Activity-dependent plasticity in adult somatic sensory cortex

Seminars in the Neurosciences

Volumn 9, Issue 1-2, 1997, Pages 47-58

  Ebner, F F ^a   Rema, V ^a   Sachdev, R ^a   Symons, F J ^a  

^a VANDERBILT UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

4 AMINOBUTYRIC ACID; CALCIUM ION; EXCITATORY AMINO ACID; GLUTAMATE RECEPTOR; NEUROTRANSMITTER;

ANIMAL CELL; CONTROLLED STUDY; DEPOLARIZATION; HUMAN; HUMAN CELL; NEOCORTEX; NERVE CELL EXCITABILITY; NERVE CELL PLASTICITY; NERVE ENDING; NEUROMODULATION; NEUROTRANSMITTER RELEASE; NONHUMAN; REVIEW; SENSORY STIMULATION; SOMATOSENSORY CORTEX; SYNAPSE;

EID: 0030930194     PISSN: 10445765     EISSN: None     Source Type: Journal    
DOI: 10.1006/smns.1997.0105     Document Type: Article

References (74)

1. Artola A., Singer W. Long term depression of excitatory synaptic transmission and its relationship to long-term potentiation. Trends Neurosci. 16:1993;480-487.
2. Castro-Alamancos M. A., Donoghue J. P., Connors B. W. Different forms of synaptic plasticity in somatosensory and motor areas of the neocortex. J. Neurosci. 15:1995;5324-5333.
3. Bliss T. V. P., Lomo T. Long-lasting potentiation of synaptic transmission in the dentate area of the anaesthetized rabbit following stimulation of the perforant path. J. Physiol. (London). 232:1973;331-356.
4. Hubel D. H., Wiesel T. N. Single-cell responses in striate cortex of kittens deprived of vision in one eye. J. Neurophysiol. 26:1963b;1003-1017.
5. Diamond M. E., Armstrong-James M., Ebner F. F. Experience-dependent plasticity in adult rat barrel. Proc. Natl. Acad. Sci. USA. 90:1993;2082-2086.
6. Recanzone G. H., Merzenich M. M., Jenkins W. M., Grajski K. A., Dinse H. R. Topographic reorganization of the hand representation in cortical area 3b of owl monkeys trained in a frequency-discrimination task. J. Neurophysiol. 67:1992;1031-1056.
7. Ramachandran V. S., Stewart M., Rogers-Ramachandran D. C. Perceptual correlates of massive cortical reorganization. Neuroreport. 3:1992;583-586.
8. Flor H., Elbert T., Wienbruch C., Pantev C., Birbaumer N., Larbig W., Taub E. Phantom-limb pain as a perceptual correlate of cortical organization following arm amputation. Nature. 375:1995;482-484.
9. Knecht S., Henningsen H., Elbert T., Flor H., Hohling C., Pantev C., Birbaumer N., Taub E. Cortical reorganization in human amputees and mislocalization of painful stimuli to the phantom limb. Neurosci. Lett. 201:1995;262-264.
10. Mogilner A., Grossman J. A., Ribary U., Joliot M., Volkmann J., Rapaport D., Beasley R. W., Llinas R. R. Somatosensory cortical plasticity in adult humans revealed by magnetoencephalography. Proc. Natl. Acad. Sci. USA. 90:1993;3593-3597.
11. Allard T. R., Clark S. A., Jenkins W. M., Merzenich M. M. Reorganization of somatosensory area 3b representation in adult owl monkeys after digital syndactyly. J. Neurophysiol. 66:1991;1048-1058.
12. Elbert T., Pantev C., Wienbruch C., Rochstroh B., Taub E. Increased cortical representation of the fingers of the left hand in string players. Science. 270:1995;305-307.
13. Pascual-Leone A., Torres F. Plasticity of the sensorimotor cortex representation of the reading finger in Braille readers. Brain. 116:1993;39-52.
14. Sadato N., Pascual-Leone A., Grafman J., Ibanez V., Deiber M. P., Dold G., Hallet M. Activation of the primary viual cortex by Braille reading in blind subjects. Nature. 11:1996;479-480.
15. Merzenich M. M., Kaas J. H., Wall J. T., Nelson R. J., Sur M., Felleman D. J. Topographic reorganization of somatosensory cortical areas 3b and 1 in adult monkeys following restricted deafferentation. Neuroscience. 8:1983;33-55.
16. Merzenich M. M., Nelson R. J., Stryker M. S., Cynader M. S., Schoppmann A., Zook J. M. Somatosensory cortical map changes following digit amputation in adult monkeys. J. Comp. Neurol. 224:1984;591-605.
17. Rasmusson D. D. Reorganization of raccoon somatosensory cortex following removal of the fifth digit. J. Comp. Neurol. 205:1982;316-326.
18. Wall J. T., Cusick C. G. Cutaneous responsiveness in primary somatosensory (SI) hindpaw cortex before and after partial hindpaw deafferentation in adult rats. J. Neurosci. 4:1984;1499-1515.
19. Calford M. B., Tweedale R. Immediate and chronic changes in responses of somatosensory cortex in adult flying-fox after digit amputation. Nature. 332:1988;446-448.
20. Wall J. T., Felleman D. J., Kaas J. H. Recovery of normal topography in the somatosensory cortex of monkeys after nerve crush and regeneration. Science. 221:1983;771-773.
21. Recanzone G. H., Jenkins W. M., Hradek G. T., Merzenich M. M. Progressive improvement in discrimination abilities in adult owl monkeys performing a tactile frequency discrimination task. J. Neurophysiol. 67:1992;1015-1030.
22. Recanzone G. H., Merzenich M. M., Jenkins W. M. Frequency discrimination training engaging a restricted skin surface results in an emergence of a cutaneous response zone in cortical area 3a. J. Neurophysiol. 67:1992;1057-1070.
23. Recanzone G. H., Merzenich M. M., Schreiner C. E. Changes in the distributed temporal response properties of SI cortical neurons reflect improvements in performance on a temporally based tactile discrimination task. J. Neurophysiol. 67:1992;1071-1091.
24. Byl N. N., Merzenich M. M., Jenkins W. M. A primate genesis model of focal dystonia and repetitive strain injury. I. Learning-induced dedifferentiation of the representation of the hand in the primary somatosensory cortex in adult monkeys. Neurology. 47:1996;508-520.
25. Delacour J., Houcine O., Talbi B. "Learned" changes in the responses of the rat barrel field neurons. Neuroscience. 23:1987;63-71.
26. Armstrong-James M., Diamond M. E., Ebner F. F. An innocuous bias in whisker use in adult rats modifies receptive fields of barrel cortex neurons. J. Neurosci. 14:1994;6978-6991.
27. Welker E., Soriano E., Dorfl J., Van der Loos H. Plasticity in the barrel cortex of the adult mouse: Effects of peripheral deprivation on GAD-immunoreactivity. Brain Res. 74:1989;441-452.
28. Ito M. Processing of vibrissa sensory information within the rat neocortex. J. Neurophysiol. 54:1985;479-490.
29. Simons D. J. Temporal and spatial integration in the rat SI Vibrissa Cortex. J. Neurophysiol. 54:1985;615-635.
30. Armstrong-James M., Fox K. Spatiotemporal convergence and divergence in the rat S1 "barrel" cortex. J. Comp. Neurol. 263:1987;265-281.
31. Armstrong-James M., Callahan C. A., Friedman M. A. Thalamo-cortical processing of vibrissal information in the rat. I. intracortical origins of surround but not centre receptive fields of layer IV neurones in the rat SI barrel field cortex. J. Comp. Neurol. 303:1991;193-210.
32. Armstrong-James M., Callahan C. A. Thalamo-cortical processing of vibrissal information in the rat. II. Spatiotemporal convergence in the thalamic ventroposterior medial nucleus (VPm) and its relevance to generation of receptive fields of S1 cortical "barrel" neurones. J. Comp. Neurol. 303:1991;211-224.
33. Diamond M. D., Huang W., Ebner F. F. Laminar comparison of somatosensory cortical plasticity. Science. 265:1994;1885-1888.
34. Huang W., Ebner F. F. The influence of early whisker sensory deprivation on cortical plasticity in the adult rat. Neurosci. Abstr. 54:1995;123.
35. Siegelbaum S. A., Kandel E. R. Learning-related synaptic plasticity: LTP and LTD. Curr. Opin. Neurobiol. 1:1991;113-120.
36. Bear M. F., Cooper L. N., Ebner F. F. A physiological basis for a theory of synapse modification. Science. 237:1987;42-48.
37. Bear M. F., Malenka R. C. Synaptic plasticity: LTP and LTD. Curr. Opin. Neurobiol. 4:1994;389-399.
38. Connor J. A., Miller L. D., Pettrozzino J., Muller W. Calcium signaling in dendritic spines of hippocampal neurons. J. Neurobiol. 25:1994;234-242.
39. Guthrie P. B., Segal M., Kater S. B. Independent regulation of calcium revealed by imaging dendritic spines. Nature. 354:1991;76-80.
40. Byrne J. H., Kandel E. R. Presynaptic facilitation revisited: State and time dependence. J. Neurosci. 16:1996;425-435.
41. Colonnier M. Synaptic patterns on different cell types in the different laminae of the cat visual cortex. An electron microscope study. Brain Res. 9:1968;268-287.
42. Valverde F. Apical dendritic spines of the visual cortex and light deprivation in the mouse. Exp. Brain Res. 3:1967;337-352.
43. Ryugo D. K., Ryugo R., Killackey H. P. Changes in pyramidal cell density consequent to vibrissae removal in the newborn rat. Brain Res. 96:1975;82-87.
44. Freire M. Effects of dark rearing on dendritic spines in layer IV of the mouse visual cortex: A quantitative electron microscopical study. J. Anat. 126:1978;193-201.
45. Marin-Padilla M. Structural abnormalities of the cerebral cortex in human chromosomal aberrations: A Golgi study. Brain Res. 44:1972;625-629.
46. Purpura D. P. Dendritic spine 'dysgenesis' and mental retardation. Science. 186:1974;1126-1128.
47. Diamond M. C. Enriching Heredity: The Impact of the Environment on the Anatomy of the Brain. 1986;Free Press, NY.
48. Greenough W. T. What's special about development? Thoughts on the bases of experience-sensitive synaptic plasticity. Developmental Neuropsychobiology. 1986;Academic Press, San Diego. p. 387-407.
49. Nakanishi S. Molecular diversity of glutamate receptors and implications for brain function. Science. 258:1992;597-603.
50. Jones K. A., Baughman R. W. Both NMDA and non-NMDA subtypes of glutamate receptors are concentrated at synapses on cerebral cortical neurons in culture. Neuron. 7:1991;593-603.
51. Jonas P., Spruston N. Mechanisms shaping glutamate-mediated excitatory postsynaptic currents in the CNS. Curr. Biol. 4:1994;366-372.
52. Sommer B., Seeburg P. H. Glutamate receptor channels: novel properties and new clones. Trends Pharmacol. Sci. 13:1992;291-296.
53. Rema V., Ebner F. F. Postnatal changes in NMDAR1 subunit expression in the rat trigeminal pathway to barrel field cortex. J. Comp. Neurol. 368:1996;165-184.
54. Armstrong-James M., Welker E. Different roles for NMDA and non-NMDA receptors in fast and slow sensory transmission by the rat SI barrel cortex neuronesin vivo. J. Physiol. 467:1993;91P.
55. Armstrong-James M., Houchen J. H., Ebner F. F. An innocuous bias in whisker use in adult rats alters relative NMDA and AMPA receptor sensory transmission in barrel field cortex. Soc. Neurosci. Abstr. 1996.
56. Rema V., Armstrong-James M., Ebner F. F. Soc. Neurosci. Abstr. 1997.
57. Garraghty P. E., Muja N. NMDA receptors and plasticity in adult primate somatosensory cortex. J. Comp. Neurol. 367:1996;319-326.
58. Akhtar N. D., Land P. W. Activity-dependent regulation of glutamic acid decarboxylase in the rat barrel cortex: Effects of neonatal versus adult sensory deprivation. J. Comp. Neurol. 307:1991;200-213.
59. Welker C. Microelectrode delineation of fine grain somatotopic organization of SmI cerebral neocortex in albino rat. Brain Res. 26:1971;259-275.
60. Welker E., Soriano E., Dorfl J., Van der Loos H. Plasticity in the barrel cortex of the adult mouse: Transient increase of GAD-immunoreactivity following sensory stimulation. Exp. Brain Res. 78:1989;659-664.
61. Lin C. S., Lu S. M., Schmechel D. E. Glutamic acid decarboxylase immunoreactivity in layer IV of barrel cortex of rat and mouse. J. Neurosci. 5:1985;1934-1939.
62. Ebner F. F., Lu S. M., Rema V., Huang W., Armstrong-James M., Bannerjee A. Localization of NMDAR1 subunit in rat layer IV barrel cells. Soc. Neurosci. Abstr. 20:1994;1384.
63. Sachdev R., Lu S.-M., Wiley R. G., Ebner F. F. Effects of acetylcholine depletion in the rat barrel cortex. Soc. Neurosci. Abstr. 21:1995;123.
64. Metherate R., Tremblay N., Dykes R. W. Transient and prolonged effects of acetylcholine on responsiveness of cat somatosensory cortical neurons. J. Neurophysiol. 59:1988a;1253-1276.
65. Jacobs S. S. E., Fine A., Juliano S. L. Cholinergic basal forebrain transplants restore diminished metabolic activity in the somatosensory cortex of rats with acetylcholine depletion. J. Neurosci. 14:1994;697-711.
66. Lu S.-M., Sachdev R., Picklo M., Robertson D., Ebner F. F. Effects of norepinephrine (NE) depletion in the rat barrel cortex. Soc. Neurosci. Abstr. 22:1996;1357.
67. Boyeson M. G., Feeney D. M. Intraventricular norepinephrine facilitates motor recovery following sensorimotor cortex injury. Pharmacol. Biochem. Behav. 35:1990;497-501.
68. Auerbach J. M., Segal M. Acetylcholine enhances NMDA evoked calcium rise in hippocampal neurons. Brain Res. 587:1992;83-87.
69. Roche K. W., Tingley W. G., Huganir R. L. Glutamate receptor phosporylation and synaptic plasticity. Curr. Opin. Neurobiol. 4:1994;383-388.
70. Soderling T. R., Tan S. E., McGlade-McCulloh E., Yamamoto H., Fukunaga K. J. Neurobiol. 25:1993;304-311.
71. Ehlers M. D., Tingley W. G., Huganir R. L. Regulated subcellular distribution of the NR1 subunit of the NMDA receptor. Science. 269:1995;1734-1737.
72. Rosen K. M., McCormack M. A., Villa-Komaroff L., Mower G. D. Brief visual experience induces immediate early gene expression in the cat visual cortex. Proc. Natl. Acad. Sci. USA. 89:1992;5437-5441.
73. Worley P. F., Christy B. A., Nakabeppu Y., Bhat R. V., Cole A. J., Baraban J. M. Constitutive expression of Zif268 in neocortex is regulated by synaptic activity. Proc. Natl. Acad. Sci. USA. 88:1991;5106-5110.
74. Chaudhuri A., Cynader M. S. Activity-dependent expression of the transcription factor Zif268 reveals ocular dominance columns in mondey visual cortex. Brain Res. 605:1993;349-353.