Conscious auditory perception related to long-range synchrony of gamma oscillations

NeuroImage

Volumn 100, Issue , 2014, Pages 435-443

  Steinmann, Saskia ^a   Leicht, Gregor ^a   Ertl, Matthias ^a   Andreou, Christina ^a   Polomac, Nenad ^a   Westerhausen, René ^b,c   Friederici, Angela D ^d   Mulert, Christoph ^a  

^a UNIVERSITY MEDICAL CENTER HAMBURG EPPENDORF   (Germany)

^b UNIVERSITY OF BERGEN   (Norway)

^c HAUKELAND UNIVERSITY HOSPITAL   (Norway)

^d MAX PLANCK INSTITUTE FOR HUMAN COGNITIVE AND BRAIN SCIENCES   (Germany)

Author keywords

Auditory cortex; Dichotic listening task; EEG; ELORETA; Functional connectivity; Gamma; Interhemispheric auditory pathways

Indexed keywords

ADULT; ALPHA RHYTHM; ARTICLE; AUDITORY DISCRIMINATION; AUDITORY STIMULATION; BETA RHYTHM; CONSCIOUSNESS; DELTA RHYTHM; DICHOTIC LISTENING; ELECTROENCEPHALOGRAPHY PHASE SYNCHRONIZATION; EVOKED AUDITORY RESPONSE; FEMALE; FREQUENCY MODULATION; GAMMA RHYTHM; HUMAN; HUMAN EXPERIMENT; INTERHEMISPHERIC TRANSFER; LEFT HEMISPHERE; MALE; MENTAL TASK; PRIMARY AUDITORY CORTEX; PRIORITY JOURNAL; RIGHT HEMISPHERE; SECONDARY AUDITORY CORTEX; THETA RHYTHM; AUDITORY CORTEX; AUDITORY NERVOUS SYSTEM; ELECTROENCEPHALOGRAPHY; HEARING; HEMISPHERIC DOMINANCE; PHYSIOLOGY; TIME;

ADULT; AUDITORY CORTEX; AUDITORY PATHWAYS; AUDITORY PERCEPTION; CONSCIOUSNESS; DICHOTIC LISTENING TESTS; ELECTROENCEPHALOGRAPHY; FEMALE; FUNCTIONAL LATERALITY; GAMMA RHYTHM; HUMANS; MALE; TIME FACTORS;

EID: 84904039126     PISSN: 10538119     EISSN: 10959572     Source Type: Journal    
DOI: 10.1016/j.neuroimage.2014.06.012     Document Type: Article

References (89)

1. Aboitiz F.A., Scheibel A.C., Fisher R.S., Zaidel E. Fiber composition of the human corpus callosum. Brain Res. 1992, 598:143-153.
2. Andersson M., Llera J.E., Rimol L.M., Hugdahl K. Using dichotic listening to study bottom-up and top-down processing in children and adults. Child Neuropsychol. 2008, 14(5):470-479.
3. Bayazit O., Oniz A., Hahn C., Güntürkün O., Ozgören M. Dichotic listening revisited: trial-by-trial ERP analyses reveal intra- and interhemispheric differences. Neuropsychologia 2009, 47(2):536-545.
4. Binder J.R., et al. Human temporal lobe activation by speech and nonspeech sounds. Cereb. Cortex 2000, 10:512-528.
5. Brancucci A., Babiloni C., Babiloni F., Galderisi S., Mucci A., Tecchio F., Zappasodi F., Pizzella V., Romani G.L., Rossini P.M. Inhibition of auditory cortical responses to ipsilateral stimuli during dichotic listening: evidence from magnetoencephalography. Eur. J. Neurosci. 2004, 19(8):2329-2336.
6. Broadbent D. The role of auditory localization in attention and memory span. J. Exp. Psychol. 1954, 47:191-196.
7. Brodal A. Neurological Anatomy in Relation to Clinical Medicine 1981, Oxford University Press, New York. 3rd ed.
8. Bryden M.P. An overview of the DL procedure and its relation to cerebral organization. Handbook of Dichotic Listening: Theory, Methods and Research 1988, 1-44. John Wiley & Sons, Chichester. K. Hugdahl (Ed.).
9. Buzsáki G., Buhl D.L., Harris K.D., Csicsvari J., Czéh B., Morozov A. Hippocampal network patterns of activity in the mouse. Neuroscience 2003, 116(1):201-211.
10. Canolty R.T., Edwards E., Dalal S.S., Soltani M., Nagarajan S.S., Kirsch H.E., Berger M.S., Barbaro N.M., Knight R.T. High gamma power is phase-locked to theta oscillations in human neocortex. Science 2006, 15;313(5793):1626-1628.
11. Canuet L., Ishii R., Pascual-Marqui R.D., Iwase M., Kurimoto R., Aoki Y., Ikeda S., Takahashi H., Nakahachi T., Takeda M. Resting-state EEG source localization and functional connectivity in schizophrenia-like psychosis of epilepsy. PLoS One 2011, 6(11):e27863.
12. Canuet L., Tellado I., Couceiro V., Fraile C., Fernandez-Novoa L., Ishii R., Takeda M., Cacabelos R. Resting-state network disruption and APOE genotype in Alzheimer's disease: a lagged functional connectivity study. PLoS One 2012, 7(9):e46289.
13. Carl C., Açik A., König P., Engel A.K., Hipp F.J. The saccadic spike artifact in MEG. NeuroImage 2012, 16;59(2):1657-1667.
14. De Diego-Balaguer R., Fuentemilla L., Rodriguez-Fornells A. Brain dynamics sustaining rapid rule extraction from speech. J. Cogn. Neurosci. 2011, 23(10):3105-3120.
15. De Ridder D., Vanneste S., Congedo M. The distressed brain: a group blind source separation analysis on tinnitus. PLoS One 2011, 6(10):e24273.
16. Doesburg S.M., Kitajo K., Ward L.M. Increased gamma-band synchrony precedes switching of conscious perceptual objects in binocular rivalry. Neuroreport 2005, 1;16(11):1139-1142.
17. Doesburg S.M., Emberson L.L., Rahi A., Cameron D., Ward L.M. Asynchrony from synchrony long-range gamma-band neural synchrony accompanies perception of audiovisual speech asynchrony. Exp. Brain Res. 2008, 185(1):11-20.
18. Engel A.K., Singer W. Temporal binding and the neural correlates of sensory awareness. Trends Cogn. Sci. 2001, 5(1):16-25.
19. Eulitz C., Maess B., Pantev C., Friederici A.D., Feige B., Elbert T. Oscillatory neuromagnetic activity induced by language and non-language stimuli. Brain Res. Cogn. Brain Res. 1996, 4(2):121-132.
20. Fisch L., Privman E., Ramot M., Harel M., Nir Y., Kipervasser S., Andelman F., Neufeld M.Y., Kramer U., Fried I., Malach R. Neural "ignition": enhanced activation linked to perceptual awareness in human ventral stream visual cortex. Neuron 2009, 64:562-574.
21. Friederici A.D. The brain basis of language processing: from structure to function. Physiol. Rev. 2011, 91(4):1357-1392.
22. Friederici A.D., von Cramon Y.D., Kotz S.A. Role of the corpus callosum in speech comprehension: interfacing syntax and prosody. Neuron 2007, 53:135-145.
23. Fries P. Neuronal gamma band synchronization as fundamental process of cortical computation. Rev. Neurosci. 2009, 32:209-224.
24. Fries P., Roelfsema P.R., Engel A.K., König P., Singer W. Synchronization of oscillatory responses in visual cortex correlates with perception in interocular rivalry. Proc. Natl. Acad. Sci. U. S. A. 1997, 11; 94(23):12699-12704.
25. Green M.F., Hugdahl K., Mitchell S. Dichotic listening during auditory hallucinations in patients with schizophrenia. Am. J. Psychiatry. 1994, 151(3):357-362.
26. Hall M.H., Taylor G., Sham P., Schulze K., Rijsdijk F., Picchioni M., Toulopoulou T., Ettinger U., Bramon E., Murray R.M., Salisbury D.F. The early auditory gamma-band response is heritable and a putative endophenotype of schizophrenia. Schizophr. Bull. 2009, 37(4):778-787.
27. Han J., Mody M., Ahlfors S.P. Gamma phase locking modulated by phonological contrast during auditory comprehension in reading disability. Neuroreport 2012, 3;23(14):851-856.
28. Henshall K.R., Sergejew A.A., McKay C.M., Rance G., Shea T.L., Hayden M.J., Innes-Brown H., Copolov D.L. Interhemispheric transfer time in patients with auditory hallucinations: an auditory event-related potential study. Int. J. Psychophysiol. 2012, 84(2):130-139.
29. Herrmann W.M., Fichte K., Kubicki S. The mathematical rationale for the clinical EEG-frequency-bands. 1. Factor analysis with EEG-power estimations for determining frequency bands. EEG EMG Z Elektroenzephalogr. Elektromyogr. Verwandte Geb 1978, 9(3):146-154.
30. Herzfeld H.D WST-Wortschatztest. Diagnostica 1992, 40(1994):293-297. Beltz Test GmbH, Weinheim, 3. S. Karl-Heinz, P. Metzler (Eds.).
31. Hipp J.F., Engel A.K., Siegel M. Oscillatory synchronization in large-scale cortical networks predicts perception. Neuron 2011, 69(2):387-396.
32. Hubl D., König T., Strik W., Federspiel A., Kreis R., Bösch C., Maier S.E., Schroth G., Lovblad K., Dierks T. Pathways that make voices. White matter changes in auditory hallucination. Arch. Gen. Psychiatry 2004, 61:658-668.
33. Hugdahl K. Dichotic listening: probing temporal lobe functional integrity. Brain Asymmetry 1995, 123-156. MIR Press, Cambridge, MA. R.J. Davidson, K. Hugdahl (Eds.).
34. Hugdahl K. Dichotic listening in the study of auditory laterality. The Asymmetrical Brain 2003, 441-475. MIT Press, Cambridge, MA. K. Hugdahl, R.J. Davidson (Eds.).
35. Hugdahl K., Andersson L. The "forced-attention paradigm" in dichotic listening to CV-syllables: a comparison between adults and children. Cortex 1986, 22:417-432.
36. Hugdahl K., Løberg E.M., Jørgensen H.A., Lundervold A., Lund A., Green M.F., Rund B. Left hemisphere lateralisation of auditory hallucinations in schizophrenia: a dichotic listening study. Cogn. Neuropsychiatry 2008, 13(2):166-179.
37. Hund-Georgiadis M., Lex U., Friederici A.D., von Cramon D.Y. Non-invasive regime for language lateralization in right- and lefthanders by means of functional MRI and dichotic listening. Exp. Brain Res. 2002, 145:166-176.
38. Johnsrude I.S., Giraud A.L., Frackowiak R.S. Functional imaging of the auditory system: the use of positron emission tomography. Audiol. Neuro Otol. 2002, 7:251-276.
39. Jokeit H., Makeig S. Different event-related patterns of gamma-band power in brain waves of fast- and slow-reacting subjects. Proc. Natl. Acad. Sci. U. S. A. 1994, 5;91(14):6339-6343.
40. Joliot M., Ribary U., Llinás R. Human oscillatory brain activity near 40Hz coexists with cognitive temporal binding. Proc. Natl. Acad. Sci. U. S. A. 1994, 22;91(24):11748-11751.
41. Keren A.S., Yuval-Greenberg S., Deoull L.Y. Saccadic spike potential in gamma-band EEG: characterization, detection and suppression. NeuroImage 2010, 49:2248-2263.
42. Kimura D. Cerebral dominance and the perception of verbal stimuli. Can. J. Psychol. 1961, 15:166-171.
43. Kimura D. Some effects of temporal-lobe damage on auditory perception. Can. J. Psychol. 1961, 15:156-165.
44. Kimura D. Functional asymmetry of the brain in dichotic listening. Cortex 1967, 3:163-168.
45. Kimura D. From ear to brain. Brain Cogn. 2011, 76(2):214-217.
46. Lazard D.S., Collette J.L., Perrot X. Speech processing: from peripheral to hemispheric asymmetry of the auditory system. Laryngoscope 2012, 122(1):167-173.
47. Leicht G., Kirsch V., Giegling I., Karch S., Hantschk I., Möller H.J., Pogarell O., Hegerl U., Rujescu D., Mulert C. Reduced early auditory evoked gamma-band response in patients with schizophrenia. Biol. Psychiatry 2010, 1; 67(3):224-231.
48. Leicht G., Karch S., Karamatskos E., Giegling I., Möller H.J., Hegerl U., Pogarell O., Rujescu D., Mulert C. Alterations of the early auditory evoked gamma-band response in first-degree relatives of patients with schizophrenia: hints to a new intermediate phenotype. J. Psychiatr. Res. 2011, 45(5):699-705.
49. Llinás R., Ribary U., Contreras D., Pedroarena C. The neuronal basis for consciousness. Philos. Trans. R. Soc. Lond. B Biol. Sci. 1998, 29; 353(1377):1841-1849.
50. Logothetis N., Pauls J., Augath M., Trinath T., Oeltermann A. Neurophysiological investigation of the basis of the fMRI signal. Nature 2001, 412:150-157.
51. Meador K.J., Ray P.G., Echauz J.R., Loring D.W., Vachtsevanos G.J. Gamma coherence and conscious perception. Neurology 2002, 59(6):847-854.
52. Mormann F., Fell J., Axmacher N., Weber B., Lehnertz K., Elger C.E., Fernández G. Phase/amplitude reset and theta-gamma interaction in the human medial temporal lobe during a continuous word recognition memory task. Hippocampus 2005, 15(7):890-900.
53. Mulert C., Jäger L., Schmitt R., Bussfeld P., Pogarell O., Möller H.J., Juckel G., Hegerla U. Integration of fMRI and simultaneous EEG: towards a comprehensive understanding of localization and time-course of brain activity in target detection. NeuroImage 2004, 22:83-94.
54. Mulert C., Jager L., Propp S., Karch S., Stormann S., Pogarell O., et al. Sound level dependence of the primary auditory cortex: simultaneous measurement with 61-channel EEG and fMRI. Neuroimage 2005, 28:49-58.
55. Mulert C., Leicht G., Hepp P., Kirsch V., Karch S., Pogarell O., Reiser M., Hegerl U., Jäger L., Moller H.J., McCarley R.W. Single-trial coupling of the gamma-band response and the corresponding BOLD signal. Neuroimage 2010, 1; 49(3):2238-2247.
56. Mulert C., Kirsch V., Whitford T.J., Alvarado J., Pelavin P., McCarley R.W., Kubicki M., Salisbury D.F., Shenton M.E. Hearing voices: a role of interhemispheric auditory connectivity?. World J. Biol. Psychiatry 2011, 13(2):153-158.
57. Mulert C., Kirsch V., Pascual-Marqui R.D., McCarley R.W., Spencer K.M. Long-range synchrony of γ oscillations and auditory hallucination symptoms in schizophrenia. Int. J. Psychophysiol. 2012, 79(1):55-63.
58. Nolte G., Bai O., Wheaton L., Mari Z., Vorbach S., et al. Identifying true brain interaction from EEG data using the imaginary part of coherency. Clin. Neurophysiol. 2004, 115:2292-2307.
59. Obleser J., Zimmermann J., Van Meter J., Rauschecker J.P. Multiple stages of auditory speech perception reflected in event-related fMRI. Cereb. Cortex 2007, 17:2251-2257.
60. Oldfield R.C. The assessment and analysis of handedness. The Edinburgh inventory. Neuropsychologia 1971, 9:97-113.
61. Panagiotaropoulos T.I., Deco G., Kapoor V., Logothetis N.K. Neuronal discharges and gamma oscillations explicitly reflect visual consciousness in the lateral prefrontal cortex. Neuron 2012, 74(5):924-935.
62. Pantev C., Makeig S., Hoke M., Galambos R., Hampson S., Gallen C. Human auditory evoked gamma-band magnetic fields. Proc. Natl. Acad. Sci. U. S. A. 1991, 88(20):8996-9000.
63. Pascual-Marqui R.D. Discrete, 3D distributed, linear imaging methods of electric neuronal activity. Part 1: Exact, Zero Error Localization 2007, (arXiv:0710.3341 [math-ph], October 17, available: http://arxiv.org/abs/0710.3341).
64. Pascual-Marqui R.D. Instantaneous and lagged measurements of linear and nonlinear dependence between groups of multivariate time series: frequency decomposition 2007, ([arXiv: 0711.1455 [stat.ME], 2007-November-09, available: http://arxiv.org/abs/0711.1455).
65. Pascual-Marqui R.D. Theory of the EEG inverse problem, Chapter 5, pp: 121-140. Quantitative EEG Analysis: Methods and Clinical Applications 2009, Artech House, Boston. S. Tong, N.V. Thakor (Eds.).
66. Pascual-Marqui R.D., Lehmann D., Koukkou M., Kochi K., Anderer P., et al. Assessing interactions in the brain with exact low resolution electromagnetic tomography (eLORETA). Philos. Trans. R. Soc. A 2011, 369:3768-3784.
67. Picton T.W., Bentin S., Berg P., Donchin E., Hillyard S.A., Johnson R., et al. Guidelines for using human event-related potentials to study cognition: recording standards and publication criteria. Psychophysiology 2000, 37(2):127-152.
68. Pollmann S., Maertens M., von Cramon D.Y., Lepsien J., Hugdahl K. Dichotic listening in patients with splenial and nonsplenial callosal lesions. Neuropsychology 2002, 16(1):56-64.
69. Pulvermüller F., Eulitz C., Pantev C., Mohr B., Feige B., Lutzenberger W., Elbert T., Birbaumer N. High-frequency cortical responses reflect lexical processing: an MEG study. Electroencephalogr. Clin. Neurophysiol. 1996, 98(1):76-85.
70. Ribary U. Dynamics of thalamo-cortical network oscillations and human perception. Prog. Brain Res. 2005, 150:127-142.
71. Ribary U., Joliot M., Miller S.L., Kronberg E., Cappell J., Tallal P., Llinás R. Cognitive temporal binding and its relation to 40Hz activity in humans: Alteration during dyslexia. Biomag96 2000, 971-974. Springer, Berlin. C. Aine, Y. Okada, G. Stroink, S. Swithenby, C.C. Wood (Eds.).
72. Rimol L.M., Eichele T., Hugdahl K. The effect of voice-onset-time on dichotic listening with consonant-vowel syllables. Neuropsychologia 2006, 44(2):191-196.
73. Rodriguez E., George N., Lachaux J.P., Martinerie J., Renault B., Varela F.J. Perception's shadow: long-distance synchronization of human brain activity. Nature 1999, 4; 397(6718):430-433.
74. Rose M., Sommer T., Büchel C. Integration of local features to a global percept by neural coupling. Cereb. Cortex 2006, 16(10):1522-1528.
75. Sauseng P., Griesmayr B., Freunberger R., Klimesch W. Control mechanisms in working memory: a possible function of EEG theta oscillations. Neurosci. Biobehav. Rev. 2010, 34(7):1015-1022.
76. Schurger A., Cowey A., Tallon-Baudry C. Induced gamma-band oscillations correlate with awareness in hemianopic patient GY. Neuropsychologia 2006, 44:1796-1803.
77. Singer W. Neuronal synchrony: a versatile code for the definition of relations?. Neuron 1999, 24(49-65):111-125.
78. Stam C.J., Nolte G., Daffertshofer A. Phase lag index: assessment of functional connectivity from multichannel EEG and MEG with diminished bias from common sources. Hum. Brain Mapp. 2007, 28:1178-1193.
79. Steinmann S., Mulert C. Functional relevance of interhemispheric fiber tracts in speech processing. J. Neurolinguistics 2012, 25(1):1-12.
80. Tallon-Baudry C., Bertrand O. Oscillatory gamma activity in humans and its role in object representation. Trends Cogn. Sci. 1999, 2:151-162.
81. Tiitinen H., Sinkkonen J., Reinikainen K., Alho K., Lavikainen J., et al. Selective attention enhances the auditory 40-Hz transient response in humans. Nature 1993, 364:59-60.
82. Trepel M. Neuroanatomie. Struktur und Funktion 1999, Urban & Fischer Verlag, München, Stuttgart, Jena, Lübeck, Ulm.
83. Van der Loo E., Gais S., Congedo M., Vanneste S., Plazier M., Menovsky T., Van de Heyning P., De Ridder D. Tinnitus intensity dependent gamma oscillations of the contralateral auditory cortex. PLoS One 2009, 9;4(10):e7396.
84. Weiss S., Mueller H.M., Schack B., King J.W., Kutas M., Rappelsberger P. Increased neuronal communication accompanying sentence comprehension. Int. J. Psychophysiol. 2005, 57(2):129-141.
85. Weisz N., Muller S., Schlee W., Dohrmann K., Hartmann T., et al. The neural code of auditory phantom perception. J. Neurosci. 2007, 27:1479-1484.
86. Westerhausen R., Woerner W., Kreuder F., Schweiger E., Hugdahl K., Wittling W. The role of the corpus callosum in dichotic listening: a combined morphological and diffusion tensor imaging study. Neuropsychology 2006, 20(3):272-279.
87. Westerhausen R., Grüner R., Specht K., Hugdahl K. Functional relevance of interindividual differences in temporal lobe callosal pathways: a DTI tractography study. Cereb. Cortex 2009, 19(6):1322-1329.
88. Yuval-Greenberg S., Tomer O., Keren A.S., Nelken I., Deouell L.Y. Transient induced gamma-band response in EEG as a manifestation of miniature saccades. Neuron 2008, 58:429-441.
89. Zaehle T., Wustenberg T., Meyer M., Jancke L. Evidence for rapid auditory perception as the foundation of speech processing: a sparse temporal sampling fMRI study. Eur. J. Neurosci. 2004, 20:2447-2456.