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D S Barth

Publications and source records attributed to D S Barth.

At least 55 records · Page 3Linked to original sources

Three-dimensional analysis of auditory-evoked potentials in rat neocortex.

1. A 8 X 8-channel microelectrode array was used to map epicortical field potentials evoked by bilaterally presented click stimuli from a 8 X 8-mm2 area in the right parietotemporal neocortex of four rats. In two rats, a 16-channel microelectrode array was also inserted into primary auditory cortex to record the laminar profile of auditory evoked potentials (AEP). 2. The epicortical responses began with a positive-negative fast wave followed by a positive-negative slow wave, similar to the previously reported P1, N1, P2, N2 complex. Topographical distributions of the potentials at the peak of each of these waves were distinct, suggesting that they were produced by separate but overlapping populations of cells. 3. Laminar recording revealed the asynchronous participation of supragranular and infragranular pyramidal cells in the generation of the evoked-response complex. The surface-recorded P1 was primarily produced by supragranular cells and the N1, by infragranular cells. The P2 and N2 were produced by temporally overlapping contributions from both cell groups. 4. We conclude that middle-latency components of the AEP complex are produced by both sequential and parallel activation of subpopulations of pyramidal cells in primary auditory cortex.

Acoustic Stimulation↗

Laminar cortical interactions during epileptic spikes studied with principal component analysis and physiological modeling.

The direct cortical responses (DCR) to electrical stimulation and electrically evoked interictal penicillin spikes (EIIS) were studied in the same rats using current source-density (CSD) analysis to directly compare regions of neuronal depolarization and hyperpolarization in neocortex. Principal component analysis (PCA) was further used to evaluate patterns of covariance in the CSD that were characteristic of interactions between pyramidal cell populations with spatially and temporally distinct transmembrane currents. A physical model was applied to the physiological interpretation of PCA results and the optimal model parameters used to estimate neuronal generators of recorded laminar field potentials. The data suggested that the DCR and EIIS were produced by the same neuronal circuit which could be represented by two anatomically distinct populations of pyramidal cells. The first of these populations was situated in the upper and middle layers (supragranular pyramidal neurons) and formed a dipolar CSD pattern that reversed polarity in layers II and III. The second deeper population (infragranular pyramidal neurons) extended throughout most of the cortical thickness and formed a dipolar CSD pattern that reversed polarity in layer V. We propose that excitatory intracortical connections of supragranular pyramidal cells may pathologically synchronize depolarization within the epileptic focus. In this way, supragranular pyramidal cells may provide a trigger mechanism for interictal spikes in neocortex.

Animals↗

Neocortical propagation in temporal lobe spike foci on magnetoencephalography and electroencephalography.

Propagation of the neuronal population of the interictal epileptic spike was quantified in 5 patients with complex partial epilepsy arising from temporal lobe using electroencephalography and magnetoencephalography. During the spike complex in each patient there was a spike at the deep sphenoidal electrode and a spike at the superficial scalp electrode on spontaneous electroencephalography. In each patient the sphenoidal spike had a different peak latency than the scalp spike, consistent with spike propagation. Electroencephalography was used to trigger two magnetoencephalographic averages of stereotyped spikes during the sphenoidal peak and the scalp peak. Magnetoencephalography discriminated the centers of two cortical spike populations at different latencies, showing deeper localization with sphenoidal trigger and more superficial localization with scalp trigger in each patient (p less than 0.05). Latency differences and propagation distances of spikes were consistent with the conduction velocity of corticocortical fibers. Noninvasive estimates of the cortical surface area of the spikes agreed with estimates obtained by electrocorticography over temporal neocortex. These findings indicate propagation of neuronal populations active during human interictal spikes between deep and superficial cortex of temporal lobe, likely by monosynaptic or oligosynaptic pathways. This interictal system appears to be partly independent of the hippocampal interictal system in complex partial epilepsy.

Cerebral Cortex↗

Neuromagnetic field modeling of multiple brain regions producing interictal spikes in human epilepsy.

A method of spatiotemporal analysis, using multiple current dipoles to represent activity in multiple brain regions, was applied to the interpretation of extracranial neuromagnetic fields generated by epileptic spikes in patients with focal seizure disorders. This method permitted the identification and approximate localization of cellular currents within single and multiple brain regions engaged over the entire duration of the human epileptic spike complex. These results suggest that spatially and temporally overlapping electrical currents in human epileptic cortex may be investigated non-invasively in the magnetoencephalogram if appropriate physical models are applied.

Brain↗

Investigation of multiple simultaneously active brain sources in the electroencephalogram.

We present a method of investigating multiple simultaneously active brain sources that overlap both in space and time in the scalp electroencephalogram (EEG). In order to identify the contributions of the individual brain sources to measured potentials, we applied principal component analysis and various methods of rotating the principal components including a newly developed rotation procedure using frequency criteria. We related the results of these multivariate statistical techniques to a new physical model using multiple current dipoles with fixed anatomical locations and time-varying activities. We thus are able to study 3-dimensional location, time activity and interaction of multiple simultaneously active brain sources in the scalp EEG.

Brain↗

Current source-density and neuromagnetic analysis of the direct cortical response in rat cortex.

The electrophysiological basis of macropotentials produced by the direct cortical response (DCR) to electrical stimulation was studied using a combination of current source-density (CSD) and neuromagnetic analysis. Current source-density analysis indicated the locations of extracellular sources and sinks in the cortical depth giving rise to each temporal component of the DCR complex. Information about intradendritic currents was obtained from extracranial magnetic field measures. These data indicate that the DCR is composed of a sequential activation of pyramidal cells at different cortical depths. The complex begins with depolarization of cells in the upper and middle layers, followed by depolarization of deeper pyramidal cells with apical dendrites extending near the cortical surface. The complex ends with a positive-negative slow wave sequence indicating possible afterhyperpolarization of surface dendrites and hyperpolarization of cell bodies and basilar dendrites in the depth. These data demonstrate a unique way in which electrical and magnetic measures may be combined to provide complementary information about the spatially and temporally organized cellular currents within local neuronal networks.

Animals↗

The magnetic and electric fields agree with intracranial localizations of somatosensory cortex.

We measured the magnetoencephalogram (MEG), electroencephalogram (EEG), and electrocorticogram (ECoG) after stimulation of contralateral median nerve in four patients with partial epilepsy evaluated for surgery. Quantitative localization estimates from equivalent source modeling were compared with locations of central fissure in hand sensorimotor area determined by cortical stimulations, intraoperative photographs, and examination after excision in frontal lobe. We also measured MEG and EEG in nine control subjects. MEG and EEG localizations were within 2.5 cm of the estimated location of central fissure in all 13 subjects. In the three patients who had complete mapping of all three fields, the average distance of localizations from central fissure was approximately 4 mm in both MEG and EEG, 3 mm in ECoG, and 3 mm in combined MEG and EEG. MEG was simpler than EEG, which was simpler than ECoG. MEG resolved ambiguities in both EEG and ECoG. The combination of the three fields added information about the spatiotemporal activity of somatosensory cortex. Localization of central fissure was essential to surgical treatment.

Brain Mapping↗

The magnetic field of epileptic spikes agrees with intracranial localizations in complex partial epilepsy.

The magnetoencephalogram (MEG) and electroencephalogram (EEG) were measured during interictal epileptic spikes in nine patients with complex partial seizures. The MEG localization estimates were compared with localizations by intraoperative cortical electrodes, subdural electrodes, stereotaxic depth electrodes, anatomic imaging, postoperative pathologic analysis, and postoperative follow-up. In all patients, MEG localization estimates were in the same lobe as the epileptic focus determined by invasive methods and EEG. In two patients, it was possible to quantify precisely the accuracy of MEG localization by mapping a spike focus that was visually indistinguishable on MEG and cortical recordings. In both patients, MEG localization was approximately 12 mm from the center of the cortical spike focus on intracranial recordings. In eight patients, MEG showed tangential dipolar field patterns on the spontaneous record, but EEG did not. In one patient, a cortical epileptic discharge was detected only on MEG for some discharges and only on EEG for other discharges. The MEG did not detect deep spikes with present levels of environmental noise.

Brain↗

The magnetic field of complex partial seizures agrees with intracranial localizations.

The magnetoencephalogram (MEG) was recorded during 63 complex partial seizures in 4 patients. The MEG showed large biomagnetic signals occurring at the same time as discharges recorded from scalp electroencephalogram (EEG). These MEG signals had the same morphology and frequency as the discharges from the EEG. The location of the seizure focus was verified by depth electrode recordings in 2 patients and by lesions shown on computed tomographic scan and magnetic resonance imaging in the other 2. In each patient, MEG localization estimates were consistent with the location of the seizure focus shown by other methods. When seizures were recorded repeatedly and mapped with a single-channel magnetometer placed at different scalp locations in a single patient, the MEG localization agreed with the electrographic seizure focus localized from depth electrodes. In the maps, the MEG resolved an ambiguity in the scalp EEG and therefore increased the confidence of localization. MEG recordings of seizures may help localize epileptic foci noninvasively.

Cerebral Cortex↗

Intracellular currents of interictal penicillin spikes: evidence from neuromagnetic mapping.

To analyze the net intracellular current produced by interictal spikes, we mapped the extracranial magnetic fields of the rat brain following application of penicillin to the right or left medial cingulate cortex. Averaged interictal spikes in both the magnetoencephalogram (MEG) and in the electrocorticogram (ECoG) were composed of 4 temporal components, a biphasic spike and slow wave. Magnetic field maps for each of these components indicated a source at the location of penicillin application, with intracellular currents oriented perpendicular to the surface of the cingulate cortex, along the axis of the major pyramidal cells. The polarity of the magnetic fields for each of the components was reversed between the two cingulate groups, reflecting the respective orientation of pyramidal cells between the juxtaposed faces of the medial cingulate cortex. This neuromagnetic study of net intracellular current complements and extends the analysis of extracellular currents within the penicillin focus obtained using laminar electrodes. These data also demonstrate how animal neuromagnetometry may provide an empirical foundation for the neurogenesis of the MEG and a new unique method for the non-invasive study of population cell physiology.

Animals↗

Magnetic localization of a dipolar current source implanted in a sphere and a human cranium.

Magnetic fields produced by a dipolar source implanted in a spherical conductor and a human cranial specimen were measured in the magnetoencephalogram (MEG). The location of the source was accurately computed in the spherical conductor from the identified magnetic field extrema using equations for a current dipole in a sphere. This same method was insufficient for localizing the source in a human cranium, where magnetic field maps appeared as distortions from the classical dipolar pattern. A more complete computer modeling procedure was used, adjusting for the non-spherical dimensions of the recording matrix on the cranium. By fitting the gradient of computer simulated fields to those measured outside the cranium, the accuracy of source localization was substantially improved. The greatest distortion of the extracranial magnetic field was an inequality in the measured amplitude of the two extrema, produced by an increased distance and angle of the MEG probe when recording over the lower face and ear. However, gross heterogeneities in the resistance of the skull due to a craniectomy and an implanted insulating balloon had a negligible effect on the extracranial magnetic field pattern.

Bone Diseases↗

Fast and slow magnetic phenomena in focal epileptic seizures.

The magnetic fields associated with penicillin-induced focal epilepsy were measured in laboratory rats. Interictal magnetic spikes were similar to those previously observed in humans with focal seizure disorders. The magnetic fields of the seizure itself displayed both slow and fast phenomena, reversing in direction on opposite sides of the head.

Animals↗

Neuromagnetic evidence of spatially distributed sources underlying epileptiform spikes in the human brain.

Neuromagnetic measurements were performed on 17 subjects with focal seizure disorders. In all of the subjects, the interictal spike in the scalp electroencephalogram was associated with an orderly extracranial magnetic field pattern. In eight of these subjects, multiple current sources underlay the magnetic spike complex. The multiple sources within a given subject displayed a fixed chronological sequence of discharge, demonstrating a high degree of spatial and temporal organization within the interictal focus.

Brain↗

A program for computing power spectra on a microcomputer.

A computer program is presented that will calculate Fourier transforms and power spectra. The program is written in assembly language for the Z-80 microprocessor and has been used on a Radio Shack TRS-80 microcomputer to analyze time-dependent data from laboratory experiments.

Animals↗

Neuromagnetic localization of epileptiform spike activity in the human brain.

Local paroxysmal discharges of epileptic tissue within the human brain, which may be electrically recorded as voltage spikes in the electroencephalogram, also generate extracranial magnetic fields. These fields were assessed by means of recently developed neuromagnetometric techniques. Surface measurements of magnetic spike field strength in the region of the focus appear sufficient to establish the location, depth, orientation, and polarity of currents underlying the paroxysmal discharge.

Brain↗