Different contributions of the corpus callosum and cerebellum to motor coordination in monkey

Journal of Neurophysiology

Volumn 98, Issue 5, 2007, Pages 2962-2973

  Soteropoulos, Demetris S ^a   Baker, Stuart N ^a,b  

^a NEWCASTLE UNIVERSITY   (United Kingdom)

^b ROYAL VICTORIA INFIRMARY   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ACCURACY; ANIMAL EXPERIMENT; ANTIDROMIC STIMULATION; ARTICLE; CEREBELLUM; CEREBELLUM NUCLEUS; COMPARATIVE STUDY; CONTROLLED STUDY; CORPUS CALLOSUM; FEMALE; HAND GRIP; MACACA; MONKEY; MOTOR CONTROL; MOTOR COORDINATION; MULTIPLE REGRESSION; MULTIVARIATE ANALYSIS; NEUROPHYSIOLOGY; NONHUMAN; PRIORITY JOURNAL; REGRESSION ANALYSIS;

ANIMALS; BEHAVIOR, ANIMAL; CEREBELLUM; CORPUS CALLOSUM; ELECTROMYOGRAPHY; FEMALE; FUNCTIONAL LATERALITY; MACACA MULATTA; NEURONS; PSYCHOMOTOR PERFORMANCE; REGRESSION ANALYSIS;

EID: 36248977069     PISSN: 00223077     EISSN: 15221598     Source Type: Journal    
DOI: 10.1152/jn.00236.2007     Document Type: Article

References (94)

1. Allison JD, Meador KJ, Loring DW, Figueroa RE, Wright JC. Functional MRI cerebral activation and deactivation during finger movement. Neurology 54: 135-142, 2000.
2. Baizer JS, Kralj-Hans I, Glickstein M. Cerebellar lesions and prism adaptation in macaque monkeys. J Neurophysiol 81: 1960-1965, 1999.
3. Baker SN, Olivier E, Lemon RN. Coherent oscillations in monkey motor cortex and hand muscle EMG show task-dependent modulation. J Physiol 501: 225-241, 1997.
4. Baker SN, Pinches EM, Lemon SN. Synchronisation in monkey motor cortex during a precision grip task. II. Effect of oscillatory activity on corticospinal output. J Neurophysiol 89: 1941-1953, 2003.
5. Baker SN, Spinks R, Jackson A, Lemon RN. Synchronization in monkey motor cortex during a precision grip task. I. Task-dependent modulation in single-unit synchrony. J Neurophysiol 85: 869-885, 2001.
6. Beloozerova IN, Sirota MG, Swadlow HA. Activity of different classes of neurons of the motor cortex during locomotion. J Neurosci 23: 1087-1097, 2003a.
7. Beloozerova IN, Sirota MG, Swadlow HA. Activity and silence of feline motor cortical efferent populations during locomotion. Soc Neurosci Abstr 921.22, 2003b.
8. Beloozerova IN, Sirota MG, Swadlow HA, Orlovsky GN, Popova LB, Deliagina TG. Activity of different classes of neurons of the motor cortex during postural corrections. J Neurosci 23: 7844-7853, 2003c.
9. Brown RG, Jahanshahi M, Marsden CD. The execution of bimanual movements in patients with Parkinson's, Huntington's and cerebellar disease. J Neurol Neurosurg Psychiatry 56: 295-297, 1993.
10. Cooper SE, Martin JH, Ghez C. Effects of inactivation of the anterior interpositus nucleus on the kinematic and dynamic control of multijoint movement. J Neurophyiol 84: 1988-2000, 2000.
11. Cui SZ, Li EZ, Zang YF, Weng XC, Ivry R, Wang JJ. Both sides of human cerebellum involved in preparation and execution of sequential movements. Neuroreport 11: 3849-3853, 2000.
12. Davies RM, Gerstein GL, Baker SN. Measurement of time-dependent changes in the irregularity of neural spiking. J Neurophysiol 96: 906-918, 2006.
13. Debaere F, Wenderoth N, Sunaert S, Van Hecke P, Swinnen SP. Internal vs external generation of movements: differential neural pathways involved in bimanual coordination performed in the presence or absence of augmented visual feedback. Neuroimage 19: 764-776, 2003.
14. Devinsky O, Laff R. Callosal lesions and behavior: history and modern concepts. Epilepsy Behav 4: 607-617, 2003.
15. Diedrichsen J, Hazeltine E, Nurss WK, Ivry RB. The role of the corpus callosum in the coupling of bimanual isometric force pulses. J Neurophysiol 90: 2409-2418, 2003.
16. Donchin O, Gribova A, Steinberg O, Bergman H, Vaadia E. Primary motor cortex is involved in bimanual coordination. Nature 395: 274-278, 1998.
17. Donchin O, Gribova A, Steinberg O, Mitz AR, Bergman H, Vaadia E. Single-unit activity related to bimanual arm movements in the primary and supplementary motor cortices. J Neurophysiol 88: 3498-3517, 2002.
18. Dyball R, Bhumbra GS. Digital spike discrimination combining size and shape elements. J Physiol 547P: D9, 2003.
19. Ehrsson HH, Kuhtz-Buschbeck JP, Forssberg H. Brain regions controlling nonsynergistic versus synergistic movement of the digits: a functional magnetic resonance imaging study. J Neurosci 22: 5074-5080, 2002.
20. Engel AK, Konig P, Kreiter AK, Singer W. Interhemispheric synchronization of oscillatory neuronal responses in cat visual cortex. Science 252: 1177-1179, 1991.
21. Fortier PA, Kalaska JF, Smith AM. Cerebellar neuronal activity related to whole-arm reaching movements in the monkey. J Neurophysiol 62: 198-211, 1989.
22. Greger B, Norris SA, Thach WT. Spike firing in the lateral cerebellar cortex correlated with movement and motor parameters irrespective of the effector limb. J Neurophysiol 91: 576-582, 2004.
23. Harvey RJ, Porter R, Rawson JA. Discharges of intracerebellar nuclear cells in monkeys. J Physiol 297: 559-580, 1979.
24. Hirata Y, Highstein SM. Acute adaptation of the vestibuloocular reflex: signal processing by floccular and ventral parafloccular Purkinje cells. J Neurophysiol 85: 2267-2288, 2001.
25. Holmes G. The cerebellum of man. Brain 62: 1-30, 1939.
26. Hore J, Vilis T. Loss of set in muscle responses to limb perturbations during cerebellar dysfunction. J Neurophysiol 51: 1137-1148, 1984.
27. Immisch I, Quintern J, Straube A. Unilateral cerebellar lesions influence arm movements bilaterally. Neuroreport 14: 837-840, 2003.
28. Immisch I, Waldvogel D, van Gelderen P, Hallett M. The role of the medial wall and its anatomical variations for bimanual antiphase and in-phase movements. Neuroimage 14: 674-684, 2001.
29. Indovina I, Sanes JN. Combined visual attention and finger movement effects on human brain representations. Exp Brain Res 140: 265-279, 2001.
30. Ivry RB, Keele SW, Diener HC. Dissociation of the lateral and medial cerebellum in movement timing and movement execution. Exp Brain Res 73: 167-180, 1988.
31. Kawashima R, Matsumura M, Sadato N, Naito E, Waki A, Nakamura S, Matsunami K, Fukuda H, Yonekura Y. Regional cerebral blood flow changes in human brain related to ipsilateral and contralateral complex hand movements - a PET study. Eur J Neurosci 10: 2254-2260, 1998.
32. Kazennikov O, Wicki U, Corboz M, Hyland B, Palmeri A, Rouiller EM, Wiesendanger M. Temporal structure of a bimanual goal-directed movement sequence in monkeys. Eur J Neurosci 6: 203-210, 1994.
33. Kelso JAS. Phase transitions and critical behavior in human bimanual coordination. Am J Physiol Regulatory Integrative Comp Physiol 246: R1000-R1004, 1984.
34. Kennerley SW, Diedrichsen J, Hazeltine E, Semjen A, Ivry RB. Callosotomy patients exhibit temporal uncoupling during continuous bimanual movements. Nat Neurosci 5: 376-381, 2002.
35. Kermadi I, Liu Y, Rouiller EM. Do bimanual motor actions involve the dorsal premotor (PMd), cingulate (CMA) and posterior parietal (PPC) cortices? Comparison with primary and supplementary motor cortical areas. Somatosens Mot Res 17: 255-271, 2000.
36. Kermadi I, Liu Y, Tempini A, Calciati E, Rouiller EM. Neuronal activity in the primate supplementary motor area and the primary motor cortex in relation to spatio-temporal bimanual coordination. Somatosens Mot Res 15: 287-308, 1998.
37. Kinoshita H, Oku N, Hashikawa K, Nishimura T. Functional brain areas used for the lifting of objects using a precision grip: a PET study. Brain Res 857: 119-130, 2000.
38. Kolb TF, Lachauer S, Schoch B, Gerwig M, Timmann D, Kolb FP. Comparison of the electrically evoked leg withdrawal reflex in cerebellar patients and healthy controls. Exp Brain Res 177: 493-508, 2007.
39. Kurata K, Wise SP. Premotor and supplementary motor cortex in rhesus monkeys: neuronal activity during externally and internally instructed motor tasks. Exp Brain Res 72: 237-248, 1988.
40. Lemon RN. Methods for Neuronal Recording in Conscious Animals (4th ed.). London: Wiley, 1984.
41. Liu J, Morel A, Wannier T, Rouiller EM. Origins of callosal projections to the supplementary motor area (SMA): a direct comparison between pre-SMA and SMA-proper in macaque monkeys. J Comp Neurol 443: 71-85, 2002.
42. MacKay WA. Unit activity in the cerebellar nuclei related to arm reaching movements. Brain Res 442: 240-254, 1988a.
43. MacKay WA. Cerebellar nuclear activity in relation to simple movements. Exp Brain Res 71: 47-58, 1988b.
44. Martin JH, Cooper SE, Hacking A, Ghez C. Differential effects of deep cerebellar nuclei inactivation on reaching and adaptive control. J Neurophysiol 83: 1886-1899, 2000.
45. Mayston MJ, Harrison LM, Stephens JA. A neurophysiological study of mirror movements in adults and children. Ann Neurol 45: 583-594, 1999.
46. Middleton FA, Strick PL. Basal ganglia and cerebellar loops: motor and cognitive circuits. Brain Res Brain Res Rev 31: 236-250, 2000.
47. Mihailoff GA. Intra- and interhemispheric collateral branching in the rat pontocerebellar system, a fluorescence double-label study. Neuroscience 10: 141-160, 1983.
48. Miller LE, Houk JC. Motor coordinates in primate red nucleus: preferential relation to muscle activation versus kinematic variables. J Physiol 488: 533-548, 1995.
49. Montgomery DC, Peck EA, Vining GG. Introduction to Linear Regression Analysis. New York: Wiley, 2001.
50. Moran DW, Schwartz AB. Motor cortical activity during drawing movements: population representation during spiral tracing. J Neurophysiol 82: 2693-2704, 1999.
51. Morrow MM, Miller LE. Prediction of muscle activity by populations of sequentially recorded primary motor cortex neurons. J Neurophysiol 89: 2279-2288, 2003.
52. Munk MH, Nowak LG, Nelson JI, Bullier J. Structural basis of cortical synchronization. II. Effects of cortical lesions. J Neurophysiol 74: 2401-2414, 1995.
53. Mushiake H, Inase M, Tanji J. Selective coding of motor sequence in the supplementary motor area of the monkey cerebral cortex. Exp Brain Res 82: 208-210, 1990.
54. Nair DG, Purcott KL, Fuchs A, Steinberg F, Kelso JA. Cortical and cerebellar activity of the human brain during imagined and executed unimanual and bimanual action sequences: a functional MRI study. Brain Res Cogn Brain Res 15: 250-260, 2003.
55. Newton JM, Sunderland A, Gowland PA. fMRI signal decreases in ipsilateral primary motor cortex during unilateral hand movements are related to duration and side of movement. Neuroimage 24: 1080-1087, 2005.
56. Oscarsson O. Functional organisation of spinocerebellar paths. In: Handbook of Sensory Physiology. Berlin: Springer Verlag, 1973, chapt. 11, p. 340-373.
57. Oulad Ben Taib N, Manto M. Hemicerebellectomy impairs the modulation of cutaneomuscular reflexes by the motor cortex following repetitive somatosensory stimulation. Brain Res 1090: 110-115, 2006.
58. Perrig S, Kazennikov O, Wiesendanger M. Time structure of a goal-directed bimanual skill and its dependence on task constraints. Behav Brain Res 103: 95-104, 1999.
59. Prut Y, Perlmutter SI. Firing properties of spinal interneurons during voluntary movement. I. State-dependent regularity of firing. J Neurosci 23: 9600-9610, 2003.
60. Ramnani N, Toni I, Passingham RE, Haggard P. The cerebellum and parietal cortex play a specific role in coordination: a PET study. Neuroimage 14: 899-911, 2001.
61. Rieke F, Warland D, de Ruyter van Steveninck R, Bialek W. Spikes: Exploring the Neural Code. Cambridge, MA: MIT Press, 1997.
62. Rouiller EM, Babalian A, Kazennikov O, Moret V, Yu XH, Wiesendanger M. Transcallosal connections of the distal forelimb representations of the primary and supplementary motor cortical areas in macaque monkeys. Exp Brain Res 102: 227-243, 1994.
63. Sadato N, Yonekura Y, Waki A, Yamada H, Ishii Y. Role of the supplementary motor area and the right premotor cortex in the coordination of bimanual finger movements. J Neurosci 17: 9667-9674, 1997.
64. Salenius S, Schnitzler A, Salmelin R, Jousmaki V, Hari R. Modulation of human cortical rolandic rhythms during natural sensorimotor tasks. Neuroimage 5: 221-228, 1997.
65. Salmelin R, Forss N, Knuutila J, Hari R. Bilateral activation of the human somatomotor cortex by distal hand movements. Electroencephalogr Clin Neurophysiol 95: 444-452, 1995.
66. Serrien DJ, Nirkko AC, Wiesendanger M. Role of the corpus callosum in bimanual coordination: a comparison of patients with congenital and acquired callosal damage. Eur J Neurosci 14: 1897-1905, 2001.
67. Serrien DJ, Wiesendanger M. Temporal control of a bimanual task in patients with cerebellar dysfunction. Neuropsychologia 38: 558-565, 2000.
68. Smith AM, Bourbonnais D. Neuronal activity in cerebellar cortex related to control of prehensile force. J Neurophysiol 45: 286-303, 1981.
69. Soteropoulos DS, Baker SN. Cortico-cerebellar coherence during a precision grip task in the monkey. J Neurophysiol 95: 1194-1206, 2006.
70. Soteropoulos DS, Rhodes SA, Baker SN. Bilateral movement representation in the deep cerebellar nuclei. Soc Neurosci Abstr 2003 Program number 75.13.
71. Spencer RM, Zelaznik HN, Diedrichsen J, Ivry RB. Disrupted timing of discontinuous but not continuous movements by cerebellar lesions. Science 300: 1437-1439, 2003.
72. Stancak A, Pfurtscheller G. Mu-rhythm changes in brisk and slow self-paced finger movements. Neuroreport 7: 1161-1164, 1996.
73. Stephan KM, Binkofski F, Halsband U, Dohle C, Wunderlich G, Schnitzler A, Tass P, Posse S, Herzog H, Sturm V, Zilles K, Seitz RJ, Freund HJ. The role of ventral medial wall motor areas in bimanual coordination. A combined lesion and activation study. Brain 122: 351-368, 1999.
74. Stern EA, Kincaid AE, Wilson CJ. Spontaneous subthreshold membrane potential fluctuations and action potential variability of rat corticostriatal and striatal neurons in vivo. J Neurophysiol 77: 1697-1715, 1997.
75. Swadlow HA. Physiological properties of individual cerebral axons studied in vivo for as long as one year. J Neurophysiol 54: 1346-1362, 1985.
76. Swadlow HA. Efferent neurons and suspected interneurons in motor cortex of the awake rabbit: axonal properties, sensory receptive fields, and subthreshold synaptic inputs. J Neurophysiol 71: 437-453, 1994.
77. Swadlow HA. Neocortical efferent neurons with very slowly conducting axons: strategies for reliable antidromic identification. J Neurosci Methods 79: 131-141, 1998.
78. Swadlow HA, Hicks TP. Subthreshold receptive fields and baseline excitability of "silent" S1 callosal neurons in awake rabbits: contributions of AMPA/kainate and NMDA receptors. Exp Brain Res 115: 403-409, 1997.
79. Swadlow HA, Rosene DL, Waxman SG. Characteristics of interhemispheric impulse conduction between prelunate gyri of the rhesus monkey. Exp Brain Res 33: 455-467, 1978.
80. Swadlow HA, Waxman SG. Variations in conduction velocity and excitability following single and multiple impulses of visual callosal axons in the rabbit. Exp Neurol 53: 128-150, 1976.
81. Tanji J. Comparison of neuronal activities in the monkey supplementary and precentral motor areas. Behav Brain Res 18: 137-142, 1985.
82. Tanji J, Kurata K. Contrasting neuronal activity in supplementary and precentral motor cortex of monkeys. I. Responses to instructions determining motor responses to forthcoming signals of different modalities. J Neurophysiol 53: 129-141, 1985.
83. Tanji J, Mushiake H. Comparison of neuronal activity in the supplementary motor area and primary motor cortex. Brain Res Cogn Brain Res 3: 143-150, 1996.
84. Tanji J, Okano K, Sato KC. Neuronal activity in cortical motor areas related to ipsilateral, contralateral, and bilateral digit movements of the monkey. J Neurophysiol 60: 325-343, 1988.
85. Thach WT. 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: 654-676, 1978.
86. Thach WT, Bastian AJ. Role of the cerebellum in the control and adaptation of gait in health and disease. Prog Brain Res 143: 353-366, 2004.
87. Toma K, Honda M, Hanakawa T, Okada T, Fukuyama H, Ikeda A, Nishizawa S, Konishi J, Shibasaki H. Activities of the primary and supplementary motor areas increase in preparation and execution of voluntary muscle relaxation: an event-related fMRI study. J Neurosci 19: 3527-3534, 1999.
88. Towe AL, Harding GW. Extracellular microelectrode sampling bias. Exp Neurol 29: 366-381, 1970.
89. Townsend BR, Paninski L, Lemon RN. Linear encoding of muscle activity in primary motor cortex and cerebellum. J Neurophysiol 96: 2578-2592, 2006.
90. Ullen F, Forssberg H, Ehrsson HH. Neural networks for the coordination of the hands in time. J Neurophysiol 89: 1126-1135, 2003.
91. Waxman SG, Bennett MVL. Relative conduction velocities of small myelinated and non-myelinated fibres in the central nervous system. Nature New Biol 238: 217-219, 1972.
92. Weiss AC, Weiller C, Liepert J. Pre-movement motor excitability is reduced ipsilateral to low force pinch grips. J Neural Transm 110: 201-208, 2003.
93. Wetmore DZ, Baker SN. Post-spike distance-to-threshold trajectories of neurones in monkey motor cortex. J Physiol 555: 831-850, 2004.
94. Yazawa S, Ikeda A, Kunieda T, Mima T, Nagamine T, Ohara S, Terada K, Taki W, Kimura J, Shibasaki H. Human supplementary motor area is active in preparation for both voluntary muscle relaxation and contraction: subdural recording of Bereitschaftspotential. Neurosci Lett 244: 145-148, 1998.