Basal forebrain stimulation induces discriminative receptive field plasticity in the auditory cortex

Behavioral Neuroscience

Volumn 113, Issue 4, 1999, Pages 691-702

  Dimyan, Michael A ^a,b   Weinberger, Norman M ^a,b  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL EXPERIMENT; ARTICLE; AUDITORY CORTEX; FOREBRAIN; GUINEA PIG; LEARNING; MALE; NERVE CELL PLASTICITY; NONHUMAN; RECEPTIVE FIELD; REINFORCEMENT;

ACOUSTIC STIMULATION; ANIMALS; AUDITORY CORTEX; CONDITIONING, CLASSICAL; ELECTRIC STIMULATION; ELECTROENCEPHALOGRAPHY; GUINEA PIGS; LEARNING; MALE; NEURONAL PLASTICITY; PROSENCEPHALON;

EID: 0032886565     PISSN: 07357044     EISSN: None     Source Type: Journal    
DOI: 10.1037/0735-7044.113.4.691     Document Type: Article

References (48)

1. Acquas, E., Wilson, C., & Fibiger, H. C. (1996). Conditioned and unconditioned stimuli increase frontal cortical and hippocampal acetylcholine release: Effects of novelty, habituation and fear. Journal of Neuroscience, 16, 3089-3096.
2. Bakin, J. S., & Weinberger, N. M. (1990). Classical conditioning induces CS-specific receptive field plasticity in the auditory cortex of the guinea pig. Brain Research, 536, 271-286.
3. Bakin, J. S., & Weinberger, N. M. (1996). Induction of a physiological memory in the cerebral cortex by stimulation of the nucleus basalis. Proceedings of the National Academy of Sciences (USA), 93, 11219-11224.
4. Beninger, R. J., Ingles, J. L., Mackenzie, P. J., Jhamandas, K., & Boegman, R. J. (1992). Muscimol injections into the nucleus basalis magnocellularis of rats: Selective impairment of working memory in the double Y-maze. Brain Research, 597, 66-73.
5. Bjordahl, T. S., Dimyan, M. A., & Weinberger, N. M. (1998). Induction of long-term receptive field plasticity in the auditory cortex of the guinea pig by stimulation of the nucleus basalis. Behavioral Neuroscience, 112, 467-479.
6. Butt, A. E., & Hodge, G. K. (1995). Acquisition, retention, and extinction of operant discriminations in rats with nucleus basalis magnocellularis lesions. Behavioral Neuroscience, 109, 699-713.
7. Deutsch, J. A. (1971, November). The cholinergic synapse and the site of memory. Science, 174, 788-794.
8. Dykes, R. W. (1997). Mechanisms controlling neuronal plasticity in somatosensory cortex. Canadian Journal of Physiological Pharmacology, 75, 535-545.
9. Edeline, J. M., & Weinberger, N. M. (1991). Subcortical adaptive filtering in the auditory system: Associative receptive field plasticity in the dorsal medial geniculate body. Behavioral Neuroscience, 105, 154-175.
10. Edeline, J. M., & Weinberger, N. M. (1993). Receptive field plasticity in the auditory cortex during frequency discrimination training: Selective retuning independent of task difficulty. Behavioral Neuroscience, 107, 82-103.
11. Essman, W. B. (1983). The cholinergic system in learning and memory. In Clinical pharmacology of learning and memory (pp. 15-42). New York: S.P. Medical.
12. Everitt, B. J., Robbins, T. W., Evenden, J. L., Marston, H. M., Jones, G. H., & Sirkia, T. A. (1987). The effects of excitotoxic lesions of the substantia innominata, ventral and dorsal globus pallidus on the acquisition and retention of a conditional visual discrimination: Implications for cholinergic hypothesis of learning and memory. Neuroscience, 22, 441-469.
13. Fisher, R. S., Buchwald, N. A., Hull, C. D., & Levine, M. S. (1988). GABAergic basal forebrain neurons project to the neocortex: The localization of glutamic acid decarboxylase and choline acetyltransferase in feline corticopetal neurons. Journal of Comparative Neurology, 272, 489-502.
14. Freund, T. F., & Meskenaite, V. (1992). g-Aminobutyric acid-containing basal forebrain neurons innervate inhibitory interneurons in the neocortex. Proceedings of the National Academy of Sciences (USA), 89, 738-742.
15. Gabriel, M., Saltwick, S., & Miller, J. (1975, September). Conditioning and reversal of short-latency multiple-unit responses in the rabbit medial geniculate nucleus. Science, 189, 1108-1109.
16. Gritti, I., Mainville, L., Mancia, M., & Jones, B. E. (1997). GABAergic and other noncholinergic basal forebrain neurons, together with cholinergic neurons, project to the mesocortex and isocortex in the rat. Journal of Comparative Neurology, 383, 163-177.
17. Hartgraves, S. L., Mensah, P. L., & Kelly, P. H. (1982). Regional decreases of cortical choline acetyltransferase after lesions of the septal area and in the area of nucleus basalis magnocellualaris. Neuroscience, 7, 2369-2376.
18. Hepler, D. J., Olton, D. S., Wenk, G. L., & Coyle, J. T. (1985). Lesions in nucleus basalis magnocellularis and medial septal area of rats produce qualitatively similar memory impairments. Journal of Neuroscience, 5, 866-873.
19. Inglis, F. M., Day, J. C., & Fibiger, H. C. (1994). Enhanced acetylcholine release in hippocampus and cortex during anticipation and consumption of a palatable meal. Neuroscience, 62, 1049-1056.
20. Jiménez-Capdeville, M. E., Dykes, R. W., & Myasnikov, A. A. (1997). Differential control of cortical activity by the basal forebrain in rats: A role for both cholinergic and inhibitory influences. Journal of Comparative Neurology, 381, 53-67.
21. Johnston, V. V., McKinney, M., & Coyle, J. T. (1979). Evidence for a cholinergic projection to neocortex from neurons in the basal forebrain. Proceedings of the National Academy of Science (USA), 76, 5392-5396.
22. Johnston, V. V., McKinney, M., & Coyle, J. T. (1981). Neocortical cholinergic innervations: A description of extrinsic and intrinsic components in the rat. Experimental Brain Research, 43, 159-172.
23. Kilgard, M. P., & Merzenich, M. M. (1998, March). Cortical map reorganization enabled by nucleus basalis activity. Science, 279, 1714-1718.
24. Lehmann, J., Nagy, J. I., Atmadja, S., & Fibiger, H. C. (1980). The nucleus basalis magnocellulais: The origin of a cholinergic projection to the neocortex of the rat. Neuroscience, 5, 1161-1174.
25. Maho, C., Hars, B., Edeline, J. M., & Hennevin, E. (1995). Conditioned changes in the basal forebrain: Relations with learning induced cortical plasticity. Psychobiology, 23, 10-25.
26. McGaugh, J. L. (1989). Involvement of hormonal and neuromodulatory systems in the regulation of memory storage. Annual Review of Neuroscience, 12, 255-287.
27. Mesulam, M. M., Mufson, E. J., Wainer, B. H., & Levey, A. I. (1983). Central cholinergic pathways in the rat: An overview based on alternative nomenclature (CH1-CH6). Neuroscience, 10, 1185-1201.
28. Miyamoto, M., Kato, J., Narumi, S., & Nagaoka, A. (1987). Characteristics of memory impairment following lesioning of the basal forebrain and medial septal nucleus in rats. Brain Research, 419, 19-31.
29. Moore, H., Sarter, M., & Bruno, J. P. (1993). Bidirectional modulation of stimulated cortical acetylcholine release by benzodiazepine receptor ligands. Brain Research, 627, 267-274.
30. Moriizumi, T., & Hattori, T. (1991). Separate neuronal populations of the rat globus pallidus projecting to the subthalamic nucleus, auditory cortex and pedunculopontine tegmental area. Neuroscience, 46, 701-710.
31. Olton, D. S. (1990). Dementia: Animal models of the cognitive impairments following damage to the basal forebrain cholinergic system. Brain Research Bulletin, 25, 499-502.
32. Rasmusson, D., & Szerb, J. C. (1975). Cortical acetylcholine release during operant behaviour in rabbits. Life Sciences, 16, 683-690.
33. Richardson, R. T., & DeLong, M. R. (1986). Nucleus basalis of Meynert neuronal activity during a delayed response task in monkey. Brain Research, 399, 364-368.
34. Roberts, A. C., Robbins, T. W., Everitt, B. J., Jones, G. H., Sirkia, T. E., Wilkinson, J., & Page, K. (1990). The effects of excitotoxic lesions of the basal forebrain on the acquisition, retention and serial reversal of visual discriminations in marmosets. Neuroscience, 34, 311-329.
35. Robertson, D., & Irvine, D. R. (1989). Plasticity of frequency organization in auditory cortex of guinea pigs with partial unilateral deafness. Journal of Comparative Neurology, 282, 456-471.
36. Ryugo, D. K., & Weinberger, N. M. (1978). Differential plasticity of morphologically distinct neuron populations in the medial geniculate body of the cat during classical conditioning. Behavioral and Neural Biology, 22, 275-301.
37. Santos-Benitez, H., Magarinos-Ascone, C. M., & Garcia-Austt, E. (1995). Nucleus basalis of Meynert cell responses in awake monkeys. Brain Research Bulletin, 37, 507-511.
38. Saper, C. B. (1984). Organization of cerebral cortical efferent systems in the rat: II. Magnocellular basal nucleus. Journal of Comparative Neurology, 222, 313-342.
39. Sarter, M. F., & Bruno, J. P. (1994). Cognitive functions of cortical ACh: Lesions from studies on trans-synaptic modulation of activated efflux. Trends in Neuroscience, 17, 217-220.
40. Siegel, S., & Castellan, N. J., Jr. (1988). Nonparametric statistics for the behavioral sciences. New York: McGraw Hill.
41. Supple, W. F, & Kapp, B. S. (1989). Response characteristics of neurons in the medial component of the medial geniculate nucleus during Pavlovian differential fear conditioning in rabbits. Behavioral Neuroscience, 103, 1276-1286.
42. Travis, R. P., & Sparks, D. L. (1968). Unitary responses and discrimination learning in the squirrel monkey: The globus pallidus. Physiology and Behavior, 3, 187-196.
43. Weinberger, N. M. (1998). Physiological memory in primary auditory cortex: characteristics and mechanisms. Neurobiology of Learning and Memory, 70, 226-251.
44. Weinberger, N. M., Ashe, J. H., Diamond, D. M., Metherate, R., McKenna, T. M., & Bakin, J. S. (1990). Retuning auditory cortex by learning: A preliminary model of receptive field plasticity. Concepts in Neuroscience, 1, 91-132.
45. Weinberger, N. M., Ashe, J. H., Metherate, R., McKenna, T. M., Diamond, D. M., Bakin, J. S., Lennartz, R. C., & Cassady, J. M. (1990). Neural adaptive information processing: A preliminary model of receptive field plasticity in auditory cortex during Pavlovian conditioning. In M. Gabriel & J. Moore (Eds.), Neurocomputation and learning: Foundations of adaptive networks (pp. 91-138). Cambridge, MA: Bradford Books/MIT Press.
46. Weinberger, N. M., & Diamond, D. M. (1987). Physiological plasticity of single neurons in auditory cortex: Rapid induction by learning. Progress in Neurobiology, 29, 1-55.
47. Whalen, P. J., Kapp, B. S., & Pascoe, J. P. (1994). Neuronal activity within the nucleus basalis and conditioned neocortical electroencephalographic activation. Journal of Neuroscience, 14, 1623-1633.
48. Wilson, F. A. W., & Rolls, E. T. (1990). Learning and memory is reflected in the responses of reinforcement-related in the primate basal forebrain. Journal of Neuroscience, 10, 1254-1267.