Processing of multiple kinematic signals in the cerebellum and motor cortices

Brain Research Reviews

Volumn 33, Issue 2-3, 2000, Pages 155-168

  Johnson, M T V ^a   Ebner, T J ^a  

^a UNIVERSITY OF MINNESOTA   (United States)

Author keywords

Cerebellum; Dorsal premotor cortex; Linear regression; Macaca Mulatta; Motor control; Primary motor cortex; Primate; Purkinje cell; Pursuit tracking

Indexed keywords

ARTICLE; CEREBELLUM; HUMAN; KINETICS; MOTOR CONTROL; MOTOR CORTEX; MOVEMENT (PHYSIOLOGY); NONHUMAN; PREMOTOR CORTEX; PRIORITY JOURNAL; PURKINJE CELL; RHESUS MONKEY; SIGNAL PROCESSING; SPIKE;

EID: 0033818204     PISSN: 01650173     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-0173(00)00027-8     Document Type: Review

References (75)

1. Albus J.S. A theory of cerebellar function. Math. Biosci. 10:1971;25-61.
2. Alexander G.E., Crutcher M.D. Neural representations of the target (goal) of visually guided arm movements in three motor areas of the monkey. J. Neurophysiol. 64:1990;164-178.
3. Allen G.I., Tsukahara N. Cerebro-cerebellar communication systems. Physiol. Rev. 54:1974;957-1006.
4. Andersen R.A. Encoding of intention and spatial location in the posterior parietal cortex. Cereb. Cortex. 5:1995;457-469.
5. Ashe J. Force and the motor cortex. Behav. Brain Res. 86:1997;1-15.
6. Ashe J., Georgopoulos A.P. Movement parameters and neural activity in motor cortex and area 5. Cereb. Cortex. 4:1994;590-600.
7. Bastian A.J., Martin T.A., Keating J.G., Thach W.T. Cerebellar ataxia: abnormal control of interaction torques across multiple joints. J. Neurophysiol. 76:1996;492-509.
8. Bloedel J.R., Courville J. A review of cerebellar afferent systems. Brooks V.B. Handbook of Physiology, Sect. 1, The Nervous System. Motor Control, Part 2. Vol. II:1981;735-830 Williams and Wilkins, Baltimore.
9. Bosco G., Poppele R. Representation of multiple kinematic parameters of the cat hind limb in spinocerebellar activity. J. Neurophysiol. 69:1997;74-94.
10. 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.
11. Carpenter A.F., Georgopoulos A.P., Pellizzer G. Motor cortical encoding of serial order in a context-recall task. Science. 283:1999;1752-1757.
12. Cheney P.D., Fetz E.E. Functional classes of primate corticomotoneuronal cells and their relation to active force. J. Neurophysiol. 44:1980;773-791.
13. Cohen D.A.D., Prud'homme M.J.L., F Kalaska J. Tactile activity in primate primary somatosensory cortex during active arm movements: correlation with receptive field properties. J. Neurophysiol. 71:1994;161-172.
14. Coltz J.D., Johnson M.T.V., Ebner T.J. Cerebellar Purkinje cell simple spike discharge encodes movement velocity in primates during visuomotor arm tracking. J. Neurosci. 19:1999;1782-1803.
15. Ebner T.J. A role for the cerebellum in the control of limb movement velocity. Curr. Opin. Neurobiol. 8:1998;762-769.
16. Ebner T.J., Fu Q.-G. What features of visually guided arm movements are encoded in the simple spike discharge of cerebellar Purkinje cells? Prog. Brain Res. 114:1997;431-447.
17. Eccles J.C., Ito M., Szentagothai J. The Cerebellum as a Neuronal Machine. 1967;Springer-Verlag, Berlin.
18. Evarts E.V., Fromm C., Kroller J., Jennings V. Relation of pyramidal tract activity to force exerted during voluntary movement. J. Neurophysiol. 31:1968;14-27.
19. Fortier P.A., Kalaska J.F., Smith A.M. Cerebellar neuronal activity related to whole-arm reaching movements in the monkey. J. Neurophysiol. 62:1989;198-210.
20. Fortier P.A., Smith A.M., Kalaska J.F. Comparison of cerebellar and motor cortex activity during reaching: directional tuning and response variability. J. Neurophysiol. 69:1993;1136-1149.
21. Freund H.-J., Hummelsheim H. Lesions of premotor cortex in man. Brain. 108:1985;697-733.
22. Fu Q.-G., Flament D., Coltz J.D., Ebner T.J. Temporal encoding of movement kinematics in the discharge of primate primary motor and premotor neurons. J. Neurophysiol. 73:1995;836-854.
23. Fu Q.-G., Flament D., Coltz J.D., Ebner T.J. Relationship of cerebellar Purkinje cell simple spike discharge to movement kinematics in the monkey. J. Neurophysiol. 78:1997;489-491.
24. Fu Q.-G., Suarez J.I., Ebner T.J. Neuronal specification of direction and distance during reaching movements in the superior precentral premotor area and primary motor cortex of monkeys. J. Neurophysiol. 70:1993;2097-2116.
25. Georgopoulos A.P. On reaching. Ann. Rev. Neurosci. 9:1986;147-170.
26. Georgopoulos A.P., Crutcher M.D., Schwartz A.B. Cognitive spatial-motor processes 3. Motor cortical prediction of movement during an instructed delay period. Exp. Brain Res. 75:1989;183-194.
27. Georgopoulos A.P., DeLong M.R., Crutcher M.D. Relations between parameters of step-tracking movements and single cell discharge in the globus pallidus and subthalamic nucleus of the behaving monkey. J. Neurosci. 3:1983;1586-1598.
28. Georgopoulos A.P., Kalaska J.F., Caminiti R., Massey J.T. On the relations between the direction of two-dimensional arm movements and cell discharge in primate motor cortex. J. Neurosci. 2:1982;1527-1537.
29. 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 of movement by a neuronal population. J. Neurosci. 8:1988;2928-2937.
30. Georgopoulos A.P., Pellizzer G. The mental and the neural: psychological and neural studies of mental rotation and memory scanning. Neuropsychologia. 33:1995;1531-1547.
31. Gilbert P.F.C., Thach W.T. Purkinje cell activity during motor learning. Brain Res. 128:1977;309-328.
32. Gomi H., Shidara M., Takemura A., Inoue Y., Kawano K., Kawato M. Temporal firing patterns of Purkinje cells in the cerebellar ventral paraflocculus during ocular following responses in monkeys. I. Simple spikes. J. Neurophysiol. 80:1998;818-831.
33. Gordon J., Ghilardi M.F., Cooper S.E., Chez C. Accuracy of planar reaching movements. II. Systematic extent errors resulting from inertial anisotropy. Exp. Brain Res. 99:1994;112-130.
34. Graf W., Simpson J.I., Leonard C.S. Spatial organization of visual messages of the rabbit's cerebellar flocculus. II. Complex and simple spike responses of Purkinje cells. J. Neurophysiol. 60:1988;2091-2121.
35. Hoffman D.S., Strick P.L. Effects of a primary motor cortex lesion on step-tracking movements of the wrist. J. Neurophysiol. 73:1995;891-895.
36. Holmes G. The cerebellum of man. Brain. 62:1939;1-30.
37. Hore J., Flament D. Changes in motor cortex neural discharge associated with the development of cerebellar limb ataxia. J. Neurophysiol. 60:1988;1285-1302.
38. Ito M. The Cerebellum and Neural Control. 1984;Raven Press, New York.
39. Johnson M.T.V., Coltz J.D., Ebner T.J. Encoding of target direction and speed during visual instruction and arm tracking in dorsal premotor and primary motor cortical neurons. Euro. J. Neurosci. 11:1999;4433-4445.
40. Johnson M.T.V., Coltz J.D., Hagen M.C., Ebner T.J. Visuomotor processing as reflected in the directional firing of cortical motor neurons. J. Neurophysiol. 81:1999;875-894.
41. Johnson P.B., Ferraina S., Bianchi L., Caminiti R. Cortical networks for visual reaching: physiological and anatomical organization of frontal and parietal lobe arm regions. Cereb. Cortex. 6:1996;102-119.
42. Kaei S., Hoffman D.S., Strick P.L. Muscle and movement representations in the primary motor cortex. Science. 285:1999;2136-2139.
43. Kalaska J.F., Caminiti R., Georgopoulos A.P. Cortical mechanisms related to the direction of two-dimensional arm movements: relations in parietal area 5 and comparison with motor cortex. Exp. Brain Res. 51:1983;247-260.
44. Kalaska J.F., Crammond D.J. Deciding not to go: neuronal correlates of response selection in a GO/NOGO task in primate premotor and parietal cortex. Cereb. Cortex. 5:1995;410-428.
45. Kawato M. Internal models for motor control and trajectory planning. Curr. Opin. Neurobiol. 9:1999;718-727.
46. Kawato M., Gomi H. A computational model of four regions of the cerebellum based on feedback-error learning. Biol. Cybern. 68:1992;95-103.
47. Keller E.L., Heinen S.J. Generation of smooth-pursuit eye movements: neuronal mechanisms and pathways. Neurosci. Res. 11:1991;79-107.
48. Lemon R.N. Neural control of dexterity: what has been achieved? Exp. Brain Res. 128:1999;6-12.
49. Lisberger S.G., Fuchs A.F. Role of primate flocculus during rapid behavioral modification of vestibulo-ocular reflex. I. Purkinje cell activity during visually guided horizontal smooth pursuit eye movement and passive head rotation. J. Neurophysiol. 46:1978;733-763.
50. Lurito J.T., Georgakopoulos T., Georgopoulos A.P. Cognitive spatial-motor processes. 7. The making of movements at an angle from a stimulus direction: studies of motor cortical activity at the single cell and population levels. Exp. Brain Res. 87:1991;562-580.
51. Marr D. A theory of cerebellar cortex. J. Physiol. (Lond.). 202:1969;437-470.
52. Miall R.C., Weir D.J., Stein J.F. Visuo-motor tracking during reversible inactivation of the cerebellum. Exp. Brain Res. 65:1987;455-464.
53. Middleton F.A., Strick P.L. Cerebellar output channels. Int. Rev. Neurobiol. 41:1997;61-82.
54. Milner A.D., Goodale M.A. Visual pathways to perception and action. Prog. Brain Res. 95:1993;317-337.
55. Moll L., Kuypers H.G.J.M. Premotor cortical ablations in monkeys: contralateral changes in visually guided reaching behavior. Science. 198:1977;317-319.
56. Moran D.W., Schwartz A.B. Motor cortical representation of speed and direction during reaching. J. Neurophysiol. 82:1999;2676-2692.
57. Mussa-Ivaldi F.A. Do neurons in the motor cortex encode movement direction? an alternative hypothesis. Neurosci. Lett. 91:1988;106-111.
58. Mussa-Ivaldi F.A., Hogan N., Bizzi E. Neural, mechanical and geometric factors subserving arm posture in humans. J. Neurosci. 5:1985;2732-2743.
59. Oscarsson O. Functional organization of olivary projection to the cerebellar anterior lobe. Courville J. The Inferior Olivary Nucleus: Anatomy and Physiology. 1980;279-290 Raven, New York.
60. Passingham R.E. Cues for movement in monkeys (Macaca mulatta) with lesions in premotor cortex. Behav. Neurosci. 100:1986;695-703.
61. Salinas E., Romo R. Conversion of sensory signals into motor commands in primary motor cortex. J. Neurosci. 18:1998;499-511.
62. Schieber M.H., Thach W.T. Trained slow tracking. II. Bidirectional discharge patterns of cerebellar nuclear, motor cortex and spindle afferent neurons. J. Neurophysiol. 54:1985;1228-1270.
63. Schwartz A.B. Direct cortical representation of drawing. Science. 265:1994;540-542.
64. Schwartz A.B. Distributed motor processing in the cerebral cortex. Curr. Opin. Neurobiol. 4:1994;840-846.
65. Schwartz A.B., Kettner R.E., Georgopoulos A.P. Primate motor cortex and free arm movements to visual targets in three-dimensional space. I. Relations between single cell discharge and direction of movement. J. Neurosci. 8:1988;2913-2927.
66. Soecting J.F., Flanders M. Sensorimotor representations for pointing to targets in three-dimensional space. J. Neurophysiol. 62:1989;582-594.
67. Stein J.F., Glickstein M. Role of the cerebellum in visual guidance of movement. Physiol. Rev. 4:1992;967-1017.
68. Stone L.S., Lisberger S.G. Visual responses of Purkinje cells in the cerebellar flocculus during smooth-pursuit eye movements. I. Simple spikes. J. Neurophysiol. 63:1990;1241-1261.
69. Thach W.T. Correlation of neural discharge with pattern and force of muscular activity, joint position and direction of intended next movement in motor cortex and cerebellum. J. Neurophysiol. 41:1978;654-676.
70. Thach W.T., Goodkin H.P., Keating J.G. The cerebellum and the adaptive coordination of movement. Annu. Rev. Neurosci. 15:1992;403-442.
71. Weinrich M., Wise S.P., Mauritz K.-H. A neurophysiological study of the premotor cortex in the rhesus monkey. Brain. 107:1984;385-414.
72. Wickelgren W.A. Webs, cell assemblies, and chunking in neural nets. Neuroscience. 1:1992;1-53.
73. Wise S.P., Boussaoud D., Johnson P.B., Caminiti R. Premotor and parietal cortex: corticocortical connectivity and combinatorial computations. Ann. Rev. Neurosci. 20:1997;25-42.
74. Wise S.P., di Pellegrino G., Boussaoud D. The premotor cortex and nonstandard sensorimotor mapping. Can. J. Physiol. Pharm. 74:1996;469-482.
75. Wise S.P., Weinrich M., Mauritz K.-H. Motor aspects of cue-related neuronal activity in premotor cortex of the rhesus monkey. Brain Res. 260:1983;301-305.