Post-activation potentiation in the neocortex of awake freely moving rats

Neuroscience and Biobehavioral Reviews

Volumn 22, Issue 2, 1998, Pages 195-207

  Campbell Teskey, G ^a   Valentine, Pamela A ^a  

^a UNIVERSITY OF CALGARY   (Canada)

Author keywords

Behaviour; Corpu s callosum; Isocortex; Kindling; Long term depression; Long term potentiation; LTD; LTP; Memory; Modulatory neurotransmitters; Neocortex; Plasticity; Posterior hypothalamus; Receptive field

Indexed keywords

4 AMINOBUTYRIC ACID; 4 AMINOBUTYRIC ACID RECEPTOR; N METHYL DEXTRO ASPARTIC ACID; N METHYL DEXTRO ASPARTIC ACID RECEPTOR; NEUROTRANSMITTER;

CORPUS CALLOSUM; ELECTROSTIMULATION; EVOKED CORTICAL RESPONSE; HIPPOCAMPUS; KINDLING; LONG TERM POTENTIATION; MEMORY; NEOCORTEX; NERVE CELL PLASTICITY; NEUROMODULATION; NONHUMAN; POSTERIOR HYPOTHALAMUS; PRIORITY JOURNAL; RAT; RECEPTIVE FIELD; REVIEW;

EID: 0344936037     PISSN: 01497634     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0149-7634(97)00004-3     Document Type: Article

References (153)

1. Abeles, M. Corticonics: Neural circuits of the cerebral cortex. Cambridge: Cambridge University Press; 1991.
2. Abeles M., Bergman H., Gat I., Meilijson I., Seidemann E., Tishby N., Vaadia E. Cortical activity flips among quasi-stationary states. Proceedings of the National Academy of Sciences of the USA. 92:1995;8616-8620.
3. Andersen P. Interhippocampal impulses: II. Apical dendritic activation of CA1 neurons. Acta Physiologica Scandinavica. 48:1960;178-208.
4. Andersen P., Holmqvist B., Voorhoeve P. E. Entorhinal activation of dentate granule cells. Acta Physiologica Scandinavica. 66:1966;448-460.
5. Artola A., Brocher S., Singer W. Different voltage-dependent thresholds for inducing long-term depression and long-term potentiation in slices of rat visual cortex. Nature. 347:1990;69-72.
6. Artola A., Singer W. The involvement of N-methyl-D-aspartate receptors in induction and maintenance of long-term potentiation in rat visual cortex. European Journal of Neuroscience. 2:1990;254-269.
7. Artola A., Singer W. Long-term potentiation and NMDA receptors in rat visual cortex. Nature. 330:1987;649-652.
8. Bair W., Koch C., Newsome W., Britten K. Power spectrum analysis of bursting cells in area MT in the behaving monkey. Journal of Neuroscience. 14:1994;2870-2892.
9. Bannerman D. M., Good M. A., Butcher S. P., Ramsay M., Morris R. G.M. NMDA receptors, long-term potentiation and spatial learning. Nature. 378:1995;182-186.
10. Barnes C. A. Involvement of LTP in memory: Are we 'searching under the street light'? Neuron. 15:1995;751-754.
11. Barnes C. A. Memory deficits associated with senescence: a neurophysiological and behavioural study in the rat. Journal of Comparative and Physiological Psychology. 93:1979;74-104.
12. Barnes C. A., Jung M. W., McNaughton B. L., Korol D. L., Andreasson K., Worley P. F. LTP saturation and spatial learning disruption: effects of task variables and saturation levels. Journal of Neuroscience. 14:1994;5793-5806.
13. Barrionuevo G., Brown T. H. Associative long-term potentiation in hippocampal slices. Proceedings of the National Academy of Sciences of the USA. 80:1983;5978-5982.
14. Bear M. F., Kirkwood A. Neocortical long-term potentiation. Current Opinions in Neurobiology. 3:1993;197-202.
15. Bear M. F., Press W. A., Connors B. W. Long-term potentiation in slices of kitten visual cortex and the effects of NMDA receptor blockade. Journal of Neurophysiology. 67:1992;1-11.
16. Bear M. F., Singer W. Modulation of visual cortical plasticity by acetylcholine and noradrenaline. Nature. 320:1986;172-176.
17. Berry R. L., Teyler T. J., Taizhen H. Induction of LTP in rat primary visual cortex: tetanus parameters. Brain Research. 481:1989;221-227.
18. Bland B. H., Vanderwolf C. H. Diencephallic and hippocampal mechanisms of motor activity in the rat: effects of posterior hypothalamic stimulation on behavior and hippocampal slow wave activity. Brain Research. 43:1972;67-88.
19. Bliss T. V.P., Gardner-Medwin A. R. Long-lasting potentiation of synaptic transmission in the dentate area of the unanesthetized rabbit following stimulation of the perforant path. Journal of Physiology (London). 232:1973;357-374.
20. Bliss T. V. P., Lømo T. Long-lasting potentiation of synaptic transmission in the dentate gyrus of the anesthetized rabbit following stimulation of the perforant path. Journal of Physiology. 232:1973;331-356.
21. Bowman D. M., Eggermont J. J., Smith G. M. Effect of stimulation on burst firing in cat primary auditory cortex. Journal of Neurophysiology. 74:1995;1841-1855.
22. Brocher S., Artola A., Singer W. Agonists of cholinergic and noradrenergic receptors facilitate synergistically the induction of long-term potentiation in slices of rat visual cortex. Brain Research. 573:1992;27-36.
23. Brown T. H., Chapman P. F., Kairiss E. W., Keenan C. L. Long-term synaptic potentiation. Science. 42:1988;724-728.
24. Burns B. D., Pritchard R. Contrast discrimination by neurones in the cat's visual cerebral cortex. Journal of Physiology. 175:1964;445-463.
25. Cain D. P. Long-term potentiation and kindling: how similar are the mechanisms. TINS. 12:1989;6-10.
26. Cain D. P., Hargreaves E. L., Boon F., Dennison Z. An examination of the relations between hippocampal long-term potentiation, kindling, afterdischarge, and place learning in the water maze. Hippocampus. 3:1993;153-164.
27. Castro-Alamancos M. A., Donoghue J. P., Connors B. W. Different forms of synaptic plasticity in somatosensory and motor areas of the neocortex. Journal of Neuroscience. 15(7):1995;5324-5333.
28. Cattaneo A., Maffei L., Morrone C. Patterns in the discharge of simple and complex visual cortical cells. Proceedings of the Royal Society (London). B 212:1981;279-297.
29. Chagnac-Amitai Y., Luhmann H. J., Prince D. A. Burst generating and regular spiking layer 5 pyramidal neurons of rat neocortex have different morphological features. Journal of Comparative Neurology. 296:1990;598-613.
30. Corcoran, M. E. Characteristics and mechanisms of kindling. In: Barnes, C.; Kavivas, P. eds. Sensitization of the nervous system. New Jersey: Telford Press; 1988:82-116.
31. Crair M. C., Malenka R. C. A critical period for long-term potentiation at thalamocortical synapses. Nature. 375:1995;325-328.
32. Cruikshank S. J., Weinberger N. M. Receptive field plasticity in the adult auditory cortex induced by Hebbian covariance. Journal of Neuroscience. 16:1996;861-875.
33. Connors B., Gutnick M., Prince D. Electrophysiological properties of neocortical neurons in vitro. Journal of Neurophysiology. 48:1982;1302-1320.
34. deJonge M., Racine R. J. The development and decay of kindling-induced increases in paired-pulse depression in the dentate gyrus. Brain Research. 412:1987;318-328.
35. B receptor feed-back on GABA release. Journal of Physiology. 412:1989;513-541.
36. Dennison Z., Teskey G. C., Cain D. P. Persistence of kindling: Effect of partial kindling, retention interval, kindling site, and stimulation parameters. Epilepsy Research. 21:1995;171-182.
37. Destrade C. Two types of diencephalically driven RSA (theta) as a means of studying memory formation in mice. Brain Research. 234:1986;486-493.
38. Edelman, G. M. Neural Darwinism: The theory of neuronal group selection. New York: Basic Books; 1987.
39. Eggermont, J. J. Is there a neural code? Neuroscience and Biobehavioral Reviews 22: 255-370; 1998.
40. Eggermont J. J., Johannesma P. I. M., Aertsen A. M. H. J. Reverse correlation methods in auditory research. Quart. Rev. Biophys. 16:1983;341-414.
41. Eggermont J. J., Smith G. M. Burst-firing sharpens frequency-tuning in primary auditory cortex. Neuroreport. 7:1996;753-757.
42. Epping W. J. M., Eggermont J. J. Coherent neural activity in the auditory midbrain of the grassfrog. Journal of Neurophysiology. 57:1987;1464-1483.
43. Fox K. The critical period for long-term potentiation in primary sensory cortex. Neuron. 15:1995;485-488.
44. Friedman A., Gutnick M. J. Low threshold calcium electrogenesis in neocortical neurons. Neuroscience Letters. 81:1987;117-122.
45. Gallistel, R. Is long-term potentiation a plausible basis for memory? In: McGaugh, J.L; Weinberger, N. M.; Lynch, G. eds. Brain and memory: Modulation and mediation of plasticity. New York: Oxford University Press; 1995:328-337.
46. Gerren R. A., Weinberger N. M. Long-term poteniation in the magnocellular medial geniculate nucleus of the anesthetized cat. Brain Research. 265:1983;138-142.
47. Goddard G. V. Development of epileptic seizures through brain stimulation at low intensity. Nature. 214:1967;1020-1021.
48. Goddard G. V., Douglas R. M. Does the engram of kindling model the engram of normal long-term memory? Canadian Journal of Neurological Science. 2:1975;385-394.
49. Goddard G. V., McIntyre D. C., Leech C. K. A permanent change in brain function resulting from daily electrical stimulation. Experimental Neurology. 25:1969;90-112.
50. Gustafsson B., Wigstrom H. Hippocampal long-lasting potentiation produced by pairing single volleys and brief conditioning tetanic evoked in separate afferents. Journal of Neuroscience. 6:1986;1575-1582.
51. Gustafsson B., Wigstrom H. Physiological mechanisms underlying long-term potentiation. TINS. 11:1988;156-162.
52. Hasselmo M. Neuromodulation and cortical function modeling the physiological basis for behavior. Behav. Brain Res. 67:1994;1-27.
53. Hebb, D. O. The organization of behavior. New York: John Wiley; 1949.
54. Iriki A., Pavlides C., Keller A., Asanuma H. Long-term potentiation of thalamic input to the motor cortex induced by coactivation of thalamocortical and corticocortical afferent. Journal of Neurophysiology. 65:1991;1435-1441.
55. James, W. Psychology: Briefer course. Cambridge, MA: Harvard University Press; 1890.
56. Kato M., Lino K., Kano M. Functional reorganization of adult cat somatosensory cortex is dependent on NMDA receptors. Neuroreport. 2:1991;77-80.
57. Keller A., Miyashita E., Asanuma H. Minimal stimulus parameters and the effects of hyperpolarization on the induction of long-term potentiation in cat motor cortex. Experimental Brain Research. 87:1991;295-302.
58. Kelso S. R., Ganong A. H., Brown T. H. Hebbian synapses in hippocampus. Proceedings of the National Academy of Sciences of the USA. 83:1986;5326-5330.
59. Kimura A., Melis F., Asanuma H. Long-lasting changes of neuronal activity in the motor cortex of cats. Neuroreport. 7:1996;869-872.
60. King G., Dingledine R., Giacchino J., McNamara J. O. Abnormal neuronal excitability in hippocampal slices from kindled rats. Journal of Neurophysiology. 54:1985;1295-1304.
61. Kirkwood A., Lee H. K., Bear M. F. Co-regulation of long-term potentiation and experience-dependent synaptic plasticity in visual cortex by age and experience. Nature. 375:1995;328-331.
62. Komatsu Y., Nakajima S., Toyama K. Induction of long-term potentiation without the participation of N-methyl-D-aspartate receptors in kitten visual cortex. Journal of Neurophysiology. 65:1991;20-32.
63. Laroche S., Doyere V., Bloch V. Linear relation between the magnitude of long-term potentiation in the dentate gyrus and associative learning in the rat: a demonstration using commissural inhibition and local infusion of an N-methyl-D-aspartate receptor antagonist. Neuroscience. 28(2):1989;375-386.
64. Laroche, S.; Doyere, V.; Redini Del Negro, C. What role for LTP in learning and the maintenance of memories? In: Baudry, M.; Davis, J. L. eds. LTP: A debate of the current issues. London: MIT Press; 1991:301-316.
65. Larson J., Lynch G. Induction of synaptic potentiation in hippocampus by patterned stimulation involves two events. Science. 232:1986;985-988.
66. Lashley, K. S. Brain mechanisms and intelligence: A quantitative study of injuries to the brain. Chicago: University of Chicago Press; 1929.
67. Lashley K. S. In search of the engram. Symp. Soc. Exp. Biol. 4:1950;454-482.
68. Levy W. B., Steward O. Synapses as associative memory elements in the hippocampal formation. Brain Research. 175(2):1979;233-245.
69. Lømo T. Frequency potentiation of excitatory synaptic activity in the dentate area of the hippocampal formation. Acta Physiologica Scandinavica. 68(suppl.277):1966;128.
70. Lømo T. Potentiation of monosynaptic EPSPs in cortical cells by single and repetitive afferent volleys. Journal of Physiology (London). 194:1966;84-85.
71. Lømo T. Patterns of activation in a monosynaptic cortical pathway: the perforant path input to the dentate area of the hippocampal formation. Experimental Brain Research. 12:1971;18-45.
72. Lømo T. Potentiation of monosynaptic EPSPs in the perforant path-dentate granule cell synapse. Experimental Brain Research. 12:1971;18-45.
73. Madison D. V., Malenka R. C., Nicoll R. A. Mechanisms underlying long-term potentiation of synaptic transmission. Annual Review of Neuroscience. 14:1991;379-397.
74. Maru E., Goddard G. V. Alteration in dentate neuronal activities associated with perforant-path kindling. I Long-term potentiation of excitatory transmission. Experimental Neurology. 96:1987;19-32.
75. McClelland J. L., McNaughton B. L., O'Reilly R. C. Why there are complimentary learning systems in the hippocampus and neocortex: Insights from the successes and failures of connectionist models of learning and memory. Psychology Review. 102:1995;419-457.
76. McIntyre D. C., Plant J. R. Pyriform cortex involvement in kindling. Neuroscience and Biobehavoral Reviews. 13:1989;277-280.
77. McIntyre D. C., Wong R. K. S. Cellular and synaptic properties of amygdala-kindled pyriform cortex in vitro. Journal of Neurophysiology. 55:1986;1295-1307.
78. McNamara J. O., Byrne M. C., Dasheiff R. M., Fitz J. G. The kindling model of epilepsy: A review. Progress in Neurobiology. 15:1978;139-159.
79. McNaughton B. L., Barnes C. A., Rao G., Baldwin J., Rasmussen M. Long-term enhancement of hippocampal synaptic transmission and the acquisition of spatial information. Journal of Neuroscience. 6:1986;563-571.
80. McNaughton B. L., Douglas R. M., Goddard G. V. Synaptic enhancement in fascia dentata: Cooperativity among coactive afferents. Brain Research. 157:1978;277-293.
81. McNaughton B. L., Miller J. J. Medial septal projections to the dentate gyrus of the rat: Electrophysiological analysis of distribution and plasticity. Experimental Brain Research. 56:1984;243-256.
82. Merzenich, M. M. Dynamic neocortical processes and the origins of higher brain functions. In: Changeux, J. P.; Konishi, M. eds. The neural and molecular basis of learning. New York: Wiley; 1987:337-358.
83. Merzenich M. M., Nelson R. J., Stryker M. P., Cynader M. S., Shoppmann A., Zook J. M. Somatosensory cortical map changes following digital amputation in adult monkey. Journal of Comparative Neurology. 224:1984;591-605.
84. Metherate R., Ashe J. H. Facilitation of a NMDA receptor-mediated EPSP by paired-pulse stimulation in rat neocortex via depression of GABAergic IPSPs. Journal of Physiology. 481(2):1994;331-348.
85. Metherate R., Ashe J. H. Synaptic interactions involving acetylcholine, glutamate, and GABA in rat auditory cortex. Experimental Brain Research. 107:1995;59-72.
86. Mitsuno K., Sasa M., Ishihara K., Ishikawa M., Kikuchi H. LTP of mossy fiber-stimulated potentials in CA3 during learning in rats. Physiology and Behavior. 55:1994;633-638.
87. Morrell, F.; de Toledo-Morrell, L. Kindling as a model of neuronal plasticity. In: Wada, J. A. ed, Kindling 3. New York: Raven; 1986.
88. Nelson S. B., Sur M. NMDA receptors in sensory information processing. Current Opinions in Neurobiology. 2:1992;484-488.
89. Nudo R. J., Jenkins W. M., Merzenich M. M. Repetitive microstimulation alters the cortical representation of movements in adult rats. Somatosens. Mot. Res. 7:1990;463-483.
90. Oddie S. D., Stefanek W., Kirk I., Bland B. H. Intraseptal procaine abolishes hypothalamic stimulation-induced wheel-running and hippocampal theta field activity in rats. Journal of Neuroscience. 16:1996;1948-1956.
91. Oddie S. D., Bland B. H., Colom L. V., Vertes R. P. The midline posterior hypothalamic region comprises a critical part of the ascending brainstem hippocampal synchronizing pathway. Hippocampus. 4:1994;454-473.
92. O'Dell T. J., Kandel E. R., Grant S. G. Long-term potentiation in the hippocampus is blocked by tyrosine kinase inhibitors. Nature. 353:1991;558-560.
93. Pei X., Vidyasagar T. R., Volgushev M., Creutzfeldt O. D. Receptive field analysis and orientation selectivity of postsynaptic potentials of simple cells in cat visual cortex. Journal of Neuroscience. 14:1994;7130-7140.
94. Patneau D. K., Stripling J. S. Functional correlates of selective long-term potentiation in the olfactory cortex and olfactory bulb. Brain Research. 585:1992;219-228.
95. Phillips D. P., Sark S. A. Separate mechanisms control spike numbers and inter-spike intervals in transient responses of cat auditory cortical neurons. Hearing Research. 53:1991;17-27.
96. Racine R. J. Modification of seizure activity by electrical stimulation II. Motor seizure. Electroencephalogr. Clin. Neurophysiol. 32:1972;281-284.
97. Racine R. J. The first decade. Neurosurgery. 3(2):1978;234-252.
98. Racine, R. J.; Burnham, W. M.; Gilbert, M.; Kairiss, E. W. Kindling mechanisms; I. Electrophysiological studies. In: Wada, J. A. ed. Kindling 3. New York: Raven; 1986:263-282.
99. Racine R. J., Chapman C. A., Trepel C., Teskey G. C., Milgram N. W. Post-activation potentiation in the neocortex. III. Kindling-induced potentiation in the chronic preparation. Brain Research. 702:1995;77-86.
100. Racine R. J., Chapman C. A., Trepel C., Teskey G. C., Milgram N. W. Post-activation potentiation in the neocortex. IV. Multiple sessions required for induction of long-term potentiation in the chronic preparation. Brain Research. 702:1995;87-93.
101. Racine, R. J.; Ivy, G. O.; Milgram, N. W. Kindling: clinical relevance and anatomical substrate. In: Bolwig, T. G.; Trimble, M. R. eds. The clinical relevance of kindling. Chichester: John Wiley and Sons Ltd; 1989:15-34.
102. Racine R. J., Milgram N. W., Hafner S. Long-term potentiation phenomena in the rat limbic forebrain. Brain Research. 260:1983;217-231.
103. Racine R. J., Moore K.-A., Evans C. Kindling-induced potentiation in the piriform cortex. Brain Research. 556:1991;218-225.
104. Racine R. J., Mosher M., Kairiss E. W. The role of the pyriform cortex in the generation of interictal spikes in the kindling preparation. Brain Research. 454:1988;251-263.
105. Racine R. J., Teskey G. C., Wilson D., Seidlitz E., Milgram N. W. Post-activation potentiation and depression in the neocortex of the rat: II Chronic preparations. Brain Research. 637:1994;83-96.
106. Racine R. J., Tuff L., Zaide J. Kindling, unit discharge and neural plasticity. Canadian Journal of Neurological Science. 2:1975;395-405.
107. Racine R. J., Wilson D., Teskey G. C., Milgram N. W. Post-activation potentiation in the neocortex: I Acute preparations. Brain Research. 637:1994;73-82.
108. Racine R. J., Wilson D. A., Gingell R., Sutherland D. Long-term potentiation in the interpoitus and septobulbar nuclei of the rat. Experimental Brain Research. 63:1986;158-162.
109. Radons G., Becker J. D., Dulfer B., Kruger J. Analysis, classification and coding of multielectrode spike trains with hidden Markov models. Biol. Cybernetics. 71:1994;359-373.
110. Recanzone G. H., Merzenich M. M., Dinse H. R. Expansion of the cortical representation of a specific skin field in primary somatosensory cortex by intracortical microstimulation. Cereb. Cort. 2:1992;181-196.
111. Robinson T. E., Whishaw I. Q. Effects of posterior hypothalamic lesions on voluntary behavior and hippocampal electroencephalograms in the rat. Journal of Comparative and Physiological Psychology. 86:1974;768-786.
112. Rogan M. T., LeDoux J. E. LTP is accompanied by commensurate enhancement of auditory-evoked responses in a fear conditioned circuit. Neuron. 15:1995;127-136.
113. Roman F. S., Chaillan F. A., Soumireu-Mourat B. Long-term potentiation in rat piriform cortex following discrimination learning. Brain Research. 601:1993;265-272.
114. Ramón y Cajal S. La fine structure des centres nerveux. Proceedings of the Royal Society (London). 55:1894;444-468.
115. Rosenzweig M. R., Bennett E. L. Psychobiology of plasticity: effects of training and experience on brain and behaviour. Behav. Brain Res. 78:1996;57-65.
116. Saper C. B. Organization of cerebral cortex cortical afferent systems in the rat I. magnocellular basal nucleus. Journal of Comparative Neurology. 222:1984;313-342.
117. Saucier D., Cain D. P. Spatial learning without NMDA receptor-dependent long-term potentiation. Nature. 378:1995;186-189.
118. Schuman E. M., Madison D. V. A requirement for the intercellular messenger nitric oxide in long-term potentiation. Science. 254:1991;1503-1506.
119. Sherman S. M. Dual response modes in lateral geniculate neurons: mechanisms and functions. Visual Neuroscience. 13:1996;205-213.
120. Sherrington, C. S. Part III. The central nervous system. In: Foster, M. ed. A text-book of physiology. London: Macmillan; 1897.
121. Squire L. R., Zola-Morgan S. The medial temporal lobe memory system. Science. 253:1991;1380-1386.
122. Steriade M., Deschenes M. The thalamus as a neuronal oscillator. Brain Res. Rev. 8:1984;1-63.
123. Stripling J. S., Patneau D. K., Gramlich C. A. Selective long-term potentiation in the piriform cortex. Brain Research. 441:1988;281-291.
124. Stripling J. S., Patneau D. K., Gramlich C. A. Characterization and anatomical distribution of selective long-term potentiation in the olfactory forebrain. Brain Research. 542:1991;107-122.
125. Sutherland R. J., Dringenberg H. C., Hoesing J. M. Induction of long-term potentiation at perforant path dentate synapses does not affect place learning and memory. Hippocampus. 3:1993;141-148.
126. Sutor B., Hablitz J. J. Long-term potentiation in frontal cortex: role of NMDA-modulated polysynaptic excitatory pathways. Neuroscience Letters. 97:1989;111-117.
127. Tanzi E. I fatti e le induzioni nell'odierna isolgia del sistema nervoso. Rev. Sper. Freniatr. Med. Leg. 19:1893;419-472.
128. Swanson, L. W. Brain maps: structure of the rat brain. Amsterdam: Elsevier; 1992.
129. Teskey G. C., Racine R. J. Increased spontaneous unit discharge rates following electrical kindling in the rat. Brain Research. 624:1993;11-18.
130. Teyler T.J., DiScenna P. Long-term potentiation. Annual Review of Neuroscience. 10:1987;131-161.
131. Traub, R. D.; Miles, R. Neuronal networks of the hippocampus. Cambridge: Cambridge University Press; 1991.
132. Trepel, C.; Racine, R. J. Induction and decay of neocortical long-term potentiation and the effects of N-methyl-D-aspartate receptor blockade in the adult, behaving rat. (in preparation).
133. Tsumoto T. Long-term potentiation and depression in the cerebral neocortex. Japanese Journal of Physiology. 40:1990;573-593.
134. Quirk G. J., Repa J. C., Laddies J. E. Fear conditioning enhances short-latency auditory responses of lateral amygdala neurons: parallel recordings in the freely behaving rat. Neuron. 15:1995;1029-1039.
135. Valentine P. A., Teskey G. C. Repeated co-activation of the corpus callosum and hypothalamus induces a long-term potentiation of the neocortex in awake behaving rats. Neuroscience Abstracts. 21:1995;1099.
136. Vanderwolf C. H. Hippocampal electrical activity and voluntary movement in the rat. Electroencephalogr. Clin. Neurophysiol. 26:1969;407-418.
137. Vanderwolf, C. H. Aminergic control of the electroencephalogram: A progress report. In: Boulton, A. A.; Baker, G. B.; Dewhurst, W.; Sandler, M. eds. Neurobiology of trace amines. Clifton: Humana Press; 1984:163-183.
138. Vanderwolf C. H. Near total loss of 'learning' and 'memory' as a result of combined cholinergic and serotonergic blockade in the rat. Behav. Brain Res. 23:1986;43-57.
139. Vanderwolf C. H., Baker G. B. Evidence that serotonin mediates non-cholinergic neocortical low-voltage fast activity, non-cholinergic hippocampal rhythmical slow activity and contributes to intelligent behavior. Brain Research. 374:1986;342-356.
140. Vanderwolf, C. H.; Leung, L.-W. S. Brain electrical activity in relation to behavior. In: Boulton, A. A.; Baker, G. B. eds. Neuromethods Vol. 1: General neurochemical techniques. Clifton: Humana Press; 1985:305-341.
141. Vanderwolf C. H., Harvey G. C., Leung L.-W. S. Transcallosal evoked potentials in relation to behaviour in the rat: Effects of atropine, p-chlorophenylalanine, reserpine, scopolamine and trifluoperazine. Behav. Brain Res. 25:1987;31-48.
142. Vertes R. P., Crane A. M., Colom L. V., Bland B. H. PHA-L analysis of ascending projections from the posterior hypothalamus in the rat. Journal of Comparative Neurology. 359:1995;1-27.
143. Vidyasagar T. R., Pei X., Volgushev M. Multiple mechanisms underlying the orientation selectivity of visual cortical neurones. TINS. 19:1996;272-277.
144. von der Malsburg C. Binding in models of perception and brain function. Current Biology. 5:1995;520-526.
145. von der Malsburg, C.; Singer, W. Principles of cortical network organization. In: Rakic, T. P.; Singer, W. eds. Neurobiology of neocortex. New York: Wiley; 1988:69-99.
146. Weinberger N. M. Learning-induced changes in auditory receptive fields. Current Biology. 3:1993;570-577.
147. Weinberger, N. M. Beyond neuronal excitability: receptive field analysis reveals that association specifically modifies the representation of auditory information. In: Squire, L. R.; Butters, N. eds. Neuropsychology of memory, 2nd Edn. New York: Guildford Press; 1992:496-510.
148. Wilhite B. L., Teyler T. J., Hendricks C. Functional relations of the rodent claustral-entorhinal-hippocampal system. Brain Research. 365:1986;54-60.
149. Whishaw, I. Q. The decorticate rat. In: Kolb, B.; Tees, R. C. eds. The cerebral cortex of the rat. Cambridge: MIT Press; 1990:239-267.
150. Wilson D. A. A comparison of the postnatal development of post-activation potentiation in the neocortex and dentate gyrus of the rat. Dev. Brain Res. 16:1984;61-68.
151. Wilson D. A., Racine R. J. The postnatal development of post-activation potentiation in the rat neocortex. Dev. Brain Res. 7:1983;271-276.
152. Wood-Jones. F.; Porteus, S. D. The matrix of the mind. Honolulu: Mercantile; 1928.
153. Zola-Morgan S., Squire L. R. Neuroanatomy of memory. Annual Review of Neuroscience. 16:1993;547-563.