BOLD coherence reveals segregated functional neural interactions when adapting to distinct torque perturbations

Journal of Neurophysiology

Volumn 97, Issue 3, 2007, Pages 2107-2120

  Tunik, Eugene ^a,b   Schmitt, Paul J ^a   Grafton, Scott T ^a,c  

^a Dartmouth College   (United States)

^b NEW YORK UNIVERSITY   (United States)

^c UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; BASAL GANGLION; BEHAVIOR; CAUDATE NUCLEUS; CONTROLLED STUDY; DENTATE NUCLEUS; FEMALE; FUNCTIONAL MAGNETIC RESONANCE IMAGING; HUMAN; HUMAN EXPERIMENT; INFORMATION PROCESSING; MALE; MOTOR CORTEX; MOTOR SYSTEM; NERVE CELL NETWORK; NEUROIMAGING; NEUROPHYSIOLOGY; NEUROSCIENCE; PHYLOGENETIC TREE; PRIORITY JOURNAL; PUTAMEN; SENSORY SYSTEM; STATISTICAL ANALYSIS; TORQUE;

ADAPTATION, PHYSIOLOGICAL; ADULT; ANALYSIS OF VARIANCE; BRAIN MAPPING; CEREBRAL CORTEX; FEMALE; HUMANS; IMAGE PROCESSING, COMPUTER-ASSISTED; MAGNETIC RESONANCE IMAGING; MALE; OXYGEN; POSTURE; PSYCHOMOTOR PERFORMANCE; TORQUE;

EID: 33947096393     PISSN: 00223077     EISSN: 15221598     Source Type: Journal    
DOI: 10.1152/jn.00405.2006     Document Type: Article

References (69)

1. Aguirre GK, Zarahn E, D'Esposito, M. Empirical analyses of BOLD fMRI statistics. II. Spatially smoothed data collected under null-hypothesis and experimental conditions. Neuroimage 5: 199-212, 1997.
2. Alexander GE, Crutcher MD. Preparation for movement: neural representations of intended direction in three motor areas of the monkey. J Neurophysiol 64: 133-150, 1990.
3. Attwell D, Iadecola C. The neural basis of functional brain imaging signals. Trends Neurosci 25: 621-625, 2002.
4. Barnard ST, Pothen A, Simon H. A spectral algorithm for envelope reduction of sparse matrices. Numer Linear Algebra Appl 2: 317-334, 1995.
5. Blakemore SJ, Sirigu A. Action prediction in the cerebellum and in the parietal lobe. Exp Brain Res 153: 239-245, 2003.
6. Boettiger CA, D'Esposito M. Frontal networks for learning and executing arbitrary stimulus-response associations. J Neurosci 25: 2723-2732, 2005.
7. Chinzei K, Kikinis R, Jolesz F. MR compatibility of mechatronic devices: design criteria. Proc MICCAI '99 Lecture Notes Comput Sci 1679: 1020-1031, 1999.
8. Clower DM, Dum RP, Strick PL. Basal ganglia and cerebellar inputs to "AIP." Cereb Cortex 15: 913-920, 2005.
9. Clower DM, Hoffman JM, Votaw JR, Faber TL, Woods RP, Alexander GE. Role of posterior parietal cortex in the recalibration of visually guided reaching. Nature 383: 618-621, 1996.
10. Clower DM, West RA, Lynch JC, Strick PL. The inferior parietal lobule is the target of output from the superior colliculus, hippocampus, and cerebellum. J Neurosci 21: 6283-6291, 2001.
11. Curtis CE, Sun FT, Miller LM, D'Esposito M. Coherence between fMRI time-series distinguishes two spatial working memory networks. Neuroimage 26: 177-183, 2005.
12. Della-Maggiore V, Malfait N, Ostry D, Paus T. Stimulation of the posterior parietal cortex interferes with arm trajectory adjustments during the learning of new dynamics. J Neurosci 24: 9971-9976, 2004.
13. DeLong MR, Alexander GE, Georgopoulos AP, Crutcher MD, Mitchell SJ, Richardson RT. Role of basal ganglia in limb movements. Hum Neurobiol 2: 235-244, 1984a.
14. DeLong MR, Georgopoulos AP, Crutcher MD, Mitchell SJ, Richardson RT, Alexander GE. Functional organization of the basal ganglia: contributions of single-cell recording studies. Ciba Found Symp 107: 64-82, 1984b.
15. Desmurget M, Epstein CM, Turner RS, Prablanc C, Alexander GE, Grafton ST. Role of the posterior parietal cortex in updating reaching movements to a visual target. Nat Neurosci 2: 563-567, 1999.
16. Desmurget M, Grafton S. Forward modeling allows feedback control for fast reaching movements. Trends Cogn Sci 4: 423-431, 2000.
17. Desmurget M, Grafton ST, Vindras P, Grea H, Turner RS. Basal ganglia network mediates the control of movement amplitude. Exp Brain Res 153: 197-209, 2003.
18. Desmurget M, Grafton ST, Vindras P, Grea H, Turner RS. The basal ganglia network mediates the planning of movement amplitude. Eur J Neurosci 19: 2871-2880, 2004.
19. Desmurget M, Pelisson D, Grethe JS, Alexander GE, Urquizar C, Prablanc C, Grafton ST. Functional adaptation of reactive saccades in humans: a PET study. Exp Brain Res 132: 243-259, 2000.
20. Diedrichsen J, Hashambhoy Y, Rane T, Shadmehr R. Neural correlates of reach errors. J Neurosci 25: 9919-9931, 2005.
21. Diedrichsen J, Verstynen T, Lehman SL, Ivry RB. Cerebellar involvement in anticipating the consequences of self-produced actions during bimanual movements. J Neurophysiol 93: 801-812, 2005.
22. Dreher JC, Grafman J. The roles of the cerebellum and basal ganglia in timing and error prediction. Eur J Neurosci 16: 1609-1619, 2002.
23. Eblen F, Graybiel AM. Highly restricted origin of prefrontal cortical inputs to striosomes in the macaque monkey. J Neurosci 15: 5999-6013, 1995.
24. Floyer-Lea A, Matthews PM. Changing brain networks for visuomotor control with increased movement automaticity. J Neurophysiol 92: 2405-2412, 2004.
25. Fu QG, Mason CR, Flament D, Coltz JD, Ebner TJ. Movement kinematics encoded in complex spike discharge of primate cerebellar Purkinje cells. Neuroreport 8: 523-529, 1997.
26. Garraux G, McKinney C, Wu T, Kansaku K, Nolte G, Hallet M. Shared brain areas but not functional connections controlling movement timing and order. J Neurosci 25: 5290-5297, 2005.
27. Gentilucci M, Negrotti A. Planning and executing an action in Parkinson's disease. Mov Disord 14: 69-79, 1999.
28. Georgopoulos AP, DeLong MR, Crutcher MD. 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: 1586-1598, 1983.
29. Ghilardi M, Ghez C, Dhawan V, Moeller J, Mentis M, Nakamura T, Antonini A, Eidelberg D. Patterns of regional brain activation associated with different forms of motor learning. Brain Res 871: 127-145, 2000.
30. Graydon FX, Friston KJ, Thomas CG, Brooks VB, Menon RS. Learning-related fMRI activation associated with a rotational visuo-motor transformation. Brain Res Cogn Brain Res 22: 373-383, 2005.
31. Grea H, Pisella L, Rossetti Y, Desmurget M, Tilikete C, Grafton S, Prablanc C, Vighetto A. A lesion of the posterior parietal cortex disrupts on-line adjustments during aiming movements. Neuropsychologia 40: 2471-2480, 2002.
32. Imamizu H, Miyauchi S, Tamada T, Sasaki Y, Takino R, Putz B, Yoshioka T, Kawato M. Human cerebellar activity reflecting an acquired internal model of a new tool. Nature 403: 192-195, 2000.
33. Inoue K, Kawashima R, Satoh K, Kinomura S, Goto R, Sugiura M, Ito M, Fukuda H. Activity in the parietal area during visuomotor learning with optical rotation. Neuroreport 8: 3979-3983, 1997.
34. Inoue, K, Kawashima R, Satoh K, Kinomura S, Sugiura M, Goto R, Ito M, Fukuda H. A PET study of visuomotor learning under optical rotation. Neuroimage 11: 505-516, 2000.
35. Johansen-Berg H, Behrens TE, Robson MD, Drobnjak I, Rushworth MF, Brady JM, Smith SM, Higham DJ, Matthews PM. Changes in connectivity profiles define functionally distinct regions in human medial frontal cortex. Proc Natl Acad Sci USA 101: 13335-13340, 2004.
36. Jueptner M, Weiller C. A review of differences between basal ganglia and cerebellar control of movements as revealed by functional imaging studies. Brain 121: 1437-1449, 1998.
37. Kimura M, Matsumoto N, Okahashi K, Ueda Y, Satoh T, Minamimoto T, Sakamoto M, Yamada H. Goal-directed, serial and synchronous activation of neurons in the primate striatum. Neuroreport 14: 799-802, 2003.
38. Krakauer JW, Ghilardi MF, Mentis M, Barnes A, Veytsman M, Eidelberg D, Ghez C. Differential cortical and subcortical activations in learning rotations and gains for reaching: a PET study. J Neurophysiol 91: 924-933, 2004.
39. Lestienne F. Effects of inertial load and velocity on the braking process of voluntary limb movements. Exp Brain Res 35: 407-418, 1979.
40. Logothetis NK. The underpinnings of the BOLD functional magnetic resonance imaging signal." J Neurosci 23: 3963-3971, 2003.
41. Martin TA, Keating JG, Goodkin HP, Bastian AJ, Thach WT. Throwing while looking through prisms. I. Focal olivocerebellar lesions impair adaptation. Brain 119: 1183-1198, 1996.
42. Menon V, Anagnoson RT, Glover GH, Pfefferbaum A. Basal ganglia involvement in memory-guided movement sequencing. Neuroreport 11: 3641-3645, 2000.
43. Messier J, Kalaska JF. Covariation of primate dorsal premotor cell activity with direction and amplitude during a memorized-delay reaching task. J Neurophysiol 84: 152-165, 2000.
44. Miall RC, Jenkinson EW. Functional imaging of changes in cerebellar activity related to learning during a novel eye-hand tracking task. Exp Brain Res 166: 170-183, 2005.
45. Miall RC, Weir DJ, Wolpert DM, Stein JF. Is the cerebellum a Smith predictor? J Mot Behav 25: 203-216, 1993.
46. Miller LM, Sun FT, Curtis CE, D'Esposito M. Functional interactions between oculomotor regions during prosaccades and antisaccades. Hum Brain Mapp 26: 119-127, 2005.
47. Milner TE, Franklin DW. Impedance control and internal model use during the initial stage of adaptation to novel dynamics in humans. J Physiol 567: 651-664, 2005.
48. Nezafat R, Shadmehr R, Holcomb HH. Long-term adaptation to dynamics of reaching movements: a PET study. Exp Brain Res 140: 66-76, 2001.
49. Nitschke MF, Stavrou G, Melchert UH, Erdmann C, Peterson D, Wessel K, Heide W. Modulation of cerebellar activation by predictive and nonpredictive sequential finger movements. Cerebellum 2: 233-240, 2003.
50. Nixon PD. The role of the cerebellum in preparing responses to predictable sensory events. Cerebellum 2: 114-122, 2003.
51. Osu R, Hirai S, Yoshioka T, Kawato M. Random presentation enables subjects to adapt to two opposing forces on the hand. Nat Neurosci 7: 111-112, 2004.
52. Rencher AC. Methods of Multivariate Analysis (2nd ed.). New York: Wiley-Interscience, 2002.
53. Sergio LE, Hamel-Paquet C, Kalaska JF. Motor cortex neural correlates of output kinematics and kinetics during isometric-force and arm-reaching tasks. J Neurophysiol 94: 2353-2378, 2005.
54. Sergio LE, Kalaska JF. Systematic changes in motor cortex cell activity with arm posture during directional isometric force generation. J Neurophysiol 89: 212-228, 2003.
55. Shadmehr R, Holcomb HH. Neural correlates of motor memory consolidation. Science 277: 821-825, 1997.
56. Shadmehr R, Holcomb HH. Inhibitory control of competing motor memories. Exp Brain Res 126: 235-251, 1999.
57. Smith MA, Shadmehr R. Intact ability to learn internal models of arm dynamics in Huntington's disease but not cerebellar degeneration. J Neurophysiol 93: 2809-2821, 2005.
58. Strick PL, Dum RP, Picard N. Motor areas on the medial wall of the hemisphere. Novartis Found Symp 218: 64-75; discussion 75-80; 104-108, 1998.
59. Sun FT, Miller LM, D'Esposito M. Measuring interregional functional connectivity using coherence and partial coherence analyses of fMRI data. Neuroimage 21: 647-658, 2004.
60. Thoenissen D, Zilles K, Toni I. Differential involvement of parietal and precentral regions in movement preparation and motor intention. J Neurosci 22: 9024-9034, 2002.
61. Timmann D, Richter S, Bestmann S, Kalveram KT, Konczak J. Predictive control of muscle responses to arm perturbations in cerebellar patients. J Neurol Neurosurg Psychiatry 69: 345-352, 2000.
62. Toni I, Passingham RE. Prefrontal-basal ganglia pathways are involved in the learning of arbitrary visuomotor associations: a PET study. Exp Brain Res 127: 19-32, 1999.
63. Toni I, Rowe J, Stephan KE, Passingham RE. Changes of cortico-striatal effective connectivity during visuomotor learning. Cereb Cortex 12: 1040-1047, 2002.
64. Toni I, Rushworth MF, Passingham RE. Neural correlates of visuomotor associations. Spatial rules compared with arbitrary rules. Exp Brain Res 141: 359-369, 2001.
65. Tunik E, Frey SH, Grafton ST. Virtual lesions of the anterior intraparietal area disrupt goal-dependent on-line adjustments of grasp. Nat Neurosci 8: 505-511, 2005.
66. Turner RS, Desmurget M, Grethe J, Crutcher MD, Grafton ST. Motor subcircuits mediating the control of movement extent and speed. J Neurophysiol 90: 3958-3966, 2003.
67. Vaillancourt DE, Mayka MA, Thulborn KR, Corcos DM. Subthalamic nucleus and internal globus pallidus scale with the rate of change of force production in humans. Neuroimage 23: 175-186, 2004.
68. Wichmann T, Bergman H, DeLong MR. The primate subthalamic nucleus. I. Functional properties in intact animals. J Neurophysiol 72: 494-506, 1994a.
69. Wichmann T, Bergman H, DeLong MR. The primate subthalamic nucleus. III. Changes in motor behavior and neuronal activity in the internal pallidum induced by subthalamic inactivation in the MPTP model of parkinsonism. J Neurophysiol 72: 521-530, 1994b.