The spinal cord and its brain: Representations and models. To what extent do forebrain mechanisms appear at brainstem spinal cord levels?

Progress in Neurobiology

Volumn 49, Issue 5, 1996, Pages 381-414

  Windhorst, U ^a,b,c,d  

^a UNIVERSITY OF CALGARY   (Canada)

^b UNIVERSITY OF GÖTTINGEN   (Germany)

^c Cyprus Neurosci and Technol Inst   (Cyprus)

^d Department of Physiology ^*  (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL EXPERIMENT; ANIMAL TISSUE; BRAIN STEM; NERVE CELL PLASTICITY; NONHUMAN; OSCILLATION; PRIORITY JOURNAL; REFLEX; REVIEW; RHYTHM; SPINAL CORD;

EID: 0030219037     PISSN: 03010082     EISSN: None     Source Type: Journal    
DOI: 10.1016/0301-0082(96)00022-6     Document Type: Article

References (254)

1. Abeles, M. (1982) Local cortical circuits. An electrophysiological study. Springer: Berlin.
2. Abeles, M. (1991) Corticonics. Neural circuits of the cerebral cortex. Cambridge University Press: Cambridge.
3. Abeles M., Bergman H., Margalit E., Vaadia E. Spatiotemporal firing patterns in the frontal cortex of behaving monkeys. J. Neurophysiol. 70:1993;1629-1638.
4. Abeles M., Gerstein G.L. Detecting spatiotemporal firing patterns among simultaneously recorded single neurons. J. Neurophysiol. 60:1988;909-924.
5. Adam D., Windhorst U., Inbar G.F. The effects of recurrent inhibition on the cross-correlated firing patterns of motoneurones (and their relation to signal transmission in the spinal cord-muscle channel). Biol. Cybern. 29:1978;229-235.
6. Aertsen A., Arndt M. Response synchronization in the visual cortex. Curr. Opin. Neurobiol. 3:1993;586-594.
7. Agarwal G.C., Gottlieb G.L. Mathematical modeling and simulation of the postural control loop: part I. CRC Crit. Rev. Biomed. Engineer. 8:1982;93-134.
8. Ahissar E., Vaadia E. Oscillatory activity of single units in a somatosensory cortex of an awake monkey and their possible role in texture analysis. Proc. Natl. Acad. Sci. USA. 87:1990;8935-8939.
9. Ahissar E., Vaadia E., Ahissar M., Bergman H., Arieli A., Abeles M. Dependence of cortical plasticity on correlated activity of single neurons and on behavioral context. Science. 257:1992;1412-1415.
10. Alexander G.E., Crutcher M.D. Neural representation of the target (goal) of visually guided arm movements in three motor areas of the monkey. J. Neurophysiol. 64:1990;164-178.
11. Arieli A., Shoham D., Hildesheim R., Grinvald A. Coherent spatiotemporal patterns of ongoing activity revealed by real-time optical imaging coupled with single-unit recording in the cat visual cortex. J. Neurophysiol. 73:1995;2072-2093.
12. Arnold D.B., Robinson D.A. A learning network model of the neural integrator of the oculomotor system. Biol. Cybern. 64:1991;447-454.
13. Artola A., Bröcher 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.
14. Artola A., Singer W. Long-term depression of excitatory synaptic transmission and its relationship to long-term potentiation. Trends Neurosci. 16:1993;480-487.
15. Bear M.F., Kirkwood A. Neocortical long-term potentiation. Curr. Opin. Neurobiol. 3:1993;197-202.
16. Bergenheim M., Johansson H., Pedersen J. The role of the γ-system for improving information transmission in populations of Ia afferents. Neurosci. Res. 23:1995;207-215.
17. Bergenheim, M., Johansson, H., Pedersen, J., Öhberg, F. and Sjölander, P. (1996) Ensemble coding of muscle stretches in afferent populations containing different types of muscle afferents. Brain Res. (in press).
18. Berkinblit M.B., Feldman A.G., Fukson O.I. Adaptability of innate motor patterns and motor control mechanisms. Behav. Brain Sci. 9:1986;585-638.
19. Bernander Ö., Douglas R.J., Martin K.A.C., Koch C. Synaptic background activity influences spatiotemporal integration in single pyramidal cells. Proc. Natl. Acad. Sci. USA. 88:1991;11569-11573.
20. Bliss T.V.P., Collingridge A. A synaptic model of memory: long-term potentiation in the hippocampus. Nature. 361:1993;31-39.
21. Bloedel J.R. Functional heterogeneity with structural homogeneity: How does the cerebellum operate? Behav. Brain Sci. 15:1992;666-678.
22. Blouin J., Bard C., Teasdale N., Paillard J., Fleury M., Forget R., Lamarre Y. Reference systems for coding spatial information in normal subjects and a deafferented patient. Expl. Brain Res. 93:1993;324-331.
23. Boorman G., Windhorst U., Kirmayer D. Waveform parameters of recurrent inhibitory postsynaptic potentials in cat motoneurones during time-varying activation patterns. Neuroscience. 63:1994;747-756.
24. Bouyer J.J., Montaron M.F., Vahnée J.M., Albert M.P., Rougeul A. Anatomical localization of cortical beta rhythms in cat. Neuroscience. 22:1987;863-869.
25. Braitenberg, V. and Schüz, A. (1991) Anatomy of the Cortex. Statistics and Geometry. Springer-Verlag: Berlin.
26. Bressler S.L. Relation of olfactory bulb and cortex. I Spatial variation of bulbocortical interdependence Brain Res. 409:1987;285-293.
27. Bruce E.N. Correlated and uncorrelated high-frequency oscillations in phrenic and recurrent laryngeal neurograms. J. Neurophysiol. 59:1988;1188-1203.
28. Bruce E.N., Ackerson L.M. High-frequency oscillations in human electromyograms during voluntary contractions. J. Neurophysiol. 56:1986;542-553.
29. Bullock T.H. Integrative systems research on the brain: resurgence and new opportunities. Annu. Rev. Neurosci. 16:1993;1-15.
30. Bullock T.H., McClune M.C. Lateral coherence of the electrocorticogram: a new measure of brain synchrony. Electroencephalogr. Clin. Neurophysiol. 73:1989;479-498.
31. Burke, R.E. (1981) Motor units: anatomy, physiology, and functional organization. In: Handbook of Physiology; Sect. 1, The Nervous System; Vol. II, Motor Control, Part 1, pp. 345-422. Ed. V.B. Brooks. American Physiological Society: Bethesda, U.S.A.
32. Buzsáki G., Horváth Z., Urioste R., Hetke J., Wise K. High-frequency network oscillation in the hippocampus. Science. 256:1992;1025-1027.
33. Caminiti R., Johnson P.B., Galli C., Ferraina S., Burnod Y. Making arm movements within different parts of space: the premotor and motor cortical representation of a coordinate system for reaching to visual targets. J. Neurosci. 11:1991;1182-1197.
34. Carp J.S., Wolpaw J.R. Motoneuron plasticity underlying operantly conditioned decrease in primate H-reflex. J. Neurophysiol. 72:1994;431-442.
35. Carp J.S., Wolpaw J.R. Motoneuron properties after operantly conditioned increase in primate H-reflex. J. Neurophysiol. 73:1995;1365-1373.
36. Chagnac-Amitai Y., Connors B.W. Synchronized excitation and inhibition driven by intrinsically bursting neurons in neocortex. J. Neurophysiol. 62:1989;1149-1162.
37. Chen D.-F., Fetz E.E. Intracellular correlates of oscillatory activity of cortical neurons in awake behaving monkeys. Soc. Neurosci. Abstr. 17:1991;310.
38. Chen X.Y., Wolpaw J.R. Operant conditioning of H-reflex in freely moving rats. J. Neurophysiol. 73:1995;411-415.
39. Christakos C.N. A study of the muscle force waveform using a population stochastic model of skeletal muscle. Biol. Cybern. 44:1982;91-106.
40. Christakos C.N. The mathematical basis of population rhythms in nervous and neuromuscular systems. Int. J. Neuroscience. 29:1986;103-107.
41. Christakos C.N., Cohen M.I., Barnhardt, Shaw C.-F. Fast rhythms in phrenic motoneuron and nerve discharges. J. Neurophysiol. 66:1991;674-687.
42. Christakos C.N., Cohen M.I., Sica A.L., Huang W.-X., See W.R., Barnhardt R. Analysis of recurrent laryngeal inspiratory discharges in relation to fast rhythms. J. Neurophysiol. 72:1994;1304-1316.
43. Cohen, A.H., Rossignol, S. and Grillner, S. (Eds.) (1988) Neural Control of Rhythmic Movements in Vertebrates. Wiley: New York.
44. Cohen M.I., See W.R., Christakos C.N., Sica A.L. High-frequency and medium-frequency components of different inspiratory nerve discharges and their modification by various inputs. Brain Res. 417:1987;148-152.
45. Collins W.F. III, Davis B.M., Mendell L.M. Amplitude modulation of EPSPs in motoneurons in response to a frequency-modulated train in single Ia afferent fibers. J. Neurosci. 6:1986;1463-1468.
46. Conway B.A., Halliday D.M., Farmer S.F., Shahani U., Maas P., Weir A.I., Rosenberg J.R. Synchronization between motor cortex and spinal motoneuronal pool during the performance of a maintained motor task in man. J. Physiol. Lond. 489:1995;917-924.
47. Crépel F., Dhanjal S.S., Sears T.A. Effect of glutamate, aspartate and related derivatives on cerebellar Purkinje cell dendrites in the rat: an in vitro study. J. Physiol. Lond. 329:1982;297-317.
48. Crépel F., Dupont J.L., Gardette R. Voltage-clamp analysis of the effect of excitatory amino acids and derivatives on Purkinje cell dendrites in rat cerebellar slices maintained in vitro. Brain Res. 279:1983;311-315.
49. Crépel F., Jaillard D. Pairing of pre- and postsynaptic activities in cerebellar Purkinje cells induces long-term changes in synaptic efficacy in vitro. J. Physiol. Lond. 432:1991;123-141.
50. Crick, F. (1994) The Astonishing Hypothesis. The Scientific Search for the Soul. Charles Scribner's Sons: New York.
51. Crutcher M.D., Alexander G.E. Movement-related neuronal activity selectively coding either direction or muscle pattern in three motor areas of the monkey. J. Neurophysiol. 64:1990;151-163.
52. Davis G.W., Murphey R.K. Long-term regulation of short-term transmitter release properties: retrograde signaling and synaptic development. Trends Neurosci. 17:1994;9-13.
53. Dawson T.M., Dawson V.L., Snyder S.H. A novel neuronal messenger molecule in brain: the free radical, nitric oxide. Ann. Neurol. 32:1992;297-311.
54. Delagrange P., Tadjer D., Bouyer J.J., Rougeul A., Conrath M. Effect of DSP4, a neurotoxic agent, on attentive behaviour and related electrocortical activity in cat. Behav. Brain Res. 33:1989;33-43.
55. DeRusso, P.M., Roy, B.J. and Close, C.M. (1965) State Variables for Engineers. John Wiley: New York.
56. De Schutter E.D. Cerebellar long-term depression might normalize excitation of Purkinje cells: a hypothesis. Trends Neurosci. 18:1995;291-295.
57. Devor M., Wall P.D. Effect of peripheral nerve injury on receptive fields of cells in the cat spinal cord. J. Comp. Neurol. 199:1981;277-291.
58. Dickinson P.S. Interactions between neural networks for behavior. Curr. Opin. Neurobiol. 5:1995;792-798.
59. Donoghue J.P. Plasticity of adult sensorimotor representations. Curr. Opin. Neurobiol. 5:1995;749-754.
60. Douglas R.J., Koch C., Mahowald M., Martin K.A.C., Suarez H.H. Recurrent excitation in neocortical circuits. Science. 269:1995;981-988.
61. Dubner R., Ruda M.A. Activity-dependent neuronal plasticity following tissue injury and inflammation. Trends Neurosci. 15:1992;96-103.
62. Du Lac S., Raymond J.L., Sejnowski T.J., Lisberger S.G. Learning and memory in the vestibulo-ocular reflex. Annu. Rev. Neurosci. 18:1995;409-441.
63. Durkovic R.G. Retention of a classically conditioned reflex response in spinal cat. Behav. Neural Biol. 43:1985;12-20.
64. Eccles J.C., Fatt P., Koketsu K. Cholinergic and inhibitory synapses in a pathway from motor-axon collaterals to motoneurons. J. Physiol., Lond. 126:1954;524-562.
65. Eckhorn R., Bauer R., Jordan W., Brosch M., Kruse W., Munk M., Reitboeck H.J. Coherent oscillations: a mechanism of feature linking in the visual cortex? Multiple electrode and correlation analyses in the cat. Biol. Cybern. 60:1988;121-130.
66. Eckhorn R., Frien A., Bauer R., Woelbern T., Kehr H. High frequency (60-90 Hz) oscillations in primary visual cortex of awake moneky. Neuro Report. 4:1993;243-246.
67. Edelman, G.M. (1987) Neural Darwinism. The Theory of Neuronal Group Selection. Basic Books, New York.
68. Edgley S.A., Jankowska E. An interneuronal relay for group I and II muscle afferents in the midlumbar segments of the cat spinal cord. J. Physiol. Lond. 389:1987;647-674.
69. Edwards F.A. LTP - a structural model to explain the inconsistencies. Trends Neurosci. 18:1995;250-255.
70. Elbert T., Ray W.J., Kowalik Z.J., Skinner J.E., Graf K.E., Birbaumer N. Chaos and physiology: deterministic chaos in excitable cell assemblies. Physiol. Rev. 74:1994;1-47.
71. Erickson, R.P. (1974) Parallel "population" neural coding in feature extraction. In: The Neurosciences, Third Study Program, pp. 155-169. Eds. F.O. Schmitt and F.G. Worden. MIT Press: Cambridge (Mass.).
72. Evatt M.L., Wolf S.L., Segal R.L. Modification of human spinal stretch reflexes: preliminary studies. Neurosci. Lett. 105:1989;350-355.
73. Farmer S.F., Bremner F.D., Halliday D.M., Rosenberg J.R., Stephens J.A. The frequency content of common synaptic inputs to motoneurones studied during voluntary isometric contractions in man. J. Physiol. Lond. 470:1993;127-155.
74. Feldman, J.L. (1986) Neurophysiology of breathing in mammals. In: The Nervous System, ed. Bloom, F.E., pp. 463-524. American Physiological Society: Bethesda (Handbook of Physiology, Intrinsic Regulatory Systems of the Brain).
75. Feldman J.L., Windhorst U., Anders K., Richter D.W. Synaptic interactions between medullary respiratory neurones during apneusis induced by NMDA-receptor blockade in cat. J. Physiol. Lond. 450:1992;303-323.
76. Ferster D., Spruston N. Cracking the neuronal code. Science. 270:1995;756-757.
77. Friedman-Hill S.R., Robertson L.C., Treisman A. Parietal contributions to visual feature binding: evidence from a patient with bilateral lesions. Science. 269:1995;853-855.
78. Fukson O.I., Berkinblit M.B., Feldman A.G. The spinal frog takes into account the scheme of its body during the wiping reflex. Science. 209:1980;1261-1263.
79. Funk G.D., Feldman J.L. Generation of respiratory rhythm and pattern in mammals: insights from developmental studies. Curr. Opin. Neurobiol. 5:1995;778-785.
80. Georgopoulos A.P., Schwartz A.B., Kettner R.E. Neuronal population coding of movement direction. Science. 233:1986;1416-1419.
81. Georgopoulos A.P., Kettner R.E., Schwartz A.B. Primate motor cortex and free arm movements to visual targets in three-dimensional space. II. Coding of the direction by a neuronal population J. Neurosci. 8:1988;2928-2937.
82. Gerstein G.L., Bedenbaugh P., Aertsen A.M.H.J. Neuronal assemblies. IEEE Trans. Biomed. Engin. 36:1989;4-14.
83. Ghez C., Gordon J., Ghilardi M.F., Christakos C.N., Cooper S.E. Roles of proprioceptive input in the programming of arm trajectories. Cold Spring Harbor Symp. Quant. Biol. 55:1990;837-847.
84. Ghose G.M., Freeman R.D. Oscillatory discharge in the visual system: does it have a functional role? J. Neurophysiol. 68:1992;1558-1574.
85. Gilbert P.F.C., Thach W.T. Purkinje cell activity during motor learning. Brain Res. 128:1977;309-328.
86. Giszter S.F., McIntyre J., Bizzi E. Kinematic strategies and sensorimotor transformations in the wiping movements of frogs. J. Neurophysiol. 62:1989;750-767.
87. Goldberger, M.E. and Murray, M. (1988) Patterns of sprouting and implications for recovery of function. In: Functional Recovery in Neurological Disease. Advances in Neurology, Vol. 47, pp. 361-385. Ed. S.G. Waxman. Raven Press: New York.
88. Goodhill G.J., Löwel S. Theory meets experiment: correlated neural activity helps determine ocular dominance column periodicity. Trends Neurosci. 18:1995;437-439.
89. Goodman C.S., Shatz C.J. Developmental mechanisms that generate precise patterns of neuronal connectivity. Cell/Neuron. 72/10((Suppl.)):1993;77-98.
90. Gritti I., Schieppati M. Short-latency inhibition of soleus motoneurones by impulses in Ia afferents from the gastrocnemius muscle in humans. J. Physiol. Lond. 416:1989;469-484.
91. Grover L.M., Teyler T.J. Two components of long-term potentiation induced by different patterns of afferent activation. Nature Lond. 347:1990;477-479.
92. Halter J.A., Carp J.S., Wolpaw J.R. Operantly conditioned motoneuron plasticity: possible role of sodium channels. J. Neurophysiol. 73:1995;867-871.
93. Harrison P.J., Jankowska E. Sources of input to interneurones mediating group I non-reciprocal inhibition of motoneurones in the cat. J. Physiol. Lond. 361:1985;403-418.
94. Havson L., Kellerth J.-O. Regeneration by supernumerary axons with synaptic terminals in spinal motoneurons of cats. Nature. 325:1987;711-714.
95. Havson L., Kellerth J.-O. Elimination of intramedullary axon collaterals of cat spinal α-motoneurons following peripheral nerve injury. Expl. Brain Res. 79:1990;65-74.
96. Havson L., Kellerth J.-O. Plasticity of recurrent inhibitory reflexes in cat spinal motoneurons following peripheral nerve injury. Expl. Brain Res. 79:1990;75-82.
97. Hebb, D.O. (1949) The Organization of Behavior. Wiley: New York.
98. Hirano T. Depression and potentiation of the synaptic transmission between a granule cell and a Purkinje cell in rat cerebellar culture. Neurosci. Lett. 119:1990;141-144.
99. Hoover J.E., Durkovic R.G. Retention of a backward classically conditioned reflex response in spinal cats. Expl. Brain Res. 77:1989;621-627.
100. Hore J., Flament D. Changes in motor cortex neural discharge associated with the development of cerebellar limb ataxia. J. Neurophysiol. 60:1988;1285-1302.
101. Hore, J. and Vilis, T. (1985) A cerebellar-dependent efference copy mechanism for generating appropriate muscle responses to limb perturbations. In: Cerebellar Functions, pp. 24-35. Eds. J.R. Bloedel, J. Dichgans and W. Precht. Springer-Verlag: Berlin.
102. Houk, J.C. and Rymer, W.Z. (1981) Neural control of muscle length and tension. In: Handbook of Physiology; Sect. 1, The Nervous System, Vol. II, Motor Control, Part 1, pp. 257-323. Ed. V.B. Brooks. American Physiological Society: Bethesda, U.S.A.
103. Huang W.-X., Christakos C.N., Cohen M.I., He Q. Possible network interactions indicated by bilaterally coherent fast rhythms in expiratory recurrent laryngeal nerve discharges. J. Neurophysiol. 70:1993;2192-2196.
104. Hulliger M. The mammalian muscle spindle and its central control. Rev. Physiol. Biochem. Pharmacol. 101:1984;1-110.
105. Inbar G.F. Muscle spindles in muscle control. 3 Analysis of adaptive system model. Kybernetik. 11:1972;130-141.
106. Iriki A., Keller A., Pavlides C., Asanuma H. Long-lasting facilitation of pyramidal tract input to spinal interneurons. NeuroReport. 1:1990;157-160.
107. Ito, M. (1984) The Cerebellum and Neural Control. Raven Press: New York.
108. Ito M. Long-term depression. Annu. Rev. Neurosci. 12:1989;85-102.
109. Ivry R.B., Baldo J.V. Is the cerebellum involved in learning and cognition? Curr. Opin. Neurobiol. 2:1992;212-216.
110. Jankowska E. Interneuronal relay in spinal pathways from proprioceptors. Progr. Neurobiol. 38:1992;335-378.
111. Jankowska E., McCrea D.A. Shared reflex pathways from Ib tendon organ afferent and Ia muscle spindle afferents in the cat. J. Physiol. Lond. 338:1983;99-111.
112. Johansson H., Bergenheim M., Djupsjöbacka M., Sjölander P. A method for analysis of encoding of stimulus separation in ensembles of afferents. J. Neurosci. Methods. 63:1995;67-74.
113. Johnston D., Williams S., Jaffe D., Gray R. NMDA-receptor-independent long-term potentiation. Annu. Rev. Physiol. 54:1992;489-505.
114. Jones E.G. The role of afferent activity in the maintenance of primate neocortical function. J. Expl. Biol. 153:1990;155-176.
115. Kano M., Rexhausen U., Dreessen J., Konnerth A. Synaptic excitation produces a long-lasting rebound potentiation of inhibitory synaptic signals in cerebellar Purkinje cells. Nature. 356:1992;601-604.
116. Katz L.C. Coordinate activity in retinal and cortical development. Curr. Opin. Neurobiol. 3:1993;93-99.
117. Katz P.S. Intrinsic and extrinsic neuromodulation of motor circuits. Curr. Opin. Neurobiol. 5:1995;799-808.
118. Keating J.G., Thach W.T. Nonclock behavior of inferior olive neurons: interspike interval of Purkinje cell complex spike discharge in the awake behaving monkey is random. J. Neurophysiol. 73:1995;1329-1340.
119. Kelly M., Zuo C.C., Bloedel J.R. Classical conditioning of the eyeblink reflex in the decerebrate-decerebellate rabbit. Behav. Brain Res. 38:1990;7-18.
120. Kelso, J.A.S. (1995) Dynamic Patterns. The Self-organization of Brain and Behavior. MIT Press: Cambridge (Mass.), London (UK).
121. Kinomura S., Larsson J., Gulyás B., Roland P.E. Activation by attention of the human reticular formation and thalamic intralaminar nuclei. Science. 271:1996;512-515.
122. Kirkwood A., Dudek S.M., Gold J.T., Aizenman C.D., Bear M.F. Common forms of synaptic plasticity in the hippocampus and neocortex in vitro. Science. 260:1993;1518-1521.
123. Koerber H.R., Mendell L.M. Modulation of synaptic transmission at Ia-afferent fiber connections on mononeurons during high-frequency stimulation: role of postsynaptic target. J. Neurophysiol. 65:1991;590-597.
124. Komatsu Y., Nakajima S., Toyama K. Induction of long-term potentiation without participation of N-methyl-D-aspartate receptors in kitten visual cortex. J. Neurophysiol. 65:1991;20-32.
125. Kristeva-Feige R., Feige B., Makeig S., Ross B., Elbert T. Oscillatory brain activity during a motor task. NeuroReport. 4:1993;1291-1294.
126. Kuba K., Kumamoto E. Long-term potentiations in vertebrate synapses: a variety of cascades with common subprocesses. Prog. Neurobiol. 34:1990;197-269.
127. Lacquaniti F., Borghese N.A., Carrozzo M. Internal models of limb geometry in the control of hand compliance. J. Neurosci. 12:1992;1750-1762.
128. Laouris Y., Windhorst U., Rissing R., Kuipers U., Meyer-Lohmann J. Time constants of facilitation and depression in Renshaw cell responses to random stimulation of motor axons. Expl. Brain Res. 72:1988;117-128.
129. Lev-Tov A., Pinco M. In vitro studies of prolonged synaptic depression in the neonatal rat spinal cord. J. Physiol. Lond. 447:1992;149-169.
130. Linden D.J., Connor J.A. Long-term synaptic depression. Annu. Rev. Neurosci. 18:1995;319-357.
131. Lippe W.R. Rhythmic spontaneous activity in the developing avian auditory system. J. Neurosci. 14:1994;1486-1495.
132. Lisberger S.G. The neural basis for motor learning in the vestubulo-ocular reflex in monkeys. Trends Neurosci. 11:1988;147-152.
133. Lisberger S.G. Neural basis for motor learning in the vestibulo-ocular reflex in monkeys. Trends Neurosci. 11:1988;147-152.
134. Lisberger S.G. Neural basis for motor learning in the vestibuloocular reflex of primates. III. Computational and behavioral analysis of the sites of learning J. Neurophysiol. 72:1994;974-998.
135. Llinás, R.R. (1991) The noncontinuous nature of movement execution. In: Motor Control: Concepts and Issues, pp. 223-242. Eds. D.R. Humphrey and H.-J. Freund. John Wiley: Chichester.
136. Lliná R.R., Grace A.A., Yarom Y. In vitro neurons in mammalian cortical layer 4 exhibit intrinsic oscillatory activity in the 10- to 50-Hz frequency range. Proc. Natl. Acad. Sci. USA. 88:1991;897-901.
137. Llinás R.R., Paré D. Of dreaming and wakefulness. Neuroscience. 44:1991;521-535.
138. Llinás R.R., Ribary U. Coherent 40-Hz oscillation characterizes dream state in humans. Proc. Natl. Acad. Sci. USA. 90:1993;2078-2081.
139. Loeb, G.E. and Levine, W.S. (1990) Linking musculoskeletal mechanics to sensorimotor neurophysiology. In: Multiple Muscle Systems. Biomechanics and Movement Organization, pp. 165-181. Eds. J.M. Winters and S.L.-Y. Woo. Springer-Verlag: New York, Berlin, Heidelberg, London, Paris, Tokyo, Hong Kong.
140. Loeb G.E., Yee W.J., Pratt C.A., Chanaud C.M., Richmond F.J.R. Cross-correlation of EMG reveals widespread synchronization of motor units during slow movements in intact cats. J. Neurosci. Meth. 21:1987;239-249.
141. Loeb G.E., He J., Levine W.S. Spinal cord circuits: are they mirrors of musculoskeletal mechanics? J. Motor Behav. 21:1989;473-491.
142. Lopes da Silva, F.H. (1996) Chapter 25. The generation of electric and magnetic signals of the brain by local networks. In: Comprehensive Human Physiology. From Cellular Mechanisms to Integration, pp. Eds. R. Greger and U. Windhorst. Springer: Berlin (in press).
143. Lozier A.P., Kendig J.J. Long-term potentiation in an isolated peripheral nerve-spinal cord preparation. J. Neurophysiol. 74:1995;1001-1009.
144. MacKay W.A., Murphy J.T. Cerebellar modulation of reflex gain. Prog. Neurobiol. 13:1979;361-417.
145. Malenka R.C., Nicoll R.A. NMDA-receptor-dependent synaptic plasticity: multiple forms and mechanisms. Trends Neurosci. 16:1993;521-527.
146. Maltenfort, M.G. (1995) Simulation of Recurrent Inhibition in Spinal Motoneuron Pools. Ph.D. Thesis. Northwestern University: Chicago.
147. Marder E., Abbott L.F. Theory in motion. Curr. Opin. Neurobiol. 5:1995;832-840.
148. Massion J. Movement, posture and equilibrium: interaction and coordination. Prog. Neurobiol. 38:1992;35-56.
149. Matthews, P.B.C. (1972) Mammalian Muscle Receptors and Their Central Actions. Arnold: London.
150. Matthews P.B.C. Proprioceptors and their contribution to somatosensory mapping: complex messages require complex processing. Can. J. Physiol. Pharmacol. 66:1988;430-438.
151. McCormick D.A., von Krosigk M. Corticothalamic activation modulates thalamic firing through glutamate "metabotropic" receptors. Proc. Natl. Acad. Sci. USA. 89:1992;2774-2778.
152. McCrea D.A. Spinal cord circuitry and motor reflexes. Exercise Sport Sci. Rev. 14:1986;105-141.
153. McKenna T.M., McMullen T.A., Shlesinger M.F. The brain as a dynamic physical system. Neuroscience. 60:1994;587-605.
154. McNaughton B.L. The mechanism of expression of long-term enhancement of hippocampal synapses: current issues and theoretical implications. Annu. Rev. Physiol. 55:1993;375-396.
155. McNaughton B.L., Barnes C.A. From cooperative synaptic enhancement to associative memory: bridging the abyss. Seminars Neurosci. 2:1990;403-416.
156. Meister M., Lagnado L., Baylor D.A. Concerted signaling by retinal ganglion cells. Science. 270:1995;1207-1210.
157. Mendell L.M. Modifiability of spinal synapses. Physiol. Rev. 64:1984;260-324.
158. Mendell, L.M. (1988) Physiological aspects of synaptic plasticity: the Ia/motoneuron connection as amodel. In: Functional Recovery in Neurological Disease. Advances in Neurology, Vol. 47, pp. 337-360. Ed. S.G. Waxman. Raven Press: New York.
159. Merton P.A. Neurophysiology on man. J. Neurol. Neurosurg. Psychiat. 44:1981;861-870.
160. Mettens P., Godaux E., Cheron G., Galiana H.L. Effect of muscimol microinjections into the prepositus hypoglossi and the medial vestibular nuclei on cat eye movements. J. Neurophysiol. 72:1994;785-802.
161. Meyer-Lohmann J., Christakos C.N., Wolf N. Dominance of the short-latency component in perturbation-induced electromyograpic responses of long-trained monkeys. Expl. Brain Res. 64:1986;393-399.
162. Misulis K.E., Durkovic R.G. Conditioned stimulus intensity: role of cutaneous fiber size in classical conditioning of the flexion reflex in the spinal cat. Expl. Neurol. 86:1984;81-92.
163. Mittelstaedt, H. (1990) Basic solutions to the problem of head-centric visual localization. In: Perception and Control of Self-motion, pp. 267-287. Eds. R. Warren and A.H. Wertheim. Erlbaum: Hillsdale NJ.
164. Mitz A.R., Godschalk M., Wise S.P. Learning-dependent neuronal activity in the premotor cortex: activity during the acquisition of conditional motor associations. J. Neurosci. 11:1991;1855-1872.
165. Montague P.R., Gally J.A., Edelman G.M. Spatial signaling in the development and function of neural connections. Cerebral Cortex. 1:1991;199-220.
166. Montague P.R., Sejnowski T.J. The predictive brain: temporal coincidence and temporal order in synaptic learning mechanisms. Learning and Memory. 1:1994;1-33.
167. Murphy P.R., Martin H.A. Fusimotor discharge patterns during rhythmic movements. Trends Neurosci. 16:1993;273-278.
168. Murthy V.N., Fetz E.E. Coherent 25-35 Hz oscillations in the sensorimotor cortex of awake behaving monkeys. Proc. Natl. Acad. Sci. USA. 89:1992;5670-5674.
169. Nozaki, D., Nakazawa, K. and Yamamoto, Y. (1996) Supraspinal effects on the fractal correlation in human H-reflex. Expl. Brain Res. (in press).
170. Nuñez A., Amzica F., Steriade M. Voltage-dependent fast (20-40 Hz) oscillations in long-axoned neocortical neurons. Neuroscience. 51:1992;7-10.
171. Okada D., Miyamoto T. Formation of long-term potentiation in superior colliculus slices from the guinea pig. Neurosci. Lett. 96:1989;108-113.
172. Parker, S.B. (ed.) (1994) McGraw-Hill Concise Encyclopedia of Science and Technology. 3rd ed. McGraw-Hill: New York.
173. Partridge L.D. How was movement controlled before Newton? Beh. Brain Sci. 5:1982;561.
174. Partridge, L.D. and Benton, L.L.A. (1981) Muscle, the motor. In Handbook of Physiology; Sect. 1, The Nervous System Vol. II, Motor Control, Part 1, pp. 43-106. Ed. V.B. Brooks. American Physiological Society: Bethesda, U.S.A.
175. Pearson K.G. Proprioceptive regulation of locomotion. Curr. Opin. Neurobiol. 5:1995;786-791.
176. Pearson, K.G. and Whelan, P.J. (1996) Plasticity in the spinal cord: alterations in polysynaptic group I pathways produced by chronic axotomy persist after spinalization. Can. J. Physiol. Pharmacol. (in press).
177. Perkel D.H., Bullock T.H. Neural coding. Neurosci. Res. Program Bull. 6:1968;221-348.
178. Perrett S.P., Ruiz B.P., Mauk M.D. Cerebellar cortex lesions disrupt learning-dependent timing of conditioned eyelid responses. J. Neurosci. 13:1993;1708-1718.
179. Pinault D., Deschênes M. Voltage-dependent 40-Hz oscillations in rat reticular thalamic neurons in vivo. Neuroscience. 51:1992;245-258.
180. Pockett S., Figurov A. Long-term potentiation and depression in the ventral horn of rat spinal cord in vitro. NeuroReport. 4:1993;97-99.
181. Racine R.J., Wilson D.A., Gingell R., Sunderland D. Long-term potentiation in the interpositus and vestibular nuclei of the rat. Expl. Brain Res. 63:1986;155-162.
182. Randić M., Jiang M.C., Cerne R. Long-term potentiation and long-term depression of primary afferent neurotransmission in the rat spinal cord. J. Neurosci. 13:1993;5228-5241.
183. Ray R.H., Doetsch G.S. Coding of stimulus location and intensity in populations of mechanosensitive nerve fibers of the raccoon: II. across-fiber response patterns Brain Res. Bull. 25:1990;533-550.
184. 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. Cerebral Cortex. 2:1992;181-196.
185. Richter, D.W. (1996) Chapter 105. Neural regulation of respiration: rhythmogenesis and afferent control. In: Comprehensive Human Physiology, From Cellular Mechanisms to Integration, pp. Eds. R. Greger and U. Windhorst. Springer-Verlag, Berlin.
186. Richter D.W., Bischoff A., Anders K., Bellingham M., Windhorst U. Response of the medullary respiratory network of the cat to hypoxia. J. Physiol. Lond. 443:1991;231-256.
187. Robinson, D.A. (1981) Control of eye movements. In: Handbook of Physiology; Sect. 1, The Nervous System, Vol. II, Motor Control, Part 2, pp. 1275-1320. Eds. J.M. Brookhart, V.B. Mountcastle, V.B. Brooks and S.R. Geiger. American Physiological Society: Bethesda, U.S.A.
188. Robinson D.A. Integrating with neurons. Annu. Rev. Neurosci. 12:1989;33-45.
189. Robinson D.A. Implications of neural networks for how we think about brain function. Behav. Brain Sci. 15:1992;644-655.
190. Robinson F.R. Role of the cerebellum in movement control and adaptation. Curr. Opin. Neurobiol. 5:1995;755-762.
191. Robson J.G., Troy J.B. Nature of the maintained discharge of Q, X, and Y retina ganglion cells of the cat. J. Opt. Soc. Am. A. 4:1987;2301-2307.
192. Rudomin P. Presynaptic inhibition of muscle spindle and tendon organ afferents in the mammalian spinal cord. Trends Neurosci. 13:1990;499-505.
193. Sakurai M. Synaptic modification of parallel fibre-Purkinje cell transmission in in vitro guinea-pig cerebellar slices. J. Physiol. Lond. 394:1987;463-480.
194. Salinas E., Abbott L.F. Transfer of coded information from sensory to motor networks. J. Neurosci. 15:1995;6461-6474.
195. Sanes J., Donoghue J. Oscillations in local field potentials of the primate motor cortex during voluntary movement. Proc. Natl. Acad. Sci. U.S.A. 90:1993;4470-4474.
196. Schotland J.L., Rymer W.Z. Wipe and flexion reflexes of the frog. II. Response to perturbations J. Neurophysiol. 69:1993;1736-1748.
197. Schreurs B.G., Alkon D.L. Rabbit cerebellar slice analysis of long-term depression and its role in classical conditioning. Brain Res. 631:1993;235-240.
198. Schuman E.M., Madison D.V. Locally distributed synaptic potentiation in the hippocampus. Science. 263:1994;532-536.
199. Schuman E.M., Madison D.V. Nitric oxide and synaptic function. Annu. Rev. Neurosci. 17:1994;153-183.
200. Seeds N.W., Williams B.L., Bickford P.C. Tissue plasminogen activator induction in Purkinje neurons after cerebellar motor learning. Science. 270:1995;1992-1994.
201. Silito A.M., Jones H.E., Gerstein G.L., West D.C. Feature-linked synchronization of thalamic relay cell firing induced by feedback from the visual cortex. Nature. 369:1994;479-482.
202. Silva L.R., Amitai Y., Connors B.W. Intrinsic oscillations of neocortex generated by layer 5 pyramdial neurons. Science. 251:1991;432-535.
203. Singer W. Synchronization of cortical activity and its putative role in information processing and learning. Annu. Rev. Physiol. 55:1993;349-374.
204. Singer W. Development and plasticity of cortical processing architectures. Science. 270:1995;758-764.
205. Singer W., Gray C.M. Visual feature integration and the temporal correlation hypothesis. Annu. Rev. Neurosci. 18:1995;555-582.
206. Smith A., Denny M. High-frequency oscillations as indicators of neural control mechanisms in human respiration, mastication, and speech. J. Neurophysiol. 63:1990;745-758.
207. Smith J.C., Ellenberger H.H., Ballanyi K., Richter D.W., Feldman J.L. Pre-Bötzinger complex: a brainstem region that may generate respiratory rhythm in mammals. Science. 254:1991;726-729.
208. Soechting J.F., Flanders M. Psychophysical approaches to motor control. Curr. Opin. Neurobiol. 5:1995;742-748.
209. Sporns O., Gally J.A., Reeke G.N., Edelman G.M. Reentrant signaling among simulated neuronal groups leads to coherency in their oscillatory activity. Proc. Natl. Acad. Sci. USA. 86:1989;7265-7269.
210. Stein J.F., Glickstein M. Role of the cerebellum in visual guidance of movement. Physiol. Rev. 72:1992;967-1017.
211. Steriade M. Central core modulation of spontaneous oscillations and sensory transmission in thalamocortical systems. Curr. Opin. Neurobiol. 3:1993;619-625.
212. Steriade M., Curró Dossi R., Paré D., Oakson G. Fast oscillations (20-40 Hz) in thalamocortical systems and their potentiation by mesopontine cholinergic nuclei in the cat. Proc. Natl. Acad. Sci. USA. 88:1991;4390-4400.
213. Steriade M., Curró Dossi R., Contreras D. Electrophysiological properties of intralaminar thalamocortical cells discharging rhythmic (40 Hz) spike-bursts at 1000 Hz during waking and rapid eye movement sleep. Neuroscience. 56:1993;1-9.
214. Taylor, A. and Gottlieb, S. (1985) Convergence of several sensory modalities in motor control. In: Feedback and Motor Control in Invertebrates and Vertebrates, pp. 77-91. Eds. W.J.P. Barnes and M.H. Gladden. Croom Helm. London Sydney Dover.
215. Thach W.T., Goodkin H.P., Keating J.G. The cerebellum and the adaptive coordination of movement. Annu. Rev. Neurosci. 15:1992;403-442.
216. Thomson A.M., Deuchars J. Temporal and spatial properties of local circuits in neocortex. Trends Neurosci. 17:1994;119-126.
217. Thompson R.F. The neural basis of basic associative learning of discrete behavioral responses. Trends Neurosci. 11:1988;152-155.
218. Thompson S.W.N., Woolf C.J., Sivilotti L.G. Small-caliber afferent inputs produce a heterosynaptic facilitation of the synaptic responses evoked by primary afferent A-fibers in the neonatal rat spinal cord in vitro. J. Neurophysiol. 69:1993;2116-2128.
219. Tsumoto T. Long-term potentiation and long-term depression in the neocortex. Prog. Neurobiol. 39:1992;209-228.
220. Urban L., Thompson S.W.N., Dray A. Modulation of spinal excitability: co-operation between neurokinin and excitatory amino acid neurotransmitters. Trends Neurosci. 17:1994;432-438.
221. von Holst E., Mittelstaedt H. Das Reafferenzprinzip (Wechselwirkungen zwischen Zentralnervensystem und Peripherie). Naturwissenschaften. 37:1950;464-476.
222. Wall, P.D. (1988) Recruitment of ineffective synapses after injury. In: Functional Recovery in Neurological Disease. Advances in Neurology, Vol. 47, pp. 387-400. Ed. S.G. Waxman. Raven Press: New York.
223. Webb C.B., Cope T.C. Modulation of Ia EPSP aamplitude: the effects of chronic synaptic inactivity. J. Neurosci. 12:1992;334-338.
224. Weinberger N.M. Dynamic regulation of receptive fields and maps in the adult sensory cortex. Annu. Rev. Neurosci. 18:1995;129-158.
225. Welsh J.P., Harvey J.A. Pavlonian conditioning in the rabbit during inactivation of the interpositus nucleus. J. Physiol. Lond. 444:1991;459-480.
226. Welsh J.P., Lang E.J., Sugihara I., Llinás R.R. Dynamic organization of motor control within the olivocerebellar system. Nature. 374:1995;453-457.
227. Whelan P.J., Hiebert G.W., Pearson K.G. Plasticity of the extensor group I pathway controlling the stance to swing transition in the cat. J. Neurophysiol. 74:1995;2782-2787.
228. Windhorst, U. (1988) How Brain-like is the Spinal Cord? Interacting Cell Assemblies in the Nervous System. Springer: Berlin.
229. Windhorst U. Activation of Renshaw cells. Prog. Neurobiol. 35:1990;135-179.
230. Windhorst, U. (1993) A new concept of the role of proprioceptive and recurrent inhibitory feedback in motor control. In: Robots and Biological Systems: Towards a New Bionics?, pp. 295-318. Eds. P. Dario, G. Sandini and P. Aebischer. Springer-Verlag: Berlin.
231. Windhorst, U. (1996a) Chapter 1. Principles of regulatory physiology. In: Comprehensive Human Physiology. From Cellular Mechanisms to Integration, pp. Eds. R. Greger and U. Windhorst. Springer-Verlag, Berlin (in press).
232. Windhorst, U. (1996b) Chapter 32. Tactile senses. In: Comprehensive Human Physiology. From Cellular Mechanisms to Integration, pp. Eds. R. Greger and U. Windhorst. Springer: Berlin (in press).
233. Windhorst, U. (1996c) Chapter 39. Central processing of vision. In: Comprehensive Human Physiology. From Cellular Mechanisms to Integration, pp. Eds. R. Greger and U. Windhorst. Springer: Berlin (in press).
234. Windhorst, U. (1996d) Chapter 48. The peripheral motor apparatus and its nervous system: General problems to be solved and general problem solvers. In: Comprehensive Human Physiology. From Cellular Mechanisms to Integration, pp. Eds. R. Greger and U. Windhorst. Springer: Berlin (in press).
235. Windhorst, U. (1996e) Chapter 49. Spinal cord and brainstem: Motor output, sensors and basic circuits. In: Comprehensive Human Physiology. From Cellular Mechanisms to Integration, pp. Eds. R. Greger and U. Windhorst. Springer: Berlin (in press).
236. Windhorst, U. (1996f) Chapter 50. Spinal cord and brainstem: Pattern generators and reflexes. In: Comprehensive Human Physiology. From Cellular Mechanisms to Integration, pp. Eds. R. Greger and U. Windhorst. Springer: Berlin (in press).
237. Windhorst, U. (1996g) Chapter 51. Cerebral cortex, basal ganglia, and cerebellum: Parallel circuits. In: Comprehensive Human Physiology. From Cellular Mechanisms to Integration, pp. Eds. R. Greger and U. Windhorst. Springer: Berlin (in press).
238. Windhorst, U. (1996h) Chapter 52. Higher psychomotor functions. In: Comprehensive Human Physiology. From Cellular Mechanisms to Integration, pp. Eds. R. Greger and U. Windhorst. Springer: Berlin (in press).
239. Windhorst, U. (1996i) Chapter 54. Specific networks of the cerebral cortex: functional organization and plasticity. In: Comprehensive Human Physiology. From Cellular Mechanisms to Integration, pp. Eds. R. Greger and U. Windhorst. Springer: Berlin (in press).
240. Windhorst U., Rissing R., Meyer-Lohmann J., Kuipers U. Facilitation and depression in the responses of spinal Renshaw cells to random stimulation of motor axons. J. Neurophysiol. 60:1988;1638-1652.
241. Windhorst, U. and Boorman, G. (1995) Overview: potential role of segmental motor circuitry in muscle fatigue. In: Fatigue. Neural and Muscular Mechanisms, pp. 241-258. Eds. S.C. Gandevia, R. M. Enoka, A.J. McComas, D.G. Stuart and C.K. Thomas. Plenum Press: New York, London.
242. Windhorst U., Boorman G., Kirmayer D. Renshaw cells and recurrent inhibition: comparison of responses to cyclic inputs. Neuroscience. 67:1995;225-233.
243. Wolpaw J.R., Carp J.S. Memory traces in the spinal cord. Trends Neurosci. 13:1990;137-142.
244. Wolpert D.M., Ghahramani Z., Jordan M.I. An internal model for sensorimotor integration. Science. 269:1995;1880-1882.
245. Wong R.O.L. The role of spatio-temporal firing patterns in neuronal development of sensory systems. Curr. Opin. Neurobiol. 3:1993;595-601.
246. Wu J.-Y., Cohen L.B., Falk C.X. Neuronal activity during different behaviors in Aplysia: a distributed organization? Science. 263:1994;820-823.
247. Yeo C.H. Cerebellum and classical conditioning of motor responses. Ann. NY Acad. Sci. 627:1991;292-304.
248. Young M.P., Tanaka K., Yamane S. On oscillating neuronal responses in the visual cortex of the monkey. J. Neurophysiol. 67:1992;1464-1474.
249. Yuste R., Peinado A., Katz L.C. Neuronal domains in developing neocortex. Science. 257:1992;665-669.
250. Zajac F.E. Muscle and tendon: properties, models, scaling, and application to biomechanics and motor control. Crit. Rev. Biomech. Engin. 17:1989;359-411.
251. Zeki, S. (1993) A Vision of the Brain. Blackwell Scientific Publications: Oxford.
252. Zheng F., Gallagher J.P. Metabotropic glutamate receptors are required for the induction of long-term potentiation. Neuron. 9:1992;163-172.
253. Zhuo M., Small S.A., Kandel E.R., Hawkins R.D. Nitric oxide and carbon monoxide produce activity-dependent long-term synaptic enhancement in hippocampus. Science. 260:1993;1946-1950.
254. Zucker R.S. Short-term synaptic plasticity. Annu. Rev. Neurosci. 12:1989;13-31.