Sec Stimulus Research Articles

Quantifying tissue temperature changes induced by infrared neural stimulation: numerical simulation and MR thermometry.

Infrared neural stimulation (INS) delivered via short pulse trains is an innovative tool that has potential for us use for studying brain function and circuitry, brain machine interface, and clinical use. The prevailing mechanism for INS involves the conversion of light energy into thermal transients, leading to neuronal membrane depolarization. Due to the potential risks of thermal damage, it is crucial to ensure that the resulting local temperature increases are within non-damaging limits for brain tissues. Previous studies have estimated damage thresholds using histological methods and have modeled thermal effects based on peripheral nerves. However, additional quantitative measurements and modeling studies are needed for the central nervous system. Here, we performed 7 T MRI thermometry on ex vivo rat brains following the delivery of infrared pulse trains at five different intensities from 0.1-1.0 J/cm2 (each pulse train 1,875 nm, 25 us/pulse, 200 Hz, 0.5 s duration, delivered through 200 µm fiber). Additionally, we utilized the General BioHeat Transfer Model (GBHTM) to simulate local temperature changes in perfused brain tissues while delivering these laser energies to tissue (with optical parameters of human skin) via three different sizes of optical fibers at five energy intensities. The simulation results clearly demonstrate that a 0.5 second INS pulse train induces an increase followed by an immediate drop in temperature at stimulation offset. The delivery of multiple pulse trains with 2.5 s interstimulus interval (ISI) leads to rising temperatures that plateau. Both thermometry and modeling results show that, using parameters that are commonly used in biological applications (200 µm diameter fiber, 0.1-1.0 J/cm2), the final temperature increase at the end of the 60 sec stimuli duration does not exceed 1°C with stimulation values of 0.1-0.5 J/cm2 and does not exceed 2°C with stimulation values of up to 1.0 J/cm2. Thus, the maximum temperature rise is consistent with the thermal damage threshold reported in previous studies. This study provides a quantitative evaluation of the temperature changes induced by INS, suggesting that existing practices pose minimal major safety concerns for biological tissues.

Assessment and Classification of Mental Workload in the Prefrontal Cortex (PFC) Using Fixed-Value Modified Beer-Lambert Law

Optical-neuro-imaging based functional Near-Infrared Spectroscopy (fNIRS) has been in use for several years in the fields of brain research to measure the functional response of brain activity and apply it in fields such as Neuro-rehabilitation, Brain-Computer Interface (BCI) and Neuro-ergonomics. In this paper we have enhanced the classification accuracy of a Mental workload task using a novel Fixed-Value Modified Beer-Lambert law (FV-MBLL) method. The hemodynamic changes corresponding to mental workload are measured from the Prefrontal Cortex (PFC) using fNIRS. The concentration changes of oxygenated and deoxygenated hemoglobin (Δc HbO (t) and Δc HbR (t)) of 20 participants are recorded for mental workload and rest. The statistical analysis shows that data obtained from fNIRS is statistically significant with p 1.97 at confidence level of 0.95. The Support Vector Machine (SVM) classifier is used to discriminate mental math (coding) task from rest. Four features, namely mean, peak, slope and variance, are calculated on data processed through two different variants of Beer-lambert Law i.e., MBLL and FVMBLL for tissue blood flow. The optimal combination of the mean and peak values classified by SVM yielded the highest accuracy, 75%. This accuracy is further enhanced using the same feature combination, to 94% when those features are calculated using the novel algorithm FV-MBLL (with its optical density modelled form the first 4 sec stimulus data). The proposed technique can be effectively used with greater accuracies in the application of fNIRS for functional brain imaging and Brain-Machine Interface.

Sleep deprivation and time-on-task performance decrement in the rat psychomotor vigilance task.

The rat psychomotor vigilance task (rPVT) was developed as a rodent analog of the human psychomotor vigilance task (hPVT). We examined whether rPVT performance displays time-on-task effects similar to those observed on the hPVT. The rPVT requires rats to respond to a randomly presented light stimulus to obtain a water reward. Rats were water deprived for 22 h prior to each 30-min rPVT session to motivate performance. We analyzed rPVT performance over time on task and as a function of the response-stimulus interval, at baseline and after sleep deprivation. The study was conducted in an academic research vivarium. Male Long-Evans rats were trained to respond to a 0.5 sec stimulus light within 3 sec of stimulus onset. Complete data were available for n = 20 rats. Rats performed the rPVT for 30 min at baseline and after 24 h total sleep deprivation by gentle handling. Compared to baseline, sleep deprived rats displayed increased performance lapses and premature responses, similar to hPVT lapses of attention and false starts. However, in contrast to hPVT performance, the time-on-task performance decrement was not significantly enhanced by sleep deprivation. Moreover, following sleep deprivation, rPVT response times were not consistently increased after short response-stimulus intervals. The rPVT manifests similarities to the hPVT in global performance outcomes, but not in post-sleep deprivation effects of time on task and response-stimulus interval.

Comparison of Diagnostic Accuracy between Octopus 900 and Goldmann Kinetic Visual Fields

Purpose. To determine diagnostic accuracy of kinetic visual field assessment by Octopus 900 perimetry compared with Goldmann perimetry. Methods. Prospective cross section evaluation of 40 control subjects with full visual fields and 50 patients with known visual field loss. Comparison of test duration and area measurement of isopters for Octopus 3, 5, and 10°/sec stimulus speeds. Comparison of test duration and type of visual field classification for Octopus versus Goldmann perimetry. Results were independently graded for presence/absence of field defect and for type and location of defect. Statistical evaluation comprised of ANOVA and paired t test for evaluation of parametric data with Bonferroni adjustment. Bland Altman and Kappa tests were used for measurement of agreement between data. Results. Octopus 5°/sec perimetry had comparable test duration to Goldmann perimetry. Octopus perimetry reliably detected type and location of visual field loss with visual fields matched to Goldmann results in 88.8% of results (K = 0.775). Conclusions. Kinetic perimetry requires individual tailoring to ensure accuracy. Octopus perimetry was reproducible for presence/absence of visual field defect. Our screening protocol when using Octopus perimetry is 5°/sec for determining boundaries of peripheral isopters and 3°/sec for blind spot mapping with further evaluation of area of field loss for defect depth and size.

Quantitative assessment of cutaneous C‐fiber function in human skin via direct sudomotor activation

Small sympathetic cholinergic C‐fiber function was examined using intradermal electrical stimulation to activate sudomotor nerves in the forearm skin of healthy humans. We measured local sweat rate (SR) with a 0.7 cm2 capsule containing a humidity sensor and a thermocouple and flushed with dry gas. Two small stainless steel needles were place into the skin (7 mm apart, 2 mm deep) and stimulated at a constant current intensity of 2.5 mA for 30 s and 120 s at frequencies of 0.2, 1, 2, 4, 8, 16, 32, and 64 Hz. The stimulus‐response characteristics were evaluated using a non‐linear four‐parameter logistic curve fitting equation. Peak local SR occurred between 32 and 64 Hz and was similar for 30 and 120 s stimulus duration averaging 0.46 ± 0.2 and 0.49 ± 0.2 mg • min−1 • cm−2, respectively. The EC50 averaged 8.3 ± 0.3 Hz during the 30 sec stimulus but decreased to 3.6 ± 0.05 Hz (p<0.05) during the 120 s stimulus. The area under the SR‐time curve following atropine sulfate (2 μg/ml) was lower than control (p<0.05) and not different from zero. These data support the hypothesis that the SR response to intradermal electrical stimulation reflects, exclusively, the effect of direct depolarization of sympathetic cholinergic C‐fibers and release of acetylcholine. As such, this model can be used to provide a quantifiable assessment of small C‐fiber function in human skin.

Kv3 Potassium Conductance is Necessary and Kinetically Optimized for High-Frequency Action Potential Generation in Hippocampal Interneurons

Kv3 channels are thought to be essential for the fast-spiking (FS) phenotype in GABAergic interneurons, but how these channels confer the ability to generate action potentials (APs) at high frequency is unknown. To address this question, we developed a fast dynamic-clamp system (approximately 50 kHz) that allowed us to add a Kv3 model conductance to CA1 oriens alveus (OA) interneurons in hippocampal slices. Selective pharmacological block of Kv3 channels by 0.3 mm 4-aminopyridine or 1 mm tetraethylammonium ions led to a marked broadening of APs during trains of short stimuli and a reduction in AP frequency during 1 sec stimuli. The addition of artificial Kv3 conductance restored the original AP pattern. Subtraction of Kv3 conductance by dynamic clamp mimicked the effects of the blockers. Application of artificial Kv3 conductance also led to FS in OA interneurons after complete K+ channel block and even induced FS in hippocampal pyramidal neurons in the absence of blockers. Adding artificial Kv3 conductance with altered deactivation kinetics revealed a nonmonotonic relationship between mean AP frequency and deactivation rate, with a maximum slightly above the original value. Insertion of artificial Kv3 conductance with either lowered activation threshold or inactivation also led to a reduction in the mean AP frequency. However, the mechanisms were distinct. Shifting the activation threshold induced adaptation, whereas adding inactivation caused frequency-dependent AP broadening. In conclusion, Kv3 channels are necessary for the FS phenotype of OA interneurons, and several of their gating properties appear to be optimized for high-frequency repetitive activity.

Odorant-Induced Olfactory Receptor Neural Oscillations and Their Modulation of Olfactory Bulbar Responses in the Channel Catfish

Peripheral waves (PWs) in the channel catfish are odorant-induced neural oscillations of synchronized populations of olfactory receptor neurons (ORNs) that appear after the initial approximately 500 msec of the response. The mean dominant frequency during the initial 2 sec of PW activity is approximately 28 Hz, declining to approximately 20 Hz in the last sec of a 5 sec stimulus. Recordings of PWs from different regions of a single olfactory lamella and simultaneously from widely separated lamellae within the olfactory organ suggest that PWs are initiated in the sensory epithelium within each olfactory lamella. Simultaneous recordings in vivo from the olfactory organ [electro-olfactogram (EOG) or integrated neural activity], local field potentials (LFPs) from the olfactory bulb (OB), and single and few-unit activity from OB neurons were performed. Cross-correlation analysis of simultaneously recorded odor-induced OB LFPs and either EOG or ORN neural activity showed that oscillations occurring within the OB were lower (<20 Hz) than those of PWs; however, during PW activity, OB LFPs increased both their magnitude and dominant frequencies and became correlated with the PWs. Also during odorant-induced PW activity, the responses of different OB neurons with similar odorant specificity became phase locked to each other and to both the PWs and OB LFPs. PWs are hypothesized to function to strengthen the synaptic transfer of olfactory information at specific glomeruli within the OB.

Electrophysiological Characterization of Chemosensory Neurons from the Mouse Vomeronasal Organ

The mechanism of sensory transduction in chemosensory neurons of the vomeronasal organ (VNO) is not known. Based on molecular data, it is likely to be different from that mediating sensory transduction in the main olfactory system. To begin to understand this system, we have characterized the electrophysiological properties of dissociated mouse VNO neurons with patch-clamp recording. Sensory neurons were distinguished from nonsensory neurons by the presence of a dendrite, by immunoreactivity for olfactory marker protein, and by the firing of action potentials. The resting potential of VNO neurons was approximately -60 mV, and the average input resistance was 3 Gomega. Current injections as small as 1-2 pA elicited steady trains of action potentials that showed no sign of elicited steady trains of action potentials that showed no sign of adaptation during a 2 sec stimulus duration. The voltage-gated conductances in VNO neurons are distinct from those in olfactory neurons. The Na+ current is composed of two components; the major component was TTX-sensitive (Ki = 3.6 nM). The outward K+ current activates at -30 mV with kinetics 10 times slower than for K+ currents in olfactory neurons. The Ca2+ current is composed of at least two components: an L-type current and a T-type current that activates at -60 mV and is not found in olfactory neurons. We find no evidence for cyclic nucleotide-gated channels in VNO neurons under a variety of experimental conditions, including those that produced large responses in mouse olfactory neurons, which is further evidence for a novel transduction pathway.

Age-associated impairments in a test of attention: evidence for involvement of cholinergic systems

We trained three groups of rats, young (Y; 3 months at the start of study), middle aged (MA; 15 months), and aged (AG; 22 months), in the serial five-choice serial reaction time task, a test of attention. There were clear age-related differences in task acquisition: Y acquired the task quicker than MA rats, which learned faster than AG rats. A subgroup of AG rats [AG(I)] could not reach criterion (> 80% correct, < 20% omissions under standard conditions of 0.5 sec stimulus duration, 5 sec limited hold). Accordingly, they were tested under conditions of 1 sec stimulus duration. Having acquired the task, under standard conditions both MA and AG groups were slower to make a correct response but not to collect the food reward. Furthermore, parameter changes, particularly reductions in stimulus duration and intensity, revealed further age-related changes in accuracy. Following completion of these studies, animals were trained in a simpler one-choice task. Importantly, reducing stimulus duration/intensity in this task revealed no differences between Y and MA/AG groups, although AG(I) rats were impaired. This dissociation between MA/AG impairments in the one- and five-choice task suggests that these animals may show attentional deficits compared with Y rats, which are independent of changes in sensory (visual), motor function, or motivation. Finally, the MA deficit in attention was partially reversed by tacrine pretreatment (3 mg/kg). Also scopolamine (0.01-0.075 mg/kg) and mecamylamine (0.3-5 mg/kg) pretreatment impaired choice accuracy of MA but not Y rats. Taken together, the drug studies imply that the attentional deficits may at least be partially due to changes in cholinergic function.

Vibration stimulus induced EEG bursts in isoflurane anaesthesia

The EEG and heart rate reactions to vibration stimulus were studied in 14 patients during moderately deep surgical isoflurane anaesthesia, at a level when EEG showed a burst suppression pattern. Vibration applied to the palm of the hand induced bursts in EEG in 12 patients, usually with a latency of about 0.5 sec from the onset, or from the end of the 3 sec stimulus. Increases in heart rate were seen at bursts related to both vibration onset and offset, as well as at spontaneous bursts. With spontaneous bursts, an initial positive wave was frequently seen. In 6 patients the vibration induced bursts were different in shape from the spontaneous bursts; no initial positive wave was seen before the negative DC shift in C z-F z recording. We conclude that EEG bursts can be evoked by a non-noxious stimulus such as vibration in patients during isoflurane anaesthesia.

Electrical potential on the papilla parotidea and Na+ and Cl- concentrations in parotid saliva and salivary flow rates in human.

Variations in the potential on the papilla parotidea (non-membrane potential), and Na+and Cl-concentrations in saliva, and the salivary flow rate in human were recorded when the tongue was stimulated at regular intervals of 60, 20, 5, 2, 1min, 30 or 15 sec. The peak in Na+concentration was generally later than that of the potential, but the time changes were not parallel. The peak in Cl-concentration was generally earlier than those of the potential at 60 and 20 min intervals, but mostly later than those of the potentials at 5, 2 and 1min and 30 sec stimulus intervals. Recovery from the increased Cl-concentration to the value before stimulation was clearly shorter than the recovery time of the potential at 60 and 20min intervals. The peak in the salivary flow rate generally appeared before those in the potentials at 60, 20 and 5min intervals, but both peaks were simultaneous at 2, 1min and 30 sec intervals. With shorter stimulus intervals, the differences between the values before stimulation and the peak values decreased. There was no clear peak at 15 sec stimulus intervals. We were not able to establish similar time changes in the variation of the potential, Na+ and Cl-concentrations in the saliva, and the salivary flow rate.

Influence of flunarizine, nicardipine and nimodipine on the anticonvulsant activity of different antiepileptic drugs in mice.

Only flunarizine (40 mg/kg, i.p.) significantly raised the threshold for electroconvulsions in mice (ear-clip electrodes, 0.2 sec stimulus duration, tonic hindlimb extension as an endpoint), whilst nicardipine and nimodipine (up to 80 mg/kg) was ineffective in this respect. Further, flunarizine (10 and 20 mg/kg) potentiated the efficacy of carbamazepine and valproate against maximum electroshock (50 mA)-induced seizures and, in the dose of 20 mg/kg, enhanced that of diphenylhydantoin. In addition, this calcium channel inhibitor was without influence upon the total levels of these antiepileptics in plasma. Nicardipine (5 and 10 mg/kg) and nimodipine (10 and 20 mg/kg) increased the protective potential of carbamazepine and nimodipine (20 mg/kg) also decreased the ED50 of diphenylhydantoin against maximum electroshock. However, nicardipine distinctly increased the level of carbamazepine in plasma, whilst nimodipine did not affect the level of both antiepileptics in plasma. The combined treatment of calcium channel inhibitors and antiepileptic drugs, providing a 50% protection against maximum electroshock, did not significantly change the motor performance of mice in the chimney test, when compared with antiepileptic drugs, given alone at their ED50s, against maximum electroshock-induced convulsions. The present results give further support to the idea of the combined use of some calcium channel inhibitors and antiepileptic drugs in the treatment of human epilepsy.

Midlatency auditory evoked responses in schizophrenia

The auditory evoked component P50 has been reported as having an abnormal recovery cycle in patients with schizophrenia. Recent studies examining the effects of stimulus rate on the midlatency response (MLR) component P1, found P1 recovery cycles in normals similar to P50. This study examined the P1 recovery cycle in patients using a rate protocol and MLR recording procedures. MLRs were recorded from 13 controls and 13 patients with schizophrenia in response to binaurally presented clicks presented at three stimulus rates: 0.9/sec, 5.1/sec, and 9.9/sec. The P1 (50–70 msec latency) in patients did not decrease as much in amplitude as in controls at the 9.9/sec stimulus rate. This lack of recovery was correlated with clinical ratings of symptomatology. Since evidence from both the human and the cat model suggests that the P1 is generated in thalamus, these findings are consistent with reports of thalamic dysfunction in schizophrenia.

Nociceptive responses in medial thalamus of the normal and arthritic rat

Recordings were obtained from 773 neurons located in the medial thalamus of rats. 23 of the 46 rats studied had been rendered arthritic by prior inoculation with Freund's adjuvant. 262 of the neurons could be activated by peripheral stimulation. In all cases but one, only stimuli considered to be nociceptive were effective in producing responses. Most of the responses were excitatory. The majority of the responsive neurons were located in the submedius (SM), mediodorsal (MD), centrolateral, paracentral, ventromedial (VM) nuclei and medial parts of the ventrolateral (VL) nucleus. A few nociceptive neurons were also recorded in anteromedial (AM), reuniens and a few other nearby regions of thalamus. Most neurons could be activated by stimuli applied bilaterally and frequently to large regions of the body. In almost all cases the responses were maintained for the entire duration of the 15 sec stimuli used and in some cases continued after cessation of the stimuli. No marked differences in incidence of responsive neurons were found between the normal and arthritic rats or between different regions. There were also no marked differences in the spontaneous rates, magnitudes of responses, or incidence of after-discharges of neurons in the various regions of medial thalamus. These findings indicate the existence of neurons responding to nociceptive stimuli in MD, AM, VM, and VL in addition to the intralaminar nuclei and SM and suggest that all these regions may be involved in mediating various aspects of nociception.

Evidence for a chronic loss of inhibition in the hippocampus after kindling: electrophysiological studies

Rats were kindled with either of 2 protocols: 1. (1) a rapidly recurring hippocampal seizure (RRHS) paradigm in which 10 sec stimulus trains were delivered every 5 min through hippocampal electrodes. 2. (2) a traditional approach in which 1 sec stimulus trains were given to the amygdala once daily. Three groups of kindled rats were prepared: 1. (1) one of amygdala-kindled rats that had experienced 9–15 seizures. 2. (2) one of RRHS-kindled rats that had experienced 96 seizures. 3. (3) one of RRHS-overkindled rats that had experienced 144–336 seizures. After a 1 month seizure-free period, the animals were anesthetized with urethane and measurements were made on the potency of paired pulse inhibition in the CA1 region of the hippocampus. All groups of kindled animals were found to have significantly less paired pulse inhibition than control rats. This decrement was confined to interpulse intervals ⩽70 msec. The amount of inhibition lost correlated with the number of seizure that had occurred. The GABAergic agonist muscimol restored paired pulse inhibition in kindled animals for interpulse intervals ⩽70 msec towards normal values. These results indicate that not only RRHS, but also other modes of kindling, reduced GABAergic inhibition in the CA1 region of the hippocampus and that this diminution was long-lasting, if not permanent.

Eye-head coordination during optokinetic stimulation in squirrel monkeys.

Head and eye movements in the yaw plane were recorded during and after optokinetic stimulation in squirrel monkeys. 1) Phasic or tonic head deviations to the side of the ocular quick phase occurred in 94% of total recordings (n = 50) during the perstimulus period, and in 75% of recordings (n = 49) during the poststimulus period. Magnitude of mean head deviation was significantly different between perstimulus and poststimulus periods. 2) Head nystagmus associated with eye nystagmus was consistently observed in seven of nine squirrel monkeys during optokinetic stimulation. Squirrel monkeys are thereby less prone to display head nystagmus than either guinea pigs, pigeons or chickens. 3) Slow phase speeds of coupled head and eye nystagmus were subjected to statistical analysis. A highly significant negative correlation was found between slow phase head and eye speeds. The correlation coefficient was - 0.81 at 60 degrees / sec stimulus (n = 119) and -0.72 at 100 degrees / sec stimulus (n = 131). The gaze speed, calculated by summing the head and eye speeds, was 59.1 plus or minus 6.8 / sec at 60 degrees / sec and 92.2 plus or minus 11.4 at 100 degrees / sec stimulus. There was no significant difference between the gaze speed in a free head condition and the eye speed when the head was fixed.

Encoding of noxious heat messages in neurons of the ventrobasal thalamic complex of the rat

Ventrobasal thalamic neurons responsive to noxious mechanical stimuli were tested with noxious heat stimuli graded in temperature, surface-area and duration. Experiments were performed by plunging the tail of intact, lightly anesthetized rats into a temperature-controlled water bath. Seventeen of 24 neurons encoded stimulus temperature by frequency of discharge although the responses of 6 of these 17 reached a plateau at the highest temperatures. Alternatively, the cell population might code stimulus temperature by a recruiting mechanism since response thresholds were distributed between 40 and 50°C. Some units also increased their discharge in parallel with an increase in stimulus area and/or duration. Analyses of discharge patterns were performed. A decrease of discharge frequency during stimulation was not observed before several tens of seconds had elapsed. Thus, the average response of the cell population to 15, 30 and 60 sec stimuli showed no clear ‘adaptation’. In our conditions, i.e. with most of the stimulations limited to a duration of 15 sec each, sensitization to heat was observed after 55 and 60°C, but not after 50°C. These data indicate that noxious heat stimulus parameters are coded at the thalamic level in the rat by both an increase in discharge and a progressive recruitment of units.

Experimental autoimmune myasthenia gravis in the rat: A preliminary report

In chronic experimental myasthenia gravis (EAMG) in rat, the decrement of electrical and mechanical responses evoked by maximal repetitive (3-167/sec) stimuli to the nerve was greater in the slow-twitch soleus (SOL) than in the fast-twitch extensor digitorum longus (EDL) muscle. Excitation-contraction coupling was impaired in moderate to severe EAMG, as evidenced by a diminished staircase phenomenon and by diminished posttetanic potentiation (PTP) of twitch tension in two EDLs. The only morphologic abnormality observed was an increase in length of the endplates in the EDLs of those animals that had had an acute phase of EAMG. The latter had more than a 90% reduction in the amplitude of the action potential and in the twitch tension of the EDL when stimuli were applied to the nerve. Stimuli applied directly to the muscle evoked a tetanic tension that was one-third of normal. The staircase and PTP were normal. Necrosis occurred in the endplate and in the adjacent segment of muscle fiber; outside the endplate region, the muscle fiber was normal.

Second-order schedules of intravenous drug self-administration in rhesus monkeys

Lever-pressing behavior was generated and maintained in 3 rhesus monkeys by intravenous infusions of morphine or cocaine under a second-order schedule of reinforcement. Under this schedule, every tenth lever-press response (FR 10) during a fixed interval of time produced a 2 sec stimulus light. The first FR 10 completed after a 60 min interval had elapsed produced the stimulus light and an intravenous infusion of morphine or cocaine. The stimulus light remained on for the duration of the drug infusion (50–60 sec). Sessions of morphine or cocaine presentation, each with distinct stimulus light conditions, alternated on a daily basis. Under this schedule, single doses of morphine from 0.125 to 1.0 mg/kg maintained high overall response rates (maximum of 40 Rs/min) in the pattern characteristic of fixed interval (FI) schedules of reinforcement. There was no functional relationship between the response-rates and the doses of morphine tested. The simultaneous infusion of naloxone (0.125 mg/kg) with morphine (0.25 mg/kg) markedly decreased response rates. However, the infusion of the same dose of naloxone five min after the presentation of morphine failed to suppress self-administration behavior. Naloxone had no effects on cocaine-reinforced responding.

Akustisch evozierte Potentiale (AEP) im Kindesalter bei periodischen und zufallsverteilten Reizintervallen

The differences between amplitudes and latencies of acoustically evoked potentials (AEP) in children, aged between 3 and 7 years, were tested using random distributed stimuli with mean interstimulus intervals (ISI) of 1.45 sec, 2.1 sec, and 4.1 sec and periodic stimuli with the same ISI. We applied three different intensities, 30, 50, and 70 dB SPL and a frequency of 1000 c/s. We determined the peak to peak amplitudes P2N2 and N2P3 and the latencies of P2, N2, and P3 for our calculation because of the typical AEP pattern in children. There were no significant differences between the mean amplitudes and mean latencies, using an error probability of 1% comparing the AEP determined by the two different ways of stimulation. The increase of the ISI from 1.45 to 4.1 sec didn't yield to a significant improvement of the AEP in both stimulation patterns. In the tested group of children the used stimulation pattern, as we already stated in adults, is without greater importance.