Synaptic and intrinsic responses of medical entorhinal cortical cells in normal and magnesium-free medium in vitro.

1. Extracellular recordings were made from slices of hippocampus plus parahippocampal regions maintained in vitro. Field potentials, recorded in the entorhinal cortex after stimulation in the subiculum, resembled those observed in vivo. 2. Washout of magnesium from the slices resulted in paroxysmal events which resembled those occurring during sustained seizures in vivo. These events were greatest in amplitude and duration in layers IV/V of the medial entorhinal cortex and could occur both spontaneously and in response to subicular stimulation. Spontaneous seizure-like events were not prevented by severing the connections between the hippocampus and entorhinal cortex, but much smaller and shorter events occurring in the dentate gyrus were stopped by this manipulation. Both spontaneous and evoked paroxysmal events were blocked by perfusion with the N-methyl-D-aspartate (NMDA) receptor antagonist, DL-2-amino-5-phosphonovalerate (2-AP5). 3. Neurons in layers IV/V were characterized by intracellular recording. Injection of depolarizing current in most cells evoked a train of nondecrementing action potentials with only weak spike frequency accommodation and little or no posttrain after hyperpolarization. 4. A small number of cells displayed burst response when depolarized by positive current. The burst consisted of a slow depolarization with superimposed action potentials which decreased in amplitude and increased in duration during the discharge. The burst was terminated by a strong after hyperpolarization and thereafter, during prolonged current pulses a train of nondecrementing spikes occurred. The burst response remained if the cell was held at hyperpolarized levels but was inactivated by holding the cell at a depolarized level. 5. Depolarizing synaptic potentials could be evoked by stimulation in the subiculum. A delayed and prolonged depolarization clearly decremented with membrane hyperpolarization and, occasionally, increased with depolarization. 6. Washout of magnesium from the slices resulted in an enhancement of the late depolarization and a reversal of its voltage dependence. Eventually a single shock to the subiculum evoked a large all-or-none paroxysmal depolarization associated with a massive increase in membrane conductance. Similar events occurred spontaneously in all cells tested. The paroxysmal depolarizations, both spontaneous and evoked, were rapidly blocked by 2-AP5. 7. It is concluded that medial entorhinal cortical cells possess several intrinsic and synaptic properties which confer an extreme susceptibility to generation of sustained seizure activity.(ABSTRACT TRUNCATED AT 400 WORDS)

[1]  Y. Ben-Ari,et al.  Is activation of N-methyl-d-aspartate receptor gated channels sufficient to induce long term potentiation? , 1987, Neuroscience Letters.

[2]  W. W. Anderson,et al.  Seizure-like events in brain slices: suppression by interictal activity , 1987, Brain Research.

[3]  I. Módy,et al.  NMDA receptors of dentate gyrus granule cells participate in synaptic transmission following kindling , 1987, Nature.

[4]  I. Módy,et al.  Low extracellular magnesium induces epileptiform activity and spreading depression in rat hippocampal slices. , 1987, Journal of neurophysiology.

[5]  M P Witter,et al.  The organization of the reciprocal connections between the subiculum and the entorhinal cortex in the cat: I. A neuroanatomical tracing study , 1986, The Journal of comparative neurology.

[6]  G. Collingridge,et al.  Frequency-dependent involvement of NMDA receptors in the hippocampus: a novel synaptic mechanism , 1986, Nature.

[7]  P. C. Schwindt,et al.  The induction and modification of voltage-sensitive responses in cat neocortical nuerons by N-methyl-d-aspartate , 1986, Brain Research.

[8]  G. Collingridge,et al.  Intracellular demonstration of an N-methyl-d-aspartate receptor mediated component of synaptic transmission in the rat hippocampus , 1985, Neuroscience Letters.

[9]  B. Connors Initiation of synchronized neuronal bursting in neocortex , 1984, Nature.

[10]  M. Mayer,et al.  Voltage-dependent block by Mg2+ of NMDA responses in spinal cord neurones , 1984, Nature.

[11]  C. Köhler,et al.  Morphological details of the projection from the presubiculum to the entorhinal area as shown with the novel PHA-L immunohistochemical tracing method in the rat , 1984, Neuroscience Letters.

[12]  L. Nowak,et al.  Magnesium gates glutamate-activated channels in mouse central neurones , 1984, Nature.

[13]  R. Dingledine N‐methyl aspartate activates voltage‐dependent calcium conductance in rat hippocampal pyramidal cells. , 1983, The Journal of physiology.

[14]  D. A. Brown,et al.  Calcium‐activated outward current in voltage‐clamped hippocampal neurones of the guinea‐pig. , 1983, The Journal of physiology.

[15]  A. Constanti,et al.  Fast inward‐rectifying current accounts for anomalous rectification in olfactory cortex neurones. , 1983, The Journal of physiology.

[16]  Paul R. Adams,et al.  Voltage-clamp analysis of muscarinic excitation in hippocampal neurons , 1982, Brain Research.

[17]  J. Ebersole,et al.  The laminar sensitivity of cat striate cortex to penicillin induced epileptogenesis , 1982, Brain Research.

[18]  T. Babb,et al.  Demonstration of caudally directed hippocampal efferents in the rat by intracellular injection of horseradish peroxidase , 1981, Brain Research.

[19]  C. Elger,et al.  Pattern of intracortical potential distribution during focal interictal epileptiform discharges (FIED) and its relation to spinal field potentials in the rat. , 1981, Electroencephalography and clinical neurophysiology.

[20]  R. H. Evans,et al.  Selective depression of excitatory amino acid induced depolarizations by magnesium ions in isolated spinal cord preparations. , 1980, The Journal of physiology.

[21]  T. Babb,et al.  Inhibition in subicular and entorhinal principal neurons in response to electrical stimulation of the fornix and hippocampus , 1980, Brain Research.

[22]  D. Johnston,et al.  Voltage clamp discloses slow inward current in hippocampal burst-firing neurones , 1980, Nature.

[23]  D. Prince,et al.  A calcium-activated hyperpolarization follows repetitive firing in hippocampal neurons. , 1980, Journal of neurophysiology.

[24]  M. T. Shipley,et al.  Projections from the subiculum to the deep layers of the lpsilateral presubicular and entorhinal cortices in the guinea pig , 1979, The Journal of comparative neurology.

[25]  D. Prince,et al.  Anomalous inward rectification in hippocampal neurons. , 1979, Journal of neurophysiology.

[26]  P. Schwartzkroin,et al.  Physiological and morphological identification of a nonpyramidal hippocampal cell type , 1978, Brain Research.

[27]  P. Schwartzkroin,et al.  Characteristics of CA1 neurons recorded intracellularly in the hippocampalin vitro slice preparation , 1975, Brain Research.

[28]  M. T. Shipley The topographical and laminar organization of the presubiculum's projection to the ipsi‐ and contralateral entorhinal cortex in the guinea pig , 1975, The Journal of comparative neurology.

[29]  A. Hjorth-Simonsen Hippocampal efferents to the ipsilateral entorhinal area: An experimental study in the rat , 1971, The Journal of comparative neurology.

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

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

[32]  A. Hodgkin,et al.  The action of calcium on the electrical properties of squid axons , 1957, The Journal of physiology.

[33]  T. Blackstad Commissural connections of the hippocampal region in the rat, with special reference to their mode of termination , 1956, The Journal of comparative neurology.