Common inhibitory prefrontal activation during inhibition of hand and foot responses

NeuroImage

Volumn 59, Issue 4, 2012, Pages 3373-3378

  Tabu, Hayato ^a   Mima, Tatsuya ^a   Aso, Toshihiko ^a   Takahashi, Ryosuke ^a   Fukuyama, Hidenao ^a  

^a KYOTO UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

Author keywords

Functional MRI; Pre supplementary motor area; Response inhibition; Stop signal task; Ventrolateral prefrontal cortex

Indexed keywords

ADULT; ARTICLE; CONTROLLED STUDY; EVENT RELATED POTENTIAL; FEMALE; FOOT; FUNCTIONAL MAGNETIC RESONANCE IMAGING; HAND; HUMAN; HUMAN EXPERIMENT; INSULA; MALE; MOTOR PERFORMANCE; NERVE CELL NETWORK; NERVOUS SYSTEM FUNCTION; NEUROIMAGING; NORMAL HUMAN; PARIETAL CORTEX; PREFRONTAL CORTEX; PRIORITY JOURNAL; RESPONSE INHIBITION; RESPONSE TIME; SUPPLEMENTARY MOTOR AREA; TASK PERFORMANCE;

ADULT; FEMALE; FOOT; HAND; HUMANS; MAGNETIC RESONANCE IMAGING; MALE; NEURAL INHIBITION; PREFRONTAL CORTEX;

EID: 84855172447     PISSN: 10538119     EISSN: 10959572     Source Type: Journal    
DOI: 10.1016/j.neuroimage.2011.10.092     Document Type: Article

References (67)

1. Aron A.R. Introducing a special issue on stopping action and cognition. Neurosci. Biobehav. Rev. 2009, 33:611-612.
2. Aron A., Poldrack R. Cortical and subcortical contributions to Stop signal response inhibition: role of the subthalamic nucleus. J. Neurosci. 2006, 26:2424-2433.
3. Aron A.R., Dowson J.H., Sahakian B.J., Robbins T.W. Methylphenidate improves response inhibition in adults with attention-deficit/hyperactivity disorder. Biol. Psychiatry 2003, 54:1465-1468.
4. Aron A.R., Fletcher P.C., Bullmore E.T., Sahakian B.J., Robbins T.W. Stop-signal inhibition disrupted by damage to right inferior frontal gyrus in humans. Nat. Neurosci. 2003, 6:115-116.
5. Aron A., Robbins T., Poldrack R. Inhibition and the right inferior frontal cortex. Trends Cogn. Sci. 2004, 8:170-177.
6. Aron A., Behrens T., Smith S., Frank M., Poldrack R. Triangulating a cognitive control network using diffusion-weighted magnetic resonance imaging (MRI) and functional MRI. J. Neurosci. 2007, 27:3743-3752.
7. Badcock J.C., Michie P.T., Johnson L., Combrinck J. Acts of control in schizophrenia: dissociating the components of inhibition. Psychol. Med. 2002, 32:287-297.
8. Badry R., Mima T., Aso T., Nakatsuka M., Abe M., Fathi D., Foly N., Nagiub H., Nagamine T., Fukuyama H. Suppression of human cortico-motoneuronal excitability during the Stop-signal task. Clin. Neurophysiol. 2009, 120:1717-1723.
9. Barkley R.A. Behavioral inhibition, sustained attention, and executive functions: constructing a unifying theory of ADHD. Psychol. Bull. 1997, 121:65-94.
10. Cai W., Leung H.C. Cortical activity during manual response inhibition guided by color and orientation cues. Brain Res. 2009, 1261:20-28.
11. Chamberlain S.R., Fineberg N.A., Blackwell A.D., Robbins T.W., Sahakian B.J. Motor inhibition and cognitive flexibility in obsessive-compulsive disorder and trichotillomania. Am. J. Psychiatry 2006, 163:1282-1284.
12. Chambers C., Bellgrove M., Stokes M., Henderson T., Garavan H., Robertson I., Morris A., Mattingley J. Executive "brake failure" following deactivation of human frontal lobe. J. Cogn. Neurosci. 2006, 18:444-455.
13. Chen C.Y., Muggleton N.G., Tzeng O.J., Hung D.L., Juan C.H. Control of prepotent responses by the superior medial frontal cortex. NeuroImage 2009, 44:537-545.
14. Chikazoe J., Konishi S., Asari T., Jimura K., Miyashita Y. Activation of right inferior frontal gyrus during response inhibition across response modalities. J. Cogn. Neurosci. 2007, 19:69-80.
15. Craig A.D. How do you feel-now? The anterior insula and human awareness. Nat. Rev. Neurosci. 2009, 10:59-70.
16. Dabrowska J. Dissociation of impairment after lateral and medial prefrontal lesions in dogs. Science 1971, 171:1037-1038.
17. Duann J.R., Ide J.S., Luo X., Li C.S. Functional connectivity delineates distinct roles of the inferior frontal cortex and presupplementary motor area in stop signal inhibition. J. Neurosci. 2009, 29:10171-10179.
18. Flaherty A.W., Graybiel A.M. Two input systems for body representations in the primate striatal matrix: experimental evidence in the squirrel monkey. J. Neurosci. 1993, 13:1120-1137.
19. Fried I., Katz A., McCarthy G., Sass K.J., Williamson P., Spencer S.S., Spencer D.D. Functional organization of human supplementary motor cortex studied by electrical stimulation. J. Neurosci. 1991, 11:3656-3666.
20. Friston K.J., Holmes A.P., Poline J.B., Grasby P.J., Williams S.C., Frackowiak R.S., Turner R. Analysis of fMRI time-series revisited. NeuroImage 1995, 2:45-53.
21. Friston K.J., Penny W.D., Glaser D.E. Conjunction revisited. NeuroImage 2005, 25:661-667.
22. Garavan H., Ross T.J., Stein E.A. Right hemispheric dominance of inhibitory control: an event-related functional MRI study. Proc. Natl. Acad. Sci. U. S. A. 1999, 96:8301-8306.
23. Gauggel S., Rieger M., Feghoff T.A. Inhibition of ongoing responses in patients with Parkinson's disease. J. Neurol. Neurosurg. Psychiatry 2004, 75:539-544.
24. Gerardin E., Lehericy S., Pochon J.B., Tezenas du Montcel S., Mangin J.F., Poupon F., Agid Y., Le Bihan D., Marsault C. Foot, hand, face and eye representation in the human striatum. Cereb. Cortex 2003, 13:162-169.
25. Godschalk M., Mitz A.R., van Duin B., van der Burg H. Somatotopy of monkey premotor cortex examined with microstimulation. Neurosci. Res. 1995, 23:269-279.
26. Hampshire A., Chamberlain S.R., Monti M.M., Duncan J., Owen A.M. The role of the right inferior frontal gyrus: inhibition and attentional control. NeuroImage 2010, 50:1313-1319.
27. Ikeda A., Luders H.O., Burgess R.C., Shibasaki H. Movement-related potentials recorded from supplementary motor area and primary motor area. Role of supplementary motor area in voluntary movements. Brain 1992, 115(Pt 4):1017-1043.
28. Ikeda A., Yazawa S., Kunieda T., Ohara S., Terada K., Mikuni N., Nagamine T., Taki W., Kimura J., Shibasaki H. Cognitive motor control in human pre-supplementary motor area studied by subdural recording of discrimination/selection-related potentials. Brain 1999, 122(Pt 5):915-931.
29. Isoda M., Hikosaka O. Switching from automatic to controlled action by monkey medial frontal cortex. Nat. Neurosci. 2007, 10:240-248.
30. Kawashima R., Satoh K., Itoh H., Ono S., Furumoto S., Gotoh R., Koyama M., Yoshioka S., Takahashi T., Takahashi K., Yanagisawa T., Fukuda H. Functional anatomy of GO/NO-GO discrimination and response selection-a PET study in man. Brain Res. 1996, 728:79-89.
31. Konishi S., Nakajima K., Uchida I., Kikyo H., Kameyama M., Miyashita Y. Common inhibitory mechanism in human inferior prefrontal cortex revealed by event-related functional MRI. Brain 1999, 122(Pt 5):981-991.
32. Kunzle H. Bilateral projections from precentral motor cortex to the putamen and other parts of the basal ganglia. An autoradiographic study in Macaca fascicularis. Brain Res. 1975, 88:195-209.
33. Leung H.C., Cai W. Common and differential ventrolateral prefrontal activity during inhibition of hand and eye movements. J. Neurosci. 2007, 27:9893-9900.
34. Li C.S., Huang C., Constable R.T., Sinha R. Imaging response inhibition in a stop-signal task: neural correlates independent of signal monitoring and post-response processing. J. Neurosci. 2006, 26:186-192.
35. Liddle P., Kiehl K., Smith A. Event-related fMRI study of response inhibition. Hum. Brain Mapp. 2001, 12:100-109.
36. Logan G.D., Cowan W.B., Davis K.A. On the ability to inhibit simple and choice reaction time responses: a model and a method. J. Exp. Psychol. Hum. Percept. Perform. 1984, 10:276-291.
37. Menon V., Adleman N.E., White C.D., Glover G.H., Reiss A.L. Error-related brain activation during a Go/NoGo response inhibition task. Hum. Brain Mapp. 2001, 12:131-143.
38. Mitz A.R., Wise S.P. The somatotopic organization of the supplementary motor area: intracortical microstimulation mapping. J. Neurosci. 1987, 7:1010-1021.
39. Morein-Zamir S., Hommersen P., Johnston C., Kingstone A. Novel measures of response performance and inhibition in children with ADHD. J. Abnorm. Child Psychol. 2008, 36:1199-1210.
40. Mostofsky S., Simmonds D. Response inhibition and response selection: two sides of the same coin. J. Cogn. Neurosci. 2008, 20:751-761.
41. Mostofsky S.H., Schafer J.G., Abrams M.T., Goldberg M.C., Flower A.A., Boyce A., Courtney S.M., Calhoun V.D., Kraut M.A., Denckla M.B., Pekar J.J. fMRI evidence that the neural basis of response inhibition is task-dependent. Brain Res. Cogn. Brain Res. 2003, 17:419-430.
42. Nachev P., Kennard C., Husain M. Functional role of the supplementary and pre-supplementary motor areas. Nat. Rev. Neurosci. 2008, 9:856-869.
43. Nakata H., Sakamoto K., Ferretti A., Gianni Perrucci M., Del Gratta C., Kakigi R., Luca Romani G. Somato-motor inhibitory processing in humans: an event-related functional MRI study. NeuroImage 2008, 39:1858-1866.
44. Nambu A., Kaneda K., Tokuno H., Takada M. Organization of corticostriatal motor inputs in monkey putamen. J. Neurophysiol. 2002, 88:1830-1842.
45. Oldfield R.C. The assessment and analysis of handedness: the Edinburgh inventory. Neuropsychologia 1971, 9:97-113.
46. Penfield W., Rasmussen T. The Cerebral Cortex of Man 1950, MacMillan, New York.
47. Petrides M. The effect of periarcuate lesions in the monkey on the performance of symmetrically and asymmetrically reinforced visual and auditory go, no-go tasks. J. Neurosci. 1986, 6:2054-2063.
48. Picton T.W., Stuss D.T., Alexander M.P., Shallice T., Binns M.A., Gillingham S. Effects of focal frontal lesions on response inhibition. Cereb. Cortex 2007, 17:826-838.
49. Raos V., Franchi G., Gallese V., Fogassi L. Somatotopic organization of the lateral part of area F2 (dorsal premotor cortex) of the macaque monkey. J. Neurophysiol. 2003, 89:1503-1518.
50. Rubia K., Russell T., Bullmore E.T., Soni W., Brammer M.J., Simmons A., Taylor E., Andrew C., Giampietro V., Sharma T. An fMRI study of reduced left prefrontal activation in schizophrenia during normal inhibitory function. Schizophr. Res. 2001, 52:47-55.
51. Rubia K., Smith A.B., Brammer M.J., Taylor E. Right inferior prefrontal cortex mediates response inhibition while mesial prefrontal cortex is responsible for error detection. NeuroImage 2003, 20:351-358.
52. Rushworth M.F., Hadland K.A., Paus T., Sipila P.K. Role of the human medial frontal cortex in task switching: a combined fMRI and TMS study. J. Neurophysiol. 2002, 87:2577-2592.
53. Sasaki K., Gemba H., Tsujimoto T. Suppression of visually initiated hand movement by stimulation of the prefrontal cortex in the monkey. Brain Res. 1989, 495:100-107.
54. Schachar R., Tannock R., Marriott M., Logan G. Deficient inhibitory control in attention deficit hyperactivity disorder. J. Abnorm. Child Psychol. 1995, 23:411-437.
55. Sharp D.J., Bonnelle V., De Boissezon X., Beckmann C.F., James S.G., Patel M.C., Mehta M.A. Distinct frontal systems for response inhibition, attentional capture, and error processing. Proc. Natl. Acad. Sci. U. S. A. 2010, 107:6106-6111.
56. Simmonds D., Pekar J., Mostofsky S. Meta-analysis of Go/No-go tasks demonstrating that fMRI activation associated with response inhibition is task-dependent. Neuropsychologia 2008, 46:224-232.
57. Solanto M.V., Abikoff H., Sonuga-Barke E., Schachar R., Logan G.D., Wigal T., Hechtman L., Hinshaw S., Turkel E. The ecological validity of delay aversion and response inhibition as measures of impulsivity in AD/HD: a supplement to the NIMH multimodal treatment study of AD/HD. J. Abnorm. Child Psychol. 2001, 29:215-228.
58. Stuphorn V., Schall J.D. Executive control of countermanding saccades by the supplementary eye field. Nat. Neurosci. 2006, 9:925-931.
59. Stuphorn V., Taylor T.L., Schall J.D. Performance monitoring by the supplementary eye field. Nature 2000, 408:857-860.
60. Swann N., Tandon N., Canolty R., Ellmore T.M., McEvoy L.K., Dreyer S., DiSano M., Aron A.R. Intracranial EEG reveals a time- and frequency-specific role for the right inferior frontal gyrus and primary motor cortex in stopping initiated responses. J. Neurosci. 2009, 29:12675-12685.
61. Tabu H., Mima T., Aso T., Takahashi R., Fukuyama H. Functional relevance of pre-supplementary motor areas for the choice to stop during Stop signal task. Neurosci. Res. 2011, 70:277-284.
62. Takada M., Tokuno H., Nambu A., Inase M. Corticostriatal projections from the somatic motor areas of the frontal cortex in the macaque monkey: segregation versus overlap of input zones from the primary motor cortex, the supplementary motor area, and the premotor cortex. Exp. Brain Res. 1998, 120:114-128.
63. van Boxtel G.J., van der Molen M.W., Jennings J.R., Brunia C.H. A psychophysiological analysis of inhibitory motor control in the stop-signal paradigm. Biol. Psychol. 2001, 58:229-262.
64. van den Wildenberg W.P., van Boxtel G.J., van der Molen M.W., Bosch D.A., Speelman J.D., Brunia C.H. Stimulation of the subthalamic region facilitates the selection and inhibition of motor responses in Parkinson's disease. J. Cogn. Neurosci. 2006, 18:626-636.
65. Verbruggen F., Logan G.D. Response inhibition in the stop-signal paradigm. Trends Cogn. Sci. 2008, 12:418-424.
66. Wager T.D., Sylvester C.Y., Lacey S.C., Nee D.E., Franklin M., Jonides J. Common and unique components of response inhibition revealed by fMRI. NeuroImage 2005, 27:323-340.
67. Yoshida S., Nambu A., Jinnai K. The distribution of the globus pallidus neurons with input from various cortical areas in the monkeys. Brain Res. 1993, 611:170-174.