Desynchronization of cortical rhythms following cutaneous stimulation: Effects of stimulus repetition and intensity, and of the size of corpus callosum

Clinical Neurophysiology

Volumn 114, Issue 10, 2003, Pages 1936-1947

  Stancák, Andrej ^a   Svoboda, Jirí ^a   Rachmanová, Rosa ^a   Vrána, Jirí ^a   Králík, Jirí ^a   Tintera, Jaroslav ^b  

^a CHARLES UNIVERSITY   (Czech Republic)

^b INSTITUTE FOR CLINICAL AND EXPERIMENTAL MEDICINE   (Czech Republic)

Author keywords

Corpus callosum; EEG; Event related desynchronization; Orienting response; Stimulus intensity

Indexed keywords

ADULT; ARTICLE; BETA RHYTHM; CORPUS CALLOSUM; CORRELATION ANALYSIS; CORTICAL SYNCHRONIZATION; ELECTRODE; ELECTROENCEPHALOGRAM; ELECTROSTIMULATION; EVOKED RESPONSE; FRONTAL CORTEX; HABITUATION; HUMAN; HUMAN EXPERIMENT; LATENT PERIOD; MALE; MU RHYTHM; NORMAL HUMAN; PAIN THRESHOLD; PRIORITY JOURNAL; RANDOMIZATION; RECORDING; SKIN STIMULATION; STATISTICAL SIGNIFICANCE; STIMULUS; STIMULUS RESPONSE; BRAIN MAPPING; CLASSIFICATION; COMPARATIVE STUDY; ELECTROENCEPHALOGRAPHY; EVOKED SOMATOSENSORY RESPONSE; FEMALE; FINGER; HEMISPHERIC DOMINANCE; HISTOLOGY; INNERVATION; METHODOLOGY; PHYSIOLOGY; RADIATION RESPONSE; SKIN;

ADULT; BRAIN MAPPING; CORPUS CALLOSUM; CORTICAL SYNCHRONIZATION; DOSE-RESPONSE RELATIONSHIP, RADIATION; ELECTRIC STIMULATION; ELECTROENCEPHALOGRAPHY; EVOKED POTENTIALS, SOMATOSENSORY; FEMALE; FINGERS; FUNCTIONAL LATERALITY; HABITUATION, PSYCHOPHYSIOLOGIC; HUMANS; MALE; RANDOM ALLOCATION; SKIN;

EID: 0642311127     PISSN: 13882457     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1388-2457(03)00201-3     Document Type: Article

References (72)

1. Aboitiz F., Scheibel A.B., Fisher R.S., Zaidel E. Fiber composition of the human corpus callosum. Brain Res. 598:1992;143-153.
2. Aboitiz F., Rodriguez E., Olivares R., Zaidel E. Age-related changes in fibre composition of the human corpus callosum: sex differences. NeuroReport. 7:1996;1761-1764.
3. Allison T., McCarthy G., Wood C.C., Williamson P.D., Spencer D.D. Human cortical potentials evoked by stimulation of the median nerve. II. Cytoarchitectonic areas generating long-latency activity. J Neurophysiol. 62:1989;711-722.
4. Allison T., McCarthy G., Wood C.C. The relationship between human long-latency somatosensory evoked potentials recorded from the cortical surface and from the scalp. Electroencephalogr clin Neurophysiol. 84:1992;301-314.
5. Bates J.F., Goldman-Rakic P.S. Prefrontal connections of medial motor areas in the rhesus monkey. J Comp Neurol. 335:1993;211-228.
6. Bouyer J.J., Montaron M.F., Vahnee J.M., Albert M.P., Rougeul A. Anatomical localization of the cortical beta rhythms in cat. Neuroscience. 22:1987;863-869.
7. Brovelli A., Battaglini P.P., Naranjo J.R., Budai R. Medium-range oscillatory network and the 20-Hz sensorimotor induced potential. Neuroimage. 16:2002;130-141.
8. Buser P., Rougeul-Buser A. EEG synchronization in cat, monkey and human during attentive states. A brief survey. Pfurtscheller G., Lopes da Silva F.H. Handbook of electroencephalography and clinical neurophysiology, revised series. Handbook of electroencephalography and clinical neurophysiology, revised series. vol. 6:1999;13-32 Elsevier, Amsterdam.
9. Chatrian G.E., Petersen M.C., Lazarte J.A. The blocking of the Rolandic wicket rhythm and some central changes related to movement. Electroenceph clin Neurophysiol. 11:1959;497-510.
10. Chen R., Corwell B., Hallett M. Modulation of motor cortex excitability by median nerve and digit stimulation. Exp Brain Res. 129:1999;77-86.
11. Franzen O., Offenloch K. Evoked response correlates of psychophysical magnitude. Estimates for tactile stimulation in man. Exp Brain Res. 8:1969;1-18.
12. Foote S.L., Berridge C.N., Adams L.M., Pineda J.A. Electrophysiological evidence for the involvement of the locus coeruleus in alertness, orienting and attention. Prog Brain Res. 88:1991;521-522.
13. Fox P., Ingham R., George M.S., Mayberg H., Ingham J., Roby J., et al. Imaging human intra-cerebral connectivity by PET during TMS. NeuroReport. 8:1997;2787-2791.
14. Gastaut H., Terzian H., Gastaut Y. Étude d'une activité arceau electroencéphalographique méconnue: 'le rythme rolandique en arceau'. Mars Med. 89:1952;296-310.
15. Geer J.H. Some basic parameters of the orienting response. Ruttkay-Nedecky I., Ciganek L., Zikmund V., Kellerova E. Mechanisms of orienting reaction in man. 1967;237-244 Publishing House of Slovak Academy of Sciences, Bratislava.
16. Gevins A., Le J., Brickett P., Reutter B., Desmond J. Seeing through the skull: advanced EEGs use MRIs to accurately measure cortical activity from the scalp. Brain Topogr. 4:1991;125-131.
17. Graham F.K., Clifton R.K. Heart-rate change as a component of the orienting response. Psychol Bull. 65:1966;305-320.
18. Graham F.K. Attention: the heartbeat, the blink, and the brain. Campbell B.A., Hayne H., Richardson R. Attention and information processing in infants and adults. Perspectives from human and animal research. 1992;3-29 Erlbaum, Hillsdale, NJ.
19. Guillery R.W., Feig S.L., Lozsadi D.A. Paying attention to the thalamic reticular nucleus. Trends Neurosci. 21:1998;28-32.
20. Heilman K.M., Van den Abel T. Right hemisphere dominance for attention: the mechanism underlying hemispheric asymmetries in inattention (neglect). Neurology. 30:1980;327-330.
21. Hirata M., Kato A., Taniguchi M., Ninomiyama H., Cheyne D., Robinson S.E., et al. Frequency-dependent spatial distribution of human somatosensory evoked neuromagnetic fields. Neurosci Lett. 318:2002;73-76.
22. Hoechstetter K., Rupp A., Meinck H.-M., Weckesser D., Bornfleth H., Stippich C., et al. Magnetic source imaging of tactile input shows task-independent attention effects in SII. NeuroReport. 11:2000;2461-2465.
23. Hunter M., Ettlinger G., Maccabe J.J. Intermanual transfer in the monkey as a function of amount of callosal sparing. Brain Res. 93:1975;223-240.
24. Iwamura Y., Iriki A., Tanaka M. Bilateral hand representation in the postcentral somatosensory cortex. Nature. 369:1994;554-556.
25. Jones E.G., Hendry S.H. Distribution of callosal fibers around the hand representations in monkey somatic sensory cortex. Neurosci Lett. 19:1980;162-172.
26. Jousmäki V., Forss N. Effects of stimulus intensity on signals from human somatosensory cortices. NeuroReport. 9:1998;3427-3431.
27. Kalcher J., Pfurtscheller G. Discrimination between phase-locked and non-phase-locked event-related EEG actitity. Electroenceph clin Neurophysiol. 94:1995;381-384.
28. Katayama Y., DeWitt D.S., Becker D.P., Hayes R.L. Behavioral evidence for a cholinoceptive pontine inhibitory area: descending control of spinal motor output and sensory input. Brain Res. 296:1984;241-262.
29. Killackey H.P., Gould H.J., Cusick C.G., Pons T.P., Kaas J.H. The relation of corpus callosum connections to architectonic fields and body surface maps in sensorimotor cortex of new and old world monkeys. J Comp Neurol. 219:1983;384-419.
30. Komssi S., Aronen H.J., Huttunen J., Kesaniemi M., Soinne L., Nikouline V.V., et al. Ipsi- and contralateral EEG reactions to transcranial magnetic stimulation. Clin Neurophysiol. 113:2002;175-184.
31. Korvenoja A., Wikstrom H., Huttunen J., Virtanan J., Laine P., Aronen H.J., et al. Activation of ipsilateral primary sensorimotor cortex by median nerve stimulation. NeuroReport. 6:1995;2589-2593.
32. Krubitzer L.A., Kaas J.F. The organization and connections of somatosensory cortex in marmosets. J Neurosci. 10:1990;952-974.
33. Lesser R.P., Koehle R., Lüders H. Effect of stimulus intensity on short latency somatosensory evoked potentials. Electroenceph clin Neurophysiol. 47:1979;377-382.
34. Mima T., Nagamine T., Nakamura K., Shibasaki H. Attention modulates both primary and second somatosensory cortical activities in humans: a magnetoencephalographic study. J Neurophysiol. 80:1998;2215-2221.
35. McGuire P.K., Bates J.F., Goldman-Rakic P.S. Interhemispheric integration: I. Symmetry and convergence of the corticocortical connections of the left and right principal sulcus (PS) and the left and right supplementary motor area (SMA) in rhesus monkey. Cereb Cortex. 1:1991;390-407.
36. Myers R.E., Ebner F.F. Localization of function in corpus callosum: tactual information processing in Macaca mulatta. Brain Res. 27:1976;455-462.
37. Neuper C., Pfurtscheller G. Evidence for distinct beta resonance frequencies in human EEG related to specific sensorimotor cortical areas. Clin Neurophysiol. 112:2001;2084-2097.
38. Nikouline V.V., Hansen K.L., Wikstrom H., Kesaniemi M., Antonova E.V., Ilmoniemi R., et al. Dynamics of mu-rhythm suppression caused by median nerve stimulation: a magnetoencephalographic study in human subjects. Neurosci Lett. 294:2000;163-166.
39. Öhman A., Eriksson A., Frederikson M., Hugdahl K., Olofson C. Habituation of the electrodermal orienting reaction to potentially phobic and supposedly neutral stimuli in normal human subjects. Biol Psychol. 2:1974;85-93.
40. Pfurtscheller G. Central beta-rhythms during sensorimotor activities in man. Electroenceph clin Neurophysiol. 51:1981;527-533.
41. Pfurtscheller G. Functional topography during sensorimotor activation studied with event-related desynchronization mapping. J Clin Neurophysiol. 6:1989;75-84.
42. Pfurtscheller G., Aranibar A. Evaluation of event-related desynchronisation (ERD) preceding and following voluntary self-paced movements. Electroenceph clin Neurophysiol. 46:1979;138-146.
43. Pfurtscheller G., Neuper C., Berger J. Source localization using event-related desynchronization (ERD) within the α-band. Brain Topogr. 6:1994;269-275.
44. Pfurtscheller G., Woertz M., Krausz G., Neuper C. Distinction of different fingers by the frequency of stimulus induced beta oscillations in the human EEG. Neurosci Lett. 307:2001;49-52.
45. Pfurtscheller G., Woertz M., Muller G., Wriessnegger S., Pfurtscheller K. Contrasting behavior of beta event-related synchronization and somatosensory evoked potential after median nerve stimulation during finger manipulation in man. Neurosci Lett. 323:2002;113-116.
46. Rohrbaugh J.W., Newlin D.B., Varner J.L., Ellingson R.J. Bilateral distribution of the O wave. Ann N Y Acad Sci. 425:1984;267-270.
47. Rougeul A., Buser J.J., Dedet L., Debray O. Fast somato-parietal rhythms during combined focal attention and immobility in baboon and squirrel monkey. Electroenceph clin Neurophysiol. 46:1979;310-319.
48. Rouiller E.M., Babalian A., Kazennikov O., Moret V., Yu X.H., Wiesendanger M. Transcallosal connections of the distal forelimb representations of the primary and supplementary motor cortical areas in macaque monkeys. Exp Brain Res. 102:1994;227-243.
49. Royston P. Approximating the Shapiro-Wilk W test for non-normality. Stat Comput. 2:1992;117-119.
50. Salmelin R., Hari R. Spatiotemporal characteristics of sensorimotor neuromagnetic rhythms related to thumb movement. Neuroscience. 60:1994;537-550.
51. Sharpless S., Jasper H.H. Habituation of the arousal reaction. Brain. 79:1956;655-680.
52. Schnitzler A., Salmelin R., Salenius S., Jousmäki V., Hari R. Tactile information from the human hand reaches the ipsilateral somatosensory cortex. Neurosci Lett. 200:1995;25-28.
53. Siebner H.R., Peller M., Bartenstein P., Willoch F., Rossmeier C., Schwaiger M., et al. Activation of frontal premotor areas during suprathreshold transcranial magnetic stimulation of the left primary sensorimotor cortex: a glucose metabolic PET study. Hum Brain Mapp. 12:2001;157-167.
54. Sokolov E.N. Perception and conditioned reflexes. 1963;Pergamon, Oxford.
55. Sokolov E.N., Nezlina N.I., Polianskij V.B., Evtikhin D.V. Orienting reflex: 'targeting reaction' and 'searchlight of attention' (in Russian). Zh Vyssh Nerv Deiat Im I P Pavlova. 51:2001;421-437.
56. Soufflet L., Toussaint R., Luthringer R., Gresser J., Minot J., Macher J.P. A statistical evaluation of the main interpolation methods applied to 3-dimensional EEG mapping. Electroenceph clin Neurophysiol. 79:1991;393-402.
57. Stancák A. Jr., Lücking C.H., Kristeva-Feige R. Lateralization of movement-related potentials and correlates with the size of corpus callosum. NeuroReport. 11:2000;329-332.
58. Stancák A. Jr., Lücking C.H., Kristeva-Feige R. The size of corpus callosum and functional connectivities of cortical regions in finger and shoulder movements. Cogn Brain Res. 13:2002;61-74.
59. Stancák A., Hoechstetter K., Tintera J., Vrana J., Rachmanova R., Kralik J., et al. Source activity in the human secondary somatosensory cortex depends on the size of corpus callosum. Brain Res. 936:2002;47-57.
60. Stancák A., Cohen E.R., Seidler R.D., Duong T.Q., Kim S.G. The size of corpus callosum correlates with functional activation of medial motor cortical areas in bimanual and unimanual movements. Cereb Cortex. 13:2003;475-485.
61. Steinmetz H.J., Jäncke L., Kleinschmidt A., Schlaug G., Volkmann J., Huang Y. Sex but no hand difference in the isthmus of the corpus callosum. Neurology. 42:1992;749-752.
62. Steingrüber H.J., Lienert G.A. Hand-Dominanztest. 1976;Hogrefe, Göttingen.
63. Thickbroom G.W., Mastaglia F.L., Carroll W.M., Davies H.D. Source derivation: application to topographic mapping of visual potentials. Electroenceph clin Neurophysiol. 59:1984;279-285.
64. Thompson R.F., Spencer W.A. Habituation: a model phenomenon for the study of neuronal substrates of behavior. Psychol Rev. 73:1966;16-43.
65. Timmermann L., Ploner M., Haucke K., Schmitz F., Baltissen R., Schitzler A. Differential coding of pain intensity in the human primary and secondary somatosensory cortex. J Neurophysiol. 86:2001;1499-1503.
66. Torquati K., Pizzella V., Della Penna S., Franciotti R., Babiloni C., Rossini P.M., et al. Comparison between SI and SII responses as a function of stimulus intensity. NeuroReport. 13:2002;813-819.
67. Weese G.D., Phillips J.M., Brown V.J. Attention orienting is impaired by unilateral lesions of the thalamic reticular nucleus. J Neurosci. 19:1999;10135-10139.
68. Wegner K., Forss N., Salenius S. Characteristics of the human contra- versus ipsilateral SII cortex. Clin Neurophysiol. 111:2000;894-900.
69. Wilson N.J., Wilson W.P. The duration of human electroencephalographic arousal responses elicited by photic stimulation. Electroenceph clin Neurophysiol. 11:1959;85-91.
70. Witelson S.F. Hand and sex differences in the isthmus and genu of the human corpus callosum. A postmortem morphological study. Brain. 112:1989;799-835.
71. Yazgan M.Y., Wexler B.E., Kinsbourne M., Peterson B., Leckman J.F. Functional significance of individual variations in callosal area. Neuropsychologia. 33:1995;769-779.
72. Zimmer H., Demmel R. Habituation and laterality of orienting processes as reflected by slow negative waves. Biol Psychol. 53:2000;161-176.