Neural correlates of auditory sensory memory and automatic change detection

NeuroImage

Volumn 21, Issue 1, 2004, Pages 69-74

  Sabri, Merav ^a,c   Kareken, David A ^a   Dzemidzic, Mario ^a   Lowe, Mark J ^a   Melara, Robert D ^b  

^a INDIANA UNIVERSITY   (United States)

^b PURDUE UNIVERSITY   (United States)

^c MEDICAL COLLEGE OF WISCONSIN   (United States)

Author keywords

Auditory sensory memory; BOLD fMRI; Change detection; Superior temporal gyrus

Indexed keywords

ADULT; ARTICLE; AUDITORY CORTEX; AUDITORY DISCRIMINATION; AUDITORY MEMORY; AUDITORY STIMULATION; AUTOANALYSIS; CLUSTER ANALYSIS; CONTROLLED STUDY; CORRELATION ANALYSIS; DATA ANALYSIS; EVOKED AUDITORY RESPONSE; FEMALE; FREQUENCY ANALYSIS; HUMAN; HUMAN EXPERIMENT; INSULA; LEFT HEMISPHERE; MALE; MISMATCH NEGATIVITY; NORMAL HUMAN; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; RANDOMIZATION; READING; RIGHT HEMISPHERE; SENSORIMOTOR CORTEX; STANDARD; STATISTICAL SIGNIFICANCE; TEMPORAL CORTEX; VISUAL STIMULATION;

EID: 1642574429     PISSN: 10538119     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neuroimage.2003.08.033     Document Type: Article

References (35)

1. Alain C., Woods D.L., Ogawa K.H. Brain indices of automatic pattern processing. NeuroReport. 6:1994;140-144.
2. Alain C., Woods D.L., Knight R.T. A distributed cortical network for auditory sensory memory in humans. Brain Res. 812:1998;23-37.
3. Alho K. Cerebral generators of mismatch negativity (MMN) and its magnetic counterpart (MMNm) elicited by sound changes. Ear Hear. 16:1995;38-60.
4. Alho K., Woods D.L., Algazi A., Knight R.T., Näätänen R. Lesions of frontal cortex diminish the auditory mismatch negativity. Electroencephalogr. Clin. Neurophysiol. 91:1994;353-362.
5. Alho K., Winkler I., Escera C., Huotilainen M., Virtanen J., Jääskeläinen I.P., Pekkonen E., Ilmoniemi R.J. Processing of novel sounds and frequency changes in the human auditory cortex: magnetoencephalographic recordings. Psychophysiology. 35:1998;211-224.
6. Bandettini P.A., Jesmanowicz A., Wong E.C., Hyde J.S. Processing strategies for time-course data sets in functional MRI of the human brain. Magn. Reson. Med. 30:1993;161-173.
7. Binder J.R., Rao S.M., Hammeke T.A., Frost J.A., Bandettini P.A., Hyde J.S. Effects of stimulus rate on signal response during functional magnetic resonance imaging of auditory cortex. Cogn. Brain Res. 2:1994;31-38.
8. Celsis P., Boulanouar K., Doyon B., Ranjeva J.P., Berry I., Nespoulous J.L., Chollet F. Differential fMRI responses in the left posterior superior temporal gyrus and left supramarginal gyrus to habituation and change detection in syllables and tones. NeuroImage. 9:1999;135-144.
9. Cowan N. Attention and Memory: An Integrated Framework. 1995;Oxford University Press.
10. Darwin C.J., Turvey M.T., Crowder R.G. An auditory analogue of the Sperling partial report procedure: evidence for brief auditory storage. Cogn. Psychol. 3:1972;255-267.
11. Downar J., Crawley A.P., Mikulis D.J., Davis K.D. A multimodal cortical network for the detection of changes in the sensory environment. Nat. Neurosci. 3:2000;277-283.
12. Downar J., Crawley A.P., Mikulis D.J., Davis K.D. A cortical network sensitive to stimulus salience in a neutral behavioral context across multiple sensory modalities. J. Neurophysiol. 87:2002;615-620.
13. Escera C., Alho K., Winkler I., Näätänen R. Neural mechanisms of involuntary attention to acoustic novelty and change. J. Cogn. Neurosci. 10:1998;590-604.
14. Fox P.T., Raichle M.E. Stimulus rate determines regional brain blood flow in striate cortex. Ann. Neurol. 17:1985;303-305.
15. Friedman D., Cycowicz Y.M., Gaeta H. The novelty P3: an event-related brain potential (ERP) sign of the brain's evaluation of novelty. Neurosci. Biobehav. Rev. 25:2001;355-373.
16. Giard M.H., Perrin F., Pernier J., Bouchet P. Brain generators implicated in processing of auditory stimulus deviance: a topographic event-related potential study. Psychophysiology. 27:1990;627-640.
17. Levänen S., Ahonen A., Hari R., McEvoy L., Sams M. Deviant auditory stimuli activate human left and right auditory cortex differently. Cereb. Cortex. 98:1996;493-501.
18. Linden D.E.J., Prvulovic D., Formisano E., Völlinger M., Zanella F.E., Goebel R., Dierks T. The functional neuroanatomy of target detection: an fMRI study of visual and auditory oddball tasks. Cereb. Cortex. 9:1999;815-823.
19. Lowe M.J., Sorenson J.A. Spatially filtering functional magnetic resonance imaging data. Magn. Reson. Med. 37:1997;723-729.
20. Müller B.W., Jüptner M., Jentzen W., Müller S.P. Cortical activation to auditory mismatch elicited by frequency deviant and complex novel sounds: a PET study. NeuroImage. 17:2002;231-239.
21. Näätänen R. The role of attention in auditory information processing as revealed by event-related potentials and other brain measures of cognitive function. Behav. Brain Sci. 13:1990;201-288.
22. Näätänen R. Attention and Brain Function. 1992;Erlbaum, Hillsdale, NJ.
23. Neisser U. Cognitive Psychology. 1967;Appleton-Century-Crofts, New York, NY.
24. Opitz B., Mecklinger A., Von Cramon D.Y., Kruggel F. Combining electrophysiological and hemodynamic measures of the auditory oddball. Psychophysiology. 36:1999;142-147.
25. Opitz B., Rinne T., Mecklinger A., von Cramon D.Y., Schröger E. Differential contribution of frontal and temporal cortices to auditory change detection: fMRI and ERP results. NeuroImage. 15:2002;167-174.
26. Price C., Wise R., Ramsay S., Friston K., Howard D., Patterson K., Frackowiak R. Regional response differences within the human auditory cortex when listening to words. Neurosci. Lett. 146:1992;179-182.
27. Rademacher J., Morosan P., Schormann T., Schleicher A., Werner C. Probabilistic mapping and volume measurement of human primary auditory cortex. NeuroImage. 13:2001;669-683.
28. Rees G., Howseman A., Josephs O., Frith C.D., Friston K.J., Frackowiak R.S.J., Turner R. Characterizing the relationship between BOLD contrast and regional cerebral blood flow measurements by varying the stimulus presentation rate. NeuroImage. 6:1997;270-278.
29. Sabri M., Campbell K.B. Effects of sequential and temporal probability of deviant occurrence on mismatch negativity. Cogn. Brain Res. 12:2001;171-180.
30. Scherg M., Vajsar J., Picton T.W. A source analysis of the late human auditory evoked potentials. J. Cogn. Neurosci. 1:1989;336-355.
31. Talairach J., Tournoux P. Co-Planar Stereotaxic Atlas of the Human Brain. 1988;Thieme, Stuttgart.
32. Tervaniemi M., Medvedev S.V., Alho K., Pakhomov S.V., Roudas M.S., van Zuijen T.L., Näätänen R. Lateralized automatic auditory processing of phonetic versus musical information: a PET study. Hum. Brain Mapp. 10:2000;74-79.
33. Winkler I., Näätänen R. The effects of auditory backward masking on event-related brain potentials. Karmos G., Csépe V., Czigler I., Molnar M., Desmedt J. Perspectives of ERP Research, EEG Suppl. 44. 1995;185-189 Elsevier, Amsterdam.
34. Woods R.P., Cherry S.R., Mazziotta J.C. Rapid automated algorithm for aligning and reslicing PET images. J. Comput. Assist. Tomogr. 16:1992;620-633.
35. Woods D.L., Knight R.T., Scabini D. Anatomical substrates of auditory selective attention: behavioral and electrophysiological effects of posterior association cortex lesions. Cogn. Brain Res. 1:1993;227-240.