A Hippocampal Mechanism for Novelty Testing and Decision About Execution of a Response

References

• Amaral D.G. A Golgi study of cell types in the hilar region of the hippocampus in the rat. Journal of Comparative Neurology 1978; 182: 851–914
   PubMed Web of Science ®Google Scholar
• Andersen P. Organization of hippocampal neurons and their inter-connections. The Hippocampus, R.L. Isaacson, K.H. Pribram. Plenum, New York 1975; 155–176
   Google Scholar
• Andersen P., Blaud B.H., Dudar J.P. Organization of the hippocampal output. Experimental Brain Research 1968; 17: 152–173
   Google Scholar
• Andersen P., Blaud B.H., Dudar J.P. Organization of the hippocampal output. Experimental Brain Research 1968; 17: 152–173
   Google Scholar
• Andersen P., Bliss T.V.P., Skede V.K. Lamellar organization of hippocampal excitatory pathways. Experimental Brain Research 1971; 13: 222–238
   PubMed Web of Science ®Google Scholar
• Andersen P., Holmquist B., Voorhoeven P.F. Excitatory synapses at hippocampal apical dendrites activated by entorhinal stimulation. Acta Physiologica Scandinavica 1966a; 66: 461–472
   PubMedGoogle Scholar
• Andersen P., Holmquist B., Voorhoeven P.F. Entorhinal activity of dentate granule cells. Acta Physiologica, Scandinavica 1966b; 66: 448–460
   PubMedGoogle Scholar
• Berger T.W., Thompson R.F. Identification of pyramidal cells as the critical elements in hippocampal neuronal plasticity during learning. Proceedings of the National Academy of Sciences 1978a; 75: 1572–1576
   PubMed Web of Science ®Google Scholar
• Berger T.W., Thompson R.F. Neuronal plasticity in the limbic system during classical conditioning of the rabbit nictitating membrane. Brain Research Bulletin 1978b; 3: 509–518
   PubMedGoogle Scholar
• Metabolic Compartmentation and Neuronal Transmission, S. Berl, D.P. Clarke, D. Schneider. Plenum, New York 1977
   Google Scholar
• Biscoe F.J., Straughan D.W. Microelectrophoretic study of neurons in the cat hippocampus. Journal of Physiology 1966; 183: 341–539
   PubMedGoogle Scholar
• Blackstad T.W. Ultrastructural studies on the hippocampal region. Progress in Brain Research 1963; 3: 122–148
   Google Scholar
• Blackstad T.W., Brink K., Hem J., Jeune B. Distribution of hippocampal mossy fibers in the rat. Journal of Comparative Neurology 1970; 138: 433–450
   PubMed Web of Science ®Google Scholar
• Brazhnik E.S., Vinogradova O.S. The effect of hippocampo-septal disconnections upon the acitvity of the hippocampal neurons. Zhurnal Vysshei Nervnoi Deyatel'nosti 1974; 24: 24–30
   Google Scholar
• Cox D.R., Lewis P.A. The Statistical Analysis of Series of Events. Wiley & Sons, New York 1966
   Google Scholar
• Cragg B.G., Hamlyn L.H. Some commissural and septal connexions of the hippocampus in the rabbit. Journal of Physiology 1957; 135: 460–485
   PubMed Web of Science ®Google Scholar
• Curtis D.R., Johnston G.A. R. Amino acid transmission in the mammalian central nervous system. Ergebnisse der Physiologie 1969; 69: 97–188
   Google Scholar
• Curtis D.R., Felix D., McLellan H. GABA and hippocampal inhibition. British Journal of Pharmacology 1970; 40: 881–886
   PubMed Web of Science ®Google Scholar
• Curtis D.R. GABAergic transmission in the mammalian central nervous system. Amino Acids as Chemical Transmitters, F. Fonnum. Plenum, New York 1978; 17–27
   Google Scholar
• Curtis D.R. Pre- and nonsynaptic activities of GABA and related amino acids in the mammalian nervous system. Amino Acids as Chemical Transmitters, F. Fonnum. Plenum, New York 1978; 55–86
   Google Scholar
• DeFrance J.F. The Septum. Advances in Behavioral Biology. Plenum, New York 1976; XX
   Google Scholar
• De France J.F., Kitai S.T., McCrea R.A., Kocsis J.D., Hatada K. Excitatory effects of 5-HT in the hippocampal circuit. Brain Research 1973; 58: 245–250
   PubMed Web of Science ®Google Scholar
• De France J.F., Kitai S.T., Shimono T. Electrophysiological analysis of the hippocampal-septal projections. Experimental Brain Research 1973; 17: 463–476
   PubMed Web of Science ®Google Scholar
• De France J.F., McCrea R.A., Yoshihara H. Effect of certain indolamines in the hippocampal-septal circuit. Experimental Neurology 1975; 48: 352–377
   PubMed Web of Science ®Google Scholar
• De France J.F., Shimono T., Kitai S.T. Hippocampal inputs to the lateral septal nucleus pattern of facilitation and inhibition. Brain Research 1972; 37: 333–339
   PubMed Web of Science ®Google Scholar
• De France J.F., Yoshihara H., McCrea R.A., Kitai D.T. Pharmacology of the inhibition in the lateral septal region. Experimental Neurology 1975; 48: 502–523
   PubMed Web of Science ®Google Scholar
• Dudar J.D. The effect of septal nuclei stimulation on the release of acetylcholine from the rabbit hippocampus. Brain Research 1975; 83: 123–133
   Web of Science ®Google Scholar
• Euler C.V., Green J.D. Excitation, inhibition and rhythmic activity in hippocampal pyramidal cells in rabbit. Acta Physiologica Scandinavica 1960; 48: 110–125
   PubMedGoogle Scholar
• Euler C.V., Green J.D., Ricci G. The role of hippocampal dendrites in evoked responses and after discharges. Acta Physiologica Scandinavica 1958; 42: 87–111
   PubMedGoogle Scholar
• Filer L.J., Jr., Kare M.R., Garattini S., Reynolds W.A., Wurtman R.J. Glutamic Acid. Raven, New York 1979
   Google Scholar
• Fonnum F. Amino Acids as Chemical Transmitters. Plenum, New York 1978
   Google Scholar
• Freeman A.R. Polyfunctional role of glutamic acid in excitatory synaptic transmission. Progress in Neurobiology 1976; 6: 137–153
   Google Scholar
• Green J.D. The hippocampus. Physiological Reviews 1964; 44: 561–608
   PubMed Web of Science ®Google Scholar
• Gormezano I. Investigation of defense and reward conditioning in the rabbit. Classical Conditioning, W.F. Prokasy. Appleton, Century, Croft, New York 1972
   Google Scholar
• Hamlyn L.H. The fine structure of the mossy fibre endings in the hippocampus of the rabbit. Journal of Anatomy 1962; 96: 112–120
   PubMed Web of Science ®Google Scholar
• Hjorth-Simonsen A. Projection of the lateral part of the entorhinal area to the hippocampus and fascia dentata. Journal of Comparative Neurology 1972; 146: 219–232
   PubMed Web of Science ®Google Scholar
• Hjorth-Simonsen A. Some intrinsic connections of the hippocampus in the rat. Journal of Comparative Neurology 1973; 147: 145–162
   PubMed Web of Science ®Google Scholar
• Hjorth-Simonsen A., Jeune B. Origin and termination of the hippocampal perforant path in the rat studied by silver impregnation. Journal of Comparative Neurology 1972; 144: 215–235
   PubMed Web of Science ®Google Scholar
• Hjorth-Simonsen A., Zimmer J. Crossed pathways from the entorhinal area to the fascia dentata. Journal of Comparative Neurology 1975; 161: 57–70
   PubMed Web of Science ®Google Scholar
• Huggins W.H. Signal flow graphs and random signals. Proceedings of the I.R.E. 1957; 45: 74–86
   Google Scholar
• Isaacson R.L., Pribram K.H. The Hippocampus. Plenum, New York, London 1975
   Google Scholar
• Kandel E.R., Spencer W.A. Electrophysiology of hippocampal neurons. Journal of Neurophysiology 1961a; 24: 243–259
   PubMed Web of Science ®Google Scholar
• Kandel E.R., Spencer W.A. Excitation and inhibition of single pyramidal cells during hippocampal seizure. Experimental Neurology 1961b; 4: 162–179
   PubMed Web of Science ®Google Scholar
• Kandel E.R., Spencer W.A., Brinley F.J. Electrophysiology of hippocampal neurons. Journal of Neurophysiology 1961c; 24: 225–242
   PubMed Web of Science ®Google Scholar
• Klemm W.R. Physiological and behavioral significance of hippocampal rhythmic slow activity (“Theta rhythm”). Progress in Neurobiology 1976; 6: 23–47
   PubMedGoogle Scholar
• Lomo T. Patterns of activation in a monosynaptic cortical pathway: the PP iput to the DF of the hippocampal formation. Experimental Brain Research 1971; 12: 18–63
   PubMed Web of Science ®Google Scholar
• Mac Gregor R.J., Lewis R. Neuronal Modeling. Plenum, New York 1975
   Google Scholar
• Moore G.P., Perkel D.H., Segundo J.B. Statistical analysis and functional interpretation of neuronal spike data. Annual Review of Physiology 1966; 28: 493–522
   PubMed Web of Science ®Google Scholar
• Mosko S., Lynch G., Cotman C.W. Distribution of the septal projection to the hippocampus. Journal of Comparative Neurology 1973; 152: 163–175
   PubMed Web of Science ®Google Scholar
• O'Keefe J., Nadel L. Hippocampus as a Cognitive Map. Oxford University Press, Oxford 1978
   Google Scholar
• Perkel D.H., Gerstein G., Moore G.P. Neuronal spike trains and stochastic point processes. Biophysical Journal 1967; 7: 391–446
   PubMed Web of Science ®Google Scholar
• Perkel D.H., Schulman J.H., Bullock T.H., Moore G.P., Segundo J.P. Pacemaker neurons: Effects of regularly spaced synaptic input. Science 1964; 145: 61–63
   PubMed Web of Science ®Google Scholar
• Poggio G.F., Viernstein L.F. J. Time series analysis of impulse sequences of somatic sensory neurons. Journal of Neurophysiology 1966; 27: 517–550
   Web of Science ®Google Scholar
• Powell E.W. Septal efferents revealed by axonal degeneration in the rat. Experimental Neurology 1963; 8: 406–422
   Web of Science ®Google Scholar
• Pribram K.H. Languages of the Brain. Prentice Hall, Englewood Cliffs, New Jersey 1971
   Google Scholar
• Ranck J.B., Jr. Behavioral correlates and firing repertoires of neurons in the dorsal hippocampal formation and septum of unrestrained rats. The Hippocampus, R.L. Isaacson, K.H. Pribram. Plenum, New York 1975; 2: 207–244
   Google Scholar
• Roberts E., Chase T.N., Tower D.B. See GABA in. Nervous System Function. Raven, New York 1976
   Google Scholar
• Sager O., Nestianu V., Florea-Ciocoiu V. EEG studies on the transmission of visual stimuli to the hippocampus. Electroencephalography and Clinical Neurophysiology 1967; 22: 576
   PubMedGoogle Scholar
• Schwartzkroin P.A., Wester K. Long-lasting facilitation of a synaptic potential following tetanization in thein vitro hippocampal slice. Brain Research 1975; 89: 107–119
   PubMed Web of Science ®Google Scholar
• Segal M. Hippocampal unit response to perforant path stimulation. Experimental Neurology 1972; 35: 541–546
   PubMed Web of Science ®Google Scholar
• Segal M. Convergence of sensory input on units in the hippocampal system of the rat. Journal of Comparative Physiology and Psychology 1974; 87: 91–99
   PubMed Web of Science ®Google Scholar
• Segal M. Physiological and pharmacological evidence for a serotonergic projection to the hippocampus. Brain Research 1975; 94: 115–132
   PubMed Web of Science ®Google Scholar
• Segal M., Bloom F.E. The action of norepinephrine in the rat hippocampus. Brain Research 1974a; 72: 79–114
   PubMed Web of Science ®Google Scholar
• Shipley M.T. The topographical and laminar organization of the subiculum's projection to the ipsiand contralateral entorhinal cortex in the guinea pig. Journal of Comparative Neurology 1975; 160: 127–146
   PubMed Web of Science ®Google Scholar
• Shute C.C.D., Lewis P.R. Cholinesterase containing systems of the brain of the rat. Nature 1963; 199: 1160–1164
   PubMed Web of Science ®Google Scholar
• Snider R.S., Niemer W.T. A Stereotaxic Atlas of the Cat Brain. University Press, Chicago 1961
   Google Scholar
• Spencer W.A., Kandel E.R. Electrophysiology of hippocampal neurons. Journal of Neurophysiology 1961; 24: 260–285
   PubMed Web of Science ®Google Scholar
• Stefanis C. Hippocampal neurons: their responsiveness to microelectrophoretically administered endogenous amines. Pharmacologist 1964; 6: 171
   Google Scholar
• Storm-Mathisen J. Quantitative neurochemistry of anticholinesterase in rat hippocampal region correlated to histochemical staining. Journal of Neurochemistry 1970; 17: 739–750
   PubMed Web of Science ®Google Scholar
• Storm-Mathisen J. Glutamate decarboxylase in the rat hippocampal region after lesion of the afferent fibre systems. Brain Research 1972; 40: 215–235
   PubMed Web of Science ®Google Scholar
• Storm-Mathisen J. Distribution of the components of the GABA system in neuronal tissue. GABA in Nervous System Function, E. Roberts, T.N. Chase, D.B. Tower. Raven, New York 1976
   Google Scholar
• Storm-Mathisen J., Fonnum F. Localisation of transmitter candidates in the hipoocampal region. Progress in Brain Research 1972; 36: 41–58
   PubMedGoogle Scholar
• Storm-Mathisen J., Guldberg H.C. 5-HT and NE in the hippocampal region. Journal of Neurochemistry 1974; 22: 793–803
   PubMedGoogle Scholar
• Stumpf Ch. Drug action on the electric activity of the hippocampus. International Review of Neurobiology 1965; 8: 77–132
   PubMedGoogle Scholar
• Thompson R.F., Berger T.W., Berry S.D., Hoehler F.K., Kettner R.E., Weisz D.J. Hippocampal substrate of classical conditioning. Physiological Psychology 1980a; 8: 262–279
   Google Scholar
• Torda C. Effects of noradrenaline and serotonin on activity of single lateral and medial geniculate neurons. General Pharmacology 1978a; 9: 455–462
   PubMedGoogle Scholar
• Torda C. Differences in acetylcholine, norepinephrine and serotonin induced activity. IRCS Journal of Medical Sciences 1978b; 6: 210
   Google Scholar
• Torda C. Serotonin and the calcium channel. Abstracts of the Society for Neurosciences 1978c; 4: 585
   Google Scholar
• Torda C. A mechanism of action of serotonin: A relationship between Ca-gating and Ca-binding. The Pharmacologist 1979a; 21: 149
   Google Scholar
• Torda C. Excitatory and inhibitory effects of serotonin rooted in calcium gating and calcium binding. IRCS Medical Science 1979b; 7: 138
   Google Scholar
• Torda C. Attenuation in central neurons: Its relationship to increased intracytoplasmic free calcium, calcium binding and memory storage. International Journal of Neuroscience 1979c; 9: 229–232
   PubMed Web of Science ®Google Scholar
• Torda C. A code for ponto-geniculo-occipital wave (PGO). International Journal of Neuroscience 1980a; 10: 197–210
   PubMed Web of Science ®Google Scholar
• Torda C. Memory and Dreams. A Modern Physics Approach. Walters, Chicago 1980b
   Google Scholar
• Traub R.D., Llinas R. Hippocampalpyramidal cells. Journal of Neurophysiology 1979; 42: 476–496
   PubMed Web of Science ®Google Scholar
• Vinogradova O.S. Functional organization of the limbic system in the process of registration of information: Facts and hypotheses. The Hypothalamus, R.L. Isaacson, K.H. Pribram. Plenum, New York, London 1975; 2: 1–70
   Google Scholar
• Winson J., Abzug C. Gating of neuronal transmission in the hippocampus. Science 1977; 196: 1223–1225
   PubMed Web of Science ®Google Scholar
• Winson J., Abzug C. Neuronal transmission through hippocampal pathways dependent on behavior. Journal of Neurophysiology 1978; 41: 716–732
   PubMed Web of Science ®Google Scholar
• Zadeh L.A. Signal flow graphs and random signals. Proceedings of I.R.E. 1957; 45: 1413–1414
   Google Scholar