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PubMed1979

[Structure and correlation of "fast" and "slow" background impulse activity of visual cortex neurons].

Background and optically modified impulse activity of neurons in visual cortex of unanaesthetized rabbits was analyzed. By means of joint interval histograms it was shown that neurons can be distinguished by the ratio of burts (intervals to 15-40 ms) and extraburst activity and by the shape of transition from one from of activity to another. The extraburst activity comprises 63% of impulses and its ratio to bursts of 2 or 3 and more impulses was 27:3:1. Burts impulse distribution showed a relative stability of timing pattern within bursts and small number of burst impulses (2.4 on the average). Bursts of 3 and more impulses (3.6 on the average) are not rhythmical and 79% of them contained long intervals (18.6 +/- 2.4 ms) before the shortest one (7.9 +/- 0.9 ms). Optical stimulation resulted in bursts containing core impulses, shorter intervals and beginning with the shortest interval in most neurons. This may testify to the increase of the EPSP steepness and amplitude. 20% of cortical neurons showed background bursts containing more impulses and shorter intervals in comparison with evoked bursts.

Animals↗

PubMed1977

Efficacy of monophasic electrical impulses with steep leading and trailing edges in cardiac defibrillation.

Experiments on dogs were performed to investigate the efficacy of various defibrillation impulse waveforms. The results showed that the decisive factors for the effectiveness of the defibrillation impulse of certain shape are its relationship to the carciac tissue accomodation and the duration of the suprathreshold current flow. For cardiac defibrillation the most convenient impulse is therefore the impulse with the highest rate of rise of the leading edge as well as the trailing edge. The amplitude of the rear trailing edge of the defibrillation impulse should be either equal or higher than the amplitude of the front leading edge. That means that rectangular or trapezoidal impulses with an ascending slope may be most conveniently used for cardiac defibrillation. The biologically optimal duration of the trapezoidal impulse with an ascending slope proved to range from 7 to 14 msec. The authors emphasize the inevitability of additional characteristics of the defibrillation impulse by its peak current and total energy contents.

Animals↗

PubMed1978

Ectopic generation of impulses and cross-talk in spinal nerve roots of "dystrophic" mice.

In "dystrophic" mice, many spinal root axons are bare and closely apposed to one another in midroot. The direction of nerve impulse traffic in lubosacral spinal nerve roots was determined by biphasic recording of spontaneous activity. In normal mice, impulse traffic in dorsal and ventral roots is directed toward and away from the spinal cord, respectively. However, in spinal root fibers of dystrophic mice, impulses also originate in midroot and are propagated toward both the spinal cord and the periphery. Impulses originate in midroot as single isolated events, in bursts at frequencies of up to 100 Hz, or as continuous activity persisting for several minutes in single fibers. Ectopically arising activity in some single fibers is consistently associated with transmission of an impulse in another fiber past the site of origin of the ectopically arising impulse. Thus impulses arise in the spinal root axons of dystrophic mice both spontaneously and as a result of cross-talk between single fibers.

Animals↗

PubMed1975

The relationship of impulse control to cognition and adjustment among institutionalized aged women.

Several dimensions of impulse control (i.e., delay of gratification, reflectivity, and motor control) were related to intelligence, mental status, and adjustment among 91 institutionalized aged women. Four different types of impulse control measures were used: Self reports of impulse control, staff ratings, interviewer's ratings, and tests of impulse control. Impulse control measures yielded statistically significant multiple correlations with all outcome measures except life satisfaction. The findings suggest that impulse control in its various forms has a consistent and significant relationship with indices of adaptation. Utilizing stepwise regression analyses, the best predictors of outcome among impulse control measures are presented.

Adaptation, Psychological↗

PubMed1975

Impulse activity of a single motor unit upon the rhythm of the summated muscle activity.

The impulses of single motor units (MUs) are recorded using the method of selective leading off with surface bipolar electrodes with small interpolar distance. Parallel recording is made of the summated EMG and of its apparatus-transformed form-the mean voltage curve of the EMG. The correct position of the electrodes with regard to the MU is controlled by means of a vector-electromyographic (VEMG) method. The statistical parameters of the impulse series of the individual MUs and of the groups of impulses in the summated EMG are determined, as well as the time interrelations between the impulses of the selected MUs and the groups of impulses in the mean voltage curve of the EMG. The delay in the appearance of the impulses from the selected MUs with regard to the beginning of the group of impulses, proved a statistically distributed value according to a bimodal type which becomes more pronounced upon rating to the intervals.

Electrodes↗

PubMed1976

Noradrenaline synthesis and utilization: control by nerve impulse flow under normal conditions and after treatment with alpha-adrenoreceptor blocking agents.

The changes in the synthesis and utilization or noradrenaline cranial and caudal to an acute section of the rat spinal cord have been used to investigate the importance of nerve impulses for these processes. 1. Cranial to a lesion of the spinal cord, the alpha-methyltyrosine-induced disappearance of noradrenaline was accelerated by the alpha-adrenoreceptor blocking agents yohimbine (10 mg/kg), piperoxan (60 mg/kg) and tolazoline (50 mg/kg). In the absence of nerve impulses caudal to a lesion of the spinal cord, this disappearance was decelerated as compared to that cranial to the lesion and it was not influenced by the three alpha-adrenoreceptor blocking agents. 2. The nialamide-induced accumulation of normetanephrine in the whole brain was increased by phenoxybenzamine (20 mg/kg) and yohimbine whereas it was decreased by the alpha-adrenoreceptor stimulating agent clonidine (0.1 mg/kg). The effect of clonidine was completely antagonized by yohimbine, but not by phenoxybenzamine, giving further evidence for the view that clonidine and yohimbine have a stronger effect than phenoxybenzamine on the alpha-adrenoreceptors regulating the release of noradrenaline induced by nerve impluses. 3. The accumulation of Dopa after decarboxylase inhibition cranial to a lesion of the spinal cord was accelerated by yohimbine, piperoxan and tolazoline, but not significantly affected by phenoxybenzamine and haloperidol (10 mg/kg). In the absence of nerve impulses caudal to a lesion of the spinal cord, the popa accumulation was decelerated as compared to that cranial to the lesion and it was not influenced by the former three alpha--adrenoreceptor blocking agents as well as by clonidine. 4. The results show that the synthesis and the utilization noradrenaline normally, as well as the accelerations of these processes by alpha-adrenoreceptor blocking agents, are dependent on nerve impulses. The stimulation of the synthesis and utilization of noradrenaline by nerve impulses might by influenced via the activity of teh alpha-adrenoreceptors located either on the nerve terminals or on the cell bodies or on both parts of the noradrenergic neurones. In the absence of nerve impulses, a receptor-mediated feedback mechanism similar to that described for the synthesis of dopamine does not appear to regulate the synthesis of noradrenaline.

Adrenergic alpha-Antagonists↗

PubMed1992

Long-term adaptation of crayfish neurons depends on the frequency and number of impulses.

Increasing the impulse activity of crustacean neurons for a few days causes long-lasting changes in transmitter release, which are termed 'long-term adaptation' (LTA) in previous studies. Both the amount of transmitter released at the beginning of a stimulus train, and synaptic fatigue during repetitive stimulation, are reduced. The present study examines the dependence of these synaptic changes on the frequency and number of impulses used to elicit LTA. Fatigue resistance develops consistently when crayfish phasic motor neurons are stimulated for 3 days with as few as 9,000 impulses per day, and occurs in response either to low frequency stimulation (0.2 or 0.5 Hz), or to stimulation in short bursts at a moderate average frequency (2.5 Hz). In contrast, the reduction in initial transmitter release does not appear consistently when the frequency and number of impulses are both low (9,000 impulses per day delivered at 0.2 Hz), but does occur at the moderate stimulus frequency (2.5 Hz) and when a larger number of impulses (18,000) are delivered at a low frequency (0.5 Hz). The data suggest that the two changes in synaptic transmission that comprise LTA have different stimulus requirements.

Action Potentials↗

PubMed1978

Growth function for human response to large-amplitude impulse noise.

The U. S. Environmental Protection Agency has proposed the use of C-weighted day/night level for the assessment of impulse noise such as the noise resulting from sonic boom, blast noise (artillery, armor, demolition, etc.) and other large-amplitude impulse sources. One remaining question pertaining to the use of C-weighting has been the growth function for human response to impulse noise. This question arises because work by Kryter and by Young using peak values and/or small amplitudes exhibited growth functions of 6--7dB for a doubling of annoyance, while the growth function for human response to common sources (planes, vehicles, etc.) increases by about 10 dB for a doubling of annoyance. Kyter's and Young's data are reanalyzed herein by using C-weighting and by including only large-amplitude data. This reanalysis results in a growth function for human response to impulse noise which increases by about 10 dB for a doubling of annoyance. This equality of growth function between common A-weighted noise and C-weighted impulse noise further supports the use of C-weighted day/night level for assessment of sonic boom, blast noise, or other large-amplitude impulse noises having similar spectral content.

Humans↗

PubMed1979

Loss of auditory sensitivity following exposure to spectrally narrow impulses.

Damage-risk criteria (DRC) for impulse noise do not presently take the spectrum of an impulse into direct account; yet it is clear that the ear is spectrally tuned. In order to establish the sensitivity of various sections of the cochlear duct to trauma from impulses, ears were exposed to 100 spectrally narrow impulses (1.0, 5.0, or 10.0 kHz) delivered in 10 min. Changes in auditory sensitivity were measured by an electrocochleographic technique in 43 cat ears and a threshold of loss established for each type of impulse. Expressed in SPL at the ear drum, the loss threshold rose at 3.2 dB/octave between 1.0 and 10.0 kHz. Expressed in stapes displacements, the loss threshold fell at 5.4 dB/octave in the same region. This curve was used to establish a tentative shape for a DRC for the human ear for impulse noise. The patterns of loss, rates of loss, lack of recovery, and loss thresholds are discussed with respect to their probable physiological basis with conclusion that mechanical displacement rather than metabolic exhaustion is the most reasonable causative factor.

Animals↗

PubMedDate not supplied

[Interaction between continuous and impulse noise: anatomic and functional evaluation in relation to the intensity of the exposure].

Interaction between continuous and impulse noise was studied. One group of chinchillas was exposed to octave band of noise of 0.5 kHz 95 dB SPL intensity. Three groups were exposed to impulse noises of 113, 119 and 125 prak SPL emitted at 1 imp/sec, 1 imp/4 sec and 1 imp/16 sec respectively. Three groups were exposed to noise created by a combination of above continuous and impulse noises. All exposures lasted for 5 days. Hearing thresholds were measured in 35 animals using auditory evoked potentials. The combined continuous and impulse noises showed equal energy contents, but the groups exposed to 119 and 125 dB impulse noise intensities developed an exacerbation of PTS and cell hair loss. Therefore, the critical level, under which the damage associated with noise exposure is related to the total noise energy (Equal Energy Hypothesis) was reduced when impulse noise was added to continuous noise.

Animals↗

PubMed1978

Influence of reflection-impulsivity and cognitive style on time estimation under different ambient conditions.

120 college students estimated seven different durations of a light by the method of reproduction. Each duration reproduction was performed while either counting fast auditory clicks, slow clicks, or with no clicks. The subjects had previously been assessed for cognitive style with the Group Embedded Figures test and for reflection-impulsively with the impulsivity scale from the Personality Research Form. Multivariate analyses of variance indicated that the rapid-tempo ambient conditions had a greater effect on estimation of duration than did either the slow tempo or control condition. There were significant differences in time estimation between reflectives and impulsives for estimations of 10, 30, and 50 sec. No interactions were observed for reflection-impulsivity by ambient conditions. Although cognitive style did not interact with ambient conditions as was predicted, it did interact with sex for three durations, 10, 20, and 30 sec. It was concluded that impulsive students tend to underestimate the brief times more than do reflective students but are not affected differently by the ambient circumstances in which the estimation is made. Cognitive style, apparently, does not have a profound influence on estimation of brief durations. However, sex and cognitive style in interaction do affect these estimations, this requires further research.

Acoustic Stimulation↗

PubMed1976

Reflective and impulsive children: strategies of information processing underlying differences in problem solving.

The hypothesis that impulsive children differ from reflective children in their preferred strategy of information processing, based on extent of stimulus analysis, was investigated. The experiments employed different age groups and a variety of tasks, including matching, grouping, recall, and concept attainment. Stimuli were presented both visually and auditorily and included both visually and aduitorily and included both verbal and pictorial matrials. The tasks required verbal and nonverbal responses and varied in the level of stimulus analysis necessary for successful performance. The subjects' strategy was assessed by the quality of their performance on tasks requiring detail versus global processing, and by the strategy they chose to adopt in tasks where either detail or global processing led to successful performance. While reflective children performed better on tasks requiring detail analysis than on tasks requiring global analysis, impulsive children showed the reverse trend. Furthermore, when successful solutions could be reached via either a global- or a detail-processing strategy, impulsive children who adopted the former were equally as successful as reflective children who adopted the latter strategy. It was concluded that, contrary to existing views, impulsive children are not inferior to reflective children in general potential or problem-solving ability. Rather, the inferior performance of impulsive children frequently reported in the literature may be due to incompatibility between their preferred global-processing strategy and the detail analysis typically required for successful performance.

Auditory Perception↗

PubMed1978

Morphine-induced regional and dose-response differences on unit impulse activity in decerebrate rats.

Previous studies have indicated that morphine alters nerve impulse activity differently in various brain areas of intact animals. Because morphine has profound effects on visceral organs and on the spinal cord, cervically transected preparations, in which hypothermia was prevented, were used for recording spontaneous impulse activity before and for 30 min after morphine simultaneously from six regions of the brain: caudate (Cau), midbrain reticular formation (MBRF), central grey (CG), cingulate cortex (CC), hippocampus (Hip), and substantia nigra (SN). Morphine (5 and 15 mg/kg, i.p.) caused a naloxone-preventable depression of impulse activity in most brain areas. The depression was, however, especially pronounced in the CG, more so with the lower than the higher dose; naloxone completely blocked the low-dose effect. The MBRF responded with increased impulse activity after 5 mg/kg, but with depression after 15 mg/kg; naloxone blocked both responses. Activity in both the Hip and CC was depressed by the low dose of morphine, but not by the high dose; naloxone blocked the depression. Both doses of morphine generally depressed the variance in impulse activity, with a clear preferential depression of CG variance; naloxone blocked the CG variance effect, but not that of other brain areas.

Animals↗

PubMed1977

Effect of post-impulse depression on background firing of sympathetic preganglionic neurons.

(1) Many of the preganglionic neurons responsible for sympathetic tone in the cat exhibit a characteristic irregular background spike activity with a low repetition rate. The properties of this activity, described by the interspike interval histogram, can be explained as the result of the responses of the neurons to random synaptic imputs. (2) Serial interspike interval correlation was used to show that additive post-impulse depression in preganglionic neurons does not enter into the timing of typical low-rate, irregular background firing. However, if cells are accelerated by anitdromic tetanization, a depressive recovery process accumulates to cause a prolonged silent period after driving of the cells has ceased. If cells are accelerated, by the action of their synaptic inputs, to rates higher than their usual basal rates, serial post-impulse depressions overlap, and summate to cause a temporal interaction between neighboring pulses which is observable by serial interval correlation. (3) By observing the effect of antidromic responses occurring at various intervals after a background spike, we showed that the time course of the summative part of post-impulse depression is shorter than the interspike intervals typically encountered in background firing. (4) At higher-than-basal levels of sympathetic activity, occurring spontaneously or during antidromic stimulation, successive post-impulse recovery periods overlap and sum to impart a negative correlation of serial interspike intervals. At the levels of sympathetic activity existing in waking animals, the damping effect of cumulative post-impulse depression is probably an important factor in stabilizing sympathetic tone.

Action Potentials↗

PubMed1979

The effect of calcium ions on the secretion of quanta evoked by an impulse at nerve terminal release sites.

A study has been made of the effects of calcium ions on the number of quanta secreted from all the release sites at an amphibian motor nerve terminal recorded with an intracellular microelectrode (m) compared with the number secreted simultaneously from a small number of release sites recorded with an extracellular microelectrode (me). If the endplate potential was made subthreshold by lowering the external calcium concentration ([Ca]o less than or equal to 0.4 mM), it was possible to find small groups of release sites for which me was comparable to m, indicating considerable nonuniformity in the probability of release of a quantum at different groups of release sites (Pe) in a given [Ca]o. Increasing [Ca]o in the range from 0.25 to 0.4 mM increased the probability of release of a quantum at groups of release sites (Pe), independent of the initial value of Pe, and the dependence of Pe on [Ca]o followed a fourth power relationship. A conditioning impulse enhanced the probability of release of a quantum by a subsequent test impulse at release sites, if Pe was less than 1.0 during the conditioning impulse. It is shown that the present observations regarding the dependence of Pe on [Ca]o and on conditioning impulses can be quantitatively predicted from previous observations regarding the dependence of the binomial parameters m, p, and n on [Ca]o and on conditioning impulses determined with intracellular electrodes, if the probability of secretion of a quantum at a release site (Pj) is different for different release sites and Pj is distributed as a beta random variable.

Action Potentials↗

PubMed1976

Prediction of propagation block on the basis of impulse shape in single unit recordings from human nerves.

The occurrence of impulse block was studied in single unit recordings and related to impulse shape when peripheral nerves were impaled with tungsten needle electrodes. Exposed nerves were exploited in frog and cat and non-exposed nerves in man. Three different impulse shapes were seen: 1. Negative spikes of very short durations which nearly all propagated. 2. Positive double peaked spikes which all propagated. 3. Positive single peaked spikes which were of two different natures: one which propagated and one which did not. The findings suggest that urinary impulses recorded witha needle electrode impaling the myelin are positive and single peaked when the injury is minimal. Gradually a propagation delay might develop at the site of impalement giving rise to a double peak. Later the propagation may be blocked which is seen as a drop out of the second peak. The collected sample of observations indicates that it was possible to predict in practically all cases whether the propagation was blocked or not from the shapes of the single unit impulses and their alterations as seen by the tungsten needle electrode.

Action Potentials↗

PubMed1977

The effect of calcium ions and temperature on the binomial parameters that control acetylcholine release by a nerve impulse at amphibian neuromuscular synapses.

1. A study has been made of the effects of changing the external calcium concentration, [Ca](o), and the temperature on both the number of quanta available for release by the nerve impulse (n) as well as the increase in release probability of a quantum p(t) during the release period (from 0 to T) following a nerve impulse at synapses in amphibian striated muscle.2. When [Ca](o) was increased in the low range from 0.25 to 0.4 mM at 18 degrees C, the average quantal content of the e.p.p. (m) increased as the fourth power of [Ca](o) and this was primarily due to a third power dependence of n on [Ca](o); the dissociation constants and power dependence of n on calcium determined in the [Ca](o) range from 0.25 to 1.0 mM were successfully used to predict the changes in size of the e.p.p. in the very high [Ca](o) range from 1 to 10 mM. When the temperature was increased from 7 to 18 degrees C in a [Ca](o) of 0.6 mM or 0.35 mM, n increased with a Q(10) of 2.5.3. When [Ca](o) was increased in the range from 0.25 to 1.0 mM at 18 degrees C, the probability that a quantum initially available for release is released during the release period (p(T)) was very sensitive to [Ca](o), increasing as the third power of [Ca](o) and with a dissociation constant of 0.13 mM. When the temperature was increased from 7 to 18 degrees C in a [Ca](o) of 0.6 mM or 0.35 mM, p(T) decreased.4. The histograms of latencies of individual quanta following a nerve impulse was very temperature dependent: the time to peak of the histograms (i.e. the interval in which most quanta fell) had a Q(10) of over 4 as did the time constant of decline of the histograms in the temperature range from 7 to 18 degrees C.5. The average number of quanta released up to time t during the release period following a nerve impulse, namely np(t), was well described by a stochastic process in which p(t) was determined by two reactions; one of these reactions released available quanta from the nerve terminal whilst the other made some of the available quanta unavailable for release by the nerve impulse.

Acetylcholine↗

PubMed1975

The role of the middle ear in acoustic trauma from impulses.

Exposure to high intensity impulse noise may produce a wide range of audiometric and histological effects in experimental animals. The objective of this study was to assess the changes in the middle ear mechanism after impulse noise exposure and to relate these changes to the audiometric and histological effects. Nine monaural chinchilla were exposed to either 161 or 166 db peak SPL impulses of 1 msec "A" duration, presented at a rate of 1 per minute for 50 minutes. The conductive mechanism of the chinchilla was assessed using standard clinical measures of static and dynamic impedance before and after the noise exposure. Auditory thresholds were measured before and after noise exposure using the average evoked response (AER) technique. At 30 days post-exposure, the animals were sacrificed for histology. Pre-exposure tympanometry showed that: 1. the total mean impedance of the chinchilla ear is considerably lower than that of man; 2. a method related hysterisis effect is present in both the susceptance and conductance tympanograms; and 3. sedation has a significant effect on the total impedance of the ear and on the shape of the tympanograms. After exposure to high level impulse noise: 1. tympanograms become irregular and double peaked, indicating tympanic membrane stress; 2. for the given exposure, 166 db is the impulse intensity needed to rupture consistently the tympanic membrane; and 3. audiometric and histological data correlate with the tympanometric findings and demonstrate a protective effect of a tympanic membrane rupture on the cochlea.

Animals↗