specific effects on auditory evoked oscillations and potentials

Background

Individuals with schizophrenia show increased smoking rates which may be due to a beneficial effect of nicotine on cognition and information processing. Decreased amplitude of the P50 and N100 auditory event-related potentials (ERPs) is observed in patients. Both measures show normalization following administration of nicotine. Recent studies identified an association between deficits in auditory evoked gamma oscillations and impaired information processing in schizophrenia, and there is evidence that nicotine normalizes gamma oscillations. Although the role of nicotine receptor subtypes in augmentation of ERPs has received some attention, less is known about how these receptor subtypes regulate the effect of nicotine on evoked gamma activity.

Methodology/Principal Findings

We examined the effects of nicotine, the α7 nicotine receptor antagonist methyllycaconitine (MLA) the α4β4/α4β2 nicotine receptor antagonist dihydro-beta-erythroidine (DHβE), and the α4β2 agonist AZD3480 on P20 and N40 amplitude as well as baseline and event-related gamma oscillations in mice, using electrodes in hippocampal CA3. Nicotine increased P20 amplitude, while DHβE blocked nicotine-induced enhancements in P20 amplitude. Conversely, MLA did not alter P20 amplitude either when presented alone or with nicotine. Administration of the α4β2 specific agonist AZD3480 did not alter any aspect of P20 response, suggesting that DHβE blocks the effects of nicotine through a non-α4β2 receptor specific mechanism. Nicotine and AZD3480 reduced N40 amplitude, which was blocked by both DHβE and MLA. Finally, nicotine significantly increased event-related gamma, as did AZD3480, while DHβE but not MLA blocked the effect of nicotine on event-related gamma.

Conclusions/Significance

These results support findings showing that nicotine-induced augmentation of P20 amplitude occurs via a DHβE sensitive mechanism, but suggests that this does not occur through activation of α4β2 receptors. Event-related gamma is strongly influenced by activation of α4β2, but not α7, receptor subtypes, while disruption of N40 amplitude requires the activation of multiple receptor subtypes.