User menu

EEG frequency-tagging to dissociate the cortical responses to nociceptive and non-nociceptive stimuli.

Bibliographic reference Colon, Elisabeth ; Legrain, Valéry ; Mouraux, André. EEG frequency-tagging to dissociate the cortical responses to nociceptive and non-nociceptive stimuli.. In: Journal of Cognitive Neuroscience, Vol. 26, no. 10, p. 2262-2274
Permanent URL
  1. Andersson S. A., Rydenhag B., Cortical Nociceptive Systems, 10.1098/rstb.1985.0035
  2. Apkarian A. Vania, Bushnell M. Catherine, Treede Rolf-Detlef, Zubieta Jon-Kar, Human brain mechanisms of pain perception and regulation in health and disease, 10.1016/j.ejpain.2004.11.001
  3. Bach Michael, Meigen Thomas, 10.1023/a:1002648202420
  4. Baumgartner U., Vogel H., Ohara S., Treede R.-D., Lenz F., Dipole source analyses of laser evoked potentials obtained from subdural grid recordings from primary somatic sensory cortex, 10.1152/jn.00135.2011
  5. Belmonte Carlos, Viana Félix, Molecular and Cellular Limits to Somatosensory Specificity, 10.1186/1744-8069-4-14
  6. Berti Stefan, Schröger Erich, Working memory controls involuntary attention switching: evidence from an auditory distraction paradigm : Working memory and involuntary attention, 10.1046/j.1460-9568.2003.02527.x
  7. Bushnell M. C., Duncan G. H., Hofbauer R. K., Ha B., Chen J.- I., Carrier B., Pain perception: Is there a role for primary somatosensory cortex?, 10.1073/pnas.96.14.7705
  8. Churyukanov Maxim, Plaghki Léon, Legrain Valéry, Mouraux André, Thermal Detection Thresholds of Aδ- and C-Fibre Afferents Activated by Brief CO2 Laser Pulses Applied onto the Human Hairy Skin, 10.1371/journal.pone.0035817
  9. Colon E., Legrain V., Mouraux A., Steady-state evoked potentials to study the processing of tactile and nociceptive somatosensory input in the human brain, 10.1016/j.neucli.2012.05.005
  10. Colon Elisabeth, Nozaradan Sylvie, Legrain Valery, Mouraux André, Steady-state evoked potentials to tag specific components of nociceptive cortical processing, 10.1016/j.neuroimage.2011.12.015
  11. de Jong Ritske, Toffanin Paolo, Harbers Marten, Dynamic crossmodal links revealed by steady-state responses in auditory–visual divided attention, 10.1016/j.ijpsycho.2009.09.013
  12. De Paepe Annick L., Crombez Geert, Spence Charles, Legrain Valéry, Mapping nociceptive stimuli in a peripersonal frame of reference: Evidence from a temporal order judgment task, 10.1016/j.neuropsychologia.2014.01.016
  13. Dong W. K., Journal of Neurophysiology, 72, 542 (1994)
  14. Driver Jon, Spence Charles, Attention and the crossmodal construction of space, 10.1016/s1364-6613(98)01188-7
  15. Eimer Martin, Crossmodal links in spatial attention between vision, audition, and touch: evidence from event-related brain potentials, 10.1016/s0028-3932(01)00118-x
  16. Garcia-Larrea L., The posterior insular-opercular region and the search of a primary cortex for pain, 10.1016/j.neucli.2012.06.001
  17. Garcia-Larrea L, Frot M, Valeriani M, Brain generators of laser-evoked potentials: from dipoles to functional significance, 10.1016/j.neucli.2003.10.008
  18. Giabbiconi Claire Marie, Dancer Chris, Zopf Regine, Gruber Thomas, Müller Matthias M, Selective spatial attention to left or right hand flutter sensation modulates the steady-state somatosensory evoked potential, 10.1016/j.cogbrainres.2004.01.004
  19. Giabbiconi C.-M., Trujillo-Barreto N.J., Gruber T., Müller M.M., Sustained spatial attention to vibration is mediated in primary somatosensory cortex, 10.1016/j.neuroimage.2006.11.022
  20. Giani Anette S., Ortiz Erick, Belardinelli Paolo, Kleiner Mario, Preissl Hubert, Noppeney Uta, Steady-state responses in MEG demonstrate information integration within but not across the auditory and visual senses, 10.1016/j.neuroimage.2012.01.114
  21. Greenspan Joel D., Lee Roland R., Lenz Fred A., Pain sensitivity alterations as a function of lesion location in the parasylvian cortex : , 10.1016/s0304-3959(99)00021-4
  22. Hillyard S. A., Vogel E. K., Luck S. J., Sensory gain control (amplification) as a mechanism of selective attention: electrophysiological and neuroimaging evidence, 10.1098/rstb.1998.0281
  23. Hofbauer R. K., Journal of Neurophysiology, 86, 402 (2001)
  24. Hutchison W. D., Davis K. D., Lozano A. M., Tasker R. R., Dostrovsky J. O., 10.1038/8065
  25. Hyvärinen A., Oja E., Independent component analysis: algorithms and applications, 10.1016/s0893-6080(00)00026-5
  26. Iannetti G. D., Mouraux A., From the neuromatrix to the pain matrix (and back), 10.1007/s00221-010-2340-1
  27. Keitel Christian, Schröger Erich, Saupe Katja, Müller Matthias M., Sustained selective intermodal attention modulates processing of language-like stimuli, 10.1007/s00221-011-2667-2
  28. Kenshalo D. R., Pain and the brain: From nociception to cognition, 21 (1995)
  29. Kenshalo D. R., Journal of Neurophysiology, 84, 719 (2000)
  30. Kenshalo Dan R., Chudler Eric H., Anton Fernand, Dubner Ronald, SI nociceptive neurons participate in the encoding process by which monkeys perceive the intensity of noxious thermal stimulation, 10.1016/0006-8993(88)90841-4
  31. Legrain Valéry, Bruyer Raymond, Guérit Jean-Michel, Plaghki Léon, Involuntary orientation of attention to unattended deviant nociceptive stimuli is modulated by concomitant visual task difficulty. Evidence from laser evoked potentials, 10.1016/j.clinph.2005.05.019
  32. Legrain Valéry, Guérit Jean-Michel, Bruyer Raymond, Plaghki Léon, Attentional modulation of the nociceptive processing into the human brain: selective spatial attention, probability of stimulus occurrence, and target detection effects on laser evoked potentials : , 10.1016/s0304-3959(02)00051-9
  33. Legrain Valéry, Iannetti Gian Domenico, Plaghki Léon, Mouraux André, The pain matrix reloaded, 10.1016/j.pneurobio.2010.10.005
  34. Legrain V., Mancini F., Sambo C.F., Torta D.M., Ronga I., Valentini E., Cognitive aspects of nociception and pain. Bridging neurophysiology with cognitive psychology, 10.1016/j.neucli.2012.06.003
  35. Liang M., Mouraux A., Iannetti G. D., Parallel Processing of Nociceptive and Non-nociceptive Somatosensory Information in the Human Primary and Secondary Somatosensory Cortices: Evidence from Dynamic Causal Modeling of Functional Magnetic Resonance Imaging Data, 10.1523/jneurosci.6207-10.2011
  36. Macmillan N. A., Detection theory: A user's guide. (2005)
  37. McMahon S. B., Wall and Melzack's textbook of pain (2013)
  38. Morgan S. T., Hansen J. C., Hillyard S. A., Selective attention to stimulus location modulates the steady-state visual evoked potential., 10.1073/pnas.93.10.4770
  39. Mountcastle V. B., Journal of Neuroscience, 10, 3032 (1990)
  40. Mouraux A., Iannetti G. D., Colon E., Nozaradan S., Legrain V., Plaghki L., Nociceptive Steady-State Evoked Potentials Elicited by Rapid Periodic Thermal Stimulation of Cutaneous Nociceptors, 10.1523/jneurosci.3977-10.2011
  41. Mouraux A., Plaghki L., Are laser-evoked brain potentials modulated by attending to first or second pain? : , 10.1016/j.pain.2006.10.018
  42. Mouraux A., Plaghki L., Cortical interactions and integration of nociceptive and non-nociceptive somatosensory inputs in humans, 10.1016/j.neuroscience.2007.08.035
  43. Mozolic Jennifer L, Joyner David, Hugenschmidt Christina E, Peiffer Ann M, Kraft Robert A, Maldjian Joseph A, Laurienti Paul J, Cross-modal deactivations during modality-specific selective attention, 10.1186/1471-2377-8-35
  44. Muller M. M., Andersen S., Trujillo N. J., Valdes-Sosa P., Malinowski P., Hillyard S. A., Feature-selective attention enhances color signals in early visual areas of the human brain, 10.1073/pnas.0606668103
  45. Nozaradan Sylvie, Peretz Isabelle, Mouraux André, Steady-state evoked potentials as an index of multisensory temporal binding, 10.1016/j.neuroimage.2011.11.065
  46. Ostrowsky K., Representation of Pain and Somatic Sensation in the Human Insula: a Study of Responses to Direct Electrical Cortical Stimulation, 10.1093/cercor/12.4.376
  47. Peyron R., Laurent B., García-Larrea L., Functional imaging of brain responses to pain. A review and meta-analysis (2000), 10.1016/s0987-7053(00)00227-6
  48. Plaghki L, Mouraux A, How do we selectively activate skin nociceptors with a high power infrared laser? Physiology and biophysics of laser stimulation, 10.1016/j.neucli.2003.10.003
  49. Plaghki L., Current Opinion in Investigational Drugs, 6, 58 (2005)
  50. Rauss Karsten S., Pourtois Gilles, Vuilleumier Patrik, Schwartz Sophie, Attentional load modifies early activity in human primary visual cortex, 10.1002/hbm.20636
  51. Regan D., Human brain electrophysiology. Evoked potentials and evoked magnetic fields in science and medicine. (1989)
  52. Regan M.P., Regan D., He P., An audio-visual convergence area in the human brain, 10.1007/bf00231071
  53. Saupe K., Frontiers in Human Neuroscience, 30 (2009)
  54. Schwent Vincent L., Hillyard Steven A., Galambos Robert, Selective attention and the auditory vertex potential. II. Effects of signal intensity and masking noise, 10.1016/0013-4694(76)90136-x
  55. Shomstein S., Control of Attention Shifts between Vision and Audition in Human Cortex, 10.1523/jneurosci.2939-04.2004
  56. Snyder Abraham Z., Steady-state vibration evoked potentials: description of technique and characterization of responses, 10.1016/0168-5597(92)90007-x
  57. Talsma Durk, Doty Tracy J., Strowd Roy, Woldorff Marty G., Attentional capacity for processing concurrent stimuli is larger across sensory modalities than within a modality, 10.1111/j.1469-8986.2006.00452.x
  58. Talsma D., Doty T. J., Woldorff M. G., Selective Attention and Audiovisual Integration: Is Attending to Both Modalities a Prerequisite for Early Integration?, 10.1093/cercor/bhk016
  59. Timmermann L., Journal of Neurophysiology, 86, 1499 (2001)
  60. Tommerdahl M., Journal of Neurophysiology, 80, 3272 (1998)
  61. Treede R.D., Apkarian A.V., Nociceptive Processing in the Cerebral Cortex, The Senses: A Comprehensive Reference (2008) ISBN:9780123708809 p.669-697, 10.1016/b978-012370880-9.00188-2
  62. Treede Rolf-Detlef, Apkarian Vania A., Bromm Burkhart, Greenspan Joel D., Lenz Frederick A., Cortical representation of pain: functional characterization of nociceptive areas near the lateral sulcus : , 10.1016/s0304-3959(00)00350-x
  63. Vialatte François-Benoît, Maurice Monique, Dauwels Justin, Cichocki Andrzej, Steady-state visually evoked potentials: Focus on essential paradigms and future perspectives, 10.1016/j.pneurobio.2009.11.005
  64. Vierck Charles J., Whitsel Barry L., Favorov Oleg V., Brown Alexander W., Tommerdahl Mark, Role of primary somatosensory cortex in the coding of pain : , 10.1016/j.pain.2012.10.021
  65. Whitsel B. L., Favorov O. V., Li Y., Quibrera M., Tommerdahl M., Area 3a Neuron Response to Skin Nociceptor Afferent Drive, 10.1093/cercor/bhn086
  66. Mouraux A., Iannetti G.D., Across-trial averaging of event-related EEG responses and beyond, 10.1016/j.mri.2008.01.011