Hippocampus and Behavioral Maturation

References

• Adey W. Neurophysiological correlates of information transaction and storage in brain tissue. Progress in Physiological psychology, E. Stellar, J. M. Sprague. Academic Press, New York 1966; I
   Google Scholar
• Altman J. Autoradiographic and histological studies of postnatal neurogenesis II. A longitudinal investigation of the kinetics, migration and transformation of cells incorporating tritiated thymidine in infant rats, with special reference to neurogenesis in some brain regions. Journal of Comparative Neurology 1966; 128: 431–473
   Web of Science ®Google Scholar
• Altman J. Postnatal growth and differentiation of a mammalian brain, with implications for a morphological theory of memory. The Neurosciences: A Study Program, G. D. Quarton, T. Melnechuk, F. O. Schnitt. Rockefeller University Press, New York 1967
   Google Scholar
• Altman J. Experimental reorganization of the cerebellar cortex I. Morphological effects of elimination of all microneurons with prolonged x-ray started at birth. Journal of Comparative Neurology. 1972; 146: 335–405
   Google Scholar
• Altman J. Experimental reorganization of the cerebellar cortex III. Regeneration of the external germinal layer and granule cells ectopia. Journal of Comparative Neurology 1972; 146: 153–180, (a)
   Google Scholar
• Altman J. Experimental reorganization of the cerebellar cortex IV. Parallel fiber reorientation following regeneration of the external germinal layer. Journal of Comparative Neurology 1973; 149: 181–192, (b)
   Google Scholar
• Altman J., Anderson W. J. Irradiation of the cerebellum in infant rats with low-level x-ray: Histological and cytological effects during infancy and adulthood. Experimental Neurology 1971; 30: 492–509
   Google Scholar
• Altman J., Anderson W. J. Experimental reorganization of the cerebellar cortex II. Effects of elimination of most microneurons with prolonged x-irradiation started at four days. Journal of Comparative Neurology 1973; 149: 123–152
   Google Scholar
• Altman J., Anderson W. J., Wright K. A. Gross morphological consequences of irradiation of the cerebellum in infant rats with repeated doses of low-level x-ray. Experimental Neurology 1968; 21: 61–91
   Google Scholar
• Altman J., Brunner R. L., Bayer S. A. The hippocampus and behavioral maturation. Behavioral Biology 1973; 8: 557–596
   PubMedGoogle Scholar
• Altman J., Das G. D. Autoradiographic and histological evidence of postnatal hippocampal neurogenesis in rats. Journal of Comparative Neurology 1965; 124: 319–335
   PubMed Web of Science ®Google Scholar
• Altman J., Das G. D. Autoradiographic and histological studies of postnatal neurogenesis I. A longitudinal investigation of the kinetics, migration and transformation of cells incorporating tritiated thymidine in neonate rats with special reference to postnatal neurogenesis in some brain regions. Journal of Comparative Neurology 1966; 126: 337–390
   PubMed Web of Science ®Google Scholar
• Altman J., Das G. D. Postnatal neurogenesis in the guinea pig. Nature 1964; 214: 1090–1101
   Google Scholar
• Barry M., Eayrs J. T. The effect of x-irradiation on the development of the cerebral cortex. Journal of Anatomy 1966; 100: 707–722
   Google Scholar
• Bayer S. A., Brunner R. L., Hine R., Altmann J. Behavioral effects of interference with the postnatal acquisition of hippocampal granule cells. Nature New Biology 1973; 242: 222–224
   Google Scholar
• Bender R., Hostetter G., Thomas G. Effects of lesions in hippocampus-entorhinal cortex on maze performance and activity in rats. Psychonomic Science 1968; 10: 13–14
   Google Scholar
• Berlyne D. E. Conflict, Arousal and Curiosity. McGraw-Hill Book Co., Inc., New York 1960
   Google Scholar
• Brizzee K. R., Jacobs L. A., Kharetchko X. Effects of total body x-irradiation in utero on early postnatal changes in neuron volumetric relationships and packing density in cerebral cortex. Radiation Research 1961; 14: 95–103
   Google Scholar
• Brodmann K. Vergleichende Lokalisationlehre der Grosshirnrinde in ihren Principien dargestellt auf Grund des Zellenbayes. J. A. Barth, Leipzig 1909
   Google Scholar
• Brunner R. L. Age differences in one-trial passive avoidance learning. Psychonomic Science 1969; 14: 134
   Google Scholar
• Buerger A. A. Effects of preoperative training in relearning successive discrimination by cats with hippocampal lesions. Journal of Comparative and Physiological Psychology 1970; 72: 462–466
   Google Scholar
• Burdach C. F. Vom Baue und Leben des Gehirns. Dyk, Leipzig 1819, 26
   Google Scholar
• Capobianco S., Worsham E., Hamilton L. W. Behavioral effects of fornix transseclion in the rat. Paper presented at 44th Annual Meeting of Eastern Psychological Association, Washington, D.C., 1943
   Google Scholar
• Cajal S. R. Studien uber die Hirnrinde des Men-schen. Leipzig 1901, 02
   Google Scholar
• Cajal S. R. Histologic du Systeme Nerveux de VHomme et des Vertebres. Instituto Ramon y Cajal, Madrid 1909, 11
   Google Scholar
• Conel J. L. Postnatal Development of the Human Cerebral Cortex. Harvard University Press, Cambridge 1939, 63
   Google Scholar
• Crosby E. C., Humphrey T., Lauer E. W. Correlative Anatomy of the Nervous System. The Macmillan Co., New York 1962
   Google Scholar
• Crowne D. P., Riddell W. I. Hippocampal lesions and the cardiac component of the orienting response in the rat. Journal of Comparative and Physiological Psychology 1969; 69: 748–755
   Google Scholar
• Douglas R. J. The hippocampus and behavior. Psychological Bulletin 1967; 67: 416–422
   PubMed Web of Science ®Google Scholar
• Douglas R. J., Isaacson R. L. Hippocampal lesions and activity. Psychonomic Science 1964; 1: 187–188
   Google Scholar
• Douglas R. J., Peterson J. J., Douglas D. P. The ontogeny of hippocampal-dependent response in two rodent species. Behavioral Biology 1973; 8: 27–34
   PubMedGoogle Scholar
• Douglas R. J., Pribram K. H. Learning and limbric lesions. Neurophysiologia 1966; 4: 197–220
   Google Scholar
• Eccles J. C. The Physiology of Synapses. Academic Press, New York 1964
   Google Scholar
• Elliott H. C. Textbook of Neuroanatomy2nd ed. J. B. Lippincott Co., Philadelphia 1969, Philadelphia
   Google Scholar
• Feder R., Ranck J. Studies on single neurons in dorsal hippocampal formation and septum in unrestrained rats: Part II. Hippocampal slow waves and theta cell firing during bar pressing and other behaviors. Experimental Neurology 1973; 41: 532–555
   PubMed Web of Science ®Google Scholar
• Fugita S. Evolution of the forebrain. Phylogenesis and Ontogenesis of the Forebrain, R. Hassler, H. Stephen. G. Thieme Verlag, Stuttgart 1966
   Google Scholar
• Gaffan D. Logs of recognition memory in rats with lesions of the fornix. Neuropsychologia 1972; 10: 327–341
   PubMed Web of Science ®Google Scholar
• Gaffan D. Inhibitory gradients and behavioral contrasts in rats with lesions of the fornix. Physiology and Behavior 1973; 11: 215–220
   Google Scholar
• Ganser S. Verglichend-anatomische Studien iiber das Gehirn des Maulwurfs. Morphol. Jahrbuch 1882; 7: 591–725
   Google Scholar
• Goldowitz D., White F. W., Steward D., Lynch G., Cotman C. Anatomical evidence for a projection from the entorhinal cortex to the contra lateral dentate gyrus of the rat. Experimental Neurology 1945; 47: 433–441
   Google Scholar
• Gordon G., Sed W. A. An investigation of nucleus gracilis of the cat by antidromic stimulation. Journal of Physiology 1961; 155: 589–601
   Google Scholar
• Grastyan E., Lissak K., Madarasz I., Donhoffer H. Hippocampal electrical activity during the development of conditioned reflexes. Electroencephalography and Clinical Neurophysiology 1959; 11: 409–430
   PubMedGoogle Scholar
• Green R., Beatty W., Schwartzbaum J. Comparative effects of septo-hippocampal and caudate lesions on avoidance behavior in rats. Journal of Comparative Physiology and Psychology 1967; 64: 444–452
   PubMed Web of Science ®Google Scholar
• Greene E., Stauff C. Behavioral role of hippocampal connections. Experimental Neurology 1974; 45: 141–160
   Google Scholar
• Haggbloom S., Brunner R., Boyer S. Affects of hippocampal granule cell agenesis on acquisition of escape from fear and one-way active avoidance responses. Journal of Comparative and Physiological Psychology 1974; 86: 447–457
   Google Scholar
• Hicks S. P. Radiation as an experimental tool in mammalian development neurology. Physiological Reviews 1958; 38: 337–356
   Google Scholar
• Hicks S. P., D'Amato C. J. Disorders of the Developing Nervous System, W. S. Field, N. M. Desmond. Charles C. Thomas, Springfield 1961
   Google Scholar
• Hicks S. P., D'Amato C. J. Advances in Teratology, D. H. M. Woollam. Logos Press, London 1966
   Google Scholar
• Himwich W. A. Biochemical and neurophysiological development of the brain in the neonatal period. International Review of Neurobiology 1962; 4: 117–158
   Google Scholar
• Hjorth-Simonsen A. Hippocampal efferents to the ipsilateral entorhinal area: An experimental study in the rat. Journal of Comparative Neurology 1971; 142: 417–438
   PubMed Web of Science ®Google Scholar
• Hjorth-Simonsen A. Projection of the lateral part of the entorhinal area to the hippocampus and the 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. An experimental analysis. 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, 172: 215–232
   Google Scholar
• Hostetter G., Thomas G. J. Evaluation of enhanced thigmetaxis as a condition of impaired maze learning by rats with hippocampal lesions. Journal of Comparative and Physiological Psychology, 63: 105–110
   Google Scholar
• Isaacson R. L., Douglas R. J., Moore R. Y. The effect of radical hippocampal oblation on acquisition of an avoidance response. Journal of Comparative and Physiological Psychology 1961; 54: 625–628
   Web of Science ®Google Scholar
• Jarrard L. E. Behavior of hippocampal lesioned rats in home cage and novel situations. Physiology and Behavior 1968; 3: 65–70
   Google Scholar
• Jarrard L. E. The hippocampus and motivation. Psychological Bulletin 1973; 79: 1–12
   PubMed Web of Science ®Google Scholar
• Kaada B., Rasmussen E., Kveim D. Impaired acquisition of passive avoidance behavior by sub-collosal, septal, hypothalamic, and insular lesions in rats. Journal of Comparative and Physiological Psychology 1962; 55: 661–670
   PubMed Web of Science ®Google Scholar
• Kappers C. U. A., Huber G. C., Crosby E. C. Comparative Anatomy of the Nervous System of Vertebrates Including Man. Hatner Publishing Co., New York 1965; Vol. III
   Google Scholar
• Kim C. Nest building, general activity, and salt preference in rats following hippocampal ablations. Journal of Comparative and Physiological Psychology 1960; 53: 11–16
   PubMed Web of Science ®Google Scholar
• Kimble D. P. The effect of bilateral hippocampal lesions in rats. Journal of Comparative and Physiological Psychology 1963; 56: 273–283
   PubMed Web of Science ®Google Scholar
• Kimble D. P. Hippocampus and internal inhibition. Psychological Bulletin 1968; 79: 285–295
   Google Scholar
• Kimura D. Effects of selective hippocampal damage on avoidance behavior in the rat. Canadian Journal of Psychology 1958; 12: 213–218
   PubMed Web of Science ®Google Scholar
• Kupffer R. 1859, (Quoted after Cajal)
   Google Scholar
• Kveim D., Setekleiv J., Kaada B. R. Differential effects of hippocampal lesions on maze and passive avoidance learning in rats. Experimental Neurology 1964; 9: 59–72
   Google Scholar
• Lanier L., Isaacson R. Activity changes related to the location of lesions in the hippocampus. Behavioral Biology 1975; 13: 59–69
   Google Scholar
• Lorente de Nó R. Studies on the structure of the cerebral cortex II. Continuation of the study of the ammonic system. Journal of Psychology and Neurology 1934; 46: 113–177
   Google Scholar
• Mahut H. A selective spatial deficit in monkeys after transection of the fornix. Neuropsychologia 1972; 10: 65–74
   PubMed Web of Science ®Google Scholar
• Meynert T. Vjschr. Psychiat. 1867, Vienna 1 and 2, 68
   Google Scholar
• Miale I. L., Sidman R. L. An autoradiographic analysis of histogenesis in the mouse and cerebellum. Experimental Neurology 1961; 4: 277–296
   PubMed Web of Science ®Google Scholar
• Milner B. Disorders of memory after brain lesions in man. Neuropsychologia 1968; 6: 175–179
   Web of Science ®Google Scholar
• Moorcroft W. H. Ontogeny of forebrain inhibition of behavioral arousal in the rat. Brain Research 1971; 35: 513–522
   Google Scholar
• Myhrer T. Locomotor and avoidance behavior in rats with partial or total hippocampal perforant paths sections. Psychiology and Behavior 1975; 15: 217–224, (a)
   Google Scholar
• Myhrer T. Locomotor, avoidance, and maze behavior in rats with selective disruption of hippocampal output. Journal of Comparative Physiology and Psychology 1975; 89: 759–777, (b)
   PubMed Web of Science ®Google Scholar
• Nadel L. Dorsal and ventral hippocampal lesions and behavior. Physiology and Behavior 1968; 3: 891–900
   Web of Science ®Google Scholar
• Nauta W. J. H. An experimental study of the fornix system in the rat. Journal of Comparative Neurology 1956; 104: 247–271
   PubMed Web of Science ®Google Scholar
• Parmeggiani P. On the functional significance of the hippocampal theta rhythm. Progress in Brain Research, W. R. Adey, T. Tokizane, 1967
   Google Scholar
• Pavlov I. P. Conditioned Reflexes. Dover Publications, Inc., New York 1924
   Google Scholar
• Penfield W., Milner B. Memory deficit produced by bilateral lesions in the hippocampal zone. Archives of Neurology and Psychiatry 1958; 79: 475–497
   PubMedGoogle Scholar
• Raisman G., Cowan W. M., Powell T. P.S. The extrinsic afferent, commissural and association fibers of the hippocampus. Brain 1965; 88: 963–976
   Web of Science ®Google Scholar
• Raisman G., Cowan W. M., Powell T. P. S. An experimental analysis of the efferent projections of the hippocampus. Brain 1966; 89: 83–108
   PubMed Web of Science ®Google Scholar
• Ranson S. W., Clark S. L. The Anatomy of the Nervous System: Its Development and Function10th ed. W. B. Saunders, Co., Philadelphia 1959
   Google Scholar
• Rich I., Thompson R. Role of the hippocampo-septal system, thalamus, and hypothalamus in avoidance conditioning. Journal of Comparative and Physiological Psychology 1965; 59: 66–72
   Google Scholar
• Riddell W. I., Rothblat L. A., Wilson W. A. Auditory and visual distraction in hippocampectomized rats. Journal of Comparative andPhysiologicalPsychology 1965; 59: 66–72
   Google Scholar
• Roberts W. W., Dember W. N., Brodwick M. Alternation and exploration in rats with hippocampal lesions. Journal of Comparative and Physiological Psychology. 1969; 67: 216–219
   Google Scholar
• Sala L. Zur feineren Anatomie des grossen Seepferde Fusses. Ztschr. Wiss. Zool 1891; 52: 18–45
   Google Scholar
• Schaffer K. Beitrag zur Histologic der Ammonshorn-formation. Arch. mikr. Anat. 1892; 39: 611–632
   Google Scholar
• Scheibel A. B. Neural correlates of psychophysiological developments in the young organism. Recent Advances in Biological Psychiatry 1962; 4: 313–327
   Google Scholar
• Scheibel M., Scheibel A. Some structural and functional substrates of development in young cats. Progress in Brain Research. Elsevier Publishing Company, New York 1964; Vol. 9
   Google Scholar
• Scoville W. B., Milner B. Loss of recent memory after bilateral hippocampal lesions. Journal of Neurosurgery and Psychiatry 1957; 20: 11–21
   PubMed Web of Science ®Google Scholar
• Smith, Elliot G. Morphology of the true limbic lobe, corpus collosum, septum pellucidum and fornix. Journal of Anatomy and Physiology 1895; 30: 157–167; 185–205
   Google Scholar
• Swanson L. W., Cowan W. M. Hippocampo-hypothalamic connections: Origin in subicular cortex, not Amnion's Horn. Science 1975; 189: 303–304
   Google Scholar
• Teitlebaum H., Milner B. Activity changes following partial hippocampal lesions in rats. Journal of Comparative and Physiological Psychology 1963; 56: 284–289
   Google Scholar
• Thomas J., McCleary R. Fornical lesions and aversely-motivated behavior in the rat. Physiology and Behavior 1974; 12: 345–350
   Google Scholar
• Tilvey F. The hippocampus and its relationship to the corpus collosum. Journal of Nervous and Mental Diseases 1939; 89: 513–533
   Google Scholar
• Towe A. L., Tabbun S. L. Cortical inhibition of neurons in dorsal column nuclei of the cat. Journal of Neuro-Physiology 1961; 24: 488–498
   Google Scholar
• Truex R. C., Carpenter M. B. Human Neuroanatomy6th ed. The Williams & Wilkins Co., Baltimore 1969
   Google Scholar
• Vanderwolf C. Hippocampal electrical activity and voluntary movement in the rat. Electroencephalography and Clinical Neurophysiology 1969; 26: 407–418
   PubMedGoogle Scholar
• Vanderwolf C. Limbic-diencephalic mechanisms of voluntary movement. Psychological Review 1971; 78: 83–113
   PubMed Web of Science ®Google Scholar
• Van Hartesveldt C. Size of reinforcement and operant responding in hippocampectomized rats. Behavioral Biology 1973; 8: 347–356
   Google Scholar
• Wallace R. B., Altman J. Behavioral effects of neonatal irradiation of the cerebellum I. Qualitative observations in infant and adolescent rats. Developmental Psychobiology 1970; 2: 257–265, (a)
   Google Scholar
• Wallace R. B., Altman J. Behavioral effects of neonatal irradiation of the cerebellum II. Quantitative studies in young adult and adult rats. Developmental Psychobiology 1970; 2: 266–272, (b)
   Google Scholar
• Wallace R. B., Altman J, Das G. D. An autoradiographic and morphological investigation of the postnatal development of the pineal body. American Journal of Anatomy 1969; 126: 175–184
   Google Scholar
• Wallace R. B., Daniels C. E., Altman J. Behavioral effects of neonatal irradiation of the cerebellum III. Qualitative observations in aged rats. DevelopmentalPsychobiology 1972; 5: 35–41
   Google Scholar
• Wallace R. B., Kaplan R., Werboff J. Behavioral correlates of focal hippocampal x-irradiation in rates. Experimental Brain Research 1976; 24: 343–349
   PubMed Web of Science ®Google Scholar
• Warwick R., Williams P. L. Gray's Anatomy35th Br. ed. W. B. Saunders Co., Philadelphia 1973
   Google Scholar
• Werboff J., Goodman I., Havlena J., Sikov M. R. Effects of prenatal x-irradiation on motor performance in the rat. American Journal of Physiology 1961; 201: 703–706
   PubMedGoogle Scholar
• Wimer C. C., Wimer R. E., Roderick T. H. Some behavioral differences associated with relative size of hippocampus in the mouse. Journal of Comparative and Physiological Psychology 1971; 76: 57–65
   PubMed Web of Science ®Google Scholar
• Yamazaki J. N., Bennett L. R., Clement C. D. Response of the Nervous System to Ionizing Radiation, T. J. Haley, R. S. Snider. Academic Press, New York 1962
   Google Scholar