Development of rabbit hippocampus: physiology.

The postnatal development of the CA1 region of rabbit hippocampus was studied using intracellular techniques in the in vitro slice preparation. Recordings from immature hippocampal neurons revealed spiking activity and functional synaptic contacts, even in the newborn animal. Resting potentials and time constants in such cells were similar to those of mature cells; input resistance was higher and action potential duration longer in the immature rabbits. These cell properties reach adult values by 2-3 weeks. Presumed calcium spikes, as well as sodium spikes, were elicited in animals as young as 1 day, so that it was not possible to determine whether calcium or sodium spikes occur earlier. Synaptic potentials recorded in immature CA1 neurons were long duration depolarizing events associated with a large conductance increase. The postsynaptic potentials (PSPs) were shown to be predominantly excitatory in nature, and could be potentiated by repetitive stimulation at slow rates and low intensities. Such stimulation in many cases could trigger seizure-like activity. Inhibitory PSPs in CA1 neurons were rare in animals less than 1-2 weeks old. Increased occurrence of hyperpolarizing inhibitory PSPs was correlated in time with the appearance of interneuron cell types in physiological recordings. These data reinforce the indication from morphological studies that inhibition is late in developing in rabbit hippocampus.

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

[2]  K. Naka Electrophysiology of the Fetal Spinal Cord : II. Interaction among peripheral inputs and recurrent inhibition , 1964 .

[3]  R. Llinás,et al.  Calcium conductances in Purkinje cell dendrites: their role in development and integration. , 1979, Progress in brain research.

[4]  J. Peacock Electrophysiology of dissociated hippocampal cultures from fetal mice , 1979, Brain Research.

[5]  D. Prince,et al.  Penicillin‐induced epileptiform activity in the hippocampal in vitro preparation , 1977, Annals of neurology.

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

[7]  D. Prince,et al.  Participation of calcium spikes during intrinsic burst firing in hippocampal neurons , 1978, Brain Research.

[8]  D. Purpura,et al.  Fine structure of neurons and synapses in the feline hippocampus during postnatal ontogenesis. , 1968, Experimental neurology.

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

[10]  E. Kandel,et al.  ELECTROPHYSIOLOGY OF HIPPOCAMPAL NEURONS: III. FIRING LEVEL AND TIME CONSTANT. , 1961, Journal of neurophysiology.

[11]  K. Naka ELECTROPHYSIOLOGY OF THE FETAL SPINAL CORD. I. ACTION POTENTIALS OF THE MOTONEURON. , 1964 .

[12]  P. Schwartzkroin,et al.  Further characteristics of hippocampal CA1 cells in vitro , 1977, Brain Research.

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

[14]  G. D. Pappas,et al.  Structural characteristics of neurons in the feline hippocampus during postnatal ontogenesis. , 1968, Experimental neurology.

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

[16]  H McLennan,et al.  Antagonism between bicuculline and GABA in the cat brain. , 1971, Brain research.

[17]  D. Prince,et al.  Changes in excitatory and inhibitory synaptic potentials leading to epileptogenic activity , 1980, Brain Research.

[18]  D. Purpura,et al.  Properties of synaptic activities and spike potentials of neurons in immature neocortex. , 1965, Journal of neurophysiology.

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

[20]  J. Eccles,et al.  The interpretation of spike potentials of motoneurones , 1957, The Journal of physiology.

[21]  E. Kandel,et al.  Electrophysiology of hippocampal neurons. I. Sequential invasion and synaptic organization. , 1961, Journal of neurophysiology.

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

[23]  M. Gutnick,et al.  Neuronal activities in epileptogenic foci of immature cortex. , 1972, Transactions of the American Neurological Association.

[24]  G. Lynch,et al.  Developmental differences in post-lesion axonal growth in the hippocampus. , 1973, Brain research.

[25]  N. Dzidzishvili,et al.  Electrophysiological signs of hippocampal development in ontogenesis. , 1968, Progress in brain research.

[26]  R. Sercombe,et al.  Slow oscillatory variations of excitability observed in vitro in immature mammalian olfactory cortex. , 1972, Brain research.

[27]  E. Kandel,et al.  Electrophysiology of hippocampal neurons. II. After-potentials and repetitive firing. , 1961, Journal of neurophysiology.

[28]  F. Crépel,et al.  Evidence for a multiple innervation of Purkinje cells by climbing fibers in the immature rat cerebellum. , 1976, Journal of neurobiology.

[29]  P. Andersen Organization of Hippocampal Neurons and Their Interconnections , 1975 .

[30]  P. Schwartzkroin,et al.  Development of kitten hippocampal neurons , 1977, Brain Research.

[31]  D. R. Curtis,et al.  Bicuculline, an antagonist of GABA and synaptic inhibition in the spinal cord of the cat. , 1971, Brain research.

[32]  M. Santini,et al.  Postsynaptic potentials and spike variations in the feline hippocampus during postnatal ontogenesis. , 1968, Experimental neurology.

[33]  K. Uchizono Axon identification in the cerebellar cortex of the cat. , 1968, Archivum histologicum Japonicum = Nihon soshikigaku kiroku.

[34]  P. Schwartzkroin,et al.  Probable calcium spikes in hippocampal neurons , 1977, Brain Research.