Evoked activity of single units and neural populations in the hippocampus of the cat.

Abstract The evoked activity of single units and neural populations in the hippocampus of cats was studied in relation to a proposed feedback circuit. The forward branch of the feedback circuit consisted of pyramidal cells which send collaterals to interneurons in a feedback branch. The pyramidal cell excitation of an interneuron pool, followed by inhibition of the pyramidal cell population, is analogous to a circuit within the prepyriform cortex. On the basis of the neural network, oscillatory wave forms were predicted under the additional assumptions that a sustained level of background activity biased the neural network and that fornix stimulation perturbed only slightly the mean activity of the cell population. The prediction was tested by recording a series of evoked potentials. Oscillatory PST histograms were recorded from 40 pyramidal cells, and oscillatory potential fields were mapped on a coronal plane through the dorsal and ventral hippocampus. A delay of a quarter of a cycle of averaged evoked potentials from cell populations with respect to poststimulus time histograms was observed following fornix stimulation. These oscillatory wave forms were consistent with the proposed feedback circuit.

[1]  G. Shepherd,et al.  Theoretical reconstruction of field potentials and dendrodendritic synaptic interactions in olfactory bulb. , 1968, Journal of neurophysiology.

[2]  W. Battersby,et al.  Neural limitations of visual excitability. V. Cerebral after-activity evoked by photic stimulation. , 1964, Vision research.

[3]  H. K. Hartline,et al.  INHIBITORY INTERACTION OF RECEPTOR UNITS IN THE EYE OF LIMULUS , 1957, The Journal of general physiology.

[4]  G. Salmoiraghi,et al.  Intracellular potentials from respiratory neurones in brain-stem of cat and mechanism of rhythmic respiration. , 1961, Journal of neurophysiology.

[5]  Lisbeth M. Kraft,et al.  The structure of Ammon's horn , 1968 .

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

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

[8]  B. Grafstein Organization of callosal connections in suprasylvian gyrus of cat. , 1959, Journal of neurophysiology.

[9]  A. Hodgkin,et al.  The after‐effects of impulses in the giant nerve fibres of Loligo , 1956, The Journal of physiology.

[10]  W. Freeman Relations between unit activity and evoked potentials in prepyriform cortex of cats. , 1968, Journal of neurophysiology.

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

[12]  P. R. Burgess,et al.  Disinhibition in the cat spinal cord. , 1962, Journal of neurophysiology.

[13]  Walter J. Freeman,et al.  Evoked potentials arising from neural population elements excited at different times on a warped surface , 1966 .

[14]  N. RafaelLorenteDe,et al.  TRANSMISSION OF IMPULSES THROUGH CRANIAL MOTOR NUCLEI , 1939 .

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

[16]  W. Freeman,et al.  Extraneuronal potential fields evoked in septal region of cat by stimulation of fornix. , 1968, Electroencephalography and clinical neurophysiology.

[17]  C. Terzuolo Cerebellar inhibitory and excitatory actions upon spinal extensor motoneurons , 1959 .

[18]  H. Petsche,et al.  [The significance of the rabbit's septum as a relay station between the midbrain and the hippocampus. I. The control of hippocampus arousal activity by the septum cells]. , 1962, Electroencephalography and clinical neurophysiology.

[19]  E. Marg A Rugged, Reliable and Sterilizable Microelectrode for recording Single Units from the Brain , 1964, Nature.

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

[21]  D. W. Bronk,et al.  CHEMICAL EXCITATION OF NERVE , 1946 .

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

[23]  W. Freeman,et al.  Superior colliculus-evoked response in anesthetized cats: space-time characteristics. , 1968, The American journal of physiology.

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

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

[26]  W. Freeman,et al.  Distribution in time and space of prepyriform electrical activity. , 1959, Journal of neurophysiology.

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

[28]  A. Hodgkin The local electric changes associated with repetitive action in a non‐medullated axon , 1948, The Journal of physiology.

[29]  A. Hodgkin,et al.  A quantitative description of membrane current and its application to conduction and excitation in nerve , 1952, The Journal of physiology.

[30]  P. Wall The origin of a spinal‐cord slow potential , 1962, The Journal of physiology.

[31]  B. Burns,et al.  The central control of respiratory movements. , 1963, British Medical Bulletin.

[32]  C. Connelly Recovery Processes and Metabolism of Nerve , 1959 .