Extracellular unit analysis of the hippocampal penicillin focus.

Abstract Extracellular recordings were made of unit activity in penicillin foci in the cat hippocampus, and the location of selected cells was ascertained by methyl blue marks. Most units demonstrated firing patterns consistent with previously reported intracellular data, consisting of a short burst of spikes followed by a period of prolonged inhibition during the inter-ictal discharge. Two additional firing patterns, suggestive of inter-neuron activity, were noted. The first of these showed prolonged trains of high frequency spikes during inter-ictal discharges occuring at low frequencies (approximately every 10 sec). As the inter-ictal discharges were evoked more frequently the spike trains became disrupted and eventually dropped out before a seizure developed. The second firing pattern consisted of short bursts of spikes coincident with the surface paroxysm, which became very long trains as the discharges were evoked slightly more frequently. Cells showing all three firing patterns were located in all layers of the hippocampus. Some cells showing all three patterns could be activated antidromically, indicating that they were pyramidal cells. When studied for several seizure periods, cells were seen to convert from one firing pattern to another. Inter-ictal firing pattern was not correlated with firing pattern during seizure. It is concluded that anatomic cell types in the hippocampus cannot be identified by their firing pattern during epileptic events. Furthermore, it appears that even during the very stereotyped inter-ictal discharges which occur in hippocampal penicillin foci, individual cells may significantly vary their firing pattern during the paroxysms.

[1]  C. A. Marsan,et al.  CORTICAL CELLULAR PHENOMENA IN EXPERIMENTAL EPILEPSY: INTERICTAL MANIFESTATIONS. , 1964, Experimental neurology.

[2]  P. Andersen,et al.  Excitatory synapses on hippocampal apical dendrites activated by entorhinal stimulation. , 1966, Acta physiologica Scandinavica.

[3]  J. Eccles,et al.  PATHWAY OF POSTSYNAPTIC INHIBITION IN THE HIPPOCAMPUS. , 1964, Journal of neurophysiology.

[4]  D. Prince The depolarization shift in "epileptic" neurons. , 1968, Experimental neurology.

[5]  Kandel Er,et al.  Cellular and integrative properties of the hippocampal pyramidal cell and the comparative electrophysiology of cortical neurons. , 1968 .

[6]  I. Sherwin Burst activity of single units in the penicillin epileptogenic focus. , 1970, Electroencephalography and clinical neurophysiology.

[7]  J. Eccles,et al.  LOCATION OF POSTSYNAPTIC INHIBITORY SYNAPSES ON HIPPOCAMPAL PYRAMIDS. , 1964, Journal of neurophysiology.

[8]  W. Spencer,et al.  Recurrent excitation in the CA3 region of cat hippocampus. , 1971, The International journal of neuroscience.

[9]  W. Spencer,et al.  Penicillin-induced interictal discharges from the cat hippocampus. II. Mechanisms underlying origin and restriction. , 1969, Journal of neurophysiology.

[10]  V. J. Wilson,et al.  Marking Single Neurons by Staining with Intracellular Recording Microelectrodes , 1966, Science.

[11]  P Andersen,et al.  Entorhinal activation of dentate granule cells. , 1966, Acta physiologica Scandinavica.

[12]  G F Ayala,et al.  Genesis of epileptic interictal spikes. New knowledge of cortical feedback systems suggests a neurophysiological explanation of brief paroxysms. , 1973, Brain research.

[13]  G. Ayala,et al.  Neuronal behavior and triggering mechanism in cortical epileptic focus. , 1969, Journal of neurophysiology.

[14]  E. Kandel,et al.  ELECTROPHYSIOLOGY OF HIPPOCAMPAL NEURONS: IV. FAST PREPOTENTIALS. , 1961, Journal of neurophysiology.

[15]  W. Spencer,et al.  Penicillin-induced interictal discharges from the cat hippocampus. I. Characteristics and topographical features. , 1969, Journal of neurophysiology.