Monitoring neuronal oscillations and signal transmission between cortical regions using time-frequency analysis of electroencephalographic activity

Oscillatory states in the electroencephalogram (EEG) reflect the rhythmic synchronous activity in large networks of neurons. Time-frequency (TF) methods, which quantify the spectral content of the EEG as a function of time, are well suited as tools for the study of spontaneous and induced changes in oscillatory states. The use of these methods provides insights into the temporal dynamics of EEG activity in both humans and experimental animals, and aids the study of the neuronal mechanisms that generate rhythmic EEG activity. Further the use of TF coherence analysts, which quantifies the consistency of phase relationships in multichannel EEG recordings, may contribute to the understanding of signal transmission between neuronal populations in different parts of the brain. We have used TF techniques to analyze the flow of activity patterns between two strongly connected brain structures: the entorhinal cortex and the hippocampus. Both of these structures are believed to be involved in information storage. By applying various frequencies of stimulation, we have found a peak in the spectral power in both sites at around 18 Hz, but the coherence between the EEG signals recorded from these sites was found to increase monotonically up to about 35 Hz. We have also found that long-term potentiation, a strong increase in the efficacy of excitatory synapses between these sites, either had no effect or decreased coherence.

[1]  John R. Knott,et al.  Fourier transforms of the electroencephalogram during sleep , 1942 .

[2]  W. R. Adey,et al.  Computer analysis of EEG data from Gemini flight GT-7. , 1967, Aerospace medicine.

[3]  N. Kawabata A nonstationary analysis of the electroencephalogram. , 1973, IEEE transactions on bio-medical engineering.

[4]  T. Bliss,et al.  Long‐lasting potentiation of synaptic transmission in the dentate area of the anaesthetized rabbit following stimulation of the perforant path , 1973, The Journal of physiology.

[5]  W. Freeman Spatial properties of an EEG event in the olfactory bulb and cortex. , 1978, Electroencephalography and clinical neurophysiology.

[6]  N Ishii,et al.  On the stationarity and normality of the electroencephalographic data during sleep stages. , 1978, Computer programs in biomedicine.

[7]  W. Freeman,et al.  Changes in spatial patterns of rabbit olfactory EEG with conditioning to odors. , 1982, Psychophysiology.

[8]  R. Racine,et al.  Long-term potentiation phenomena in the rat limbic forebrain , 1983, Brain Research.

[9]  Alan S. Gevins,et al.  Analysis of the Electromagnetic Signals of the Human Brain: Milestones, Obstacles, and Goals , 1984, IEEE Transactions on Biomedical Engineering.

[10]  S L Bressler,et al.  Spatial organization of EEGs from olfactory bulb and cortex. , 1984, Electroencephalography and clinical neurophysiology.

[11]  M. Schuckit,et al.  EEG spectral characteristics following ethanol administration in young men. , 1989, Electroencephalography and clinical neurophysiology.

[12]  M. Riley Speech Time-Frequency Representations , 1989 .

[13]  M. Witter,et al.  Functional organization of the extrinsic and intrinsic circuitry of the parahippocampal region , 1989, Progress in Neurobiology.

[14]  J. Bronzino,et al.  Bispectral analysis of the rat EEG during various vigilance states , 1989, IEEE Transactions on Biomedical Engineering.

[15]  W. Singer,et al.  Stimulus-specific neuronal oscillations in orientation columns of cat visual cortex. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[16]  W. Singer,et al.  Oscillatory responses in cat visual cortex exhibit inter-columnar synchronization which reflects global stimulus properties , 1989, Nature.

[17]  H Petsche,et al.  Periodicity analysis of sleep EEG in the second and minute ranges--example of application in different alpha activities in sleep. , 1990, Electroencephalography and clinical neurophysiology.

[18]  Taikang Ning,et al.  Cross-bispectra Of The Rat EEG During Rem Sleep , 1991, Proceedings of the Annual International Conference of the IEEE Engineering in Medicine and Biology Society Volume 13: 1991.

[19]  F. D. Silva Neural mechanisms underlying brain waves: from neural membranes to networks. , 1991 .

[20]  W. J. Williams,et al.  Cross Time-frequency Representation Of Electrocorticograms In Temporal Lobe Epilepsy , 1991 .

[21]  P Hilfiker,et al.  Detection and evolution of rhythmic components in ictal EEG using short segment spectra and discriminant analysis. , 1992, Electroencephalography and clinical neurophysiology.

[22]  C. H. Vanderwolf The electrocorticogram in relation to physiology and behavior: a new analysis. , 1992, Electroencephalography and clinical neurophysiology.

[23]  I. Gath,et al.  On the tracking of rapid dynamic changes in seizure EEG , 1992, IEEE Transactions on Biomedical Engineering.

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

[25]  R. Llinás,et al.  Coherent 40-Hz oscillation characterizes dream state in humans. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[26]  S. Bressler,et al.  Episodic multiregional cortical coherence at multiple frequencies during visual task performance , 1993, Nature.

[27]  C. H. Vanderwolf,et al.  Components of weasel and fox odors elicit fast wave bursts in the dentate gyrus of rats , 1994, Behavioural Brain Research.

[28]  Bernat Kocsis,et al.  Separation of hippocampal theta dipoles by partial coherence analysis in the rat , 1994, Brain Research.