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Results for “Cortical Synchronization”

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At least 883 records · Page 49Linked to original sources
PubMedDate not supplied

Rhythmic activity of the brain evoked by local injections of carbachol into subcortical nuclei.

The effect of local injections of carbachol into the caudate nucleus and individual nuclei of the thalamus on the electrocorticogram of the anterior portion of the brain was investigated in unanesthetized, immobilized cats. It was shown that chemical stimulation of subcortical structures, like electrical stimulation, can induce spindle-like activity and a recruitment response. The appearance of these reactions after injections of carbachol both into the caudate nucleus and into individual nuclei of the thalamus indicates the existence of a functionally unified caudate-thalamic cholinoreceptive system, responsible for the slow wave rhythmic activity.

Animals↗
PubMedDate not supplied

Role of hyperactive determinant structures in the creation of functional complexes of seizure activity in the cerebral cortex.

Foci of enhanced excitability, with independent discharge patterns, were created by subconvulsive strychninization in experiments on cats. A focus of more powerful excitation created with the same strychnine played the role of determinant despatch station (DDS). Its importance is that it determines the character of activity of the other foci of excitation, strengthens excitation in them, combines them into a single functional complex, and determines the character of activity of the whole complex. This complex can be destroyed by suppressing the DDS with pentobarbital. Blocking individual destination stations included in the complex does not lead to its destruction.

Animals↗
PubMed1994

Spatiotemporal study of Bereitschaftspotential and event-related desynchronization during voluntary movement in Parkinson's disease.

Bereitschaftspotential (BP) and Event-Related Desynchronization (ERD) were simultaneously recorded during a voluntary wrist flexion in 10 patients with Parkinson's disease (PD) treated with L-Dopa therapy and 10 control subjects. BP and ERD were analyzed 2 s before and 0.5 s after the movement, during two successive left and right experimental conditions. ERD (9-11 Hz) was computed from 11 source derivations (frontocentral, central, parietocentral). The BP was averaged from these 11 electrodes. For the BP, no spatiotemporal difference was found between the two groups. BP began bilaterally over the 3 groups of electrodes, 1250 ms before movement onset for the right flexion and 1500 ms for the left flexion. A contralateral predominance appeared 500 ms before movement onset over the central area. ERD began in the control group 1750 ms before movement over the contralateral central area, and then appeared bilaterally after its execution. In the PD group, the ERD appeared with a shorter latency than in the control group, 1250 ms (left flexion) and 1000 ms (right flexion) before movement onset; diffusion over the ipsilateral side was found 500 ms before movement onset. ERD also involved the frontocentral area and could be interpreted as a compensatory activity of the supplementary motor area. These findings suggest that with Parkinsonian and control subjects, ERD gives additional and maybe more information than the BP about changes of cortical activity during the motor preparation period. In the PD group the delay of ERD appearance seems to confirm that the programming of movement would be affected, thus explaining partially akinesia.

Aged↗
PubMedDate not supplied

The influence of high-frequency stimulation of the midbrain reticular formation on the interaction of neurons of the neocortex.

The influence of the stimulation of the midbrain reticular formation (NRT) at a frequency of 75-100 Hz, current strength 33-400 microA, on the interaction of neurons of the visual and sensorimotor areas of the neocortex of rabbits was investigated. Cross- and autocorrelation histograms of the impulse sequences were plotted. Stimulation of the NRT led to an increase in the number of pairs of neurons functioning in correlation and an increase in the probability of discharges of neurons one after the other with delays from 100 to 400 msec as compared with resting wakefulness. The mechanisms of the interaction of the cells were not altered in the process. Comparison with previously obtained data made it possible to conclude that activation of the NRT may lead to specific changes in the interaction of neurons which are observable during pseudoconditioning and at the beginning of the development of a conditioned reflex.

Animals↗
PubMed1994

Source localization using event-related desynchronization (ERD) within the alpha band.

Voluntary finger movements result in a maximal ERD in the 10-12 Hz band close to electrodes C3 and C4, overlying the sensorimotor hand areas. This ERD focus is not very pronounced with EEG data recorded against a common reference electrode (monopolar recording). After transformation of the raw data using common average, local average and weighted average reference and the Hjorth method, respectively, the ERD becomes enhanced over electrodes C3 or C4. Movement-related EEG data were studied with 17, 19, 30 and 56 electrode montages using large and small interelectrode distances. The best focused ERD was obtained with a 56 electrode montage with small interelectrode distances and local average reference data.

Alpha Rhythm↗
PubMed1994

Diphenylhydantoin potentiates the EEG and behavioural effects induced by N-methyl-D-aspartate antagonists in rats.

The N-methyl-D-aspartate (NMDA) subtype of excitatory amino acid receptors are involved in the electrical and behavioural generalization of epileptiform activity within the brain. In rats, both competitive and non-competitive NMDA antagonists induce three dose-dependent stages of EEG patterns: 1) increase in cortical desynchronization periods; 2) increase in amplitude of cortical high frequency (20-30 Hz), low voltage (30-50 microV) background activity; 3) appearance of cortical slow (2-3 Hz) wave-sharp wave complexes. These EEG changes are accompanied by stimulatory-depressive behavioural effects such as stereotypy (circling, head weaving) and ataxia. In the present study, the influence of the prototypic anticonvulsant diphenylhydantoin (DPH) has been tested on the EEG and behavioural effects induced by the non-competitive NMDA antagonists phencyclidine (PCP) and dizocilpine (MK-801) and by the competitive NMDA antagonist cis-4-phosphonomethyl-2-piperidine-carboxylic acid (CGS 19755). Even though DPH (up to 100 mg/kg IP) did not markedly affect basal cortical EEG activity, at doses of 10-100 mg/kg IP it potentiated all the EEG effects induced by the NMDA antagonists. These data support involvement of NMDA neurotransmission in the pharmacological effects of DPH.

Animals↗
PubMed2001

Effect of luminance level on electro-encephalogram alpha-wave synchronisation.

A control system for the remote activation of electronic devices, based on alpha-wave synchronisation, must be robust over a wide range of lighting conditions. This study investigates the effect that low light levels have on the increase in amplitude of the occipital alpha-wave component of the human electro-encephalogram spectrum in response to eye closure. Measurements of the time required for the amplitude of the occipital alpha wave to increase above a predetermined threshold, upon eye closure, were taken from 21 subjects and at four illuminances, ranging from 2 x 10(-1) lx to 2 x 10(-5) lx. The light source used to provide these illuminances was a featureless, uniformly illuminated white paper that subtended 30 degrees of the visual field. Statistical analysis showed that the time to exceed threshold (TTET) upon eye closure was not independent (p< 0.001) of illuminance, and that the main source of this lack of independence occurred at the lowest illuminance, 2 x 10(-5) lx. At this luminance, the median TTET value was 15.0s. However, at 2 x 10(-4) lx, the median value of the TTET was 4.2s. This is a sufficiently short time for device activation, and therefore a control system based on alpha-wave synchronisation is functional at very low light levels.

Adolescent↗
PubMedDate not supplied

Spatial organization of electrical processes in the brain: problems and solutions.

Theoretical questions of the spatial organization of electrical activity in the brain are discussed in terms of a multilevel realization of the synergetic principle for formation of functional systems underlying behavior and mental function. The role of the spatial-temporal superimposition of coherent structures of biopotentials in generating fields of increased activity in the cerebral cortex is discussed, these being responsible for integrative and associative functions. A hypothesis is proposed regarding the relationship between the energy and information factors of coherent structures as one of the important characteristics describing the efficiency of energy-informational processes. Emphasis is placed on the need for considering not only linear, but also nonlinear associations of biopotentials in considerations of the form and functional sense of their spatial organization.

Brain↗
PubMed2003

Adaptive changes in the reactivity of 5-HT1A and 5-HT2 receptors induced in rat frontal cortex by repeated imipramine and citalopram.

Using extracellular ex vivo recording we studied changes in the reactivity of rat frontal cortical neurons to the 5-HT(1A), 5-HT(2) and 5-HT(4) receptor agonists (+/-)-2-dipropyloamino-8-hydroxy-1,2,3,4-tetrahydronaphtalene hydrobromide (8-OH-DPAT), (+/-)-2,5-dimethoxy-4-iodoamphetamine hydrochloride (DOI) and zacopride, respectively, induced by a repeated treatment with imipramine or citalopram. Rats were treated with imipramine or citalopram for 14 days (10 mg/kg p.o.) twice daily. Frontal cortical slices were prepared 2 days after the last drug administration. Spontaneous epileptiform discharges were induced in slices by perfusion with a medium devoid of Mg(2+) ions and with added picrotoxin (30 microM). While the application of 2 microM 8-OH-DPAT resulted in a reversible decrease of the discharge frequency, in the presence of DOI (1 microM) or zacopride (5 microM), the discharge frequency was increased. Both repeated imipramine and citalopram enhanced the effect of the activation of 5-HT(1A) receptor and attenuated the effect related to 5-HT(2) receptor activation, while the effect of the activation of 5-HT(4) receptor remained unchanged. Moreover, imipramine, but not citalopram, induced a reduction of epileptiform discharge frequency and an increase of the time of occurrence of epileptiform activity. These data indicate that antidepressants enhance the 5-HT-mediated inhibition in neuronal circuitry of the frontal cortex.

8-Hydroxy-2-(di-n-propylamino)tetralin↗