Perception of pain coincides with the spatial expansion of electroencephalographic dynamics in human subjects

The dynamics of cortex driven by painful median nerve stimulation were investigated in event-related oscillation (ERO). We applied a wavelet time-frequency analysis to differentiate the brain dynamics between painful and non-painful somatosensory stimulation. The observed pattern to pain-induced effects exhibited a stepwise decrease of frequencies over time, starting around 26 ms over somatosensory cortex at 80 Hz, intermediate oscillations at 40 and 20 Hz around 40 ms, and reaching down to 10 Hz after 160 ms. This step-wise frequency decrease of ERO, coincident with spatial shift from the contralateral somatosensory area at 80 Hz to the centro-frontal brain at 40/20 Hz and final spatial expansion to the large region of centro-parietal areas at 10 Hz, may represent the cortical processes necessary to transfer sensory information from perceptual stages to subsequent cognitive stages in consciousness.

[1]  M. Steriade,et al.  Fast (mainly 30–100 Hz) oscillations in the cat cerebellothalamic pathway and their synchronization with cortical potentials , 1997, The Journal of physiology.

[2]  I Shimoyama,et al.  Attention changes the peak latency of the visual gamma-band oscillation of the EEG. , 1999, Neuroreport.

[3]  W. Singer Synchronization of cortical activity and its putative role in information processing and learning. , 1993, Annual review of physiology.

[4]  E. Basar,et al.  Are cognitive processes manifested in event-related gamma, alpha, theta and delta oscillations in the EEG? , 1999, Neuroscience Letters.

[5]  Christoph Braun,et al.  Coherence of gamma-band EEG activity as a basis for associative learning , 1999, Nature.

[6]  W Singer,et al.  Consciousness and the structure of neuronal representations. , 1998, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[7]  C Braun,et al.  Gamma-band MEG activity to coherent motion depends on task-driven attention. , 1999, Neuroreport.

[8]  B. Oken,et al.  Statistical issues concerning computerized analysis of brainwave topography , 1986, Annals of neurology.

[9]  Matthias M. Müller,et al.  Human Gamma Band Activity and Perception of a Gestalt , 1999, The Journal of Neuroscience.

[10]  W. Klimesch Brain Function and Oscillations, Vol. II: Integrative Brain Function. Neurophysiology and Cognitive Processes, edited by Erol Basar , 1999, Trends in Cognitive Sciences.

[11]  R. Lesser,et al.  Functional mapping of human sensorimotor cortex with electrocorticographic spectral analysis. I. Alpha and beta event-related desynchronization. , 1998, Brain : a journal of neurology.

[12]  R. Traub,et al.  On the Mechanism of the γ → β Frequency Shift in Neuronal Oscillations Induced in Rat Hippocampal Slices by Tetanic Stimulation , 1999, The Journal of Neuroscience.

[13]  C. Herrmann,et al.  Gamma responses and ERPs in a visual classification task , 1999, Clinical Neurophysiology.

[14]  T. Baldeweg,et al.  γ-band electroencephalographic oscillations in a patient with somatic hallucinations , 1998, The Lancet.

[15]  R. Lesser,et al.  Functional mapping of human sensorimotor cortex with electrocorticographic spectral analysis. II. Event-related synchronization in the gamma band. , 1998, Brain : a journal of neurology.

[16]  O. Bertrand,et al.  Sustained and transient oscillatory responses in the gamma and beta bands in a visual short-term memory task in humans , 1999, Visual Neuroscience.

[17]  J. Desmedt,et al.  Transient phase-locking of 40 Hz electrical oscillations in prefrontal and parietal human cortex reflects the process of conscious somatic perception , 1994, Neuroscience Letters.

[18]  F. Varela,et al.  Perception's shadow: long-distance synchronization of human brain activity , 1999, Nature.

[19]  E. Basar,et al.  Oscillatory Brain Dynamics, Wavelet Analysis, and Cognition , 1999, Brain and Language.