A parietal-premotor network for movement intention and motor awareness

Trends in Cognitive Sciences

Volumn 13, Issue 10, 2009, Pages 411-419

  Desmurget, Michel ^a,b   Sirigu, Angela ^a,b  

^a INSTITUT DES SCIENCES COGNITIVES   (France)

^b UNIVERSITÉ LYON 1   (France)

Author keywords

[No Author keywords available]

Indexed keywords

BRAIN REGIONS; NEURAL PROCESS; POSTERIOR PARIETAL CORTICES;

MOTORS;

BRAIN;

ARTICLE; AWARENESS; BEHAVIOR; BRAIN FUNCTION; BRAIN REGION; COGNITION; CONSCIOUSNESS; ELECTRODE; ELECTROSTIMULATION; HUMAN; MONITORING; MOTOR SYSTEM; MOVEMENT (PHYSIOLOGY); NERVE CELL NETWORK; NEUROSCIENCE; NONHUMAN; PARIETAL LOBE; PREMOTOR CORTEX;

ANIMALS; AWARENESS; BRAIN MAPPING; COGNITIVE SCIENCE; ELECTRIC STIMULATION; HUMANS; INTENTION; MODELS, BIOLOGICAL; MOTOR CORTEX; MOVEMENT; PARIETAL LOBE;

EID: 70349404208     PISSN: 13646613     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tics.2009.08.001     Document Type: Article

References (77)

1. Sirigu A., et al. Perception of self-generated movement following left parietal lesion. Brain 122 Pt 10 (1999) 1867-1874
2. Sirigu A., et al. Altered awareness of voluntary action after damage to the parietal cortex. Nat. Neurosci. 7 (2004) 80-84
3. Lau H.C., et al. Attention to intention. Science 303 (2004) 1208-1210
4. Assal F., et al. Moving with or without will: functional neural correlates of alien hand syndrome. Ann. Neurol. 62 (2007) 301-306
5. Berti A., et al. Shared cortical anatomy for motor awareness and motor control. Science 309 (2005) 488-491
6. Appelros P., et al. Anosognosia versus unilateral neglect. Coexistence and their relations to age, stroke severity, lesion site and cognition. Eur. J. Neurol 14 (2007) 54-59
7. Haggard P., and Magno E. Localising awareness of action with transcranial magnetic stimulation. Exp. Brain Res. 127 (1999) 102-107
8. Haggard P., et al. Voluntary action and conscious awareness. Nat. Neurosci. 5 (2002) 382-385
9. Singer W. Consciousness and the binding problem. Ann. N. Y. Acad. Sci. 929 (2001) 123-146
10. Fried I., et al. Functional organization of human supplementary motor cortex studied by electrical stimulation. J. Neurosci. 11 (1991) 3656-3666
11. Desmurget M., et al. Movement intention after parietal cortex stimulation in humans. Science 324 (2009) 811-813
12. Haggard P. Human volition: towards a neuroscience of will. Nat. Rev. Neurosci. 9 (2008) 934-946
13. Soon C.S., et al. Unconscious determinants of free decisions in the human brain. Nat. Neurosci. 11 (2008) 543-545
14. Haggard P., and Eimer M. On the relation between brain potentials and the awareness of voluntary movements. Exp. Brain Res. 126 (1999) 128-133
15. Eimer M. The lateralized readiness potential as an on-line measure of central response activation processes. Behavioral Research Methods, Intruments & Computer 30 (1998) 146-156
16. Libet B., et al. Time of conscious intention to act in relation to onset of cerebral activity (readiness-potential). The unconscious initiation of a freely voluntary act. Brain 106 Pt 3 (1983) 623-642
17. Ballanger B., et al. Paradoxical kinesis" is not a hallmark of Parkinson's disease but a general property of the motor system. Mov Disord. 21 (2006) 1490-1495
18. Desmurget M., et al. Updating target location at the end of an orienting saccade affects the characteristics of simple point-to-point movements. J. Exp. Psychol. Hum. Percept. Perform. 31 (2005) 1510-1536
19. Desmurget M., et al. The basal ganglia network mediates the planning of movement amplitude. Eur. J. Neurosci. 19 (2004) 2871-2880
20. Thobois S., et al. Functional anatomy of motor urgency. Neuroimage. 37 (2007) 243-252
21. Ikeda A., et al. Movement-related potentials recorded from supplementary motor area and primary motor area. Role of supplementary motor area in voluntary movements. Brain 115 Pt 4 (1992) 1017-1043
22. Goldberg G., et al. Medial frontal cortex infarction and the alien hand sign. Arch. Neurol. 38 (1981) 683-686
23. Scepkowski L.A., and Cronin-Golomb A. The alien hand: cases, categorizations, and anatomical correlates. Behav. Cogn Neurosci. Rev. 2 (2003) 261-277
24. Ball T., et al. The role of higher-order motor areas in voluntary movement as revealed by high-resolution EEG and fMRI. Neuroimage 10 (1999) 682-694
25. Sirigu A., et al. A selective impairment of hand posture for object utilization in apraxia. Cortex 31 (1995) 41-55
26. Rothi L.J., et al. A cognitive neurpsychological model of limb praxis and apraxia. In: Rothi L.J., and Heilman K.M. (Eds). Apraxia: the neuropsychology of action (1997), Psychology Press 29-49
27. Haggard P. Neuroscience. The sources of human volition. Science 324 (2009) 731-733
28. Carota, F. et al. (2009) Forward modeling mediates motor awareness. In Conscious Will and Responsibility: A Tribute to Benjamin Libet (Nadel, L. and Sinnott-Armstrong, W., eds), Oxford University Press, in press
29. Frith C.D., et al. Abnormalities in the awareness and control of action. Philos. Trans. R. Soc. Lond B Biol. Sci. 355 (2000) 1771-1788
30. Blakemore S.J., and Frith C. Self-awareness and action. Curr. Opin. Neurobiol. 13 (2003) 219-224
31. Fourneret P., and Jeannerod M. Limited conscious monitoring of motor performance in normal subjects. Neuropsychologia 36 (1998) 1133-1140
32. Lafargue G., et al. Production and perception of grip force without proprioception: is there a sense of effort in deafferented subjects?. Eur. J. Neurosci. 17 (2003) 2741-2749
33. Kristeva R., et al. Is the movement-evoked potential mandatory for movement execution? A high-resolution EEG study in a deafferented patient. Neuroimage. 31 (2006) 677-685
34. Sarlegna F.R., et al. Internally driven control of reaching movements: a study on a proprioceptively deafferented subject. Brain Res. Bull. 69 (2006) 404-415
35. Bisiach E., and Geniniani G. Anosognosia related to hemiplegia and heminopia. In: Prigatano G.P., and Scahcter D.L. (Eds). Awareness of deficit after brain injury (1991), Oxford University Press 17-39
36. Orfei M.D., et al. Anosognosia for hemiplegia after stroke is a multifaceted phenomenon: a systematic review of the literature. Brain 130 (2007) 3075-3090
37. Fotopoulou A., et al. The role of motor intention in motor awareness: an experimental study on anosognosia for hemiplegia. Brain 131 (2008) 3432-3442
38. Wolpert D.M., and Flanagan J.R. Motor prediction. Curr. Biol. 11 (2001) R729-R732
39. Desmurget M., and Grafton S. Forward modeling allows feedback control for fast reaching movements. Trends Cogn Sci. 4 (2000) 423-431
40. Desmurget M., and Grafton S. Feedback or forward control: end of a dichotomie. In: Johnson S. (Ed). Cognitive Neuroscience Perspectives on the Problem of Intentional Action (2003), MIT press 289-338
41. Wolpert D.M., et al. Maintaining internal representations: the role of the human superior parietal lobe. Nat. Neurosci. 1 (1998) 529-533
42. Pellijeff A., et al. Parietal updating of limb posture: an event-related fMRI study. Neuropsychologia 44 (2006) 2685-2690
43. Ogawa K., et al. Neural correlates of state estimation in visually guided movements: an event-related fMRI study. Cortex 43 (2007) 289-300
44. Todorov E. Optimality principles in sensorimotor control. Nat. Neurosci 7 (2004) 907-915
45. Guigon E., et al. Computational motor control: redundancy and invariance. J. Neurophysiol. 97 (2007) 331-347
46. Guigon E., et al. Computational motor control: feedback and accuracy. Eur. J. Neurosci 27 (2008) 1003-1016
47. Stratton, G. (1897) Vision without inversion of the retinal image. Psychological Review, 341-360, 463-481
48. Sekiyama K., et al. Body image as a visuomotor transformation device revealed in adaptation to reversed vision. Nature 407 (2000) 374-377
49. Richter H., et al. Long-term adaptation to prism-induced inversion of the retinal images. Exp Brain Res. 144 (2002) 445-457
50. Malfait N., and Ostry D.J. Is interlimb transfer of force-field adaptation a cognitive response to the sudden introduction of load?. J. Neurosci. 24 (2004) 8084-8089
51. Michel C., et al. Enhancing visuomotor adaptation by reducing error signals: single-step (aware) versus multiple-step (unaware) exposure to wedge prisms. J. Cogn Neurosci. 19 (2007) 341-350
52. Berti A., et al. Motor awareness and motor intention in anosognosia for hemiplegia. In: Haggard P., et al. (Ed). Sensorimotor foundations of higher cognition series: attention and performance XXII (2007), Oxford University Press 163-181
53. Christensen M.S., et al. Premotor cortex modulates somatosensory cortex during voluntary movements without proprioceptive feedback. Nat. Neurosci. 10 (2007) 417-419
54. Hummelsheim H., et al. Sensory inputs to the agranular motor fields: a comparison between precentral, supplementary-motor and premotor areas in the monkey. Exp. Brain Res. 69 (1988) 289-298
55. Fogassi L., et al. Visual responses in the dorsal premotor area F2 of the macaque monkey. Exp. Brain Res. 128 (1999) 194-199
56. Giraux P., and Sirigu A. Illusory movements of the paralyzed limb restore motor cortex activity. Neuroimage 20 Suppl 1 (2003) S107-S111
57. Klockgether T., et al. A defect of kinesthesia in Parkinson's disease. Mov Disord. 10 (1995) 460-465
58. Albert F., et al. The Ia afferent feedback of a given movement evokes the illusion of the same movement when returned to the subject via muscle tendon vibration. Exp. Brain Res. 172 (2006) 163-174
59. Crapse T.B., and Sommer M.A. Corollary discharge across the animal kingdom. Nat. Rev. Neurosci. 9 (2008) 587-600
60. Searle J.R. Consciousness. Annu. Rev. Neurosci 23 (2000) 557-578
61. Brass M., and Haggard P. The what, when, whether model of intentional action. Neuroscientist 14 (2008) 319-325
62. Jahanshahi M., et al. Self-initiated versus externally triggered movements. I. An investigation using measurement of regional cerebral blood flow with PET and movement-related potentials in normal and Parkinson's disease subjects. Brain 118 Pt 4 (1995) 913-933
63. Kringelbach M.L. The human orbitofrontal cortex: linking reward to hedonic experience. Nat. Rev. Neurosci. 6 (2005) 691-702
64. Selemon L.D., and Goldman-Rakic P.S. Common cortical and subcortical targets of the dorsolateral prefrontal and posterior parietal cortices in the rhesus monkey: evidence for a distributed neural network subserving spatially guided behavior. J. Neurosci. 8 (1988) 4049-4068
65. Turner R.S., and Anderson M.E. Context-dependent modulation of movement-related discharge in the primate globus pallidus. J. Neurosci. 25 (2005) 2965-2976
66. Penfield W., and Boldrey E. Somatic motor and sensory representation in the cerebral cortex of man as studied by electrical stimulation. Brain 60 (1937) 389-443
67. Duffau H. Lessons from brain mapping in surgery for low-grade glioma: insights into associations between tumour and brain plasticity. Lancet Neurol. 4 (2005) 476-486
68. Jankowska E., et al. The mode of activation of pyramidal tract cells by intracortical stimuli. J. Physiol 249 (1975) 617-636
69. Haglund M.M., et al. Optical imaging of bipolar cortical stimulation. J. Neurosurg. 78 (1993) 785-793
70. Tolias A.S., et al. Mapping cortical activity elicited with electrical microstimulation using FMRI in the macaque. Neuron 48 (2005) 901-911
71. Goffart L., et al. Saccade dysmetria during functional perturbation of the caudal fastigial nucleus in the monkey. Ann. N. Y. Acad. Sci 1004 (2003) 220-228
72. Duffau H., et al. New insights into the anatomo-functional connectivity of the semantic system: a study using cortico-subcortical electrostimulations. Brain 128 (2005) 797-810
73. Graziano M. The organization of behavioral repertoire in motor cortex. Annu. Rev. Neurosci. 29 (2006) 105-134
74. Stark E., et al. Encoding of reach and grasp by single neurons in premotor cortex is independent of recording site. J. Neurophysiol. 97 (2007) 3351-3364
75. Wolpert D.M., et al. An internal model for sensorimotor integration. Science 269 (1995) 1880-1882
76. Sirigu A., et al. The mental representation of hand movements after parietal cortex damage. Science 273 (1996) 1564-1568
77. Desmurget M., et al. Role of the posterior parietal cortex in updating reaching movements to a visual target. Nat. Neurosci. 2 (1999) 563-567